Hmdb loader

Showing metabocard for CDP-glucose (HMDB0003369)

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Record Information
Version5.0
StatusExpected but not Quantified
Creation Date2006-08-12 19:25:22 UTC
Update Date2021-09-14 15:48:15 UTC
HMDB IDHMDB0003369
Secondary Accession Numbers
  • HMDB03369
Metabolite Identification
Common NameCDP-glucose
DescriptionCDP-glucose, also known as CDP-D-glucose or CDP-GLC, belongs to the class of organic compounds known as pyrimidine nucleotide sugars. These are pyrimidine nucleotides bound to a saccharide derivative through the terminal phosphate group. CDP-glucose has been detected, but not quantified in, a few different foods, such as anatidaes (Anatidae), chickens (Gallus gallus), and domestic pigs (Sus scrofa domestica). This could make CDP-glucose a potential biomarker for the consumption of these foods. CDP-glucose is a primary metabolite. Primary metabolites are metabolically or physiologically essential metabolites. They are directly involved in an organism’s growth, development or reproduction. Based on a literature review a significant number of articles have been published on CDP-glucose.
Structure
Data?1582752273
MOL3D MOLSDF3D SDFPDB3D PDBSMILESInChI

MOL for HMDB0003369 (CDP-glucose)


  Mrv0541 02231219422D          

 36 38  0  0  1  0            999 V2000
   26.6177  -10.3971    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   27.0696   -9.2999    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
   25.9372   -9.9056    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   26.3682  -11.1684    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   26.3514   -8.8803    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   27.7918   -8.8954    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   25.2754  -10.3858    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   25.5364  -11.1684    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   26.8559  -11.8301    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   26.3551   -8.0560    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
   25.6367   -9.2886    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   27.7918   -8.0598    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   24.4891   -9.8648    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   25.0637  -11.8376    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   27.0735   -7.6401    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   23.6686   -9.8648    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   27.0735   -6.8196    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
   22.8444   -9.8648    0.0000 P   0  0  0  0  0  0  0  0  0  0  0  0
   22.0239   -9.8648    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   22.8444  -10.7273    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   22.8444   -8.9985    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   21.1959   -9.8648    0.0000 P   0  0  0  0  0  0  0  0  0  0  0  0
   20.3754   -9.8610    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   21.1921  -10.7273    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   21.1959   -8.9985    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   19.6608  -10.2693    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   18.9425   -9.8610    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   19.6608  -11.0899    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   18.2316  -10.2732    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   18.9425  -11.5057    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   20.3754  -11.5057    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   18.2316  -11.0936    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   17.5284   -9.8610    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   18.9425  -12.3262    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   17.5284  -11.5057    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   16.8970  -10.3904    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  1  0  0  0
  1  3  1  0  0  0  0
  1  4  1  0  0  0  0
  2  5  1  0  0  0  0
  2  6  1  0  0  0  0
  3  7  1  0  0  0  0
  4  8  1  0  0  0  0
  4  9  1  6  0  0  0
  5 10  1  0  0  0  0
  5 11  2  0  0  0  0
  6 12  2  0  0  0  0
  7 13  1  1  0  0  0
  8 14  1  6  0  0  0
 10 15  2  0  0  0  0
 13 16  1  0  0  0  0
 15 17  1  0  0  0  0
 16 18  1  0  0  0  0
 18 19  1  0  0  0  0
 18 20  1  0  0  0  0
 18 21  2  0  0  0  0
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 33 36  1  0  0  0  0
  7  8  1  0  0  0  0
 12 15  1  0  0  0  0
 30 32  1  0  0  0  0
M  END
Download

3D MOL for HMDB0003369 (CDP-glucose)

HMDB0003369
     RDKit          3D
CDP-glucose
 61 63  0  0  0  0  0  0  0  0999 V2000
   -9.6016   -1.8166    0.5792 N   0  0  0  0  0  0  0  0  0  0  0  0
   -8.3081   -1.3559    0.2044 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.7640   -0.2246    0.7776 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.4902    0.2162    0.3987 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.7646   -0.4389   -0.5238 N   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4662   -0.0488   -0.9567 C   0  0  2  0  0  0  0  0  0  0  0  0
   -3.4280   -0.4631   -0.1527 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3146    0.1934   -0.6057 C   0  0  2  0  0  0  0  0  0  0  0  0
   -1.3269    0.5093    0.5033 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8694   -0.6187    1.1421 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.2141   -0.1282    2.3446 P   0  0  0  0  0  5  0  0  0  0  0  0
   -0.3794    1.0547    3.1132 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.3776   -1.3893    3.4506 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.6849    0.3715    1.7298 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.9527   -0.6713    2.2064 P   0  0  0  0  0  5  0  0  0  0  0  0
    3.6184   -0.1135    3.4433 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.3517   -2.2185    2.5279 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.1105   -0.7228    0.9753 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.2406    0.5132    0.3716 C   0  0  1  0  0  0  0  0  0  0  0  0
    5.5225    1.0240    0.5028 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.4805    0.0792    0.1028 C   0  0  2  0  0  0  0  0  0  0  0  0
    7.7873    0.8440   -0.0469 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.8241    0.0215   -0.4414 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.1144   -0.5805   -1.1915 C   0  0  1  0  0  0  0  0  0  0  0  0
    5.5727   -1.8422   -0.9193 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.1119    0.2505   -1.9450 C   0  0  2  0  0  0  0  0  0  0  0  0
    5.7333    1.4698   -2.2569 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.8729    0.4613   -1.1031 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.9735   -0.5746   -1.2694 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7380    1.5046   -1.2098 C   0  0  1  0  0  0  0  0  0  0  0  0
   -2.5424    1.4649   -2.6034 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2526    1.4669   -0.9589 C   0  0  1  0  0  0  0  0  0  0  0  0
   -4.9552    2.0864   -1.9702 O   0  0  0  0  0  0  0  0  0  0  0  0
   -6.3304   -1.5479   -1.0674 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.6608   -2.1866   -1.9453 O   0  0  0  0  0  0  0  0  0  0  0  0
   -7.5530   -1.9854   -0.7148 N   0  0  0  0  0  0  0  0  0  0  0  0
  -10.4696   -1.2970    0.2987 H   0  0  0  0  0  0  0  0  0  0  0  0
   -9.7645   -2.6821    1.1447 H   0  0  0  0  0  0  0  0  0  0  0  0
   -8.3223    0.3156    1.5157 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.0717    1.1004    0.8507 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2287   -0.3727   -1.9941 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8167   -0.4404   -1.3838 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8491    1.1820    1.2150 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5217    1.1146    0.0394 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3253   -2.0691    3.3187 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.6859   -2.5025    1.8639 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.5412    1.2177    0.8630 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.5786   -0.6285    0.9460 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.0277    1.3377    0.9269 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.6941    1.6606   -0.7884 H   0  0  0  0  0  0  0  0  0  0  0  0
    9.0012    0.0756   -1.4229 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.0053   -0.7246   -1.8384 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.1339   -2.3622   -0.3104 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.7876   -0.2915   -2.8621 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.1667    2.1978   -1.9475 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.3564    1.4044   -1.3933 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.2274   -1.2292   -1.9410 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2658    2.3796   -0.7629 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3975    1.3572   -3.0921 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3924    1.9118    0.0358 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.5790    2.7410   -1.5440 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  1  0
  3  4  2  0
  4  5  1  0
  5  6  1  0
  6  7  1  0
  7  8  1  0
  8  9  1  0
  9 10  1  0
 10 11  1  0
 11 12  2  0
 11 13  1  0
 11 14  1  0
 14 15  1  0
 15 16  2  0
 15 17  1  0
 15 18  1  0
 18 19  1  0
 19 20  1  0
 20 21  1  0
 21 22  1  0
 22 23  1  0
 21 24  1  0
 24 25  1  0
 24 26  1  0
 26 27  1  0
 26 28  1  0
 28 29  1  0
  8 30  1  0
 30 31  1  0
 30 32  1  0
 32 33  1  0
  5 34  1  0
 34 35  2  0
 34 36  1  0
 36  2  2  0
 32  6  1  0
 28 19  1  0
  1 37  1  0
  1 38  1  0
  3 39  1  0
  4 40  1  0
  6 41  1  6
  8 42  1  6
  9 43  1  0
  9 44  1  0
 13 45  1  0
 17 46  1  0
 19 47  1  1
 21 48  1  1
 22 49  1  0
 22 50  1  0
 23 51  1  0
 24 52  1  6
 25 53  1  0
 26 54  1  6
 27 55  1  0
 28 56  1  6
 29 57  1  0
 30 58  1  1
 31 59  1  0
 32 60  1  1
 33 61  1  0
M  END
Download

3D SDF for HMDB0003369 (CDP-glucose)


  Mrv0541 02231219422D          

 36 38  0  0  1  0            999 V2000
   26.6177  -10.3971    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   27.0696   -9.2999    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
   25.9372   -9.9056    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   26.3682  -11.1684    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   26.3514   -8.8803    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   27.7918   -8.8954    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   25.2754  -10.3858    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   25.5364  -11.1684    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   26.8559  -11.8301    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   26.3551   -8.0560    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
   25.6367   -9.2886    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   27.7918   -8.0598    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   24.4891   -9.8648    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   25.0637  -11.8376    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   27.0735   -7.6401    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   23.6686   -9.8648    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   27.0735   -6.8196    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
   22.8444   -9.8648    0.0000 P   0  0  0  0  0  0  0  0  0  0  0  0
   22.0239   -9.8648    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   22.8444  -10.7273    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   22.8444   -8.9985    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   21.1959   -9.8648    0.0000 P   0  0  0  0  0  0  0  0  0  0  0  0
   20.3754   -9.8610    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   21.1921  -10.7273    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   21.1959   -8.9985    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   19.6608  -10.2693    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   18.9425   -9.8610    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   19.6608  -11.0899    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   18.2316  -10.2732    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   18.9425  -11.5057    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   20.3754  -11.5057    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   18.2316  -11.0936    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   17.5284   -9.8610    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   18.9425  -12.3262    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   17.5284  -11.5057    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   16.8970  -10.3904    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  1  0  0  0
  1  3  1  0  0  0  0
  1  4  1  0  0  0  0
  2  5  1  0  0  0  0
  2  6  1  0  0  0  0
  3  7  1  0  0  0  0
  4  8  1  0  0  0  0
  4  9  1  6  0  0  0
  5 10  1  0  0  0  0
  5 11  2  0  0  0  0
  6 12  2  0  0  0  0
  7 13  1  1  0  0  0
  8 14  1  6  0  0  0
 10 15  2  0  0  0  0
 13 16  1  0  0  0  0
 15 17  1  0  0  0  0
 16 18  1  0  0  0  0
 18 19  1  0  0  0  0
 18 20  1  0  0  0  0
 18 21  2  0  0  0  0
 19 22  1  0  0  0  0
 22 23  1  0  0  0  0
 22 24  1  0  0  0  0
 22 25  2  0  0  0  0
 26 23  1  6  0  0  0
 26 27  1  0  0  0  0
 26 28  1  0  0  0  0
 27 29  1  0  0  0  0
 28 30  1  0  0  0  0
 28 31  1  6  0  0  0
 29 32  1  0  0  0  0
 29 33  1  1  0  0  0
 30 34  1  1  0  0  0
 32 35  1  6  0  0  0
 33 36  1  0  0  0  0
  7  8  1  0  0  0  0
 12 15  1  0  0  0  0
 30 32  1  0  0  0  0
M  END
> <DATABASE_ID>
HMDB0003369

> <DATABASE_NAME>
hmdb

> <SMILES>
NC1=NC(=O)N(C=C1)[C@@H]1O[C@H](COP(O)(=O)OP(O)(=O)O[C@H]2O[C@H](CO)[C@@H](O)[C@H](O)[C@H]2O)[C@@H](O)[C@H]1O

> <INCHI_IDENTIFIER>
InChI=1S/C15H25N3O16P2/c16-7-1-2-18(15(25)17-7)13-11(23)9(21)6(31-13)4-30-35(26,27)34-36(28,29)33-14-12(24)10(22)8(20)5(3-19)32-14/h1-2,5-6,8-14,19-24H,3-4H2,(H,26,27)(H,28,29)(H2,16,17,25)/t5-,6-,8-,9-,10+,11-,12-,13-,14-/m1/s1

> <INCHI_KEY>
CGPHZDRCVSLMCF-JZMIEXBBSA-N

> <FORMULA>
C15H25N3O16P2

> <MOLECULAR_WEIGHT>
565.317

> <EXACT_MASS>
565.071004791

> <JCHEM_ACCEPTOR_COUNT>
15

> <JCHEM_AVERAGE_POLARIZABILITY>
45.941490450985455

> <JCHEM_BIOAVAILABILITY>
0

> <JCHEM_DONOR_COUNT>
9

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
{[(2R,3S,4R,5R)-5-(4-amino-2-oxo-1,2-dihydropyrimidin-1-yl)-3,4-dihydroxyoxolan-2-yl]methoxy}({[hydroxy({[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy})phosphoryl]oxy})phosphinic acid

> <ALOGPS_LOGP>
-1.36

> <JCHEM_LOGP>
-5.6687219669634725

> <ALOGPS_LOGS>
-1.30

> <JCHEM_MDDR_LIKE_RULE>
1

> <JCHEM_NUMBER_OF_RINGS>
3

> <JCHEM_PHYSIOLOGICAL_CHARGE>
-2

> <JCHEM_PKA>
3.158312053500531

> <JCHEM_PKA_STRONGEST_ACIDIC>
1.7346226959637967

> <JCHEM_PKA_STRONGEST_BASIC>
-0.5844091015948797

> <JCHEM_POLAR_SURFACE_AREA>
300.82

> <JCHEM_REFRACTIVITY>
108.43499999999999

> <JCHEM_ROTATABLE_BOND_COUNT>
9

> <JCHEM_RULE_OF_FIVE>
0

> <ALOGPS_SOLUBILITY>
2.86e+01 g/l

> <JCHEM_TRADITIONAL_IUPAC>
cytidine diphosphate glucose

> <JCHEM_VEBER_RULE>
0

$$$$
Download

3D-SDF for HMDB0003369 (CDP-glucose)

HMDB0003369
     RDKit          3D
CDP-glucose
 61 63  0  0  0  0  0  0  0  0999 V2000
   -9.6016   -1.8166    0.5792 N   0  0  0  0  0  0  0  0  0  0  0  0
   -8.3081   -1.3559    0.2044 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.7640   -0.2246    0.7776 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.4902    0.2162    0.3987 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.7646   -0.4389   -0.5238 N   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4662   -0.0488   -0.9567 C   0  0  2  0  0  0  0  0  0  0  0  0
   -3.4280   -0.4631   -0.1527 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3146    0.1934   -0.6057 C   0  0  2  0  0  0  0  0  0  0  0  0
   -1.3269    0.5093    0.5033 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8694   -0.6187    1.1421 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.2141   -0.1282    2.3446 P   0  0  0  0  0  5  0  0  0  0  0  0
   -0.3794    1.0547    3.1132 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.3776   -1.3893    3.4506 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.6849    0.3715    1.7298 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.9527   -0.6713    2.2064 P   0  0  0  0  0  5  0  0  0  0  0  0
    3.6184   -0.1135    3.4433 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.3517   -2.2185    2.5279 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.1105   -0.7228    0.9753 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.2406    0.5132    0.3716 C   0  0  1  0  0  0  0  0  0  0  0  0
    5.5225    1.0240    0.5028 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.4805    0.0792    0.1028 C   0  0  2  0  0  0  0  0  0  0  0  0
    7.7873    0.8440   -0.0469 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.8241    0.0215   -0.4414 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.1144   -0.5805   -1.1915 C   0  0  1  0  0  0  0  0  0  0  0  0
    5.5727   -1.8422   -0.9193 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.1119    0.2505   -1.9450 C   0  0  2  0  0  0  0  0  0  0  0  0
    5.7333    1.4698   -2.2569 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.8729    0.4613   -1.1031 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.9735   -0.5746   -1.2694 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7380    1.5046   -1.2098 C   0  0  1  0  0  0  0  0  0  0  0  0
   -2.5424    1.4649   -2.6034 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2526    1.4669   -0.9589 C   0  0  1  0  0  0  0  0  0  0  0  0
   -4.9552    2.0864   -1.9702 O   0  0  0  0  0  0  0  0  0  0  0  0
   -6.3304   -1.5479   -1.0674 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.6608   -2.1866   -1.9453 O   0  0  0  0  0  0  0  0  0  0  0  0
   -7.5530   -1.9854   -0.7148 N   0  0  0  0  0  0  0  0  0  0  0  0
  -10.4696   -1.2970    0.2987 H   0  0  0  0  0  0  0  0  0  0  0  0
   -9.7645   -2.6821    1.1447 H   0  0  0  0  0  0  0  0  0  0  0  0
   -8.3223    0.3156    1.5157 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.0717    1.1004    0.8507 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2287   -0.3727   -1.9941 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8167   -0.4404   -1.3838 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8491    1.1820    1.2150 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5217    1.1146    0.0394 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3253   -2.0691    3.3187 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.6859   -2.5025    1.8639 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.5412    1.2177    0.8630 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.5786   -0.6285    0.9460 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.0277    1.3377    0.9269 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.6941    1.6606   -0.7884 H   0  0  0  0  0  0  0  0  0  0  0  0
    9.0012    0.0756   -1.4229 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.0053   -0.7246   -1.8384 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.1339   -2.3622   -0.3104 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.7876   -0.2915   -2.8621 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.1667    2.1978   -1.9475 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.3564    1.4044   -1.3933 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.2274   -1.2292   -1.9410 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2658    2.3796   -0.7629 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3975    1.3572   -3.0921 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3924    1.9118    0.0358 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.5790    2.7410   -1.5440 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  1  0
  3  4  2  0
  4  5  1  0
  5  6  1  0
  6  7  1  0
  7  8  1  0
  8  9  1  0
  9 10  1  0
 10 11  1  0
 11 12  2  0
 11 13  1  0
 11 14  1  0
 14 15  1  0
 15 16  2  0
 15 17  1  0
 15 18  1  0
 18 19  1  0
 19 20  1  0
 20 21  1  0
 21 22  1  0
 22 23  1  0
 21 24  1  0
 24 25  1  0
 24 26  1  0
 26 27  1  0
 26 28  1  0
 28 29  1  0
  8 30  1  0
 30 31  1  0
 30 32  1  0
 32 33  1  0
  5 34  1  0
 34 35  2  0
 34 36  1  0
 36  2  2  0
 32  6  1  0
 28 19  1  0
  1 37  1  0
  1 38  1  0
  3 39  1  0
  4 40  1  0
  6 41  1  6
  8 42  1  6
  9 43  1  0
  9 44  1  0
 13 45  1  0
 17 46  1  0
 19 47  1  1
 21 48  1  1
 22 49  1  0
 22 50  1  0
 23 51  1  0
 24 52  1  6
 25 53  1  0
 26 54  1  6
 27 55  1  0
 28 56  1  6
 29 57  1  0
 30 58  1  1
 31 59  1  0
 32 60  1  1
 33 61  1  0
M  END
Download

PDB for HMDB0003369 (CDP-glucose)

HEADER    PROTEIN                                 23-FEB-12   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   23-FEB-12         0                                  
HETATM    1  C   UNK     0      49.686 -19.408   0.000  0.00  0.00           C+0
HETATM    2  N   UNK     0      50.530 -17.360   0.000  0.00  0.00           N+0
HETATM    3  O   UNK     0      48.416 -18.490   0.000  0.00  0.00           O+0
HETATM    4  C   UNK     0      49.221 -20.848   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0      49.189 -16.577   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0      51.878 -16.605   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0      47.181 -19.387   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0      47.668 -20.848   0.000  0.00  0.00           C+0
HETATM    9  O   UNK     0      50.131 -22.083   0.000  0.00  0.00           O+0
HETATM   10  N   UNK     0      49.196 -15.038   0.000  0.00  0.00           N+0
HETATM   11  O   UNK     0      47.855 -17.339   0.000  0.00  0.00           O+0
HETATM   12  C   UNK     0      51.878 -15.045   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0      45.713 -18.414   0.000  0.00  0.00           C+0
HETATM   14  O   UNK     0      46.786 -22.097   0.000  0.00  0.00           O+0
HETATM   15  C   UNK     0      50.537 -14.262   0.000  0.00  0.00           C+0
HETATM   16  O   UNK     0      44.181 -18.414   0.000  0.00  0.00           O+0
HETATM   17  N   UNK     0      50.537 -12.730   0.000  0.00  0.00           N+0
HETATM   18  P   UNK     0      42.643 -18.414   0.000  0.00  0.00           P+0
HETATM   19  O   UNK     0      41.111 -18.414   0.000  0.00  0.00           O+0
HETATM   20  O   UNK     0      42.643 -20.024   0.000  0.00  0.00           O+0
HETATM   21  O   UNK     0      42.643 -16.797   0.000  0.00  0.00           O+0
HETATM   22  P   UNK     0      39.566 -18.414   0.000  0.00  0.00           P+0
HETATM   23  O   UNK     0      38.034 -18.407   0.000  0.00  0.00           O+0
HETATM   24  O   UNK     0      39.559 -20.024   0.000  0.00  0.00           O+0
HETATM   25  O   UNK     0      39.566 -16.797   0.000  0.00  0.00           O+0
HETATM   26  C   UNK     0      36.700 -19.169   0.000  0.00  0.00           C+0
HETATM   27  O   UNK     0      35.359 -18.407   0.000  0.00  0.00           O+0
HETATM   28  C   UNK     0      36.700 -20.701   0.000  0.00  0.00           C+0
HETATM   29  C   UNK     0      34.032 -19.177   0.000  0.00  0.00           C+0
HETATM   30  C   UNK     0      35.359 -21.477   0.000  0.00  0.00           C+0
HETATM   31  O   UNK     0      38.034 -21.477   0.000  0.00  0.00           O+0
HETATM   32  C   UNK     0      34.032 -20.708   0.000  0.00  0.00           C+0
HETATM   33  C   UNK     0      32.720 -18.407   0.000  0.00  0.00           C+0
HETATM   34  O   UNK     0      35.359 -23.009   0.000  0.00  0.00           O+0
HETATM   35  O   UNK     0      32.720 -21.477   0.000  0.00  0.00           O+0
HETATM   36  O   UNK     0      31.541 -19.395   0.000  0.00  0.00           O+0
CONECT    1    2    3    4                                                  
CONECT    2    1    5    6                                                  
CONECT    3    1    7                                                       
CONECT    4    1    8    9                                                  
CONECT    5    2   10   11                                                  
CONECT    6    2   12                                                       
CONECT    7    3   13    8                                                  
CONECT    8    4   14    7                                                  
CONECT    9    4                                                            
CONECT   10    5   15                                                       
CONECT   11    5                                                            
CONECT   12    6   15                                                       
CONECT   13    7   16                                                       
CONECT   14    8                                                            
CONECT   15   10   17   12                                                  
CONECT   16   13   18                                                       
CONECT   17   15                                                            
CONECT   18   16   19   20   21                                             
CONECT   19   18   22                                                       
CONECT   20   18                                                            
CONECT   21   18                                                            
CONECT   22   19   23   24   25                                             
CONECT   23   22   26                                                       
CONECT   24   22                                                            
CONECT   25   22                                                            
CONECT   26   23   27   28                                                  
CONECT   27   26   29                                                       
CONECT   28   26   30   31                                                  
CONECT   29   27   32   33                                                  
CONECT   30   28   34   32                                                  
CONECT   31   28                                                            
CONECT   32   29   35   30                                                  
CONECT   33   29   36                                                       
CONECT   34   30                                                            
CONECT   35   32                                                            
CONECT   36   33                                                            
MASTER        0    0    0    0    0    0    0    0   36    0   76    0
END
Download

3D PDB for HMDB0003369 (CDP-glucose)

COMPND    HMDB0003369
HETATM    1  N1  UNL     1      -9.602  -1.817   0.579  1.00  0.00           N  
HETATM    2  C1  UNL     1      -8.308  -1.356   0.204  1.00  0.00           C  
HETATM    3  C2  UNL     1      -7.764  -0.225   0.778  1.00  0.00           C  
HETATM    4  C3  UNL     1      -6.490   0.216   0.399  1.00  0.00           C  
HETATM    5  N2  UNL     1      -5.765  -0.439  -0.524  1.00  0.00           N  
HETATM    6  C4  UNL     1      -4.466  -0.049  -0.957  1.00  0.00           C  
HETATM    7  O1  UNL     1      -3.428  -0.463  -0.153  1.00  0.00           O  
HETATM    8  C5  UNL     1      -2.315   0.193  -0.606  1.00  0.00           C  
HETATM    9  C6  UNL     1      -1.327   0.509   0.503  1.00  0.00           C  
HETATM   10  O2  UNL     1      -0.869  -0.619   1.142  1.00  0.00           O  
HETATM   11  P1  UNL     1       0.214  -0.128   2.345  1.00  0.00           P  
HETATM   12  O3  UNL     1      -0.379   1.055   3.113  1.00  0.00           O  
HETATM   13  O4  UNL     1       0.378  -1.389   3.451  1.00  0.00           O  
HETATM   14  O5  UNL     1       1.685   0.372   1.730  1.00  0.00           O  
HETATM   15  P2  UNL     1       2.953  -0.671   2.206  1.00  0.00           P  
HETATM   16  O6  UNL     1       3.618  -0.113   3.443  1.00  0.00           O  
HETATM   17  O7  UNL     1       2.352  -2.218   2.528  1.00  0.00           O  
HETATM   18  O8  UNL     1       4.111  -0.723   0.975  1.00  0.00           O  
HETATM   19  C7  UNL     1       4.241   0.513   0.372  1.00  0.00           C  
HETATM   20  O9  UNL     1       5.523   1.024   0.503  1.00  0.00           O  
HETATM   21  C8  UNL     1       6.480   0.079   0.103  1.00  0.00           C  
HETATM   22  C9  UNL     1       7.787   0.844  -0.047  1.00  0.00           C  
HETATM   23  O10 UNL     1       8.824   0.021  -0.441  1.00  0.00           O  
HETATM   24  C10 UNL     1       6.114  -0.581  -1.191  1.00  0.00           C  
HETATM   25  O11 UNL     1       5.573  -1.842  -0.919  1.00  0.00           O  
HETATM   26  C11 UNL     1       5.112   0.251  -1.945  1.00  0.00           C  
HETATM   27  O12 UNL     1       5.733   1.470  -2.257  1.00  0.00           O  
HETATM   28  C12 UNL     1       3.873   0.461  -1.103  1.00  0.00           C  
HETATM   29  O13 UNL     1       2.973  -0.575  -1.269  1.00  0.00           O  
HETATM   30  C13 UNL     1      -2.738   1.505  -1.210  1.00  0.00           C  
HETATM   31  O14 UNL     1      -2.542   1.465  -2.603  1.00  0.00           O  
HETATM   32  C14 UNL     1      -4.253   1.467  -0.959  1.00  0.00           C  
HETATM   33  O15 UNL     1      -4.955   2.086  -1.970  1.00  0.00           O  
HETATM   34  C15 UNL     1      -6.330  -1.548  -1.067  1.00  0.00           C  
HETATM   35  O16 UNL     1      -5.661  -2.187  -1.945  1.00  0.00           O  
HETATM   36  N3  UNL     1      -7.553  -1.985  -0.715  1.00  0.00           N  
HETATM   37  H1  UNL     1     -10.470  -1.297   0.299  1.00  0.00           H  
HETATM   38  H2  UNL     1      -9.765  -2.682   1.145  1.00  0.00           H  
HETATM   39  H3  UNL     1      -8.322   0.316   1.516  1.00  0.00           H  
HETATM   40  H4  UNL     1      -6.072   1.100   0.851  1.00  0.00           H  
HETATM   41  H5  UNL     1      -4.229  -0.373  -1.994  1.00  0.00           H  
HETATM   42  H6  UNL     1      -1.817  -0.440  -1.384  1.00  0.00           H  
HETATM   43  H7  UNL     1      -1.849   1.182   1.215  1.00  0.00           H  
HETATM   44  H8  UNL     1      -0.522   1.115   0.039  1.00  0.00           H  
HETATM   45  H9  UNL     1      -0.325  -2.069   3.319  1.00  0.00           H  
HETATM   46  H10 UNL     1       1.686  -2.503   1.864  1.00  0.00           H  
HETATM   47  H11 UNL     1       3.541   1.218   0.863  1.00  0.00           H  
HETATM   48  H12 UNL     1       6.579  -0.629   0.946  1.00  0.00           H  
HETATM   49  H13 UNL     1       8.028   1.338   0.927  1.00  0.00           H  
HETATM   50  H14 UNL     1       7.694   1.661  -0.788  1.00  0.00           H  
HETATM   51  H15 UNL     1       9.001   0.076  -1.423  1.00  0.00           H  
HETATM   52  H16 UNL     1       7.005  -0.725  -1.838  1.00  0.00           H  
HETATM   53  H17 UNL     1       6.134  -2.362  -0.310  1.00  0.00           H  
HETATM   54  H18 UNL     1       4.788  -0.292  -2.862  1.00  0.00           H  
HETATM   55  H19 UNL     1       5.167   2.198  -1.948  1.00  0.00           H  
HETATM   56  H20 UNL     1       3.356   1.404  -1.393  1.00  0.00           H  
HETATM   57  H21 UNL     1       3.227  -1.229  -1.941  1.00  0.00           H  
HETATM   58  H22 UNL     1      -2.266   2.380  -0.763  1.00  0.00           H  
HETATM   59  H23 UNL     1      -3.398   1.357  -3.092  1.00  0.00           H  
HETATM   60  H24 UNL     1      -4.392   1.912   0.036  1.00  0.00           H  
HETATM   61  H25 UNL     1      -5.579   2.741  -1.544  1.00  0.00           H  
CONECT    1    2   37   38
CONECT    2    3   36   36
CONECT    3    4    4   39
CONECT    4    5   40
CONECT    5    6   34
CONECT    6    7   32   41
CONECT    7    8
CONECT    8    9   30   42
CONECT    9   10   43   44
CONECT   10   11
CONECT   11   12   12   13   14
CONECT   13   45
CONECT   14   15
CONECT   15   16   16   17   18
CONECT   17   46
CONECT   18   19
CONECT   19   20   28   47
CONECT   20   21
CONECT   21   22   24   48
CONECT   22   23   49   50
CONECT   23   51
CONECT   24   25   26   52
CONECT   25   53
CONECT   26   27   28   54
CONECT   27   55
CONECT   28   29   56
CONECT   29   57
CONECT   30   31   32   58
CONECT   31   59
CONECT   32   33   60
CONECT   33   61
CONECT   34   35   35   36
END
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SMILES for HMDB0003369 (CDP-glucose)

NC1=NC(=O)N(C=C1)[C@@H]1O[C@H](COP(O)(=O)OP(O)(=O)O[C@H]2O[C@H](CO)[C@@H](O)[C@H](O)[C@H]2O)[C@@H](O)[C@H]1O
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INCHI for HMDB0003369 (CDP-glucose)

InChI=1S/C15H25N3O16P2/c16-7-1-2-18(15(25)17-7)13-11(23)9(21)6(31-13)4-30-35(26,27)34-36(28,29)33-14-12(24)10(22)8(20)5(3-19)32-14/h1-2,5-6,8-14,19-24H,3-4H2,(H,26,27)(H,28,29)(H2,16,17,25)/t5-,6-,8-,9-,10+,11-,12-,13-,14-/m1/s1
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View in JSmolView NMR AssignmentsView Stereo Labels
Synonyms
ValueSource
CDP-D-GlucoseChEBI
CDP-GLCChEBI
Cytidine diphosphate-glucoseMeSH, HMDB
CDP-a-D-GlucoseGenerator, HMDB
CDP-Α-D-glucoseGenerator, HMDB
CDP-GlucoseMeSH
Chemical FormulaC15H25N3O16P2
Average Molecular Weight565.317
Monoisotopic Molecular Weight565.071004791
IUPAC Name{[(2R,3S,4R,5R)-5-(4-amino-2-oxo-1,2-dihydropyrimidin-1-yl)-3,4-dihydroxyoxolan-2-yl]methoxy}({[hydroxy({[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy})phosphoryl]oxy})phosphinic acid
Traditional Namecytidine diphosphate glucose
CAS Registry Number2906-23-2
SMILES
NC1=NC(=O)N(C=C1)[C@@H]1O[C@H](COP(O)(=O)OP(O)(=O)O[C@H]2O[C@H](CO)[C@@H](O)[C@H](O)[C@H]2O)[C@@H](O)[C@H]1O
InChI Identifier
InChI=1S/C15H25N3O16P2/c16-7-1-2-18(15(25)17-7)13-11(23)9(21)6(31-13)4-30-35(26,27)34-36(28,29)33-14-12(24)10(22)8(20)5(3-19)32-14/h1-2,5-6,8-14,19-24H,3-4H2,(H,26,27)(H,28,29)(H2,16,17,25)/t5-,6-,8-,9-,10+,11-,12-,13-,14-/m1/s1
InChI KeyCGPHZDRCVSLMCF-JZMIEXBBSA-N
Chemical Taxonomy
Description Belongs to the class of organic compounds known as pyrimidine nucleotide sugars. These are pyrimidine nucleotides bound to a saccharide derivative through the terminal phosphate group.
KingdomOrganic compounds
Super ClassNucleosides, nucleotides, and analogues
ClassPyrimidine nucleotides
Sub ClassPyrimidine nucleotide sugars
Direct ParentPyrimidine nucleotide sugars
Alternative Parents
Substituents
  • Pyrimidine nucleotide sugar
  • Pyrimidine ribonucleoside diphosphate
  • Pentose phosphate
  • Pentose-5-phosphate
  • Glycosyl compound
  • N-glycosyl compound
  • Monosaccharide phosphate
  • Organic pyrophosphate
  • Aminopyrimidine
  • Pyrimidone
  • Monoalkyl phosphate
  • Hydropyrimidine
  • Monosaccharide
  • Organic phosphoric acid derivative
  • Oxane
  • Phosphoric acid ester
  • Pyrimidine
  • Imidolactam
  • Alkyl phosphate
  • Tetrahydrofuran
  • Heteroaromatic compound
  • Secondary alcohol
  • Polyol
  • Oxacycle
  • Organoheterocyclic compound
  • Azacycle
  • Organic oxide
  • Organonitrogen compound
  • Hydrocarbon derivative
  • Organic nitrogen compound
  • Amine
  • Primary amine
  • Organooxygen compound
  • Organopnictogen compound
  • Alcohol
  • Organic oxygen compound
  • Primary alcohol
  • Aromatic heteromonocyclic compound
Molecular FrameworkAromatic heteromonocyclic compounds
External Descriptors
Ontology
Physiological effectNot Available
Disposition
Biological locationSource
ProcessNot Available
RoleNot Available
Physical Properties
StateSolid
Experimental Molecular Properties
PropertyValueReference
Melting PointNot AvailableNot Available
Boiling PointNot AvailableNot Available
Water SolubilityNot AvailableNot Available
LogPNot AvailableNot Available
Experimental Chromatographic PropertiesNot Available
Predicted Molecular Properties
PropertyValueSource
Water Solubility28.6 g/LALOGPS
logP-1.4ALOGPS
logP-5.7ChemAxon
logS-1.3ALOGPS
pKa (Strongest Acidic)1.73ChemAxon
pKa (Strongest Basic)-0.58ChemAxon
Physiological Charge-2ChemAxon
Hydrogen Acceptor Count15ChemAxon
Hydrogen Donor Count9ChemAxon
Polar Surface Area300.82 ŲChemAxon
Rotatable Bond Count9ChemAxon
Refractivity108.44 m³·mol⁻¹ChemAxon
Polarizability45.94 ųChemAxon
Number of Rings3ChemAxon
BioavailabilityNoChemAxon
Rule of FiveNoChemAxon
Ghose FilterNoChemAxon
Veber's RuleNoChemAxon
MDDR-like RuleYesChemAxon
Predicted Chromatographic Properties

Predicted Collision Cross Sections

PredictorAdduct TypeCCS Value (Å2)Reference
DeepCCS[M+H]+176.06730932474
DeepCCS[M-H]-174.24230932474
DeepCCS[M-2H]-208.0830932474
DeepCCS[M+Na]+181.85630932474
AllCCS[M+H]+215.132859911
AllCCS[M+H-H2O]+213.732859911
AllCCS[M+NH4]+216.432859911
AllCCS[M+Na]+216.832859911
AllCCS[M-H]-208.532859911
AllCCS[M+Na-2H]-209.532859911
AllCCS[M+HCOO]-210.732859911

Predicted Kovats Retention Indices

Underivatized

MetaboliteSMILESKovats RI ValueColumn TypeReference
CDP-glucoseNC1=NC(=O)N(C=C1)[C@@H]1O[C@H](COP(O)(=O)OP(O)(=O)O[C@H]2O[C@H](CO)[C@@H](O)[C@H](O)[C@H]2O)[C@@H](O)[C@H]1O4573.4Standard polar33892256
CDP-glucoseNC1=NC(=O)N(C=C1)[C@@H]1O[C@H](COP(O)(=O)OP(O)(=O)O[C@H]2O[C@H](CO)[C@@H](O)[C@H](O)[C@H]2O)[C@@H](O)[C@H]1O3691.7Standard non polar33892256
CDP-glucoseNC1=NC(=O)N(C=C1)[C@@H]1O[C@H](COP(O)(=O)OP(O)(=O)O[C@H]2O[C@H](CO)[C@@H](O)[C@H](O)[C@H]2O)[C@@H](O)[C@H]1O4943.4Semi standard non polar33892256

Derivatized

Derivative Name / StructureSMILESKovats RI ValueColumn TypeReference
CDP-glucose,1TMS,isomer #1C[Si](C)(C)OC[C@H]1O[C@H](OP(=O)(O)OP(=O)(O)OC[C@H]2O[C@@H](N3C=CC(N)=NC3=O)[C@H](O)[C@@H]2O)[C@H](O)[C@@H](O)[C@@H]1O4415.4Semi standard non polar33892256
CDP-glucose,1TMS,isomer #2C[Si](C)(C)O[C@@H]1[C@@H](CO)O[C@H](OP(=O)(O)OP(=O)(O)OC[C@H]2O[C@@H](N3C=CC(N)=NC3=O)[C@H](O)[C@@H]2O)[C@H](O)[C@H]1O4384.2Semi standard non polar33892256
CDP-glucose,1TMS,isomer #3C[Si](C)(C)O[C@H]1[C@H](O)[C@@H](CO)O[C@H](OP(=O)(O)OP(=O)(O)OC[C@H]2O[C@@H](N3C=CC(N)=NC3=O)[C@H](O)[C@@H]2O)[C@@H]1O4362.3Semi standard non polar33892256
CDP-glucose,1TMS,isomer #4C[Si](C)(C)O[C@@H]1[C@@H](O)[C@H](O)[C@@H](CO)O[C@@H]1OP(=O)(O)OP(=O)(O)OC[C@H]1O[C@@H](N2C=CC(N)=NC2=O)[C@H](O)[C@@H]1O4387.3Semi standard non polar33892256
CDP-glucose,1TMS,isomer #5C[Si](C)(C)O[C@@H]1[C@@H](COP(=O)(O)OP(=O)(O)O[C@H]2O[C@H](CO)[C@@H](O)[C@H](O)[C@H]2O)O[C@@H](N2C=CC(N)=NC2=O)[C@@H]1O4413.6Semi standard non polar33892256
CDP-glucose,1TMS,isomer #6C[Si](C)(C)O[C@@H]1[C@H](O)[C@@H](COP(=O)(O)OP(=O)(O)O[C@H]2O[C@H](CO)[C@@H](O)[C@H](O)[C@H]2O)O[C@H]1N1C=CC(N)=NC1=O4407.4Semi standard non polar33892256
CDP-glucose,1TMS,isomer #7C[Si](C)(C)OP(=O)(OC[C@H]1O[C@@H](N2C=CC(N)=NC2=O)[C@H](O)[C@@H]1O)OP(=O)(O)O[C@H]1O[C@H](CO)[C@@H](O)[C@H](O)[C@H]1O4461.7Semi standard non polar33892256
CDP-glucose,1TMS,isomer #8C[Si](C)(C)OP(=O)(O[C@H]1O[C@H](CO)[C@@H](O)[C@H](O)[C@H]1O)OP(=O)(O)OC[C@H]1O[C@@H](N2C=CC(N)=NC2=O)[C@H](O)[C@@H]1O4471.9Semi standard non polar33892256
CDP-glucose,1TMS,isomer #9C[Si](C)(C)NC1=NC(=O)N([C@@H]2O[C@H](COP(=O)(O)OP(=O)(O)O[C@H]3O[C@H](CO)[C@@H](O)[C@H](O)[C@H]3O)[C@@H](O)[C@H]2O)C=C14510.5Semi standard non polar33892256
CDP-glucose,2TMS,isomer #1C[Si](C)(C)OC[C@H]1O[C@H](OP(=O)(O)OP(=O)(O)OC[C@H]2O[C@@H](N3C=CC(N)=NC3=O)[C@H](O[Si](C)(C)C)[C@@H]2O)[C@H](O)[C@@H](O)[C@@H]1O4291.5Semi standard non polar33892256
CDP-glucose,2TMS,isomer #10C[Si](C)(C)O[C@@H]1[C@@H](CO)O[C@H](OP(=O)(O)OP(=O)(O)OC[C@H]2O[C@@H](N3C=CC(N)=NC3=O)[C@H](O)[C@@H]2O[Si](C)(C)C)[C@H](O)[C@H]1O4268.4Semi standard non polar33892256
CDP-glucose,2TMS,isomer #11C[Si](C)(C)O[C@H]1[C@H](O)[C@@H](O[Si](C)(C)C)[C@@H](OP(=O)(O)OP(=O)(O)OC[C@H]2O[C@@H](N3C=CC(N)=NC3=O)[C@H](O)[C@@H]2O)O[C@@H]1CO4239.5Semi standard non polar33892256
CDP-glucose,2TMS,isomer #12C[Si](C)(C)O[C@@H]1[C@@H](CO)O[C@H](OP(=O)(O)OP(=O)(O)OC[C@H]2O[C@@H](N3C=CC(N)=NC3=O)[C@H](O)[C@@H]2O)[C@H](O)[C@H]1O[Si](C)(C)C4237.1Semi standard non polar33892256
CDP-glucose,2TMS,isomer #13C[Si](C)(C)O[C@@H]1[C@@H](CO)O[C@H](OP(=O)(O[Si](C)(C)C)OP(=O)(O)OC[C@H]2O[C@@H](N3C=CC(N)=NC3=O)[C@H](O)[C@@H]2O)[C@H](O)[C@H]1O4322.8Semi standard non polar33892256
CDP-glucose,2TMS,isomer #14C[Si](C)(C)O[C@@H]1[C@@H](CO)O[C@H](OP(=O)(O)OP(=O)(OC[C@H]2O[C@@H](N3C=CC(N)=NC3=O)[C@H](O)[C@@H]2O)O[Si](C)(C)C)[C@H](O)[C@H]1O4317.3Semi standard non polar33892256
CDP-glucose,2TMS,isomer #15C[Si](C)(C)NC1=NC(=O)N([C@@H]2O[C@H](COP(=O)(O)OP(=O)(O)O[C@H]3O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@H](O)[C@H]3O)[C@@H](O)[C@H]2O)C=C14402.7Semi standard non polar33892256
CDP-glucose,2TMS,isomer #16C[Si](C)(C)O[C@H]1[C@H](O)[C@@H](CO)O[C@H](OP(=O)(O)OP(=O)(O)OC[C@H]2O[C@@H](N3C=CC(N)=NC3=O)[C@H](O[Si](C)(C)C)[C@@H]2O)[C@@H]1O4228.5Semi standard non polar33892256
CDP-glucose,2TMS,isomer #17C[Si](C)(C)O[C@H]1[C@H](O)[C@@H](CO)O[C@H](OP(=O)(O)OP(=O)(O)OC[C@H]2O[C@@H](N3C=CC(N)=NC3=O)[C@H](O)[C@@H]2O[Si](C)(C)C)[C@@H]1O4239.6Semi standard non polar33892256
CDP-glucose,2TMS,isomer #18C[Si](C)(C)O[C@H]1[C@H](O)[C@@H](CO)O[C@H](OP(=O)(O)OP(=O)(O)OC[C@H]2O[C@@H](N3C=CC(N)=NC3=O)[C@H](O)[C@@H]2O)[C@@H]1O[Si](C)(C)C4256.8Semi standard non polar33892256
CDP-glucose,2TMS,isomer #19C[Si](C)(C)O[C@H]1[C@H](O)[C@@H](CO)O[C@H](OP(=O)(O[Si](C)(C)C)OP(=O)(O)OC[C@H]2O[C@@H](N3C=CC(N)=NC3=O)[C@H](O)[C@@H]2O)[C@@H]1O4297.2Semi standard non polar33892256
CDP-glucose,2TMS,isomer #2C[Si](C)(C)OC[C@H]1O[C@H](OP(=O)(O)OP(=O)(O)OC[C@H]2O[C@@H](N3C=CC(N)=NC3=O)[C@H](O)[C@@H]2O[Si](C)(C)C)[C@H](O)[C@@H](O)[C@@H]1O4302.2Semi standard non polar33892256
CDP-glucose,2TMS,isomer #20C[Si](C)(C)O[C@H]1[C@H](O)[C@@H](CO)O[C@H](OP(=O)(O)OP(=O)(OC[C@H]2O[C@@H](N3C=CC(N)=NC3=O)[C@H](O)[C@@H]2O)O[Si](C)(C)C)[C@@H]1O4288.0Semi standard non polar33892256
CDP-glucose,2TMS,isomer #21C[Si](C)(C)NC1=NC(=O)N([C@@H]2O[C@H](COP(=O)(O)OP(=O)(O)O[C@H]3O[C@H](CO)[C@@H](O)[C@H](O[Si](C)(C)C)[C@H]3O)[C@@H](O)[C@H]2O)C=C14390.5Semi standard non polar33892256
CDP-glucose,2TMS,isomer #22C[Si](C)(C)O[C@@H]1[C@@H](O)[C@H](O)[C@@H](CO)O[C@@H]1OP(=O)(O)OP(=O)(O)OC[C@H]1O[C@@H](N2C=CC(N)=NC2=O)[C@H](O[Si](C)(C)C)[C@@H]1O4260.7Semi standard non polar33892256
CDP-glucose,2TMS,isomer #23C[Si](C)(C)O[C@@H]1[C@@H](COP(=O)(O)OP(=O)(O)O[C@H]2O[C@H](CO)[C@@H](O)[C@H](O)[C@H]2O[Si](C)(C)C)O[C@@H](N2C=CC(N)=NC2=O)[C@@H]1O4271.8Semi standard non polar33892256
CDP-glucose,2TMS,isomer #24C[Si](C)(C)O[C@@H]1[C@@H](O)[C@H](O)[C@@H](CO)O[C@@H]1OP(=O)(O[Si](C)(C)C)OP(=O)(O)OC[C@H]1O[C@@H](N2C=CC(N)=NC2=O)[C@H](O)[C@@H]1O4330.9Semi standard non polar33892256
CDP-glucose,2TMS,isomer #25C[Si](C)(C)O[C@@H]1[C@@H](O)[C@H](O)[C@@H](CO)O[C@@H]1OP(=O)(O)OP(=O)(OC[C@H]1O[C@@H](N2C=CC(N)=NC2=O)[C@H](O)[C@@H]1O)O[Si](C)(C)C4319.7Semi standard non polar33892256
CDP-glucose,2TMS,isomer #26C[Si](C)(C)NC1=NC(=O)N([C@@H]2O[C@H](COP(=O)(O)OP(=O)(O)O[C@H]3O[C@H](CO)[C@@H](O)[C@H](O)[C@H]3O[Si](C)(C)C)[C@@H](O)[C@H]2O)C=C14409.6Semi standard non polar33892256
CDP-glucose,2TMS,isomer #27C[Si](C)(C)O[C@@H]1[C@@H](COP(=O)(O)OP(=O)(O)O[C@H]2O[C@H](CO)[C@@H](O)[C@H](O)[C@H]2O)O[C@@H](N2C=CC(N)=NC2=O)[C@@H]1O[Si](C)(C)C4304.3Semi standard non polar33892256
CDP-glucose,2TMS,isomer #28C[Si](C)(C)O[C@@H]1[C@@H](COP(=O)(O[Si](C)(C)C)OP(=O)(O)O[C@H]2O[C@H](CO)[C@@H](O)[C@H](O)[C@H]2O)O[C@@H](N2C=CC(N)=NC2=O)[C@@H]1O4345.0Semi standard non polar33892256
CDP-glucose,2TMS,isomer #29C[Si](C)(C)O[C@@H]1[C@@H](COP(=O)(O)OP(=O)(O[C@H]2O[C@H](CO)[C@@H](O)[C@H](O)[C@H]2O)O[Si](C)(C)C)O[C@@H](N2C=CC(N)=NC2=O)[C@@H]1O4352.4Semi standard non polar33892256
CDP-glucose,2TMS,isomer #3C[Si](C)(C)OC[C@H]1O[C@H](OP(=O)(O)OP(=O)(O)OC[C@H]2O[C@@H](N3C=CC(N)=NC3=O)[C@H](O)[C@@H]2O)[C@H](O[Si](C)(C)C)[C@@H](O)[C@@H]1O4290.9Semi standard non polar33892256
CDP-glucose,2TMS,isomer #30C[Si](C)(C)NC1=NC(=O)N([C@@H]2O[C@H](COP(=O)(O)OP(=O)(O)O[C@H]3O[C@H](CO)[C@@H](O)[C@H](O)[C@H]3O)[C@@H](O[Si](C)(C)C)[C@H]2O)C=C14425.4Semi standard non polar33892256
CDP-glucose,2TMS,isomer #31C[Si](C)(C)O[C@@H]1[C@H](O)[C@@H](COP(=O)(O[Si](C)(C)C)OP(=O)(O)O[C@H]2O[C@H](CO)[C@@H](O)[C@H](O)[C@H]2O)O[C@H]1N1C=CC(N)=NC1=O4332.3Semi standard non polar33892256
CDP-glucose,2TMS,isomer #32C[Si](C)(C)O[C@@H]1[C@H](O)[C@@H](COP(=O)(O)OP(=O)(O[C@H]2O[C@H](CO)[C@@H](O)[C@H](O)[C@H]2O)O[Si](C)(C)C)O[C@H]1N1C=CC(N)=NC1=O4339.2Semi standard non polar33892256
CDP-glucose,2TMS,isomer #33C[Si](C)(C)NC1=NC(=O)N([C@@H]2O[C@H](COP(=O)(O)OP(=O)(O)O[C@H]3O[C@H](CO)[C@@H](O)[C@H](O)[C@H]3O)[C@@H](O)[C@H]2O[Si](C)(C)C)C=C14418.5Semi standard non polar33892256
CDP-glucose,2TMS,isomer #34C[Si](C)(C)OP(=O)(OC[C@H]1O[C@@H](N2C=CC(N)=NC2=O)[C@H](O)[C@@H]1O)OP(=O)(O[C@H]1O[C@H](CO)[C@@H](O)[C@H](O)[C@H]1O)O[Si](C)(C)C4393.0Semi standard non polar33892256
CDP-glucose,2TMS,isomer #35C[Si](C)(C)NC1=NC(=O)N([C@@H]2O[C@H](COP(=O)(O[Si](C)(C)C)OP(=O)(O)O[C@H]3O[C@H](CO)[C@@H](O)[C@H](O)[C@H]3O)[C@@H](O)[C@H]2O)C=C14470.4Semi standard non polar33892256
CDP-glucose,2TMS,isomer #36C[Si](C)(C)NC1=NC(=O)N([C@@H]2O[C@H](COP(=O)(O)OP(=O)(O[C@H]3O[C@H](CO)[C@@H](O)[C@H](O)[C@H]3O)O[Si](C)(C)C)[C@@H](O)[C@H]2O)C=C14476.5Semi standard non polar33892256
CDP-glucose,2TMS,isomer #37C[Si](C)(C)N(C1=NC(=O)N([C@@H]2O[C@H](COP(=O)(O)OP(=O)(O)O[C@H]3O[C@H](CO)[C@@H](O)[C@H](O)[C@H]3O)[C@@H](O)[C@H]2O)C=C1)[Si](C)(C)C4436.7Semi standard non polar33892256
CDP-glucose,2TMS,isomer #4C[Si](C)(C)OC[C@H]1O[C@H](OP(=O)(O)OP(=O)(O)OC[C@H]2O[C@@H](N3C=CC(N)=NC3=O)[C@H](O)[C@@H]2O)[C@H](O)[C@@H](O[Si](C)(C)C)[C@@H]1O4256.5Semi standard non polar33892256
CDP-glucose,2TMS,isomer #5C[Si](C)(C)OC[C@H]1O[C@H](OP(=O)(O)OP(=O)(O)OC[C@H]2O[C@@H](N3C=CC(N)=NC3=O)[C@H](O)[C@@H]2O)[C@H](O)[C@@H](O)[C@@H]1O[Si](C)(C)C4298.6Semi standard non polar33892256
CDP-glucose,2TMS,isomer #6C[Si](C)(C)OC[C@H]1O[C@H](OP(=O)(O[Si](C)(C)C)OP(=O)(O)OC[C@H]2O[C@@H](N3C=CC(N)=NC3=O)[C@H](O)[C@@H]2O)[C@H](O)[C@@H](O)[C@@H]1O4356.3Semi standard non polar33892256
CDP-glucose,2TMS,isomer #7C[Si](C)(C)OC[C@H]1O[C@H](OP(=O)(O)OP(=O)(OC[C@H]2O[C@@H](N3C=CC(N)=NC3=O)[C@H](O)[C@@H]2O)O[Si](C)(C)C)[C@H](O)[C@@H](O)[C@@H]1O4341.6Semi standard non polar33892256
CDP-glucose,2TMS,isomer #8C[Si](C)(C)NC1=NC(=O)N([C@@H]2O[C@H](COP(=O)(O)OP(=O)(O)O[C@H]3O[C@H](CO[Si](C)(C)C)[C@@H](O)[C@H](O)[C@H]3O)[C@@H](O)[C@H]2O)C=C14420.1Semi standard non polar33892256
CDP-glucose,2TMS,isomer #9C[Si](C)(C)O[C@@H]1[C@@H](CO)O[C@H](OP(=O)(O)OP(=O)(O)OC[C@H]2O[C@@H](N3C=CC(N)=NC3=O)[C@H](O[Si](C)(C)C)[C@@H]2O)[C@H](O)[C@H]1O4257.9Semi standard non polar33892256
CDP-glucose,3TMS,isomer #1C[Si](C)(C)OC[C@H]1O[C@H](OP(=O)(O)OP(=O)(O)OC[C@H]2O[C@@H](N3C=CC(N)=NC3=O)[C@H](O[Si](C)(C)C)[C@@H]2O[Si](C)(C)C)[C@H](O)[C@@H](O)[C@@H]1O4166.7Semi standard non polar33892256
CDP-glucose,3TMS,isomer #10C[Si](C)(C)OC[C@H]1O[C@H](OP(=O)(O)OP(=O)(O)OC[C@H]2O[C@@H](N3C=CC(N)=NC3=O)[C@H](O)[C@@H]2O[Si](C)(C)C)[C@H](O)[C@@H](O)[C@@H]1O[Si](C)(C)C4148.2Semi standard non polar33892256
CDP-glucose,3TMS,isomer #11C[Si](C)(C)OC[C@H]1O[C@H](OP(=O)(O[Si](C)(C)C)OP(=O)(O)OC[C@H]2O[C@@H](N3C=CC(N)=NC3=O)[C@H](O)[C@@H]2O[Si](C)(C)C)[C@H](O)[C@@H](O)[C@@H]1O4195.9Semi standard non polar33892256
CDP-glucose,3TMS,isomer #12C[Si](C)(C)OC[C@H]1O[C@H](OP(=O)(O)OP(=O)(OC[C@H]2O[C@@H](N3C=CC(N)=NC3=O)[C@H](O)[C@@H]2O[Si](C)(C)C)O[Si](C)(C)C)[C@H](O)[C@@H](O)[C@@H]1O4187.2Semi standard non polar33892256
CDP-glucose,3TMS,isomer #13C[Si](C)(C)NC1=NC(=O)N([C@@H]2O[C@H](COP(=O)(O)OP(=O)(O)O[C@H]3O[C@H](CO[Si](C)(C)C)[C@@H](O)[C@H](O)[C@H]3O)[C@@H](O[Si](C)(C)C)[C@H]2O)C=C14287.8Semi standard non polar33892256
CDP-glucose,3TMS,isomer #14C[Si](C)(C)OC[C@H]1O[C@H](OP(=O)(O)OP(=O)(O)OC[C@H]2O[C@@H](N3C=CC(N)=NC3=O)[C@H](O)[C@@H]2O)[C@H](O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@@H]1O4145.6Semi standard non polar33892256
CDP-glucose,3TMS,isomer #15C[Si](C)(C)OC[C@H]1O[C@H](OP(=O)(O)OP(=O)(O)OC[C@H]2O[C@@H](N3C=CC(N)=NC3=O)[C@H](O)[C@@H]2O)[C@H](O[Si](C)(C)C)[C@@H](O)[C@@H]1O[Si](C)(C)C4142.9Semi standard non polar33892256
CDP-glucose,3TMS,isomer #16C[Si](C)(C)OC[C@H]1O[C@H](OP(=O)(O[Si](C)(C)C)OP(=O)(O)OC[C@H]2O[C@@H](N3C=CC(N)=NC3=O)[C@H](O)[C@@H]2O)[C@H](O[Si](C)(C)C)[C@@H](O)[C@@H]1O4189.8Semi standard non polar33892256
CDP-glucose,3TMS,isomer #17C[Si](C)(C)OC[C@H]1O[C@H](OP(=O)(O)OP(=O)(OC[C@H]2O[C@@H](N3C=CC(N)=NC3=O)[C@H](O)[C@@H]2O)O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@@H](O)[C@@H]1O4177.2Semi standard non polar33892256
CDP-glucose,3TMS,isomer #18C[Si](C)(C)NC1=NC(=O)N([C@@H]2O[C@H](COP(=O)(O)OP(=O)(O)O[C@H]3O[C@H](CO[Si](C)(C)C)[C@@H](O)[C@H](O)[C@H]3O[Si](C)(C)C)[C@@H](O)[C@H]2O)C=C14292.4Semi standard non polar33892256
CDP-glucose,3TMS,isomer #19C[Si](C)(C)OC[C@H]1O[C@H](OP(=O)(O)OP(=O)(O)OC[C@H]2O[C@@H](N3C=CC(N)=NC3=O)[C@H](O)[C@@H]2O)[C@H](O)[C@@H](O[Si](C)(C)C)[C@@H]1O[Si](C)(C)C4136.0Semi standard non polar33892256
CDP-glucose,3TMS,isomer #2C[Si](C)(C)OC[C@H]1O[C@H](OP(=O)(O)OP(=O)(O)OC[C@H]2O[C@@H](N3C=CC(N)=NC3=O)[C@H](O[Si](C)(C)C)[C@@H]2O)[C@H](O[Si](C)(C)C)[C@@H](O)[C@@H]1O4139.6Semi standard non polar33892256
CDP-glucose,3TMS,isomer #20C[Si](C)(C)OC[C@H]1O[C@H](OP(=O)(O[Si](C)(C)C)OP(=O)(O)OC[C@H]2O[C@@H](N3C=CC(N)=NC3=O)[C@H](O)[C@@H]2O)[C@H](O)[C@@H](O[Si](C)(C)C)[C@@H]1O4159.0Semi standard non polar33892256
CDP-glucose,3TMS,isomer #21C[Si](C)(C)OC[C@H]1O[C@H](OP(=O)(O)OP(=O)(OC[C@H]2O[C@@H](N3C=CC(N)=NC3=O)[C@H](O)[C@@H]2O)O[Si](C)(C)C)[C@H](O)[C@@H](O[Si](C)(C)C)[C@@H]1O4143.9Semi standard non polar33892256
CDP-glucose,3TMS,isomer #22C[Si](C)(C)NC1=NC(=O)N([C@@H]2O[C@H](COP(=O)(O)OP(=O)(O)O[C@H]3O[C@H](CO[Si](C)(C)C)[C@@H](O)[C@H](O[Si](C)(C)C)[C@H]3O)[C@@H](O)[C@H]2O)C=C14273.1Semi standard non polar33892256
CDP-glucose,3TMS,isomer #23C[Si](C)(C)OC[C@H]1O[C@H](OP(=O)(O[Si](C)(C)C)OP(=O)(O)OC[C@H]2O[C@@H](N3C=CC(N)=NC3=O)[C@H](O)[C@@H]2O)[C@H](O)[C@@H](O)[C@@H]1O[Si](C)(C)C4193.5Semi standard non polar33892256
CDP-glucose,3TMS,isomer #24C[Si](C)(C)OC[C@H]1O[C@H](OP(=O)(O)OP(=O)(OC[C@H]2O[C@@H](N3C=CC(N)=NC3=O)[C@H](O)[C@@H]2O)O[Si](C)(C)C)[C@H](O)[C@@H](O)[C@@H]1O[Si](C)(C)C4183.9Semi standard non polar33892256
CDP-glucose,3TMS,isomer #25C[Si](C)(C)NC1=NC(=O)N([C@@H]2O[C@H](COP(=O)(O)OP(=O)(O)O[C@H]3O[C@H](CO[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@H](O)[C@H]3O)[C@@H](O)[C@H]2O)C=C14298.8Semi standard non polar33892256
CDP-glucose,3TMS,isomer #26C[Si](C)(C)OC[C@H]1O[C@H](OP(=O)(O[Si](C)(C)C)OP(=O)(OC[C@H]2O[C@@H](N3C=CC(N)=NC3=O)[C@H](O)[C@@H]2O)O[Si](C)(C)C)[C@H](O)[C@@H](O)[C@@H]1O4221.8Semi standard non polar33892256
CDP-glucose,3TMS,isomer #27C[Si](C)(C)NC1=NC(=O)N([C@@H]2O[C@H](COP(=O)(O)OP(=O)(O[C@H]3O[C@H](CO[Si](C)(C)C)[C@@H](O)[C@H](O)[C@H]3O)O[Si](C)(C)C)[C@@H](O)[C@H]2O)C=C14330.9Semi standard non polar33892256
CDP-glucose,3TMS,isomer #28C[Si](C)(C)NC1=NC(=O)N([C@@H]2O[C@H](COP(=O)(O[Si](C)(C)C)OP(=O)(O)O[C@H]3O[C@H](CO[Si](C)(C)C)[C@@H](O)[C@H](O)[C@H]3O)[C@@H](O)[C@H]2O)C=C14327.4Semi standard non polar33892256
CDP-glucose,3TMS,isomer #29C[Si](C)(C)OC[C@H]1O[C@H](OP(=O)(O)OP(=O)(O)OC[C@H]2O[C@@H](N3C=CC(N([Si](C)(C)C)[Si](C)(C)C)=NC3=O)[C@H](O)[C@@H]2O)[C@H](O)[C@@H](O)[C@@H]1O4308.8Semi standard non polar33892256
CDP-glucose,3TMS,isomer #3C[Si](C)(C)OC[C@H]1O[C@H](OP(=O)(O)OP(=O)(O)OC[C@H]2O[C@@H](N3C=CC(N)=NC3=O)[C@H](O[Si](C)(C)C)[C@@H]2O)[C@H](O)[C@@H](O[Si](C)(C)C)[C@@H]1O4108.6Semi standard non polar33892256
CDP-glucose,3TMS,isomer #30C[Si](C)(C)O[C@@H]1[C@@H](CO)O[C@H](OP(=O)(O)OP(=O)(O)OC[C@H]2O[C@@H](N3C=CC(N)=NC3=O)[C@H](O[Si](C)(C)C)[C@@H]2O[Si](C)(C)C)[C@H](O)[C@H]1O4127.4Semi standard non polar33892256
CDP-glucose,3TMS,isomer #31C[Si](C)(C)O[C@H]1[C@H](O)[C@@H](O[Si](C)(C)C)[C@@H](OP(=O)(O)OP(=O)(O)OC[C@H]2O[C@@H](N3C=CC(N)=NC3=O)[C@H](O[Si](C)(C)C)[C@@H]2O)O[C@@H]1CO4094.9Semi standard non polar33892256
CDP-glucose,3TMS,isomer #32C[Si](C)(C)O[C@@H]1[C@@H](CO)O[C@H](OP(=O)(O)OP(=O)(O)OC[C@H]2O[C@@H](N3C=CC(N)=NC3=O)[C@H](O[Si](C)(C)C)[C@@H]2O)[C@H](O)[C@H]1O[Si](C)(C)C4086.2Semi standard non polar33892256
CDP-glucose,3TMS,isomer #33C[Si](C)(C)O[C@@H]1[C@@H](CO)O[C@H](OP(=O)(O[Si](C)(C)C)OP(=O)(O)OC[C@H]2O[C@@H](N3C=CC(N)=NC3=O)[C@H](O[Si](C)(C)C)[C@@H]2O)[C@H](O)[C@H]1O4153.9Semi standard non polar33892256
CDP-glucose,3TMS,isomer #34C[Si](C)(C)O[C@@H]1[C@@H](CO)O[C@H](OP(=O)(O)OP(=O)(OC[C@H]2O[C@@H](N3C=CC(N)=NC3=O)[C@H](O[Si](C)(C)C)[C@@H]2O)O[Si](C)(C)C)[C@H](O)[C@H]1O4146.6Semi standard non polar33892256
CDP-glucose,3TMS,isomer #35C[Si](C)(C)NC1=NC(=O)N([C@@H]2O[C@H](COP(=O)(O)OP(=O)(O)O[C@H]3O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@H](O)[C@H]3O)[C@@H](O)[C@H]2O[Si](C)(C)C)C=C14271.7Semi standard non polar33892256
CDP-glucose,3TMS,isomer #36C[Si](C)(C)O[C@H]1[C@H](O)[C@@H](O[Si](C)(C)C)[C@@H](OP(=O)(O)OP(=O)(O)OC[C@H]2O[C@@H](N3C=CC(N)=NC3=O)[C@H](O)[C@@H]2O[Si](C)(C)C)O[C@@H]1CO4098.3Semi standard non polar33892256
CDP-glucose,3TMS,isomer #37C[Si](C)(C)O[C@@H]1[C@@H](COP(=O)(O)OP(=O)(O)O[C@H]2O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]2O)O[C@@H](N2C=CC(N)=NC2=O)[C@@H]1O4090.8Semi standard non polar33892256
CDP-glucose,3TMS,isomer #38C[Si](C)(C)O[C@@H]1[C@@H](CO)O[C@H](OP(=O)(O[Si](C)(C)C)OP(=O)(O)OC[C@H]2O[C@@H](N3C=CC(N)=NC3=O)[C@H](O)[C@@H]2O[Si](C)(C)C)[C@H](O)[C@H]1O4161.3Semi standard non polar33892256
CDP-glucose,3TMS,isomer #39C[Si](C)(C)O[C@@H]1[C@@H](CO)O[C@H](OP(=O)(O)OP(=O)(OC[C@H]2O[C@@H](N3C=CC(N)=NC3=O)[C@H](O)[C@@H]2O[Si](C)(C)C)O[Si](C)(C)C)[C@H](O)[C@H]1O4156.1Semi standard non polar33892256
CDP-glucose,3TMS,isomer #4C[Si](C)(C)OC[C@H]1O[C@H](OP(=O)(O)OP(=O)(O)OC[C@H]2O[C@@H](N3C=CC(N)=NC3=O)[C@H](O[Si](C)(C)C)[C@@H]2O)[C@H](O)[C@@H](O)[C@@H]1O[Si](C)(C)C4140.7Semi standard non polar33892256
CDP-glucose,3TMS,isomer #40C[Si](C)(C)NC1=NC(=O)N([C@@H]2O[C@H](COP(=O)(O)OP(=O)(O)O[C@H]3O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@H](O)[C@H]3O)[C@@H](O[Si](C)(C)C)[C@H]2O)C=C14278.4Semi standard non polar33892256
CDP-glucose,3TMS,isomer #41C[Si](C)(C)O[C@H]1[C@H](O[Si](C)(C)C)[C@@H](CO)O[C@H](OP(=O)(O)OP(=O)(O)OC[C@H]2O[C@@H](N3C=CC(N)=NC3=O)[C@H](O)[C@@H]2O)[C@@H]1O[Si](C)(C)C4126.2Semi standard non polar33892256
CDP-glucose,3TMS,isomer #42C[Si](C)(C)O[C@H]1[C@H](O)[C@@H](O[Si](C)(C)C)[C@@H](OP(=O)(O[Si](C)(C)C)OP(=O)(O)OC[C@H]2O[C@@H](N3C=CC(N)=NC3=O)[C@H](O)[C@@H]2O)O[C@@H]1CO4144.3Semi standard non polar33892256
CDP-glucose,3TMS,isomer #43C[Si](C)(C)O[C@H]1[C@H](O)[C@@H](O[Si](C)(C)C)[C@@H](OP(=O)(O)OP(=O)(OC[C@H]2O[C@@H](N3C=CC(N)=NC3=O)[C@H](O)[C@@H]2O)O[Si](C)(C)C)O[C@@H]1CO4132.1Semi standard non polar33892256
CDP-glucose,3TMS,isomer #44C[Si](C)(C)NC1=NC(=O)N([C@@H]2O[C@H](COP(=O)(O)OP(=O)(O)O[C@H]3O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@H](O)[C@H]3O[Si](C)(C)C)[C@@H](O)[C@H]2O)C=C14265.0Semi standard non polar33892256
CDP-glucose,3TMS,isomer #45C[Si](C)(C)O[C@@H]1[C@@H](CO)O[C@H](OP(=O)(O[Si](C)(C)C)OP(=O)(O)OC[C@H]2O[C@@H](N3C=CC(N)=NC3=O)[C@H](O)[C@@H]2O)[C@H](O)[C@H]1O[Si](C)(C)C4139.7Semi standard non polar33892256
CDP-glucose,3TMS,isomer #46C[Si](C)(C)O[C@@H]1[C@@H](CO)O[C@H](OP(=O)(O)OP(=O)(OC[C@H]2O[C@@H](N3C=CC(N)=NC3=O)[C@H](O)[C@@H]2O)O[Si](C)(C)C)[C@H](O)[C@H]1O[Si](C)(C)C4126.0Semi standard non polar33892256
CDP-glucose,3TMS,isomer #47C[Si](C)(C)NC1=NC(=O)N([C@@H]2O[C@H](COP(=O)(O)OP(=O)(O)O[C@H]3O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]3O)[C@@H](O)[C@H]2O)C=C14261.1Semi standard non polar33892256
CDP-glucose,3TMS,isomer #48C[Si](C)(C)O[C@@H]1[C@@H](CO)O[C@H](OP(=O)(O[Si](C)(C)C)OP(=O)(OC[C@H]2O[C@@H](N3C=CC(N)=NC3=O)[C@H](O)[C@@H]2O)O[Si](C)(C)C)[C@H](O)[C@H]1O4193.5Semi standard non polar33892256
CDP-glucose,3TMS,isomer #49C[Si](C)(C)NC1=NC(=O)N([C@@H]2O[C@H](COP(=O)(O)OP(=O)(O[C@H]3O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@H](O)[C@H]3O)O[Si](C)(C)C)[C@@H](O)[C@H]2O)C=C14324.9Semi standard non polar33892256
CDP-glucose,3TMS,isomer #5C[Si](C)(C)OC[C@H]1O[C@H](OP(=O)(O[Si](C)(C)C)OP(=O)(O)OC[C@H]2O[C@@H](N3C=CC(N)=NC3=O)[C@H](O[Si](C)(C)C)[C@@H]2O)[C@H](O)[C@@H](O)[C@@H]1O4186.5Semi standard non polar33892256
CDP-glucose,3TMS,isomer #50C[Si](C)(C)NC1=NC(=O)N([C@@H]2O[C@H](COP(=O)(O[Si](C)(C)C)OP(=O)(O)O[C@H]3O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@H](O)[C@H]3O)[C@@H](O)[C@H]2O)C=C14321.9Semi standard non polar33892256
CDP-glucose,3TMS,isomer #51C[Si](C)(C)O[C@@H]1[C@@H](CO)O[C@H](OP(=O)(O)OP(=O)(O)OC[C@H]2O[C@@H](N3C=CC(N([Si](C)(C)C)[Si](C)(C)C)=NC3=O)[C@H](O)[C@@H]2O)[C@H](O)[C@H]1O4273.2Semi standard non polar33892256
CDP-glucose,3TMS,isomer #52C[Si](C)(C)O[C@H]1[C@H](O)[C@@H](CO)O[C@H](OP(=O)(O)OP(=O)(O)OC[C@H]2O[C@@H](N3C=CC(N)=NC3=O)[C@H](O[Si](C)(C)C)[C@@H]2O[Si](C)(C)C)[C@@H]1O4103.4Semi standard non polar33892256
CDP-glucose,3TMS,isomer #53C[Si](C)(C)O[C@H]1[C@H](O)[C@@H](CO)O[C@H](OP(=O)(O)OP(=O)(O)OC[C@H]2O[C@@H](N3C=CC(N)=NC3=O)[C@H](O[Si](C)(C)C)[C@@H]2O)[C@@H]1O[Si](C)(C)C4106.3Semi standard non polar33892256
CDP-glucose,3TMS,isomer #54C[Si](C)(C)O[C@H]1[C@H](O)[C@@H](CO)O[C@H](OP(=O)(O[Si](C)(C)C)OP(=O)(O)OC[C@H]2O[C@@H](N3C=CC(N)=NC3=O)[C@H](O[Si](C)(C)C)[C@@H]2O)[C@@H]1O4134.9Semi standard non polar33892256
CDP-glucose,3TMS,isomer #55C[Si](C)(C)O[C@H]1[C@H](O)[C@@H](CO)O[C@H](OP(=O)(O)OP(=O)(OC[C@H]2O[C@@H](N3C=CC(N)=NC3=O)[C@H](O[Si](C)(C)C)[C@@H]2O)O[Si](C)(C)C)[C@@H]1O4123.0Semi standard non polar33892256
CDP-glucose,3TMS,isomer #56C[Si](C)(C)NC1=NC(=O)N([C@@H]2O[C@H](COP(=O)(O)OP(=O)(O)O[C@H]3O[C@H](CO)[C@@H](O)[C@H](O[Si](C)(C)C)[C@H]3O)[C@@H](O)[C@H]2O[Si](C)(C)C)C=C14256.1Semi standard non polar33892256
CDP-glucose,3TMS,isomer #57C[Si](C)(C)O[C@@H]1[C@@H](COP(=O)(O)OP(=O)(O)O[C@H]2O[C@H](CO)[C@@H](O)[C@H](O[Si](C)(C)C)[C@H]2O[Si](C)(C)C)O[C@@H](N2C=CC(N)=NC2=O)[C@@H]1O4111.1Semi standard non polar33892256
CDP-glucose,3TMS,isomer #58C[Si](C)(C)O[C@H]1[C@H](O)[C@@H](CO)O[C@H](OP(=O)(O[Si](C)(C)C)OP(=O)(O)OC[C@H]2O[C@@H](N3C=CC(N)=NC3=O)[C@H](O)[C@@H]2O[Si](C)(C)C)[C@@H]1O4143.4Semi standard non polar33892256
CDP-glucose,3TMS,isomer #59C[Si](C)(C)O[C@H]1[C@H](O)[C@@H](CO)O[C@H](OP(=O)(O)OP(=O)(OC[C@H]2O[C@@H](N3C=CC(N)=NC3=O)[C@H](O)[C@@H]2O[Si](C)(C)C)O[Si](C)(C)C)[C@@H]1O4133.0Semi standard non polar33892256
CDP-glucose,3TMS,isomer #6C[Si](C)(C)OC[C@H]1O[C@H](OP(=O)(O)OP(=O)(OC[C@H]2O[C@@H](N3C=CC(N)=NC3=O)[C@H](O[Si](C)(C)C)[C@@H]2O)O[Si](C)(C)C)[C@H](O)[C@@H](O)[C@@H]1O4177.0Semi standard non polar33892256
CDP-glucose,3TMS,isomer #60C[Si](C)(C)NC1=NC(=O)N([C@@H]2O[C@H](COP(=O)(O)OP(=O)(O)O[C@H]3O[C@H](CO)[C@@H](O)[C@H](O[Si](C)(C)C)[C@H]3O)[C@@H](O[Si](C)(C)C)[C@H]2O)C=C14264.4Semi standard non polar33892256
CDP-glucose,3TMS,isomer #61C[Si](C)(C)O[C@H]1[C@H](O)[C@@H](CO)O[C@H](OP(=O)(O[Si](C)(C)C)OP(=O)(O)OC[C@H]2O[C@@H](N3C=CC(N)=NC3=O)[C@H](O)[C@@H]2O)[C@@H]1O[Si](C)(C)C4157.3Semi standard non polar33892256
CDP-glucose,3TMS,isomer #62C[Si](C)(C)O[C@H]1[C@H](O)[C@@H](CO)O[C@H](OP(=O)(O)OP(=O)(OC[C@H]2O[C@@H](N3C=CC(N)=NC3=O)[C@H](O)[C@@H]2O)O[Si](C)(C)C)[C@@H]1O[Si](C)(C)C4145.7Semi standard non polar33892256
CDP-glucose,3TMS,isomer #63C[Si](C)(C)NC1=NC(=O)N([C@@H]2O[C@H](COP(=O)(O)OP(=O)(O)O[C@H]3O[C@H](CO)[C@@H](O)[C@H](O[Si](C)(C)C)[C@H]3O[Si](C)(C)C)[C@@H](O)[C@H]2O)C=C14278.1Semi standard non polar33892256
CDP-glucose,3TMS,isomer #64C[Si](C)(C)O[C@H]1[C@H](O)[C@@H](CO)O[C@H](OP(=O)(O[Si](C)(C)C)OP(=O)(OC[C@H]2O[C@@H](N3C=CC(N)=NC3=O)[C@H](O)[C@@H]2O)O[Si](C)(C)C)[C@@H]1O4170.9Semi standard non polar33892256
CDP-glucose,3TMS,isomer #65C[Si](C)(C)NC1=NC(=O)N([C@@H]2O[C@H](COP(=O)(O)OP(=O)(O[C@H]3O[C@H](CO)[C@@H](O)[C@H](O[Si](C)(C)C)[C@H]3O)O[Si](C)(C)C)[C@@H](O)[C@H]2O)C=C14313.9Semi standard non polar33892256
CDP-glucose,3TMS,isomer #66C[Si](C)(C)NC1=NC(=O)N([C@@H]2O[C@H](COP(=O)(O[Si](C)(C)C)OP(=O)(O)O[C@H]3O[C@H](CO)[C@@H](O)[C@H](O[Si](C)(C)C)[C@H]3O)[C@@H](O)[C@H]2O)C=C14308.1Semi standard non polar33892256
CDP-glucose,3TMS,isomer #67C[Si](C)(C)O[C@H]1[C@H](O)[C@@H](CO)O[C@H](OP(=O)(O)OP(=O)(O)OC[C@H]2O[C@@H](N3C=CC(N([Si](C)(C)C)[Si](C)(C)C)=NC3=O)[C@H](O)[C@@H]2O)[C@@H]1O4247.9Semi standard non polar33892256
CDP-glucose,3TMS,isomer #68C[Si](C)(C)O[C@@H]1[C@@H](O)[C@H](O)[C@@H](CO)O[C@@H]1OP(=O)(O)OP(=O)(O)OC[C@H]1O[C@@H](N2C=CC(N)=NC2=O)[C@H](O[Si](C)(C)C)[C@@H]1O[Si](C)(C)C4139.1Semi standard non polar33892256
CDP-glucose,3TMS,isomer #69C[Si](C)(C)O[C@@H]1[C@@H](O)[C@H](O)[C@@H](CO)O[C@@H]1OP(=O)(O[Si](C)(C)C)OP(=O)(O)OC[C@H]1O[C@@H](N2C=CC(N)=NC2=O)[C@H](O[Si](C)(C)C)[C@@H]1O4164.6Semi standard non polar33892256
CDP-glucose,3TMS,isomer #7C[Si](C)(C)NC1=NC(=O)N([C@@H]2O[C@H](COP(=O)(O)OP(=O)(O)O[C@H]3O[C@H](CO[Si](C)(C)C)[C@@H](O)[C@H](O)[C@H]3O)[C@@H](O)[C@H]2O[Si](C)(C)C)C=C14279.5Semi standard non polar33892256
CDP-glucose,3TMS,isomer #70C[Si](C)(C)O[C@@H]1[C@@H](O)[C@H](O)[C@@H](CO)O[C@@H]1OP(=O)(O)OP(=O)(OC[C@H]1O[C@@H](N2C=CC(N)=NC2=O)[C@H](O[Si](C)(C)C)[C@@H]1O)O[Si](C)(C)C4152.6Semi standard non polar33892256
CDP-glucose,3TMS,isomer #71C[Si](C)(C)NC1=NC(=O)N([C@@H]2O[C@H](COP(=O)(O)OP(=O)(O)O[C@H]3O[C@H](CO)[C@@H](O)[C@H](O)[C@H]3O[Si](C)(C)C)[C@@H](O)[C@H]2O[Si](C)(C)C)C=C14274.6Semi standard non polar33892256
CDP-glucose,3TMS,isomer #72C[Si](C)(C)O[C@@H]1[C@@H](COP(=O)(O[Si](C)(C)C)OP(=O)(O)O[C@H]2O[C@H](CO)[C@@H](O)[C@H](O)[C@H]2O[Si](C)(C)C)O[C@@H](N2C=CC(N)=NC2=O)[C@@H]1O4161.8Semi standard non polar33892256
CDP-glucose,3TMS,isomer #73C[Si](C)(C)O[C@@H]1[C@@H](COP(=O)(O)OP(=O)(O[C@H]2O[C@H](CO)[C@@H](O)[C@H](O)[C@H]2O[Si](C)(C)C)O[Si](C)(C)C)O[C@@H](N2C=CC(N)=NC2=O)[C@@H]1O4171.5Semi standard non polar33892256
CDP-glucose,3TMS,isomer #74C[Si](C)(C)NC1=NC(=O)N([C@@H]2O[C@H](COP(=O)(O)OP(=O)(O)O[C@H]3O[C@H](CO)[C@@H](O)[C@H](O)[C@H]3O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@H]2O)C=C14282.1Semi standard non polar33892256
CDP-glucose,3TMS,isomer #75C[Si](C)(C)O[C@@H]1[C@@H](O)[C@H](O)[C@@H](CO)O[C@@H]1OP(=O)(O[Si](C)(C)C)OP(=O)(OC[C@H]1O[C@@H](N2C=CC(N)=NC2=O)[C@H](O)[C@@H]1O)O[Si](C)(C)C4199.5Semi standard non polar33892256
CDP-glucose,3TMS,isomer #76C[Si](C)(C)NC1=NC(=O)N([C@@H]2O[C@H](COP(=O)(O)OP(=O)(O[C@H]3O[C@H](CO)[C@@H](O)[C@H](O)[C@H]3O[Si](C)(C)C)O[Si](C)(C)C)[C@@H](O)[C@H]2O)C=C14332.1Semi standard non polar33892256
CDP-glucose,3TMS,isomer #77C[Si](C)(C)NC1=NC(=O)N([C@@H]2O[C@H](COP(=O)(O[Si](C)(C)C)OP(=O)(O)O[C@H]3O[C@H](CO)[C@@H](O)[C@H](O)[C@H]3O[Si](C)(C)C)[C@@H](O)[C@H]2O)C=C14324.1Semi standard non polar33892256
CDP-glucose,3TMS,isomer #78C[Si](C)(C)O[C@@H]1[C@@H](O)[C@H](O)[C@@H](CO)O[C@@H]1OP(=O)(O)OP(=O)(O)OC[C@H]1O[C@@H](N2C=CC(N([Si](C)(C)C)[Si](C)(C)C)=NC2=O)[C@H](O)[C@@H]1O4280.5Semi standard non polar33892256
CDP-glucose,3TMS,isomer #79C[Si](C)(C)O[C@@H]1[C@@H](COP(=O)(O[Si](C)(C)C)OP(=O)(O)O[C@H]2O[C@H](CO)[C@@H](O)[C@H](O)[C@H]2O)O[C@@H](N2C=CC(N)=NC2=O)[C@@H]1O[Si](C)(C)C4190.3Semi standard non polar33892256
CDP-glucose,3TMS,isomer #8C[Si](C)(C)OC[C@H]1O[C@H](OP(=O)(O)OP(=O)(O)OC[C@H]2O[C@@H](N3C=CC(N)=NC3=O)[C@H](O)[C@@H]2O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@@H](O)[C@@H]1O4145.5Semi standard non polar33892256
CDP-glucose,3TMS,isomer #80C[Si](C)(C)O[C@@H]1[C@@H](COP(=O)(O)OP(=O)(O[C@H]2O[C@H](CO)[C@@H](O)[C@H](O)[C@H]2O)O[Si](C)(C)C)O[C@@H](N2C=CC(N)=NC2=O)[C@@H]1O[Si](C)(C)C4196.0Semi standard non polar33892256
CDP-glucose,3TMS,isomer #81C[Si](C)(C)NC1=NC(=O)N([C@@H]2O[C@H](COP(=O)(O)OP(=O)(O)O[C@H]3O[C@H](CO)[C@@H](O)[C@H](O)[C@H]3O)[C@@H](O[Si](C)(C)C)[C@H]2O[Si](C)(C)C)C=C14304.2Semi standard non polar33892256
CDP-glucose,3TMS,isomer #82C[Si](C)(C)O[C@@H]1[C@@H](COP(=O)(O[Si](C)(C)C)OP(=O)(O[C@H]2O[C@H](CO)[C@@H](O)[C@H](O)[C@H]2O)O[Si](C)(C)C)O[C@@H](N2C=CC(N)=NC2=O)[C@@H]1O4221.6Semi standard non polar33892256
CDP-glucose,3TMS,isomer #83C[Si](C)(C)NC1=NC(=O)N([C@@H]2O[C@H](COP(=O)(O[Si](C)(C)C)OP(=O)(O)O[C@H]3O[C@H](CO)[C@@H](O)[C@H](O)[C@H]3O)[C@@H](O[Si](C)(C)C)[C@H]2O)C=C14336.8Semi standard non polar33892256
CDP-glucose,3TMS,isomer #84C[Si](C)(C)NC1=NC(=O)N([C@@H]2O[C@H](COP(=O)(O)OP(=O)(O[C@H]3O[C@H](CO)[C@@H](O)[C@H](O)[C@H]3O)O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@H]2O)C=C14338.9Semi standard non polar33892256
CDP-glucose,3TMS,isomer #85C[Si](C)(C)O[C@@H]1[C@@H](COP(=O)(O)OP(=O)(O)O[C@H]2O[C@H](CO)[C@@H](O)[C@H](O)[C@H]2O)O[C@@H](N2C=CC(N([Si](C)(C)C)[Si](C)(C)C)=NC2=O)[C@@H]1O4290.6Semi standard non polar33892256
CDP-glucose,3TMS,isomer #86C[Si](C)(C)O[C@@H]1[C@H](O)[C@@H](COP(=O)(O[Si](C)(C)C)OP(=O)(O[C@H]2O[C@H](CO)[C@@H](O)[C@H](O)[C@H]2O)O[Si](C)(C)C)O[C@H]1N1C=CC(N)=NC1=O4211.0Semi standard non polar33892256
CDP-glucose,3TMS,isomer #87C[Si](C)(C)NC1=NC(=O)N([C@@H]2O[C@H](COP(=O)(O[Si](C)(C)C)OP(=O)(O)O[C@H]3O[C@H](CO)[C@@H](O)[C@H](O)[C@H]3O)[C@@H](O)[C@H]2O[Si](C)(C)C)C=C14329.0Semi standard non polar33892256
CDP-glucose,3TMS,isomer #88C[Si](C)(C)NC1=NC(=O)N([C@@H]2O[C@H](COP(=O)(O)OP(=O)(O[C@H]3O[C@H](CO)[C@@H](O)[C@H](O)[C@H]3O)O[Si](C)(C)C)[C@@H](O)[C@H]2O[Si](C)(C)C)C=C14332.2Semi standard non polar33892256
CDP-glucose,3TMS,isomer #89C[Si](C)(C)O[C@@H]1[C@H](O)[C@@H](COP(=O)(O)OP(=O)(O)O[C@H]2O[C@H](CO)[C@@H](O)[C@H](O)[C@H]2O)O[C@H]1N1C=CC(N([Si](C)(C)C)[Si](C)(C)C)=NC1=O4294.2Semi standard non polar33892256
CDP-glucose,3TMS,isomer #9C[Si](C)(C)OC[C@H]1O[C@H](OP(=O)(O)OP(=O)(O)OC[C@H]2O[C@@H](N3C=CC(N)=NC3=O)[C@H](O)[C@@H]2O[Si](C)(C)C)[C@H](O)[C@@H](O[Si](C)(C)C)[C@@H]1O4114.5Semi standard non polar33892256
CDP-glucose,3TMS,isomer #90C[Si](C)(C)NC1=NC(=O)N([C@@H]2O[C@H](COP(=O)(O[Si](C)(C)C)OP(=O)(O[C@H]3O[C@H](CO)[C@@H](O)[C@H](O)[C@H]3O)O[Si](C)(C)C)[C@@H](O)[C@H]2O)C=C14373.1Semi standard non polar33892256
CDP-glucose,3TMS,isomer #91C[Si](C)(C)OP(=O)(OC[C@H]1O[C@@H](N2C=CC(N([Si](C)(C)C)[Si](C)(C)C)=NC2=O)[C@H](O)[C@@H]1O)OP(=O)(O)O[C@H]1O[C@H](CO)[C@@H](O)[C@H](O)[C@H]1O4350.4Semi standard non polar33892256
CDP-glucose,3TMS,isomer #92C[Si](C)(C)OP(=O)(O[C@H]1O[C@H](CO)[C@@H](O)[C@H](O)[C@H]1O)OP(=O)(O)OC[C@H]1O[C@@H](N2C=CC(N([Si](C)(C)C)[Si](C)(C)C)=NC2=O)[C@H](O)[C@@H]1O4359.0Semi standard non polar33892256
CDP-glucose,4TMS,isomer #1C[Si](C)(C)OC[C@H]1O[C@H](OP(=O)(O)OP(=O)(O)OC[C@H]2O[C@@H](N3C=CC(N)=NC3=O)[C@H](O[Si](C)(C)C)[C@@H]2O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@@H](O)[C@@H]1O4045.1Semi standard non polar33892256
CDP-glucose,4TMS,isomer #10C[Si](C)(C)OC[C@H]1O[C@H](OP(=O)(O)OP(=O)(OC[C@H]2O[C@@H](N3C=CC(N)=NC3=O)[C@H](O[Si](C)(C)C)[C@@H]2O)O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@@H](O)[C@@H]1O4044.5Semi standard non polar33892256
CDP-glucose,4TMS,isomer #100C[Si](C)(C)NC1=NC(=O)N([C@@H]2O[C@H](COP(=O)(O[Si](C)(C)C)OP(=O)(O)O[C@H]3O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]3O)[C@@H](O)[C@H]2O)C=C14181.8Semi standard non polar33892256
CDP-glucose,4TMS,isomer #101C[Si](C)(C)O[C@@H]1[C@@H](CO)O[C@H](OP(=O)(O)OP(=O)(O)OC[C@H]2O[C@@H](N3C=CC(N([Si](C)(C)C)[Si](C)(C)C)=NC3=O)[C@H](O)[C@@H]2O)[C@H](O)[C@H]1O[Si](C)(C)C4125.5Semi standard non polar33892256
CDP-glucose,4TMS,isomer #102C[Si](C)(C)NC1=NC(=O)N([C@@H]2O[C@H](COP(=O)(O[Si](C)(C)C)OP(=O)(O[C@H]3O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@H](O)[C@H]3O)O[Si](C)(C)C)[C@@H](O)[C@H]2O)C=C14237.9Semi standard non polar33892256
CDP-glucose,4TMS,isomer #103C[Si](C)(C)O[C@@H]1[C@@H](CO)O[C@H](OP(=O)(O[Si](C)(C)C)OP(=O)(O)OC[C@H]2O[C@@H](N3C=CC(N([Si](C)(C)C)[Si](C)(C)C)=NC3=O)[C@H](O)[C@@H]2O)[C@H](O)[C@H]1O4181.0Semi standard non polar33892256
CDP-glucose,4TMS,isomer #104C[Si](C)(C)O[C@@H]1[C@@H](CO)O[C@H](OP(=O)(O)OP(=O)(OC[C@H]2O[C@@H](N3C=CC(N([Si](C)(C)C)[Si](C)(C)C)=NC3=O)[C@H](O)[C@@H]2O)O[Si](C)(C)C)[C@H](O)[C@H]1O4175.0Semi standard non polar33892256
CDP-glucose,4TMS,isomer #105C[Si](C)(C)O[C@H]1[C@H](O)[C@@H](CO)O[C@H](OP(=O)(O)OP(=O)(O)OC[C@H]2O[C@@H](N3C=CC(N)=NC3=O)[C@H](O[Si](C)(C)C)[C@@H]2O[Si](C)(C)C)[C@@H]1O[Si](C)(C)C4040.6Semi standard non polar33892256
CDP-glucose,4TMS,isomer #106C[Si](C)(C)O[C@H]1[C@H](O)[C@@H](CO)O[C@H](OP(=O)(O[Si](C)(C)C)OP(=O)(O)OC[C@H]2O[C@@H](N3C=CC(N)=NC3=O)[C@H](O[Si](C)(C)C)[C@@H]2O[Si](C)(C)C)[C@@H]1O4061.6Semi standard non polar33892256
CDP-glucose,4TMS,isomer #107C[Si](C)(C)O[C@H]1[C@H](O)[C@@H](CO)O[C@H](OP(=O)(O)OP(=O)(OC[C@H]2O[C@@H](N3C=CC(N)=NC3=O)[C@H](O[Si](C)(C)C)[C@@H]2O[Si](C)(C)C)O[Si](C)(C)C)[C@@H]1O4048.8Semi standard non polar33892256
CDP-glucose,4TMS,isomer #108C[Si](C)(C)NC1=NC(=O)N([C@@H]2O[C@H](COP(=O)(O)OP(=O)(O)O[C@H]3O[C@H](CO)[C@@H](O)[C@H](O[Si](C)(C)C)[C@H]3O)[C@@H](O[Si](C)(C)C)[C@H]2O[Si](C)(C)C)C=C14172.7Semi standard non polar33892256
CDP-glucose,4TMS,isomer #109C[Si](C)(C)O[C@H]1[C@H](O)[C@@H](CO)O[C@H](OP(=O)(O[Si](C)(C)C)OP(=O)(O)OC[C@H]2O[C@@H](N3C=CC(N)=NC3=O)[C@H](O[Si](C)(C)C)[C@@H]2O)[C@@H]1O[Si](C)(C)C4055.8Semi standard non polar33892256
CDP-glucose,4TMS,isomer #11C[Si](C)(C)NC1=NC(=O)N([C@@H]2O[C@H](COP(=O)(O)OP(=O)(O)O[C@H]3O[C@H](CO[Si](C)(C)C)[C@@H](O)[C@H](O)[C@H]3O[Si](C)(C)C)[C@@H](O)[C@H]2O[Si](C)(C)C)C=C14168.1Semi standard non polar33892256
CDP-glucose,4TMS,isomer #110C[Si](C)(C)O[C@H]1[C@H](O)[C@@H](CO)O[C@H](OP(=O)(O)OP(=O)(OC[C@H]2O[C@@H](N3C=CC(N)=NC3=O)[C@H](O[Si](C)(C)C)[C@@H]2O)O[Si](C)(C)C)[C@@H]1O[Si](C)(C)C4044.4Semi standard non polar33892256
CDP-glucose,4TMS,isomer #111C[Si](C)(C)NC1=NC(=O)N([C@@H]2O[C@H](COP(=O)(O)OP(=O)(O)O[C@H]3O[C@H](CO)[C@@H](O)[C@H](O[Si](C)(C)C)[C@H]3O[Si](C)(C)C)[C@@H](O)[C@H]2O[Si](C)(C)C)C=C14158.4Semi standard non polar33892256
CDP-glucose,4TMS,isomer #112C[Si](C)(C)O[C@H]1[C@H](O)[C@@H](CO)O[C@H](OP(=O)(O[Si](C)(C)C)OP(=O)(OC[C@H]2O[C@@H](N3C=CC(N)=NC3=O)[C@H](O[Si](C)(C)C)[C@@H]2O)O[Si](C)(C)C)[C@@H]1O4067.7Semi standard non polar33892256
CDP-glucose,4TMS,isomer #113C[Si](C)(C)NC1=NC(=O)N([C@@H]2O[C@H](COP(=O)(O)OP(=O)(O[C@H]3O[C@H](CO)[C@@H](O)[C@H](O[Si](C)(C)C)[C@H]3O)O[Si](C)(C)C)[C@@H](O)[C@H]2O[Si](C)(C)C)C=C14199.7Semi standard non polar33892256
CDP-glucose,4TMS,isomer #114C[Si](C)(C)NC1=NC(=O)N([C@@H]2O[C@H](COP(=O)(O[Si](C)(C)C)OP(=O)(O)O[C@H]3O[C@H](CO)[C@@H](O)[C@H](O[Si](C)(C)C)[C@H]3O)[C@@H](O)[C@H]2O[Si](C)(C)C)C=C14191.2Semi standard non polar33892256
CDP-glucose,4TMS,isomer #115C[Si](C)(C)O[C@H]1[C@H](O)[C@@H](CO)O[C@H](OP(=O)(O)OP(=O)(O)OC[C@H]2O[C@@H](N3C=CC(N([Si](C)(C)C)[Si](C)(C)C)=NC3=O)[C@H](O[Si](C)(C)C)[C@@H]2O)[C@@H]1O4139.3Semi standard non polar33892256
CDP-glucose,4TMS,isomer #116C[Si](C)(C)O[C@@H]1[C@@H](COP(=O)(O[Si](C)(C)C)OP(=O)(O)O[C@H]2O[C@H](CO)[C@@H](O)[C@H](O[Si](C)(C)C)[C@H]2O[Si](C)(C)C)O[C@@H](N2C=CC(N)=NC2=O)[C@@H]1O4059.0Semi standard non polar33892256
CDP-glucose,4TMS,isomer #117C[Si](C)(C)O[C@@H]1[C@@H](COP(=O)(O)OP(=O)(O[C@H]2O[C@H](CO)[C@@H](O)[C@H](O[Si](C)(C)C)[C@H]2O[Si](C)(C)C)O[Si](C)(C)C)O[C@@H](N2C=CC(N)=NC2=O)[C@@H]1O4067.7Semi standard non polar33892256
CDP-glucose,4TMS,isomer #118C[Si](C)(C)NC1=NC(=O)N([C@@H]2O[C@H](COP(=O)(O)OP(=O)(O)O[C@H]3O[C@H](CO)[C@@H](O)[C@H](O[Si](C)(C)C)[C@H]3O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@H]2O)C=C14163.8Semi standard non polar33892256
CDP-glucose,4TMS,isomer #119C[Si](C)(C)O[C@H]1[C@H](O)[C@@H](CO)O[C@H](OP(=O)(O[Si](C)(C)C)OP(=O)(OC[C@H]2O[C@@H](N3C=CC(N)=NC3=O)[C@H](O)[C@@H]2O[Si](C)(C)C)O[Si](C)(C)C)[C@@H]1O4084.0Semi standard non polar33892256
CDP-glucose,4TMS,isomer #12C[Si](C)(C)OC[C@H]1O[C@H](OP(=O)(O)OP(=O)(O)OC[C@H]2O[C@@H](N3C=CC(N)=NC3=O)[C@H](O[Si](C)(C)C)[C@@H]2O)[C@H](O)[C@@H](O[Si](C)(C)C)[C@@H]1O[Si](C)(C)C4036.9Semi standard non polar33892256
CDP-glucose,4TMS,isomer #120C[Si](C)(C)NC1=NC(=O)N([C@@H]2O[C@H](COP(=O)(O)OP(=O)(O[C@H]3O[C@H](CO)[C@@H](O)[C@H](O[Si](C)(C)C)[C@H]3O)O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@H]2O)C=C14205.2Semi standard non polar33892256
CDP-glucose,4TMS,isomer #121C[Si](C)(C)NC1=NC(=O)N([C@@H]2O[C@H](COP(=O)(O[Si](C)(C)C)OP(=O)(O)O[C@H]3O[C@H](CO)[C@@H](O)[C@H](O[Si](C)(C)C)[C@H]3O)[C@@H](O[Si](C)(C)C)[C@H]2O)C=C14198.5Semi standard non polar33892256
CDP-glucose,4TMS,isomer #122C[Si](C)(C)O[C@H]1[C@H](O)[C@@H](CO)O[C@H](OP(=O)(O)OP(=O)(O)OC[C@H]2O[C@@H](N3C=CC(N([Si](C)(C)C)[Si](C)(C)C)=NC3=O)[C@H](O)[C@@H]2O[Si](C)(C)C)[C@@H]1O4136.6Semi standard non polar33892256
CDP-glucose,4TMS,isomer #123C[Si](C)(C)O[C@H]1[C@H](O)[C@@H](CO)O[C@H](OP(=O)(O[Si](C)(C)C)OP(=O)(OC[C@H]2O[C@@H](N3C=CC(N)=NC3=O)[C@H](O)[C@@H]2O)O[Si](C)(C)C)[C@@H]1O[Si](C)(C)C4072.9Semi standard non polar33892256
CDP-glucose,4TMS,isomer #124C[Si](C)(C)NC1=NC(=O)N([C@@H]2O[C@H](COP(=O)(O)OP(=O)(O[C@H]3O[C@H](CO)[C@@H](O)[C@H](O[Si](C)(C)C)[C@H]3O[Si](C)(C)C)O[Si](C)(C)C)[C@@H](O)[C@H]2O)C=C14198.3Semi standard non polar33892256
CDP-glucose,4TMS,isomer #125C[Si](C)(C)NC1=NC(=O)N([C@@H]2O[C@H](COP(=O)(O[Si](C)(C)C)OP(=O)(O)O[C@H]3O[C@H](CO)[C@@H](O)[C@H](O[Si](C)(C)C)[C@H]3O[Si](C)(C)C)[C@@H](O)[C@H]2O)C=C14189.1Semi standard non polar33892256
CDP-glucose,4TMS,isomer #126C[Si](C)(C)O[C@H]1[C@H](O)[C@@H](CO)O[C@H](OP(=O)(O)OP(=O)(O)OC[C@H]2O[C@@H](N3C=CC(N([Si](C)(C)C)[Si](C)(C)C)=NC3=O)[C@H](O)[C@@H]2O)[C@@H]1O[Si](C)(C)C4135.8Semi standard non polar33892256
CDP-glucose,4TMS,isomer #127C[Si](C)(C)NC1=NC(=O)N([C@@H]2O[C@H](COP(=O)(O[Si](C)(C)C)OP(=O)(O[C@H]3O[C@H](CO)[C@@H](O)[C@H](O[Si](C)(C)C)[C@H]3O)O[Si](C)(C)C)[C@@H](O)[C@H]2O)C=C14233.7Semi standard non polar33892256
CDP-glucose,4TMS,isomer #128C[Si](C)(C)O[C@H]1[C@H](O)[C@@H](CO)O[C@H](OP(=O)(O[Si](C)(C)C)OP(=O)(O)OC[C@H]2O[C@@H](N3C=CC(N([Si](C)(C)C)[Si](C)(C)C)=NC3=O)[C@H](O)[C@@H]2O)[C@@H]1O4173.5Semi standard non polar33892256
CDP-glucose,4TMS,isomer #129C[Si](C)(C)O[C@H]1[C@H](O)[C@@H](CO)O[C@H](OP(=O)(O)OP(=O)(OC[C@H]2O[C@@H](N3C=CC(N([Si](C)(C)C)[Si](C)(C)C)=NC3=O)[C@H](O)[C@@H]2O)O[Si](C)(C)C)[C@@H]1O4162.4Semi standard non polar33892256
CDP-glucose,4TMS,isomer #13C[Si](C)(C)OC[C@H]1O[C@H](OP(=O)(O[Si](C)(C)C)OP(=O)(O)OC[C@H]2O[C@@H](N3C=CC(N)=NC3=O)[C@H](O[Si](C)(C)C)[C@@H]2O)[C@H](O)[C@@H](O[Si](C)(C)C)[C@@H]1O4049.8Semi standard non polar33892256
CDP-glucose,4TMS,isomer #130C[Si](C)(C)O[C@@H]1[C@@H](O)[C@H](O)[C@@H](CO)O[C@@H]1OP(=O)(O[Si](C)(C)C)OP(=O)(O)OC[C@H]1O[C@@H](N2C=CC(N)=NC2=O)[C@H](O[Si](C)(C)C)[C@@H]1O[Si](C)(C)C4069.6Semi standard non polar33892256
CDP-glucose,4TMS,isomer #131C[Si](C)(C)O[C@@H]1[C@@H](O)[C@H](O)[C@@H](CO)O[C@@H]1OP(=O)(O)OP(=O)(OC[C@H]1O[C@@H](N2C=CC(N)=NC2=O)[C@H](O[Si](C)(C)C)[C@@H]1O[Si](C)(C)C)O[Si](C)(C)C4056.8Semi standard non polar33892256
CDP-glucose,4TMS,isomer #132C[Si](C)(C)NC1=NC(=O)N([C@@H]2O[C@H](COP(=O)(O)OP(=O)(O)O[C@H]3O[C@H](CO)[C@@H](O)[C@H](O)[C@H]3O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@H]2O[Si](C)(C)C)C=C14179.2Semi standard non polar33892256
CDP-glucose,4TMS,isomer #133C[Si](C)(C)O[C@@H]1[C@@H](O)[C@H](O)[C@@H](CO)O[C@@H]1OP(=O)(O[Si](C)(C)C)OP(=O)(OC[C@H]1O[C@@H](N2C=CC(N)=NC2=O)[C@H](O[Si](C)(C)C)[C@@H]1O)O[Si](C)(C)C4070.4Semi standard non polar33892256
CDP-glucose,4TMS,isomer #134C[Si](C)(C)NC1=NC(=O)N([C@@H]2O[C@H](COP(=O)(O)OP(=O)(O[C@H]3O[C@H](CO)[C@@H](O)[C@H](O)[C@H]3O[Si](C)(C)C)O[Si](C)(C)C)[C@@H](O)[C@H]2O[Si](C)(C)C)C=C14205.0Semi standard non polar33892256
CDP-glucose,4TMS,isomer #135C[Si](C)(C)NC1=NC(=O)N([C@@H]2O[C@H](COP(=O)(O[Si](C)(C)C)OP(=O)(O)O[C@H]3O[C@H](CO)[C@@H](O)[C@H](O)[C@H]3O[Si](C)(C)C)[C@@H](O)[C@H]2O[Si](C)(C)C)C=C14195.8Semi standard non polar33892256
CDP-glucose,4TMS,isomer #136C[Si](C)(C)O[C@@H]1[C@@H](O)[C@H](O)[C@@H](CO)O[C@@H]1OP(=O)(O)OP(=O)(O)OC[C@H]1O[C@@H](N2C=CC(N([Si](C)(C)C)[Si](C)(C)C)=NC2=O)[C@H](O[Si](C)(C)C)[C@@H]1O4149.0Semi standard non polar33892256
CDP-glucose,4TMS,isomer #137C[Si](C)(C)O[C@@H]1[C@@H](COP(=O)(O[Si](C)(C)C)OP(=O)(O[C@H]2O[C@H](CO)[C@@H](O)[C@H](O)[C@H]2O[Si](C)(C)C)O[Si](C)(C)C)O[C@@H](N2C=CC(N)=NC2=O)[C@@H]1O4086.6Semi standard non polar33892256
CDP-glucose,4TMS,isomer #138C[Si](C)(C)NC1=NC(=O)N([C@@H]2O[C@H](COP(=O)(O[Si](C)(C)C)OP(=O)(O)O[C@H]3O[C@H](CO)[C@@H](O)[C@H](O)[C@H]3O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@H]2O)C=C14201.1Semi standard non polar33892256
CDP-glucose,4TMS,isomer #139C[Si](C)(C)NC1=NC(=O)N([C@@H]2O[C@H](COP(=O)(O)OP(=O)(O[C@H]3O[C@H](CO)[C@@H](O)[C@H](O)[C@H]3O[Si](C)(C)C)O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@H]2O)C=C14209.6Semi standard non polar33892256
CDP-glucose,4TMS,isomer #14C[Si](C)(C)OC[C@H]1O[C@H](OP(=O)(O)OP(=O)(OC[C@H]2O[C@@H](N3C=CC(N)=NC3=O)[C@H](O[Si](C)(C)C)[C@@H]2O)O[Si](C)(C)C)[C@H](O)[C@@H](O[Si](C)(C)C)[C@@H]1O4035.1Semi standard non polar33892256
CDP-glucose,4TMS,isomer #140C[Si](C)(C)O[C@@H]1[C@@H](COP(=O)(O)OP(=O)(O)O[C@H]2O[C@H](CO)[C@@H](O)[C@H](O)[C@H]2O[Si](C)(C)C)O[C@@H](N2C=CC(N([Si](C)(C)C)[Si](C)(C)C)=NC2=O)[C@@H]1O4144.0Semi standard non polar33892256
CDP-glucose,4TMS,isomer #141C[Si](C)(C)NC1=NC(=O)N([C@@H]2O[C@H](COP(=O)(O[Si](C)(C)C)OP(=O)(O[C@H]3O[C@H](CO)[C@@H](O)[C@H](O)[C@H]3O[Si](C)(C)C)O[Si](C)(C)C)[C@@H](O)[C@H]2O)C=C14237.6Semi standard non polar33892256
CDP-glucose,4TMS,isomer #142C[Si](C)(C)O[C@@H]1[C@@H](O)[C@H](O)[C@@H](CO)O[C@@H]1OP(=O)(O[Si](C)(C)C)OP(=O)(O)OC[C@H]1O[C@@H](N2C=CC(N([Si](C)(C)C)[Si](C)(C)C)=NC2=O)[C@H](O)[C@@H]1O4185.8Semi standard non polar33892256
CDP-glucose,4TMS,isomer #143C[Si](C)(C)O[C@@H]1[C@@H](O)[C@H](O)[C@@H](CO)O[C@@H]1OP(=O)(O)OP(=O)(OC[C@H]1O[C@@H](N2C=CC(N([Si](C)(C)C)[Si](C)(C)C)=NC2=O)[C@H](O)[C@@H]1O)O[Si](C)(C)C4175.2Semi standard non polar33892256
CDP-glucose,4TMS,isomer #144C[Si](C)(C)O[C@@H]1[C@@H](COP(=O)(O[Si](C)(C)C)OP(=O)(O[C@H]2O[C@H](CO)[C@@H](O)[C@H](O)[C@H]2O)O[Si](C)(C)C)O[C@@H](N2C=CC(N)=NC2=O)[C@@H]1O[Si](C)(C)C4093.1Semi standard non polar33892256
CDP-glucose,4TMS,isomer #145C[Si](C)(C)NC1=NC(=O)N([C@@H]2O[C@H](COP(=O)(O[Si](C)(C)C)OP(=O)(O)O[C@H]3O[C@H](CO)[C@@H](O)[C@H](O)[C@H]3O)[C@@H](O[Si](C)(C)C)[C@H]2O[Si](C)(C)C)C=C14220.2Semi standard non polar33892256
CDP-glucose,4TMS,isomer #146C[Si](C)(C)NC1=NC(=O)N([C@@H]2O[C@H](COP(=O)(O)OP(=O)(O[C@H]3O[C@H](CO)[C@@H](O)[C@H](O)[C@H]3O)O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@H]2O[Si](C)(C)C)C=C14224.8Semi standard non polar33892256
CDP-glucose,4TMS,isomer #147C[Si](C)(C)O[C@@H]1[C@@H](COP(=O)(O)OP(=O)(O)O[C@H]2O[C@H](CO)[C@@H](O)[C@H](O)[C@H]2O)O[C@@H](N2C=CC(N([Si](C)(C)C)[Si](C)(C)C)=NC2=O)[C@@H]1O[Si](C)(C)C4181.5Semi standard non polar33892256
CDP-glucose,4TMS,isomer #148C[Si](C)(C)NC1=NC(=O)N([C@@H]2O[C@H](COP(=O)(O[Si](C)(C)C)OP(=O)(O[C@H]3O[C@H](CO)[C@@H](O)[C@H](O)[C@H]3O)O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@H]2O)C=C14247.5Semi standard non polar33892256
CDP-glucose,4TMS,isomer #149C[Si](C)(C)O[C@@H]1[C@@H](COP(=O)(O[Si](C)(C)C)OP(=O)(O)O[C@H]2O[C@H](CO)[C@@H](O)[C@H](O)[C@H]2O)O[C@@H](N2C=CC(N([Si](C)(C)C)[Si](C)(C)C)=NC2=O)[C@@H]1O4197.3Semi standard non polar33892256
CDP-glucose,4TMS,isomer #15C[Si](C)(C)NC1=NC(=O)N([C@@H]2O[C@H](COP(=O)(O)OP(=O)(O)O[C@H]3O[C@H](CO[Si](C)(C)C)[C@@H](O)[C@H](O[Si](C)(C)C)[C@H]3O)[C@@H](O)[C@H]2O[Si](C)(C)C)C=C14159.1Semi standard non polar33892256
CDP-glucose,4TMS,isomer #150C[Si](C)(C)O[C@@H]1[C@@H](COP(=O)(O)OP(=O)(O[C@H]2O[C@H](CO)[C@@H](O)[C@H](O)[C@H]2O)O[Si](C)(C)C)O[C@@H](N2C=CC(N([Si](C)(C)C)[Si](C)(C)C)=NC2=O)[C@@H]1O4198.5Semi standard non polar33892256
CDP-glucose,4TMS,isomer #151C[Si](C)(C)NC1=NC(=O)N([C@@H]2O[C@H](COP(=O)(O[Si](C)(C)C)OP(=O)(O[C@H]3O[C@H](CO)[C@@H](O)[C@H](O)[C@H]3O)O[Si](C)(C)C)[C@@H](O)[C@H]2O[Si](C)(C)C)C=C14243.2Semi standard non polar33892256
CDP-glucose,4TMS,isomer #152C[Si](C)(C)O[C@@H]1[C@H](O)[C@@H](COP(=O)(O[Si](C)(C)C)OP(=O)(O)O[C@H]2O[C@H](CO)[C@@H](O)[C@H](O)[C@H]2O)O[C@H]1N1C=CC(N([Si](C)(C)C)[Si](C)(C)C)=NC1=O4196.1Semi standard non polar33892256
CDP-glucose,4TMS,isomer #153C[Si](C)(C)O[C@@H]1[C@H](O)[C@@H](COP(=O)(O)OP(=O)(O[C@H]2O[C@H](CO)[C@@H](O)[C@H](O)[C@H]2O)O[Si](C)(C)C)O[C@H]1N1C=CC(N([Si](C)(C)C)[Si](C)(C)C)=NC1=O4201.8Semi standard non polar33892256
CDP-glucose,4TMS,isomer #154C[Si](C)(C)OP(=O)(OC[C@H]1O[C@@H](N2C=CC(N([Si](C)(C)C)[Si](C)(C)C)=NC2=O)[C@H](O)[C@@H]1O)OP(=O)(O[C@H]1O[C@H](CO)[C@@H](O)[C@H](O)[C@H]1O)O[Si](C)(C)C4226.7Semi standard non polar33892256
CDP-glucose,4TMS,isomer #16C[Si](C)(C)OC[C@H]1O[C@H](OP(=O)(O[Si](C)(C)C)OP(=O)(O)OC[C@H]2O[C@@H](N3C=CC(N)=NC3=O)[C@H](O[Si](C)(C)C)[C@@H]2O)[C@H](O)[C@@H](O)[C@@H]1O[Si](C)(C)C4056.6Semi standard non polar33892256
CDP-glucose,4TMS,isomer #17C[Si](C)(C)OC[C@H]1O[C@H](OP(=O)(O)OP(=O)(OC[C@H]2O[C@@H](N3C=CC(N)=NC3=O)[C@H](O[Si](C)(C)C)[C@@H]2O)O[Si](C)(C)C)[C@H](O)[C@@H](O)[C@@H]1O[Si](C)(C)C4046.5Semi standard non polar33892256
CDP-glucose,4TMS,isomer #18C[Si](C)(C)NC1=NC(=O)N([C@@H]2O[C@H](COP(=O)(O)OP(=O)(O)O[C@H]3O[C@H](CO[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@H](O)[C@H]3O)[C@@H](O)[C@H]2O[Si](C)(C)C)C=C14173.9Semi standard non polar33892256
CDP-glucose,4TMS,isomer #19C[Si](C)(C)OC[C@H]1O[C@H](OP(=O)(O[Si](C)(C)C)OP(=O)(OC[C@H]2O[C@@H](N3C=CC(N)=NC3=O)[C@H](O[Si](C)(C)C)[C@@H]2O)O[Si](C)(C)C)[C@H](O)[C@@H](O)[C@@H]1O4067.4Semi standard non polar33892256
CDP-glucose,4TMS,isomer #2C[Si](C)(C)OC[C@H]1O[C@H](OP(=O)(O)OP(=O)(O)OC[C@H]2O[C@@H](N3C=CC(N)=NC3=O)[C@H](O[Si](C)(C)C)[C@@H]2O[Si](C)(C)C)[C@H](O)[C@@H](O[Si](C)(C)C)[C@@H]1O4033.1Semi standard non polar33892256
CDP-glucose,4TMS,isomer #20C[Si](C)(C)NC1=NC(=O)N([C@@H]2O[C@H](COP(=O)(O)OP(=O)(O[C@H]3O[C@H](CO[Si](C)(C)C)[C@@H](O)[C@H](O)[C@H]3O)O[Si](C)(C)C)[C@@H](O)[C@H]2O[Si](C)(C)C)C=C14203.7Semi standard non polar33892256
CDP-glucose,4TMS,isomer #21C[Si](C)(C)NC1=NC(=O)N([C@@H]2O[C@H](COP(=O)(O[Si](C)(C)C)OP(=O)(O)O[C@H]3O[C@H](CO[Si](C)(C)C)[C@@H](O)[C@H](O)[C@H]3O)[C@@H](O)[C@H]2O[Si](C)(C)C)C=C14198.4Semi standard non polar33892256
CDP-glucose,4TMS,isomer #22C[Si](C)(C)OC[C@H]1O[C@H](OP(=O)(O)OP(=O)(O)OC[C@H]2O[C@@H](N3C=CC(N([Si](C)(C)C)[Si](C)(C)C)=NC3=O)[C@H](O[Si](C)(C)C)[C@@H]2O)[C@H](O)[C@@H](O)[C@@H]1O4159.3Semi standard non polar33892256
CDP-glucose,4TMS,isomer #23C[Si](C)(C)OC[C@H]1O[C@H](OP(=O)(O)OP(=O)(O)OC[C@H]2O[C@@H](N3C=CC(N)=NC3=O)[C@H](O)[C@@H]2O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@@H]1O4050.6Semi standard non polar33892256
CDP-glucose,4TMS,isomer #24C[Si](C)(C)OC[C@H]1O[C@H](OP(=O)(O)OP(=O)(O)OC[C@H]2O[C@@H](N3C=CC(N)=NC3=O)[C@H](O)[C@@H]2O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@@H](O)[C@@H]1O[Si](C)(C)C4047.2Semi standard non polar33892256
CDP-glucose,4TMS,isomer #25C[Si](C)(C)OC[C@H]1O[C@H](OP(=O)(O[Si](C)(C)C)OP(=O)(O)OC[C@H]2O[C@@H](N3C=CC(N)=NC3=O)[C@H](O)[C@@H]2O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@@H](O)[C@@H]1O4069.4Semi standard non polar33892256
CDP-glucose,4TMS,isomer #26C[Si](C)(C)OC[C@H]1O[C@H](OP(=O)(O)OP(=O)(OC[C@H]2O[C@@H](N3C=CC(N)=NC3=O)[C@H](O)[C@@H]2O[Si](C)(C)C)O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@@H](O)[C@@H]1O4057.5Semi standard non polar33892256
CDP-glucose,4TMS,isomer #27C[Si](C)(C)NC1=NC(=O)N([C@@H]2O[C@H](COP(=O)(O)OP(=O)(O)O[C@H]3O[C@H](CO[Si](C)(C)C)[C@@H](O)[C@H](O)[C@H]3O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@H]2O)C=C14171.8Semi standard non polar33892256
CDP-glucose,4TMS,isomer #28C[Si](C)(C)OC[C@H]1O[C@H](OP(=O)(O)OP(=O)(O)OC[C@H]2O[C@@H](N3C=CC(N)=NC3=O)[C@H](O)[C@@H]2O[Si](C)(C)C)[C@H](O)[C@@H](O[Si](C)(C)C)[C@@H]1O[Si](C)(C)C4044.3Semi standard non polar33892256
CDP-glucose,4TMS,isomer #29C[Si](C)(C)OC[C@H]1O[C@H](OP(=O)(O[Si](C)(C)C)OP(=O)(O)OC[C@H]2O[C@@H](N3C=CC(N)=NC3=O)[C@H](O)[C@@H]2O[Si](C)(C)C)[C@H](O)[C@@H](O[Si](C)(C)C)[C@@H]1O4061.0Semi standard non polar33892256
CDP-glucose,4TMS,isomer #3C[Si](C)(C)OC[C@H]1O[C@H](OP(=O)(O)OP(=O)(O)OC[C@H]2O[C@@H](N3C=CC(N)=NC3=O)[C@H](O[Si](C)(C)C)[C@@H]2O[Si](C)(C)C)[C@H](O)[C@@H](O)[C@@H]1O[Si](C)(C)C4043.2Semi standard non polar33892256
CDP-glucose,4TMS,isomer #30C[Si](C)(C)OC[C@H]1O[C@H](OP(=O)(O)OP(=O)(OC[C@H]2O[C@@H](N3C=CC(N)=NC3=O)[C@H](O)[C@@H]2O[Si](C)(C)C)O[Si](C)(C)C)[C@H](O)[C@@H](O[Si](C)(C)C)[C@@H]1O4049.9Semi standard non polar33892256
CDP-glucose,4TMS,isomer #31C[Si](C)(C)NC1=NC(=O)N([C@@H]2O[C@H](COP(=O)(O)OP(=O)(O)O[C@H]3O[C@H](CO[Si](C)(C)C)[C@@H](O)[C@H](O[Si](C)(C)C)[C@H]3O)[C@@H](O[Si](C)(C)C)[C@H]2O)C=C14165.2Semi standard non polar33892256
CDP-glucose,4TMS,isomer #32C[Si](C)(C)OC[C@H]1O[C@H](OP(=O)(O[Si](C)(C)C)OP(=O)(O)OC[C@H]2O[C@@H](N3C=CC(N)=NC3=O)[C@H](O)[C@@H]2O[Si](C)(C)C)[C@H](O)[C@@H](O)[C@@H]1O[Si](C)(C)C4068.9Semi standard non polar33892256
CDP-glucose,4TMS,isomer #33C[Si](C)(C)OC[C@H]1O[C@H](OP(=O)(O)OP(=O)(OC[C@H]2O[C@@H](N3C=CC(N)=NC3=O)[C@H](O)[C@@H]2O[Si](C)(C)C)O[Si](C)(C)C)[C@H](O)[C@@H](O)[C@@H]1O[Si](C)(C)C4060.9Semi standard non polar33892256
CDP-glucose,4TMS,isomer #34C[Si](C)(C)NC1=NC(=O)N([C@@H]2O[C@H](COP(=O)(O)OP(=O)(O)O[C@H]3O[C@H](CO[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@H](O)[C@H]3O)[C@@H](O[Si](C)(C)C)[C@H]2O)C=C14178.0Semi standard non polar33892256
CDP-glucose,4TMS,isomer #35C[Si](C)(C)OC[C@H]1O[C@H](OP(=O)(O[Si](C)(C)C)OP(=O)(OC[C@H]2O[C@@H](N3C=CC(N)=NC3=O)[C@H](O)[C@@H]2O[Si](C)(C)C)O[Si](C)(C)C)[C@H](O)[C@@H](O)[C@@H]1O4083.1Semi standard non polar33892256
CDP-glucose,4TMS,isomer #36C[Si](C)(C)NC1=NC(=O)N([C@@H]2O[C@H](COP(=O)(O)OP(=O)(O[C@H]3O[C@H](CO[Si](C)(C)C)[C@@H](O)[C@H](O)[C@H]3O)O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@H]2O)C=C14208.5Semi standard non polar33892256
CDP-glucose,4TMS,isomer #37C[Si](C)(C)NC1=NC(=O)N([C@@H]2O[C@H](COP(=O)(O[Si](C)(C)C)OP(=O)(O)O[C@H]3O[C@H](CO[Si](C)(C)C)[C@@H](O)[C@H](O)[C@H]3O)[C@@H](O[Si](C)(C)C)[C@H]2O)C=C14205.0Semi standard non polar33892256
CDP-glucose,4TMS,isomer #38C[Si](C)(C)OC[C@H]1O[C@H](OP(=O)(O)OP(=O)(O)OC[C@H]2O[C@@H](N3C=CC(N([Si](C)(C)C)[Si](C)(C)C)=NC3=O)[C@H](O)[C@@H]2O[Si](C)(C)C)[C@H](O)[C@@H](O)[C@@H]1O4157.6Semi standard non polar33892256
CDP-glucose,4TMS,isomer #39C[Si](C)(C)OC[C@H]1O[C@H](OP(=O)(O)OP(=O)(O)OC[C@H]2O[C@@H](N3C=CC(N)=NC3=O)[C@H](O)[C@@H]2O)[C@H](O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@@H]1O[Si](C)(C)C4068.4Semi standard non polar33892256
CDP-glucose,4TMS,isomer #4C[Si](C)(C)OC[C@H]1O[C@H](OP(=O)(O[Si](C)(C)C)OP(=O)(O)OC[C@H]2O[C@@H](N3C=CC(N)=NC3=O)[C@H](O[Si](C)(C)C)[C@@H]2O[Si](C)(C)C)[C@H](O)[C@@H](O)[C@@H]1O4069.7Semi standard non polar33892256
CDP-glucose,4TMS,isomer #40C[Si](C)(C)OC[C@H]1O[C@H](OP(=O)(O[Si](C)(C)C)OP(=O)(O)OC[C@H]2O[C@@H](N3C=CC(N)=NC3=O)[C@H](O)[C@@H]2O)[C@H](O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@@H]1O4066.0Semi standard non polar33892256
CDP-glucose,4TMS,isomer #41C[Si](C)(C)OC[C@H]1O[C@H](OP(=O)(O)OP(=O)(OC[C@H]2O[C@@H](N3C=CC(N)=NC3=O)[C@H](O)[C@@H]2O)O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@@H]1O4055.1Semi standard non polar33892256
CDP-glucose,4TMS,isomer #42C[Si](C)(C)NC1=NC(=O)N([C@@H]2O[C@H](COP(=O)(O)OP(=O)(O)O[C@H]3O[C@H](CO[Si](C)(C)C)[C@@H](O)[C@H](O[Si](C)(C)C)[C@H]3O[Si](C)(C)C)[C@@H](O)[C@H]2O)C=C14176.5Semi standard non polar33892256
CDP-glucose,4TMS,isomer #43C[Si](C)(C)OC[C@H]1O[C@H](OP(=O)(O[Si](C)(C)C)OP(=O)(O)OC[C@H]2O[C@@H](N3C=CC(N)=NC3=O)[C@H](O)[C@@H]2O)[C@H](O[Si](C)(C)C)[C@@H](O)[C@@H]1O[Si](C)(C)C4064.7Semi standard non polar33892256
CDP-glucose,4TMS,isomer #44C[Si](C)(C)OC[C@H]1O[C@H](OP(=O)(O)OP(=O)(OC[C@H]2O[C@@H](N3C=CC(N)=NC3=O)[C@H](O)[C@@H]2O)O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@@H](O)[C@@H]1O[Si](C)(C)C4051.2Semi standard non polar33892256
CDP-glucose,4TMS,isomer #45C[Si](C)(C)NC1=NC(=O)N([C@@H]2O[C@H](COP(=O)(O)OP(=O)(O)O[C@H]3O[C@H](CO[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@H](O)[C@H]3O[Si](C)(C)C)[C@@H](O)[C@H]2O)C=C14177.1Semi standard non polar33892256
CDP-glucose,4TMS,isomer #46C[Si](C)(C)OC[C@H]1O[C@H](OP(=O)(O[Si](C)(C)C)OP(=O)(OC[C@H]2O[C@@H](N3C=CC(N)=NC3=O)[C@H](O)[C@@H]2O)O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@@H](O)[C@@H]1O4068.0Semi standard non polar33892256
CDP-glucose,4TMS,isomer #47C[Si](C)(C)NC1=NC(=O)N([C@@H]2O[C@H](COP(=O)(O)OP(=O)(O[C@H]3O[C@H](CO[Si](C)(C)C)[C@@H](O)[C@H](O)[C@H]3O[Si](C)(C)C)O[Si](C)(C)C)[C@@H](O)[C@H]2O)C=C14213.4Semi standard non polar33892256
CDP-glucose,4TMS,isomer #48C[Si](C)(C)NC1=NC(=O)N([C@@H]2O[C@H](COP(=O)(O[Si](C)(C)C)OP(=O)(O)O[C@H]3O[C@H](CO[Si](C)(C)C)[C@@H](O)[C@H](O)[C@H]3O[Si](C)(C)C)[C@@H](O)[C@H]2O)C=C14203.1Semi standard non polar33892256
CDP-glucose,4TMS,isomer #49C[Si](C)(C)OC[C@H]1O[C@H](OP(=O)(O)OP(=O)(O)OC[C@H]2O[C@@H](N3C=CC(N([Si](C)(C)C)[Si](C)(C)C)=NC3=O)[C@H](O)[C@@H]2O)[C@H](O[Si](C)(C)C)[C@@H](O)[C@@H]1O4152.8Semi standard non polar33892256
CDP-glucose,4TMS,isomer #5C[Si](C)(C)OC[C@H]1O[C@H](OP(=O)(O)OP(=O)(OC[C@H]2O[C@@H](N3C=CC(N)=NC3=O)[C@H](O[Si](C)(C)C)[C@@H]2O[Si](C)(C)C)O[Si](C)(C)C)[C@H](O)[C@@H](O)[C@@H]1O4057.8Semi standard non polar33892256
CDP-glucose,4TMS,isomer #50C[Si](C)(C)OC[C@H]1O[C@H](OP(=O)(O[Si](C)(C)C)OP(=O)(O)OC[C@H]2O[C@@H](N3C=CC(N)=NC3=O)[C@H](O)[C@@H]2O)[C@H](O)[C@@H](O[Si](C)(C)C)[C@@H]1O[Si](C)(C)C4065.0Semi standard non polar33892256
CDP-glucose,4TMS,isomer #51C[Si](C)(C)OC[C@H]1O[C@H](OP(=O)(O)OP(=O)(OC[C@H]2O[C@@H](N3C=CC(N)=NC3=O)[C@H](O)[C@@H]2O)O[Si](C)(C)C)[C@H](O)[C@@H](O[Si](C)(C)C)[C@@H]1O[Si](C)(C)C4050.0Semi standard non polar33892256
CDP-glucose,4TMS,isomer #52C[Si](C)(C)NC1=NC(=O)N([C@@H]2O[C@H](COP(=O)(O)OP(=O)(O)O[C@H]3O[C@H](CO[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]3O)[C@@H](O)[C@H]2O)C=C14174.3Semi standard non polar33892256
CDP-glucose,4TMS,isomer #53C[Si](C)(C)OC[C@H]1O[C@H](OP(=O)(O[Si](C)(C)C)OP(=O)(OC[C@H]2O[C@@H](N3C=CC(N)=NC3=O)[C@H](O)[C@@H]2O)O[Si](C)(C)C)[C@H](O)[C@@H](O[Si](C)(C)C)[C@@H]1O4062.5Semi standard non polar33892256
CDP-glucose,4TMS,isomer #54C[Si](C)(C)NC1=NC(=O)N([C@@H]2O[C@H](COP(=O)(O)OP(=O)(O[C@H]3O[C@H](CO[Si](C)(C)C)[C@@H](O)[C@H](O[Si](C)(C)C)[C@H]3O)O[Si](C)(C)C)[C@@H](O)[C@H]2O)C=C14200.5Semi standard non polar33892256
CDP-glucose,4TMS,isomer #55C[Si](C)(C)NC1=NC(=O)N([C@@H]2O[C@H](COP(=O)(O[Si](C)(C)C)OP(=O)(O)O[C@H]3O[C@H](CO[Si](C)(C)C)[C@@H](O)[C@H](O[Si](C)(C)C)[C@H]3O)[C@@H](O)[C@H]2O)C=C14191.5Semi standard non polar33892256
CDP-glucose,4TMS,isomer #56C[Si](C)(C)OC[C@H]1O[C@H](OP(=O)(O)OP(=O)(O)OC[C@H]2O[C@@H](N3C=CC(N([Si](C)(C)C)[Si](C)(C)C)=NC3=O)[C@H](O)[C@@H]2O)[C@H](O)[C@@H](O[Si](C)(C)C)[C@@H]1O4135.8Semi standard non polar33892256
CDP-glucose,4TMS,isomer #57C[Si](C)(C)OC[C@H]1O[C@H](OP(=O)(O[Si](C)(C)C)OP(=O)(OC[C@H]2O[C@@H](N3C=CC(N)=NC3=O)[C@H](O)[C@@H]2O)O[Si](C)(C)C)[C@H](O)[C@@H](O)[C@@H]1O[Si](C)(C)C4072.0Semi standard non polar33892256
CDP-glucose,4TMS,isomer #58C[Si](C)(C)NC1=NC(=O)N([C@@H]2O[C@H](COP(=O)(O)OP(=O)(O[C@H]3O[C@H](CO[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@H](O)[C@H]3O)O[Si](C)(C)C)[C@@H](O)[C@H]2O)C=C14218.6Semi standard non polar33892256
CDP-glucose,4TMS,isomer #59C[Si](C)(C)NC1=NC(=O)N([C@@H]2O[C@H](COP(=O)(O[Si](C)(C)C)OP(=O)(O)O[C@H]3O[C@H](CO[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@H](O)[C@H]3O)[C@@H](O)[C@H]2O)C=C14213.9Semi standard non polar33892256
CDP-glucose,4TMS,isomer #6C[Si](C)(C)NC1=NC(=O)N([C@@H]2O[C@H](COP(=O)(O)OP(=O)(O)O[C@H]3O[C@H](CO[Si](C)(C)C)[C@@H](O)[C@H](O)[C@H]3O)[C@@H](O[Si](C)(C)C)[C@H]2O[Si](C)(C)C)C=C14179.2Semi standard non polar33892256
CDP-glucose,4TMS,isomer #60C[Si](C)(C)OC[C@H]1O[C@H](OP(=O)(O)OP(=O)(O)OC[C@H]2O[C@@H](N3C=CC(N([Si](C)(C)C)[Si](C)(C)C)=NC3=O)[C@H](O)[C@@H]2O)[C@H](O)[C@@H](O)[C@@H]1O[Si](C)(C)C4157.7Semi standard non polar33892256
CDP-glucose,4TMS,isomer #61C[Si](C)(C)NC1=NC(=O)N([C@@H]2O[C@H](COP(=O)(O[Si](C)(C)C)OP(=O)(O[C@H]3O[C@H](CO[Si](C)(C)C)[C@@H](O)[C@H](O)[C@H]3O)O[Si](C)(C)C)[C@@H](O)[C@H]2O)C=C14232.4Semi standard non polar33892256
CDP-glucose,4TMS,isomer #62C[Si](C)(C)OC[C@H]1O[C@H](OP(=O)(O[Si](C)(C)C)OP(=O)(O)OC[C@H]2O[C@@H](N3C=CC(N([Si](C)(C)C)[Si](C)(C)C)=NC3=O)[C@H](O)[C@@H]2O)[C@H](O)[C@@H](O)[C@@H]1O4194.4Semi standard non polar33892256
CDP-glucose,4TMS,isomer #63C[Si](C)(C)OC[C@H]1O[C@H](OP(=O)(O)OP(=O)(OC[C@H]2O[C@@H](N3C=CC(N([Si](C)(C)C)[Si](C)(C)C)=NC3=O)[C@H](O)[C@@H]2O)O[Si](C)(C)C)[C@H](O)[C@@H](O)[C@@H]1O4188.6Semi standard non polar33892256
CDP-glucose,4TMS,isomer #64C[Si](C)(C)O[C@H]1[C@H](O)[C@@H](O[Si](C)(C)C)[C@@H](OP(=O)(O)OP(=O)(O)OC[C@H]2O[C@@H](N3C=CC(N)=NC3=O)[C@H](O[Si](C)(C)C)[C@@H]2O[Si](C)(C)C)O[C@@H]1CO4028.9Semi standard non polar33892256
CDP-glucose,4TMS,isomer #65C[Si](C)(C)O[C@@H]1[C@@H](CO)O[C@H](OP(=O)(O)OP(=O)(O)OC[C@H]2O[C@@H](N3C=CC(N)=NC3=O)[C@H](O[Si](C)(C)C)[C@@H]2O[Si](C)(C)C)[C@H](O)[C@H]1O[Si](C)(C)C4027.2Semi standard non polar33892256
CDP-glucose,4TMS,isomer #66C[Si](C)(C)O[C@@H]1[C@@H](CO)O[C@H](OP(=O)(O[Si](C)(C)C)OP(=O)(O)OC[C@H]2O[C@@H](N3C=CC(N)=NC3=O)[C@H](O[Si](C)(C)C)[C@@H]2O[Si](C)(C)C)[C@H](O)[C@H]1O4063.4Semi standard non polar33892256
CDP-glucose,4TMS,isomer #67C[Si](C)(C)O[C@@H]1[C@@H](CO)O[C@H](OP(=O)(O)OP(=O)(OC[C@H]2O[C@@H](N3C=CC(N)=NC3=O)[C@H](O[Si](C)(C)C)[C@@H]2O[Si](C)(C)C)O[Si](C)(C)C)[C@H](O)[C@H]1O4054.0Semi standard non polar33892256
CDP-glucose,4TMS,isomer #68C[Si](C)(C)NC1=NC(=O)N([C@@H]2O[C@H](COP(=O)(O)OP(=O)(O)O[C@H]3O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@H](O)[C@H]3O)[C@@H](O[Si](C)(C)C)[C@H]2O[Si](C)(C)C)C=C14177.9Semi standard non polar33892256
CDP-glucose,4TMS,isomer #69C[Si](C)(C)O[C@H]1[C@H](O[Si](C)(C)C)[C@@H](CO)O[C@H](OP(=O)(O)OP(=O)(O)OC[C@H]2O[C@@H](N3C=CC(N)=NC3=O)[C@H](O[Si](C)(C)C)[C@@H]2O)[C@@H]1O[Si](C)(C)C4039.2Semi standard non polar33892256
CDP-glucose,4TMS,isomer #7C[Si](C)(C)OC[C@H]1O[C@H](OP(=O)(O)OP(=O)(O)OC[C@H]2O[C@@H](N3C=CC(N)=NC3=O)[C@H](O[Si](C)(C)C)[C@@H]2O)[C@H](O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@@H]1O4043.0Semi standard non polar33892256
CDP-glucose,4TMS,isomer #70C[Si](C)(C)O[C@H]1[C@H](O)[C@@H](O[Si](C)(C)C)[C@@H](OP(=O)(O[Si](C)(C)C)OP(=O)(O)OC[C@H]2O[C@@H](N3C=CC(N)=NC3=O)[C@H](O[Si](C)(C)C)[C@@H]2O)O[C@@H]1CO4047.7Semi standard non polar33892256
CDP-glucose,4TMS,isomer #71C[Si](C)(C)O[C@H]1[C@H](O)[C@@H](O[Si](C)(C)C)[C@@H](OP(=O)(O)OP(=O)(OC[C@H]2O[C@@H](N3C=CC(N)=NC3=O)[C@H](O[Si](C)(C)C)[C@@H]2O)O[Si](C)(C)C)O[C@@H]1CO4037.9Semi standard non polar33892256
CDP-glucose,4TMS,isomer #72C[Si](C)(C)NC1=NC(=O)N([C@@H]2O[C@H](COP(=O)(O)OP(=O)(O)O[C@H]3O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@H](O)[C@H]3O[Si](C)(C)C)[C@@H](O)[C@H]2O[Si](C)(C)C)C=C14154.6Semi standard non polar33892256
CDP-glucose,4TMS,isomer #73C[Si](C)(C)O[C@@H]1[C@@H](CO)O[C@H](OP(=O)(O[Si](C)(C)C)OP(=O)(O)OC[C@H]2O[C@@H](N3C=CC(N)=NC3=O)[C@H](O[Si](C)(C)C)[C@@H]2O)[C@H](O)[C@H]1O[Si](C)(C)C4049.9Semi standard non polar33892256
CDP-glucose,4TMS,isomer #74C[Si](C)(C)O[C@@H]1[C@@H](CO)O[C@H](OP(=O)(O)OP(=O)(OC[C@H]2O[C@@H](N3C=CC(N)=NC3=O)[C@H](O[Si](C)(C)C)[C@@H]2O)O[Si](C)(C)C)[C@H](O)[C@H]1O[Si](C)(C)C4035.2Semi standard non polar33892256
CDP-glucose,4TMS,isomer #75C[Si](C)(C)NC1=NC(=O)N([C@@H]2O[C@H](COP(=O)(O)OP(=O)(O)O[C@H]3O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]3O)[C@@H](O)[C@H]2O[Si](C)(C)C)C=C14151.3Semi standard non polar33892256
CDP-glucose,4TMS,isomer #76C[Si](C)(C)O[C@@H]1[C@@H](CO)O[C@H](OP(=O)(O[Si](C)(C)C)OP(=O)(OC[C@H]2O[C@@H](N3C=CC(N)=NC3=O)[C@H](O[Si](C)(C)C)[C@@H]2O)O[Si](C)(C)C)[C@H](O)[C@H]1O4069.8Semi standard non polar33892256
CDP-glucose,4TMS,isomer #77C[Si](C)(C)NC1=NC(=O)N([C@@H]2O[C@H](COP(=O)(O)OP(=O)(O[C@H]3O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@H](O)[C@H]3O)O[Si](C)(C)C)[C@@H](O)[C@H]2O[Si](C)(C)C)C=C14202.3Semi standard non polar33892256
CDP-glucose,4TMS,isomer #78C[Si](C)(C)NC1=NC(=O)N([C@@H]2O[C@H](COP(=O)(O[Si](C)(C)C)OP(=O)(O)O[C@H]3O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@H](O)[C@H]3O)[C@@H](O)[C@H]2O[Si](C)(C)C)C=C14197.2Semi standard non polar33892256
CDP-glucose,4TMS,isomer #79C[Si](C)(C)O[C@@H]1[C@@H](CO)O[C@H](OP(=O)(O)OP(=O)(O)OC[C@H]2O[C@@H](N3C=CC(N([Si](C)(C)C)[Si](C)(C)C)=NC3=O)[C@H](O[Si](C)(C)C)[C@@H]2O)[C@H](O)[C@H]1O4147.5Semi standard non polar33892256
CDP-glucose,4TMS,isomer #8C[Si](C)(C)OC[C@H]1O[C@H](OP(=O)(O)OP(=O)(O)OC[C@H]2O[C@@H](N3C=CC(N)=NC3=O)[C@H](O[Si](C)(C)C)[C@@H]2O)[C@H](O[Si](C)(C)C)[C@@H](O)[C@@H]1O[Si](C)(C)C4037.4Semi standard non polar33892256
CDP-glucose,4TMS,isomer #80C[Si](C)(C)O[C@@H]1[C@@H](COP(=O)(O)OP(=O)(O)O[C@H]2O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]2O[Si](C)(C)C)O[C@@H](N2C=CC(N)=NC2=O)[C@@H]1O4045.4Semi standard non polar33892256
CDP-glucose,4TMS,isomer #81C[Si](C)(C)O[C@H]1[C@H](O)[C@@H](O[Si](C)(C)C)[C@@H](OP(=O)(O[Si](C)(C)C)OP(=O)(O)OC[C@H]2O[C@@H](N3C=CC(N)=NC3=O)[C@H](O)[C@@H]2O[Si](C)(C)C)O[C@@H]1CO4060.5Semi standard non polar33892256
CDP-glucose,4TMS,isomer #82C[Si](C)(C)O[C@H]1[C@H](O)[C@@H](O[Si](C)(C)C)[C@@H](OP(=O)(O)OP(=O)(OC[C@H]2O[C@@H](N3C=CC(N)=NC3=O)[C@H](O)[C@@H]2O[Si](C)(C)C)O[Si](C)(C)C)O[C@@H]1CO4053.5Semi standard non polar33892256
CDP-glucose,4TMS,isomer #83C[Si](C)(C)NC1=NC(=O)N([C@@H]2O[C@H](COP(=O)(O)OP(=O)(O)O[C@H]3O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@H](O)[C@H]3O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@H]2O)C=C14159.6Semi standard non polar33892256
CDP-glucose,4TMS,isomer #84C[Si](C)(C)O[C@@H]1[C@@H](COP(=O)(O[Si](C)(C)C)OP(=O)(O)O[C@H]2O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]2O)O[C@@H](N2C=CC(N)=NC2=O)[C@@H]1O4050.0Semi standard non polar33892256
CDP-glucose,4TMS,isomer #85C[Si](C)(C)O[C@@H]1[C@@H](COP(=O)(O)OP(=O)(O[C@H]2O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]2O)O[Si](C)(C)C)O[C@@H](N2C=CC(N)=NC2=O)[C@@H]1O4061.2Semi standard non polar33892256
CDP-glucose,4TMS,isomer #86C[Si](C)(C)NC1=NC(=O)N([C@@H]2O[C@H](COP(=O)(O)OP(=O)(O)O[C@H]3O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]3O)[C@@H](O[Si](C)(C)C)[C@H]2O)C=C14156.4Semi standard non polar33892256
CDP-glucose,4TMS,isomer #87C[Si](C)(C)O[C@@H]1[C@@H](CO)O[C@H](OP(=O)(O[Si](C)(C)C)OP(=O)(OC[C@H]2O[C@@H](N3C=CC(N)=NC3=O)[C@H](O)[C@@H]2O[Si](C)(C)C)O[Si](C)(C)C)[C@H](O)[C@H]1O4086.7Semi standard non polar33892256
CDP-glucose,4TMS,isomer #88C[Si](C)(C)NC1=NC(=O)N([C@@H]2O[C@H](COP(=O)(O)OP(=O)(O[C@H]3O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@H](O)[C@H]3O)O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@H]2O)C=C14207.9Semi standard non polar33892256
CDP-glucose,4TMS,isomer #89C[Si](C)(C)NC1=NC(=O)N([C@@H]2O[C@H](COP(=O)(O[Si](C)(C)C)OP(=O)(O)O[C@H]3O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@H](O)[C@H]3O)[C@@H](O[Si](C)(C)C)[C@H]2O)C=C14202.9Semi standard non polar33892256
CDP-glucose,4TMS,isomer #9C[Si](C)(C)OC[C@H]1O[C@H](OP(=O)(O[Si](C)(C)C)OP(=O)(O)OC[C@H]2O[C@@H](N3C=CC(N)=NC3=O)[C@H](O[Si](C)(C)C)[C@@H]2O)[C@H](O[Si](C)(C)C)[C@@H](O)[C@@H]1O4057.9Semi standard non polar33892256
CDP-glucose,4TMS,isomer #90C[Si](C)(C)O[C@@H]1[C@@H](CO)O[C@H](OP(=O)(O)OP(=O)(O)OC[C@H]2O[C@@H](N3C=CC(N([Si](C)(C)C)[Si](C)(C)C)=NC3=O)[C@H](O)[C@@H]2O[Si](C)(C)C)[C@H](O)[C@H]1O4143.2Semi standard non polar33892256
CDP-glucose,4TMS,isomer #91C[Si](C)(C)O[C@H]1[C@H](O[Si](C)(C)C)[C@@H](CO)O[C@H](OP(=O)(O[Si](C)(C)C)OP(=O)(O)OC[C@H]2O[C@@H](N3C=CC(N)=NC3=O)[C@H](O)[C@@H]2O)[C@@H]1O[Si](C)(C)C4063.1Semi standard non polar33892256
CDP-glucose,4TMS,isomer #92C[Si](C)(C)O[C@H]1[C@H](O[Si](C)(C)C)[C@@H](CO)O[C@H](OP(=O)(O)OP(=O)(OC[C@H]2O[C@@H](N3C=CC(N)=NC3=O)[C@H](O)[C@@H]2O)O[Si](C)(C)C)[C@@H]1O[Si](C)(C)C4050.9Semi standard non polar33892256
CDP-glucose,4TMS,isomer #93C[Si](C)(C)NC1=NC(=O)N([C@@H]2O[C@H](COP(=O)(O)OP(=O)(O)O[C@H]3O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]3O[Si](C)(C)C)[C@@H](O)[C@H]2O)C=C14169.7Semi standard non polar33892256
CDP-glucose,4TMS,isomer #94C[Si](C)(C)O[C@H]1[C@H](O)[C@@H](O[Si](C)(C)C)[C@@H](OP(=O)(O[Si](C)(C)C)OP(=O)(OC[C@H]2O[C@@H](N3C=CC(N)=NC3=O)[C@H](O)[C@@H]2O)O[Si](C)(C)C)O[C@@H]1CO4064.8Semi standard non polar33892256
CDP-glucose,4TMS,isomer #95C[Si](C)(C)NC1=NC(=O)N([C@@H]2O[C@H](COP(=O)(O)OP(=O)(O[C@H]3O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@H](O)[C@H]3O[Si](C)(C)C)O[Si](C)(C)C)[C@@H](O)[C@H]2O)C=C14195.4Semi standard non polar33892256
CDP-glucose,4TMS,isomer #96C[Si](C)(C)NC1=NC(=O)N([C@@H]2O[C@H](COP(=O)(O[Si](C)(C)C)OP(=O)(O)O[C@H]3O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@H](O)[C@H]3O[Si](C)(C)C)[C@@H](O)[C@H]2O)C=C14186.2Semi standard non polar33892256
CDP-glucose,4TMS,isomer #97C[Si](C)(C)O[C@H]1[C@H](O)[C@@H](O[Si](C)(C)C)[C@@H](OP(=O)(O)OP(=O)(O)OC[C@H]2O[C@@H](N3C=CC(N([Si](C)(C)C)[Si](C)(C)C)=NC3=O)[C@H](O)[C@@H]2O)O[C@@H]1CO4130.5Semi standard non polar33892256
CDP-glucose,4TMS,isomer #98C[Si](C)(C)O[C@@H]1[C@@H](CO)O[C@H](OP(=O)(O[Si](C)(C)C)OP(=O)(OC[C@H]2O[C@@H](N3C=CC(N)=NC3=O)[C@H](O)[C@@H]2O)O[Si](C)(C)C)[C@H](O)[C@H]1O[Si](C)(C)C4067.9Semi standard non polar33892256
CDP-glucose,4TMS,isomer #99C[Si](C)(C)NC1=NC(=O)N([C@@H]2O[C@H](COP(=O)(O)OP(=O)(O[C@H]3O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]3O)O[Si](C)(C)C)[C@@H](O)[C@H]2O)C=C14191.3Semi standard non polar33892256
CDP-glucose,1TBDMS,isomer #1CC(C)(C)[Si](C)(C)OC[C@H]1O[C@H](OP(=O)(O)OP(=O)(O)OC[C@H]2O[C@@H](N3C=CC(N)=NC3=O)[C@H](O)[C@@H]2O)[C@H](O)[C@@H](O)[C@@H]1O4613.2Semi standard non polar33892256
CDP-glucose,1TBDMS,isomer #2CC(C)(C)[Si](C)(C)O[C@@H]1[C@@H](CO)O[C@H](OP(=O)(O)OP(=O)(O)OC[C@H]2O[C@@H](N3C=CC(N)=NC3=O)[C@H](O)[C@@H]2O)[C@H](O)[C@H]1O4589.8Semi standard non polar33892256
CDP-glucose,1TBDMS,isomer #3CC(C)(C)[Si](C)(C)O[C@H]1[C@H](O)[C@@H](CO)O[C@H](OP(=O)(O)OP(=O)(O)OC[C@H]2O[C@@H](N3C=CC(N)=NC3=O)[C@H](O)[C@@H]2O)[C@@H]1O4568.7Semi standard non polar33892256
CDP-glucose,1TBDMS,isomer #4CC(C)(C)[Si](C)(C)O[C@@H]1[C@@H](O)[C@H](O)[C@@H](CO)O[C@@H]1OP(=O)(O)OP(=O)(O)OC[C@H]1O[C@@H](N2C=CC(N)=NC2=O)[C@H](O)[C@@H]1O4590.3Semi standard non polar33892256
CDP-glucose,1TBDMS,isomer #5CC(C)(C)[Si](C)(C)O[C@@H]1[C@@H](COP(=O)(O)OP(=O)(O)O[C@H]2O[C@H](CO)[C@@H](O)[C@H](O)[C@H]2O)O[C@@H](N2C=CC(N)=NC2=O)[C@@H]1O4632.7Semi standard non polar33892256
CDP-glucose,1TBDMS,isomer #6CC(C)(C)[Si](C)(C)O[C@@H]1[C@H](O)[C@@H](COP(=O)(O)OP(=O)(O)O[C@H]2O[C@H](CO)[C@@H](O)[C@H](O)[C@H]2O)O[C@H]1N1C=CC(N)=NC1=O4629.3Semi standard non polar33892256
CDP-glucose,1TBDMS,isomer #7CC(C)(C)[Si](C)(C)OP(=O)(OC[C@H]1O[C@@H](N2C=CC(N)=NC2=O)[C@H](O)[C@@H]1O)OP(=O)(O)O[C@H]1O[C@H](CO)[C@@H](O)[C@H](O)[C@H]1O4685.0Semi standard non polar33892256
CDP-glucose,1TBDMS,isomer #8CC(C)(C)[Si](C)(C)OP(=O)(O[C@H]1O[C@H](CO)[C@@H](O)[C@H](O)[C@H]1O)OP(=O)(O)OC[C@H]1O[C@@H](N2C=CC(N)=NC2=O)[C@H](O)[C@@H]1O4694.2Semi standard non polar33892256
CDP-glucose,1TBDMS,isomer #9CC(C)(C)[Si](C)(C)NC1=NC(=O)N([C@@H]2O[C@H](COP(=O)(O)OP(=O)(O)O[C@H]3O[C@H](CO)[C@@H](O)[C@H](O)[C@H]3O)[C@@H](O)[C@H]2O)C=C14767.2Semi standard non polar33892256
CDP-glucose,2TBDMS,isomer #1CC(C)(C)[Si](C)(C)OC[C@H]1O[C@H](OP(=O)(O)OP(=O)(O)OC[C@H]2O[C@@H](N3C=CC(N)=NC3=O)[C@H](O[Si](C)(C)C(C)(C)C)[C@@H]2O)[C@H](O)[C@@H](O)[C@@H]1O4656.2Semi standard non polar33892256
CDP-glucose,2TBDMS,isomer #10CC(C)(C)[Si](C)(C)O[C@@H]1[C@@H](CO)O[C@H](OP(=O)(O)OP(=O)(O)OC[C@H]2O[C@@H](N3C=CC(N)=NC3=O)[C@H](O)[C@@H]2O[Si](C)(C)C(C)(C)C)[C@H](O)[C@H]1O4635.6Semi standard non polar33892256
CDP-glucose,2TBDMS,isomer #11CC(C)(C)[Si](C)(C)O[C@H]1[C@H](O)[C@@H](O[Si](C)(C)C(C)(C)C)[C@@H](OP(=O)(O)OP(=O)(O)OC[C@H]2O[C@@H](N3C=CC(N)=NC3=O)[C@H](O)[C@@H]2O)O[C@@H]1CO4590.7Semi standard non polar33892256
CDP-glucose,2TBDMS,isomer #12CC(C)(C)[Si](C)(C)O[C@@H]1[C@@H](CO)O[C@H](OP(=O)(O)OP(=O)(O)OC[C@H]2O[C@@H](N3C=CC(N)=NC3=O)[C@H](O)[C@@H]2O)[C@H](O)[C@H]1O[Si](C)(C)C(C)(C)C4580.5Semi standard non polar33892256
CDP-glucose,2TBDMS,isomer #13CC(C)(C)[Si](C)(C)O[C@@H]1[C@@H](CO)O[C@H](OP(=O)(O[Si](C)(C)C(C)(C)C)OP(=O)(O)OC[C@H]2O[C@@H](N3C=CC(N)=NC3=O)[C@H](O)[C@@H]2O)[C@H](O)[C@H]1O4669.4Semi standard non polar33892256
CDP-glucose,2TBDMS,isomer #14CC(C)(C)[Si](C)(C)O[C@@H]1[C@@H](CO)O[C@H](OP(=O)(O)OP(=O)(OC[C@H]2O[C@@H](N3C=CC(N)=NC3=O)[C@H](O)[C@@H]2O)O[Si](C)(C)C(C)(C)C)[C@H](O)[C@H]1O4665.7Semi standard non polar33892256
CDP-glucose,2TBDMS,isomer #15CC(C)(C)[Si](C)(C)NC1=NC(=O)N([C@@H]2O[C@H](COP(=O)(O)OP(=O)(O)O[C@H]3O[C@H](CO)[C@@H](O[Si](C)(C)C(C)(C)C)[C@H](O)[C@H]3O)[C@@H](O)[C@H]2O)C=C14776.5Semi standard non polar33892256
CDP-glucose,2TBDMS,isomer #16CC(C)(C)[Si](C)(C)O[C@H]1[C@H](O)[C@@H](CO)O[C@H](OP(=O)(O)OP(=O)(O)OC[C@H]2O[C@@H](N3C=CC(N)=NC3=O)[C@H](O[Si](C)(C)C(C)(C)C)[C@@H]2O)[C@@H]1O4613.3Semi standard non polar33892256
CDP-glucose,2TBDMS,isomer #17CC(C)(C)[Si](C)(C)O[C@H]1[C@H](O)[C@@H](CO)O[C@H](OP(=O)(O)OP(=O)(O)OC[C@H]2O[C@@H](N3C=CC(N)=NC3=O)[C@H](O)[C@@H]2O[Si](C)(C)C(C)(C)C)[C@@H]1O4613.4Semi standard non polar33892256
CDP-glucose,2TBDMS,isomer #18CC(C)(C)[Si](C)(C)O[C@H]1[C@H](O)[C@@H](CO)O[C@H](OP(=O)(O)OP(=O)(O)OC[C@H]2O[C@@H](N3C=CC(N)=NC3=O)[C@H](O)[C@@H]2O)[C@@H]1O[Si](C)(C)C(C)(C)C4603.1Semi standard non polar33892256
CDP-glucose,2TBDMS,isomer #19CC(C)(C)[Si](C)(C)O[C@H]1[C@H](O)[C@@H](CO)O[C@H](OP(=O)(O[Si](C)(C)C(C)(C)C)OP(=O)(O)OC[C@H]2O[C@@H](N3C=CC(N)=NC3=O)[C@H](O)[C@@H]2O)[C@@H]1O4652.8Semi standard non polar33892256
CDP-glucose,2TBDMS,isomer #2CC(C)(C)[Si](C)(C)OC[C@H]1O[C@H](OP(=O)(O)OP(=O)(O)OC[C@H]2O[C@@H](N3C=CC(N)=NC3=O)[C@H](O)[C@@H]2O[Si](C)(C)C(C)(C)C)[C@H](O)[C@@H](O)[C@@H]1O4660.3Semi standard non polar33892256
CDP-glucose,2TBDMS,isomer #20CC(C)(C)[Si](C)(C)O[C@H]1[C@H](O)[C@@H](CO)O[C@H](OP(=O)(O)OP(=O)(OC[C@H]2O[C@@H](N3C=CC(N)=NC3=O)[C@H](O)[C@@H]2O)O[Si](C)(C)C(C)(C)C)[C@@H]1O4644.4Semi standard non polar33892256
CDP-glucose,2TBDMS,isomer #21CC(C)(C)[Si](C)(C)NC1=NC(=O)N([C@@H]2O[C@H](COP(=O)(O)OP(=O)(O)O[C@H]3O[C@H](CO)[C@@H](O)[C@H](O[Si](C)(C)C(C)(C)C)[C@H]3O)[C@@H](O)[C@H]2O)C=C14765.8Semi standard non polar33892256
CDP-glucose,2TBDMS,isomer #22CC(C)(C)[Si](C)(C)O[C@@H]1[C@@H](O)[C@H](O)[C@@H](CO)O[C@@H]1OP(=O)(O)OP(=O)(O)OC[C@H]1O[C@@H](N2C=CC(N)=NC2=O)[C@H](O[Si](C)(C)C(C)(C)C)[C@@H]1O4631.5Semi standard non polar33892256
CDP-glucose,2TBDMS,isomer #23CC(C)(C)[Si](C)(C)O[C@@H]1[C@@H](COP(=O)(O)OP(=O)(O)O[C@H]2O[C@H](CO)[C@@H](O)[C@H](O)[C@H]2O[Si](C)(C)C(C)(C)C)O[C@@H](N2C=CC(N)=NC2=O)[C@@H]1O4632.3Semi standard non polar33892256
CDP-glucose,2TBDMS,isomer #24CC(C)(C)[Si](C)(C)O[C@@H]1[C@@H](O)[C@H](O)[C@@H](CO)O[C@@H]1OP(=O)(O[Si](C)(C)C(C)(C)C)OP(=O)(O)OC[C@H]1O[C@@H](N2C=CC(N)=NC2=O)[C@H](O)[C@@H]1O4672.2Semi standard non polar33892256
CDP-glucose,2TBDMS,isomer #25CC(C)(C)[Si](C)(C)O[C@@H]1[C@@H](O)[C@H](O)[C@@H](CO)O[C@@H]1OP(=O)(O)OP(=O)(OC[C@H]1O[C@@H](N2C=CC(N)=NC2=O)[C@H](O)[C@@H]1O)O[Si](C)(C)C(C)(C)C4663.1Semi standard non polar33892256
CDP-glucose,2TBDMS,isomer #26CC(C)(C)[Si](C)(C)NC1=NC(=O)N([C@@H]2O[C@H](COP(=O)(O)OP(=O)(O)O[C@H]3O[C@H](CO)[C@@H](O)[C@H](O)[C@H]3O[Si](C)(C)C(C)(C)C)[C@@H](O)[C@H]2O)C=C14776.8Semi standard non polar33892256
CDP-glucose,2TBDMS,isomer #27CC(C)(C)[Si](C)(C)O[C@@H]1[C@@H](COP(=O)(O)OP(=O)(O)O[C@H]2O[C@H](CO)[C@@H](O)[C@H](O)[C@H]2O)O[C@@H](N2C=CC(N)=NC2=O)[C@@H]1O[Si](C)(C)C(C)(C)C4671.3Semi standard non polar33892256
CDP-glucose,2TBDMS,isomer #28CC(C)(C)[Si](C)(C)O[C@@H]1[C@@H](COP(=O)(O[Si](C)(C)C(C)(C)C)OP(=O)(O)O[C@H]2O[C@H](CO)[C@@H](O)[C@H](O)[C@H]2O)O[C@@H](N2C=CC(N)=NC2=O)[C@@H]1O4705.7Semi standard non polar33892256
CDP-glucose,2TBDMS,isomer #29CC(C)(C)[Si](C)(C)O[C@@H]1[C@@H](COP(=O)(O)OP(=O)(O[C@H]2O[C@H](CO)[C@@H](O)[C@H](O)[C@H]2O)O[Si](C)(C)C(C)(C)C)O[C@@H](N2C=CC(N)=NC2=O)[C@@H]1O4710.8Semi standard non polar33892256
CDP-glucose,2TBDMS,isomer #3CC(C)(C)[Si](C)(C)OC[C@H]1O[C@H](OP(=O)(O)OP(=O)(O)OC[C@H]2O[C@@H](N3C=CC(N)=NC3=O)[C@H](O)[C@@H]2O)[C@H](O[Si](C)(C)C(C)(C)C)[C@@H](O)[C@@H]1O4635.1Semi standard non polar33892256
CDP-glucose,2TBDMS,isomer #30CC(C)(C)[Si](C)(C)NC1=NC(=O)N([C@@H]2O[C@H](COP(=O)(O)OP(=O)(O)O[C@H]3O[C@H](CO)[C@@H](O)[C@H](O)[C@H]3O)[C@@H](O[Si](C)(C)C(C)(C)C)[C@H]2O)C=C14818.3Semi standard non polar33892256
CDP-glucose,2TBDMS,isomer #31CC(C)(C)[Si](C)(C)O[C@@H]1[C@H](O)[C@@H](COP(=O)(O[Si](C)(C)C(C)(C)C)OP(=O)(O)O[C@H]2O[C@H](CO)[C@@H](O)[C@H](O)[C@H]2O)O[C@H]1N1C=CC(N)=NC1=O4704.1Semi standard non polar33892256
CDP-glucose,2TBDMS,isomer #32CC(C)(C)[Si](C)(C)O[C@@H]1[C@H](O)[C@@H](COP(=O)(O)OP(=O)(O[C@H]2O[C@H](CO)[C@@H](O)[C@H](O)[C@H]2O)O[Si](C)(C)C(C)(C)C)O[C@H]1N1C=CC(N)=NC1=O4707.9Semi standard non polar33892256
CDP-glucose,2TBDMS,isomer #33CC(C)(C)[Si](C)(C)NC1=NC(=O)N([C@@H]2O[C@H](COP(=O)(O)OP(=O)(O)O[C@H]3O[C@H](CO)[C@@H](O)[C@H](O)[C@H]3O)[C@@H](O)[C@H]2O[Si](C)(C)C(C)(C)C)C=C14817.3Semi standard non polar33892256
CDP-glucose,2TBDMS,isomer #34CC(C)(C)[Si](C)(C)OP(=O)(OC[C@H]1O[C@@H](N2C=CC(N)=NC2=O)[C@H](O)[C@@H]1O)OP(=O)(O[C@H]1O[C@H](CO)[C@@H](O)[C@H](O)[C@H]1O)O[Si](C)(C)C(C)(C)C4742.3Semi standard non polar33892256
CDP-glucose,2TBDMS,isomer #35CC(C)(C)[Si](C)(C)NC1=NC(=O)N([C@@H]2O[C@H](COP(=O)(O[Si](C)(C)C(C)(C)C)OP(=O)(O)O[C@H]3O[C@H](CO)[C@@H](O)[C@H](O)[C@H]3O)[C@@H](O)[C@H]2O)C=C14869.7Semi standard non polar33892256
CDP-glucose,2TBDMS,isomer #36CC(C)(C)[Si](C)(C)NC1=NC(=O)N([C@@H]2O[C@H](COP(=O)(O)OP(=O)(O[C@H]3O[C@H](CO)[C@@H](O)[C@H](O)[C@H]3O)O[Si](C)(C)C(C)(C)C)[C@@H](O)[C@H]2O)C=C14873.9Semi standard non polar33892256
CDP-glucose,2TBDMS,isomer #37CC(C)(C)[Si](C)(C)N(C1=NC(=O)N([C@@H]2O[C@H](COP(=O)(O)OP(=O)(O)O[C@H]3O[C@H](CO)[C@@H](O)[C@H](O)[C@H]3O)[C@@H](O)[C@H]2O)C=C1)[Si](C)(C)C(C)(C)C4790.9Semi standard non polar33892256
CDP-glucose,2TBDMS,isomer #4CC(C)(C)[Si](C)(C)OC[C@H]1O[C@H](OP(=O)(O)OP(=O)(O)OC[C@H]2O[C@@H](N3C=CC(N)=NC3=O)[C@H](O)[C@@H]2O)[C@H](O)[C@@H](O[Si](C)(C)C(C)(C)C)[C@@H]1O4611.4Semi standard non polar33892256
CDP-glucose,2TBDMS,isomer #5CC(C)(C)[Si](C)(C)OC[C@H]1O[C@H](OP(=O)(O)OP(=O)(O)OC[C@H]2O[C@@H](N3C=CC(N)=NC3=O)[C@H](O)[C@@H]2O)[C@H](O)[C@@H](O)[C@@H]1O[Si](C)(C)C(C)(C)C4630.9Semi standard non polar33892256
CDP-glucose,2TBDMS,isomer #6CC(C)(C)[Si](C)(C)OC[C@H]1O[C@H](OP(=O)(O[Si](C)(C)C(C)(C)C)OP(=O)(O)OC[C@H]2O[C@@H](N3C=CC(N)=NC3=O)[C@H](O)[C@@H]2O)[C@H](O)[C@@H](O)[C@@H]1O4698.4Semi standard non polar33892256
CDP-glucose,2TBDMS,isomer #7CC(C)(C)[Si](C)(C)OC[C@H]1O[C@H](OP(=O)(O)OP(=O)(OC[C@H]2O[C@@H](N3C=CC(N)=NC3=O)[C@H](O)[C@@H]2O)O[Si](C)(C)C(C)(C)C)[C@H](O)[C@@H](O)[C@@H]1O4690.1Semi standard non polar33892256
CDP-glucose,2TBDMS,isomer #8CC(C)(C)[Si](C)(C)NC1=NC(=O)N([C@@H]2O[C@H](COP(=O)(O)OP(=O)(O)O[C@H]3O[C@H](CO[Si](C)(C)C(C)(C)C)[C@@H](O)[C@H](O)[C@H]3O)[C@@H](O)[C@H]2O)C=C14786.3Semi standard non polar33892256
CDP-glucose,2TBDMS,isomer #9CC(C)(C)[Si](C)(C)O[C@@H]1[C@@H](CO)O[C@H](OP(=O)(O)OP(=O)(O)OC[C@H]2O[C@@H](N3C=CC(N)=NC3=O)[C@H](O[Si](C)(C)C(C)(C)C)[C@@H]2O)[C@H](O)[C@H]1O4633.6Semi standard non polar33892256
Spectra

GC-MS Spectra

Spectrum TypeDescriptionSplash KeyDeposition DateSourceView
Predicted GC-MSPredicted GC-MS Spectrum - CDP-glucose GC-MS (Non-derivatized) - 70eV, Positivesplash10-055b-4932470000-cc78435fdf80ab84337a2017-09-01Wishart LabView Spectrum
Predicted GC-MSPredicted GC-MS Spectrum - CDP-glucose GC-MS (1 TMS) - 70eV, Positivesplash10-0uk9-4941706000-2564988c7dc10b34ba162017-10-06Wishart LabView Spectrum
Predicted GC-MSPredicted GC-MS Spectrum - CDP-glucose GC-MS ("CDP-glucose,1TMS,#1" TMS) - 70eV, PositiveNot Available2021-10-14Wishart LabView Spectrum
Predicted GC-MSPredicted GC-MS Spectrum - CDP-glucose GC-MS (TMS_1_2) - 70eV, PositiveNot Available2021-10-15Wishart LabView Spectrum
Predicted GC-MSPredicted GC-MS Spectrum - CDP-glucose GC-MS (TMS_1_3) - 70eV, PositiveNot Available2021-10-15Wishart LabView Spectrum
Predicted GC-MSPredicted GC-MS Spectrum - CDP-glucose GC-MS (TMS_1_4) - 70eV, PositiveNot Available2021-10-15Wishart LabView Spectrum
Predicted GC-MSPredicted GC-MS Spectrum - CDP-glucose GC-MS (TMS_1_5) - 70eV, PositiveNot Available2021-10-15Wishart LabView Spectrum
Predicted GC-MSPredicted GC-MS Spectrum - CDP-glucose GC-MS (TMS_1_6) - 70eV, PositiveNot Available2021-10-15Wishart LabView Spectrum
Predicted GC-MSPredicted GC-MS Spectrum - CDP-glucose GC-MS (TMS_1_7) - 70eV, PositiveNot Available2021-10-15Wishart LabView Spectrum
Predicted GC-MSPredicted GC-MS Spectrum - CDP-glucose GC-MS (TMS_1_8) - 70eV, PositiveNot Available2021-10-15Wishart LabView Spectrum
Predicted GC-MSPredicted GC-MS Spectrum - CDP-glucose GC-MS (TMS_1_9) - 70eV, PositiveNot Available2021-10-15Wishart LabView Spectrum
Predicted GC-MSPredicted GC-MS Spectrum - CDP-glucose GC-MS (TMS_2_1) - 70eV, PositiveNot Available2021-10-15Wishart LabView Spectrum
Predicted GC-MSPredicted GC-MS Spectrum - CDP-glucose GC-MS (TMS_2_2) - 70eV, PositiveNot Available2021-10-15Wishart LabView Spectrum
Predicted GC-MSPredicted GC-MS Spectrum - CDP-glucose GC-MS (TMS_2_3) - 70eV, PositiveNot Available2021-10-15Wishart LabView Spectrum
Predicted GC-MSPredicted GC-MS Spectrum - CDP-glucose GC-MS (TMS_2_4) - 70eV, PositiveNot Available2021-10-15Wishart LabView Spectrum
Predicted GC-MSPredicted GC-MS Spectrum - CDP-glucose GC-MS (TMS_2_5) - 70eV, PositiveNot Available2021-10-15Wishart LabView Spectrum
Predicted GC-MSPredicted GC-MS Spectrum - CDP-glucose GC-MS (TMS_2_6) - 70eV, PositiveNot Available2021-10-15Wishart LabView Spectrum
Predicted GC-MSPredicted GC-MS Spectrum - CDP-glucose GC-MS (TMS_2_7) - 70eV, PositiveNot Available2021-10-15Wishart LabView Spectrum
Predicted GC-MSPredicted GC-MS Spectrum - CDP-glucose GC-MS (TMS_2_8) - 70eV, PositiveNot Available2021-10-15Wishart LabView Spectrum
Predicted GC-MSPredicted GC-MS Spectrum - CDP-glucose GC-MS (TMS_2_9) - 70eV, PositiveNot Available2021-10-15Wishart LabView Spectrum
Predicted GC-MSPredicted GC-MS Spectrum - CDP-glucose GC-MS (TMS_2_10) - 70eV, PositiveNot Available2021-10-15Wishart LabView Spectrum
Predicted GC-MSPredicted GC-MS Spectrum - CDP-glucose GC-MS (TMS_2_11) - 70eV, PositiveNot Available2021-10-15Wishart LabView Spectrum
Predicted GC-MSPredicted GC-MS Spectrum - CDP-glucose GC-MS (TMS_2_12) - 70eV, PositiveNot Available2021-10-15Wishart LabView Spectrum
Predicted GC-MSPredicted GC-MS Spectrum - CDP-glucose GC-MS (TMS_2_13) - 70eV, PositiveNot Available2021-10-15Wishart LabView Spectrum
Predicted GC-MSPredicted GC-MS Spectrum - CDP-glucose GC-MS (TMS_2_14) - 70eV, PositiveNot Available2021-10-15Wishart LabView Spectrum

MS/MS Spectra

Spectrum TypeDescriptionSplash KeyDeposition DateSourceView
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - CDP-glucose 10V, Positive-QTOFsplash10-03di-0901110000-13d2effadf491f35035a2017-09-01Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - CDP-glucose 20V, Positive-QTOFsplash10-03di-2910000000-ed5b462d0c312d6a5bdb2017-09-01Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - CDP-glucose 40V, Positive-QTOFsplash10-03di-4900000000-90a7ac808c5d4858589b2017-09-01Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - CDP-glucose 10V, Negative-QTOFsplash10-08fr-0901160000-e111a674ae2d2089a6412017-09-01Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - CDP-glucose 20V, Negative-QTOFsplash10-03di-7906020000-e0153c693f7146c107322017-09-01Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - CDP-glucose 40V, Negative-QTOFsplash10-0bvl-4900000000-8c5119b6eaadc19d832e2017-09-01Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - CDP-glucose 10V, Positive-QTOFsplash10-03di-0900040000-3c275dd6786692e75a8c2021-09-23Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - CDP-glucose 20V, Positive-QTOFsplash10-01p9-1621930000-bee26ae88105c78462e42021-09-23Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - CDP-glucose 40V, Positive-QTOFsplash10-03di-3981100000-b03d0b63bd4aa6c9d3b72021-09-23Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - CDP-glucose 10V, Negative-QTOFsplash10-03di-0000090000-769bfaf73b856e460e162021-09-25Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - CDP-glucose 20V, Negative-QTOFsplash10-03xr-2200950000-004d310719ae6596dd7e2021-09-25Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - CDP-glucose 40V, Negative-QTOFsplash10-0563-6928110000-8bd90dbd63502af05e8a2021-09-25Wishart LabView Spectrum

NMR Spectra

Spectrum TypeDescriptionDeposition DateSourceView
Predicted 1D NMR13C NMR Spectrum (1D, 100 MHz, D2O, predicted)2021-09-24Wishart LabView Spectrum
Predicted 1D NMR1H NMR Spectrum (1D, 100 MHz, D2O, predicted)2021-09-24Wishart LabView Spectrum
Predicted 1D NMR13C NMR Spectrum (1D, 1000 MHz, D2O, predicted)2021-09-24Wishart LabView Spectrum
Predicted 1D NMR1H NMR Spectrum (1D, 1000 MHz, D2O, predicted)2021-09-24Wishart LabView Spectrum
Predicted 1D NMR13C NMR Spectrum (1D, 200 MHz, D2O, predicted)2021-09-24Wishart LabView Spectrum
Predicted 1D NMR1H NMR Spectrum (1D, 200 MHz, D2O, predicted)2021-09-24Wishart LabView Spectrum
Predicted 1D NMR13C NMR Spectrum (1D, 300 MHz, D2O, predicted)2021-09-24Wishart LabView Spectrum
Predicted 1D NMR1H NMR Spectrum (1D, 300 MHz, D2O, predicted)2021-09-24Wishart LabView Spectrum
Predicted 1D NMR13C NMR Spectrum (1D, 400 MHz, D2O, predicted)2021-09-24Wishart LabView Spectrum
Predicted 1D NMR1H NMR Spectrum (1D, 400 MHz, D2O, predicted)2021-09-24Wishart LabView Spectrum
Predicted 1D NMR13C NMR Spectrum (1D, 500 MHz, D2O, predicted)2021-09-24Wishart LabView Spectrum
Predicted 1D NMR1H NMR Spectrum (1D, 500 MHz, D2O, predicted)2021-09-24Wishart LabView Spectrum
Predicted 1D NMR13C NMR Spectrum (1D, 600 MHz, D2O, predicted)2021-09-24Wishart LabView Spectrum
Predicted 1D NMR1H NMR Spectrum (1D, 600 MHz, D2O, predicted)2021-09-24Wishart LabView Spectrum
Predicted 1D NMR13C NMR Spectrum (1D, 700 MHz, D2O, predicted)2021-09-24Wishart LabView Spectrum
Predicted 1D NMR1H NMR Spectrum (1D, 700 MHz, D2O, predicted)2021-09-24Wishart LabView Spectrum
Predicted 1D NMR13C NMR Spectrum (1D, 800 MHz, D2O, predicted)2021-09-24Wishart LabView Spectrum
Predicted 1D NMR1H NMR Spectrum (1D, 800 MHz, D2O, predicted)2021-09-24Wishart LabView Spectrum
Predicted 1D NMR13C NMR Spectrum (1D, 900 MHz, D2O, predicted)2021-09-24Wishart LabView Spectrum
Predicted 1D NMR1H NMR Spectrum (1D, 900 MHz, D2O, predicted)2021-09-24Wishart LabView Spectrum
Biological Properties
Cellular Locations
  • Cytoplasm (predicted from logP)
Biospecimen LocationsNot Available
Tissue LocationsNot Available
Pathways
Normal Concentrations
Not Available
Abnormal Concentrations
Not Available
Associated Disorders and Diseases
Disease ReferencesNone
Associated OMIM IDsNone
DrugBank IDNot Available
Phenol Explorer Compound IDNot Available
FooDB IDFDB023155
KNApSAcK IDC00019342
Chemspider ID388381
KEGG Compound IDC00501
BioCyc IDCDP-D-GLUCOSE
BiGG IDNot Available
Wikipedia LinkCytidine diphosphate glucose
METLIN ID6907
PubChem Compound439244
PDB IDNot Available
ChEBI ID28942
Food Biomarker OntologyNot Available
VMH IDCDPGLC
MarkerDB IDNot Available
Good Scents IDNot Available
References
Synthesis ReferenceGinsburg, Victor; O'Brien, Paul J.; Hall, Clara W. Enzymic synthesis of cytidine 5'-diphosphate glucose. Biocherns Biophys. Res. Communs. (1962), 7 1-4.
Material Safety Data Sheet (MSDS)Not Available
General References
  1. Chandra GR, Mandava N, Warthen JD Jr: Uridine diphosphate glucose:fatty acid glucosyl transferase activity of rape (Brassica napus L.) anther tissue. Biochim Biophys Acta. 1978 Oct 12;526(2):387-97. [PubMed:718943 ]
  2. Wojciechowski ZA, Zimowski J, Zimowski JG, Lyznik A: Specificity of sterol-glucosylating enzymes from Sinapis alba and Physarum polycephalum. Biochim Biophys Acta. 1979 Oct 11;570(2):363-70. [PubMed:497231 ]
  3. Mookerjea S: Effect of nucleotides on UDP-N-acetylglucosamine pyrophosphatase and N-acetylglucosaminyltransferase activities in microsomal membranes. Can J Biochem. 1979 Jun;57(6):557-65. [PubMed:476505 ]