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Record Information

Version

5.0

Status

Expected but not Quantified

Creation Date

2017-03-16 03:41:20 UTC

Update Date

2021-09-14 15:46:45 UTC

HMDB ID

HMDB0062276

Secondary Accession Numbers

HMDB62276

Metabolite Identification

Common Name

10-Hydroxy-E4-neuroprostane

Description

10-Hydroxy-E4-neuroprostane, also known as 10-E4-NeuroP or 10H-E4np, is a member of the class of compounds known as prostaglandins and related compounds. Prostaglandins and related compounds are unsaturated carboxylic acids consisting of a 20 carbon skeleton that also contains a five-member ring, and are based upon the fatty acid arachidonic acid. 10-Hydroxy-E4-neuroprostane is practically insoluble (in water) and a weakly acidic compound (based on its pKa). Within the cell, 10-hydroxy-E4-neuroprostane is primarily located in the membrane (predicted from logP). It can also be found in the extracellular space.

Structure

MOL 3D MOL SDF 3D SDF PDB 3D PDB SMILES InChI

                                    
  Mrv1652307041817302D          

 27 27  0  0  1  0            999 V2000
   13.1422   -8.6265    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   12.4331   -9.0412    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   13.9710   -8.6276    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.7880   -8.7851    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.3030   -9.4526    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.7880  -10.1201    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   10.2871   -8.6278    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.5726   -9.0402    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   11.0015   -9.0402    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.5726   -9.8651    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   11.7160   -8.6278    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   11.7160   -7.8028    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   15.3947   -8.6255    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   14.6854   -9.0400    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   16.2234   -8.6264    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   16.9378   -9.0390    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   17.6523   -8.6265    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   18.3668   -9.0391    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   18.3666   -9.8642    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   19.0813   -8.6268    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   10.9974   -9.8650    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.2913  -10.2778    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   11.8223   -9.8659    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   12.5336  -10.2767    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   13.2482   -9.8643    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.5319   -7.9969    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    8.5318  -10.9083    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  3  1  2  0  0  0  0
  1  2  1  0  0  0  0
  4  5  1  0  0  0  0
  5  6  1  0  0  0  0
  7  9  2  0  0  0  0
  4  8  1  0  0  0  0
  6 10  1  0  0  0  0
 10  8  1  0  0  0  0
  8  7  1  1  0  0  0
  9 11  1  0  0  0  0
 11 12  1  1  0  0  0
 11  2  1  0  0  0  0
 15 16  1  0  0  0  0
 15 13  2  0  0  0  0
 13 14  1  0  0  0  0
  3 14  1  0  0  0  0
 16 17  1  0  0  0  0
 17 18  1  0  0  0  0
 18 19  2  0  0  0  0
 18 20  1  0  0  0  0
 23 21  2  0  0  0  0
 21 22  1  0  0  0  0
 23 24  1  0  0  0  0
 10 22  1  1  0  0  0
 24 25  1  0  0  0  0
  4 26  2  0  0  0  0
  6 27  1  6  0  0  0
M  END

HMDB0062276
     RDKit          3D
10-Hydroxy-E4-neuroprostane
 59 59  0  0  0  0  0  0  0  0999 V2000
   -7.5036    0.9880   -0.0564 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.3687    0.9416    0.9818 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.1973   -0.4640    1.3428 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0733   -1.0975    1.1645 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8613   -0.5178    0.5982 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4548   -1.2716   -0.6694 C   0  0  2  0  0  0  0  0  0  0  0  0
   -2.2162   -0.6988   -1.2739 C   0  0  2  0  0  0  0  0  0  0  0  0
   -1.2175   -0.3249   -0.2400 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7377    0.8597   -0.0381 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2676    1.2020    1.0115 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.3941    1.3495    2.2273 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.3043    0.1033    1.1748 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2883    0.4574    2.2123 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5799    0.5849    2.0170 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2330    0.3860    0.7018 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.2313   -0.7071    0.7973 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.5168   -0.5727    0.5575 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.1201    0.6949    0.1621 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.7889    0.5515   -1.2246 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.8392   -0.4964   -1.1407 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.9138   -0.1971   -0.5597 O   0  0  0  0  0  0  0  0  0  0  0  0
    8.5876   -1.7390   -1.6997 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6673    0.3922   -2.1366 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9991    1.2693   -2.6511 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1359    0.2839   -2.3166 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4709   -1.1186   -1.7725 C   0  0  1  0  0  0  0  0  0  0  0  0
   -4.1767   -2.0109   -2.7828 O   0  0  0  0  0  0  0  0  0  0  0  0
   -7.4083    0.0766   -0.6820 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.3708    1.8558   -0.7380 H   0  0  0  0  0  0  0  0  0  0  0  0
   -8.4895    1.0600    0.4491 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.5431    1.4570    0.5207 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.7904    1.4819    1.8679 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.0371   -1.0386    1.7863 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0314   -2.1669    1.4682 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0263   -0.7826    1.3257 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7983    0.5523    0.4884 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3307   -2.3324   -0.3642 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7839   -1.5283   -1.9092 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8648   -1.1344    0.4015 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0649    1.6921   -0.6475 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.7830    2.1553    0.7949 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.0582    1.9441    2.8457 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.7980   -0.8327    1.5503 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.7383   -0.1238    0.2140 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.9458    0.6348    3.2408 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.2419    0.8536    2.8559 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.7341    1.3108    0.3915 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.5478    0.0924   -0.1189 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.9123   -1.7344    1.0907 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.2063   -1.4322    0.6475 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.9984    0.8713    0.8555 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.5104    1.5723    0.1208 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.0380    0.2820   -1.9798 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.2326    1.5335   -1.4316 H   0  0  0  0  0  0  0  0  0  0  0  0
    9.3530   -2.4093   -1.8408 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7075    0.9874   -1.6759 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4495    0.3707   -3.3682 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.5062   -1.1801   -1.4239 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0918   -2.9354   -2.4127 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  2  0
  9 10  1  0
 10 11  1  0
 10 12  1  0
 12 13  1  0
 13 14  2  0
 14 15  1  0
 15 16  1  0
 16 17  2  0
 17 18  1  0
 18 19  1  0
 19 20  1  0
 20 21  2  0
 20 22  1  0
  7 23  1  0
 23 24  2  0
 23 25  1  0
 25 26  1  0
 26 27  1  0
 26  6  1  0
  1 28  1  0
  1 29  1  0
  1 30  1  0
  2 31  1  0
  2 32  1  0
  3 33  1  0
  4 34  1  0
  5 35  1  0
  5 36  1  0
  6 37  1  1
  7 38  1  6
  8 39  1  0
  9 40  1  0
 10 41  1  6
 11 42  1  0
 12 43  1  0
 12 44  1  0
 13 45  1  0
 14 46  1  0
 15 47  1  0
 15 48  1  0
 16 49  1  0
 17 50  1  0
 18 51  1  0
 18 52  1  0
 19 53  1  0
 19 54  1  0
 22 55  1  0
 25 56  1  0
 25 57  1  0
 26 58  1  1
 27 59  1  0
M  END

                                    
  Mrv1652307041817302D          

 27 27  0  0  1  0            999 V2000
   13.1422   -8.6265    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   12.4331   -9.0412    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   13.9710   -8.6276    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.7880   -8.7851    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.3030   -9.4526    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.7880  -10.1201    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   10.2871   -8.6278    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.5726   -9.0402    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   11.0015   -9.0402    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.5726   -9.8651    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   11.7160   -8.6278    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   11.7160   -7.8028    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   15.3947   -8.6255    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   14.6854   -9.0400    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   16.2234   -8.6264    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   16.9378   -9.0390    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   17.6523   -8.6265    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   18.3668   -9.0391    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   18.3666   -9.8642    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   19.0813   -8.6268    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   10.9974   -9.8650    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.2913  -10.2778    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   11.8223   -9.8659    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   12.5336  -10.2767    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   13.2482   -9.8643    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.5319   -7.9969    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    8.5318  -10.9083    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  3  1  2  0  0  0  0
  1  2  1  0  0  0  0
  4  5  1  0  0  0  0
  5  6  1  0  0  0  0
  7  9  2  0  0  0  0
  4  8  1  0  0  0  0
  6 10  1  0  0  0  0
 10  8  1  0  0  0  0
  8  7  1  1  0  0  0
  9 11  1  0  0  0  0
 11 12  1  1  0  0  0
 11  2  1  0  0  0  0
 15 16  1  0  0  0  0
 15 13  2  0  0  0  0
 13 14  1  0  0  0  0
  3 14  1  0  0  0  0
 16 17  1  0  0  0  0
 17 18  1  0  0  0  0
 18 19  2  0  0  0  0
 18 20  1  0  0  0  0
 23 21  2  0  0  0  0
 21 22  1  0  0  0  0
 23 24  1  0  0  0  0
 10 22  1  1  0  0  0
 24 25  1  0  0  0  0
  4 26  2  0  0  0  0
  6 27  1  6  0  0  0
M  END
> <DATABASE_ID>
HMDB0062276

> <DATABASE_NAME>
hmdb

> <SMILES>
CC\C=C/C[C@H]1[C@H](O)CC(=O)[C@H]1\C=C\[C@@H](O)C\C=C/C\C=C/CCC(O)=O

> <INCHI_IDENTIFIER>
InChI=1S/C22H32O5/c1-2-3-8-12-18-19(21(25)16-20(18)24)15-14-17(23)11-9-6-4-5-7-10-13-22(26)27/h3,5-9,14-15,17-20,23-24H,2,4,10-13,16H2,1H3,(H,26,27)/b7-5-,8-3-,9-6-,15-14+/t17-,18+,19-,20+/m0/s1

> <INCHI_KEY>
IFQRUHXGXJVRNV-ZNQQBSSQSA-N

> <FORMULA>
C22H32O5

> <MOLECULAR_WEIGHT>
376.493

> <EXACT_MASS>
376.22497413

> <JCHEM_ACCEPTOR_COUNT>
5

> <JCHEM_ATOM_COUNT>
59

> <JCHEM_AVERAGE_POLARIZABILITY>
42.23308394163923

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
3

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
(4Z,7Z,10S,11E)-10-hydroxy-12-[(1S,2R,3R)-3-hydroxy-5-oxo-2-[(2Z)-pent-2-en-1-yl]cyclopentyl]dodeca-4,7,11-trienoic acid

> <ALOGPS_LOGP>
3.53

> <JCHEM_LOGP>
3.3905641536666664

> <ALOGPS_LOGS>
-4.19

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
1

> <JCHEM_PHYSIOLOGICAL_CHARGE>
-1

> <JCHEM_PKA>
13.98051567191775

> <JCHEM_PKA_STRONGEST_ACIDIC>
4.815639900947735

> <JCHEM_PKA_STRONGEST_BASIC>
-1.6358492144245247

> <JCHEM_POLAR_SURFACE_AREA>
94.83

> <JCHEM_REFRACTIVITY>
110.87029999999999

> <JCHEM_ROTATABLE_BOND_COUNT>
12

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
2.42e-02 g/l

> <JCHEM_TRADITIONAL_IUPAC>
(4Z,7Z,10S,11E)-10-hydroxy-12-[(1S,2R,3R)-3-hydroxy-5-oxo-2-[(2Z)-pent-2-en-1-yl]cyclopentyl]dodeca-4,7,11-trienoic acid

> <JCHEM_VEBER_RULE>
0

$$$$

HMDB0062276
     RDKit          3D
10-Hydroxy-E4-neuroprostane
 59 59  0  0  0  0  0  0  0  0999 V2000
   -7.5036    0.9880   -0.0564 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.3687    0.9416    0.9818 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.1973   -0.4640    1.3428 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0733   -1.0975    1.1645 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8613   -0.5178    0.5982 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4548   -1.2716   -0.6694 C   0  0  2  0  0  0  0  0  0  0  0  0
   -2.2162   -0.6988   -1.2739 C   0  0  2  0  0  0  0  0  0  0  0  0
   -1.2175   -0.3249   -0.2400 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7377    0.8597   -0.0381 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2676    1.2020    1.0115 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.3941    1.3495    2.2273 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.3043    0.1033    1.1748 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2883    0.4574    2.2123 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5799    0.5849    2.0170 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2330    0.3860    0.7018 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.2313   -0.7071    0.7973 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.5168   -0.5727    0.5575 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.1201    0.6949    0.1621 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.7889    0.5515   -1.2246 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.8392   -0.4964   -1.1407 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.9138   -0.1971   -0.5597 O   0  0  0  0  0  0  0  0  0  0  0  0
    8.5876   -1.7390   -1.6997 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6673    0.3922   -2.1366 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9991    1.2693   -2.6511 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1359    0.2839   -2.3166 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4709   -1.1186   -1.7725 C   0  0  1  0  0  0  0  0  0  0  0  0
   -4.1767   -2.0109   -2.7828 O   0  0  0  0  0  0  0  0  0  0  0  0
   -7.4083    0.0766   -0.6820 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.3708    1.8558   -0.7380 H   0  0  0  0  0  0  0  0  0  0  0  0
   -8.4895    1.0600    0.4491 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.5431    1.4570    0.5207 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.7904    1.4819    1.8679 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.0371   -1.0386    1.7863 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0314   -2.1669    1.4682 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0263   -0.7826    1.3257 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7983    0.5523    0.4884 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3307   -2.3324   -0.3642 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7839   -1.5283   -1.9092 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8648   -1.1344    0.4015 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0649    1.6921   -0.6475 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.7830    2.1553    0.7949 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.0582    1.9441    2.8457 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.7980   -0.8327    1.5503 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.7383   -0.1238    0.2140 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.9458    0.6348    3.2408 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.2419    0.8536    2.8559 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.7341    1.3108    0.3915 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.5478    0.0924   -0.1189 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.9123   -1.7344    1.0907 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.2063   -1.4322    0.6475 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.9984    0.8713    0.8555 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.5104    1.5723    0.1208 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.0380    0.2820   -1.9798 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.2326    1.5335   -1.4316 H   0  0  0  0  0  0  0  0  0  0  0  0
    9.3530   -2.4093   -1.8408 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7075    0.9874   -1.6759 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4495    0.3707   -3.3682 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.5062   -1.1801   -1.4239 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0918   -2.9354   -2.4127 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  2  0
  9 10  1  0
 10 11  1  0
 10 12  1  0
 12 13  1  0
 13 14  2  0
 14 15  1  0
 15 16  1  0
 16 17  2  0
 17 18  1  0
 18 19  1  0
 19 20  1  0
 20 21  2  0
 20 22  1  0
  7 23  1  0
 23 24  2  0
 23 25  1  0
 25 26  1  0
 26 27  1  0
 26  6  1  0
  1 28  1  0
  1 29  1  0
  1 30  1  0
  2 31  1  0
  2 32  1  0
  3 33  1  0
  4 34  1  0
  5 35  1  0
  5 36  1  0
  6 37  1  1
  7 38  1  6
  8 39  1  0
  9 40  1  0
 10 41  1  6
 11 42  1  0
 12 43  1  0
 12 44  1  0
 13 45  1  0
 14 46  1  0
 15 47  1  0
 15 48  1  0
 16 49  1  0
 17 50  1  0
 18 51  1  0
 18 52  1  0
 19 53  1  0
 19 54  1  0
 22 55  1  0
 25 56  1  0
 25 57  1  0
 26 58  1  1
 27 59  1  0
M  END

HEADER    PROTEIN                                 04-JUL-18   NONE
TITLE     NULL                                                        
COMPND    MOLECULE:                                                   
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   04-JUL-18         0                                  
HETATM    1  C   UNK     0      24.532 -16.103   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0      23.208 -16.877   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0      26.079 -16.105   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0      16.404 -16.399   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0      15.499 -17.645   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0      16.404 -18.891   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0      19.203 -16.105   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0      17.869 -16.875   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0      20.536 -16.875   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0      17.869 -18.415   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0      21.870 -16.105   0.000  0.00  0.00           C+0
HETATM   12  O   UNK     0      21.870 -14.565   0.000  0.00  0.00           O+0
HETATM   13  C   UNK     0      28.737 -16.101   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0      27.413 -16.875   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0      30.284 -16.103   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0      31.617 -16.873   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0      32.951 -16.103   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0      34.285 -16.873   0.000  0.00  0.00           C+0
HETATM   19  O   UNK     0      34.284 -18.413   0.000  0.00  0.00           O+0
HETATM   20  O   UNK     0      35.618 -16.103   0.000  0.00  0.00           O+0
HETATM   21  C   UNK     0      20.528 -18.415   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0      19.210 -19.185   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0      22.068 -18.416   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0      23.396 -19.183   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0      24.730 -18.413   0.000  0.00  0.00           C+0
HETATM   26  O   UNK     0      15.926 -14.928   0.000  0.00  0.00           O+0
HETATM   27  O   UNK     0      15.926 -20.362   0.000  0.00  0.00           O+0
CONECT    1    3    2                                                       
CONECT    2    1   11                                                       
CONECT    3    1   14                                                       
CONECT    4    5    8   26                                                  
CONECT    5    4    6                                                       
CONECT    6    5   10   27                                                  
CONECT    7    9    8                                                       
CONECT    8    4   10    7                                                  
CONECT    9    7   11                                                       
CONECT   10    6    8   22                                                  
CONECT   11    9   12    2                                                  
CONECT   12   11                                                            
CONECT   13   15   14                                                       
CONECT   14   13    3                                                       
CONECT   15   16   13                                                       
CONECT   16   15   17                                                       
CONECT   17   16   18                                                       
CONECT   18   17   19   20                                                  
CONECT   19   18                                                            
CONECT   20   18                                                            
CONECT   21   23   22                                                       
CONECT   22   21   10                                                       
CONECT   23   21   24                                                       
CONECT   24   23   25                                                       
CONECT   25   24                                                            
CONECT   26    4                                                            
CONECT   27    6                                                            
MASTER        0    0    0    0    0    0    0    0   27    0   54    0
END

COMPND    HMDB0062276
HETATM    1  C1  UNL     1      -7.504   0.988  -0.056  1.00  0.00           C  
HETATM    2  C2  UNL     1      -6.369   0.942   0.982  1.00  0.00           C  
HETATM    3  C3  UNL     1      -6.197  -0.464   1.343  1.00  0.00           C  
HETATM    4  C4  UNL     1      -5.073  -1.098   1.165  1.00  0.00           C  
HETATM    5  C5  UNL     1      -3.861  -0.518   0.598  1.00  0.00           C  
HETATM    6  C6  UNL     1      -3.455  -1.272  -0.669  1.00  0.00           C  
HETATM    7  C7  UNL     1      -2.216  -0.699  -1.274  1.00  0.00           C  
HETATM    8  C8  UNL     1      -1.217  -0.325  -0.240  1.00  0.00           C  
HETATM    9  C9  UNL     1      -0.738   0.860  -0.038  1.00  0.00           C  
HETATM   10  C10 UNL     1       0.268   1.202   1.012  1.00  0.00           C  
HETATM   11  O1  UNL     1      -0.394   1.349   2.227  1.00  0.00           O  
HETATM   12  C11 UNL     1       1.304   0.103   1.175  1.00  0.00           C  
HETATM   13  C12 UNL     1       2.288   0.457   2.212  1.00  0.00           C  
HETATM   14  C13 UNL     1       3.580   0.585   2.017  1.00  0.00           C  
HETATM   15  C14 UNL     1       4.233   0.386   0.702  1.00  0.00           C  
HETATM   16  C15 UNL     1       5.231  -0.707   0.797  1.00  0.00           C  
HETATM   17  C16 UNL     1       6.517  -0.573   0.558  1.00  0.00           C  
HETATM   18  C17 UNL     1       7.120   0.695   0.162  1.00  0.00           C  
HETATM   19  C18 UNL     1       7.789   0.552  -1.225  1.00  0.00           C  
HETATM   20  C19 UNL     1       8.839  -0.496  -1.141  1.00  0.00           C  
HETATM   21  O2  UNL     1       9.914  -0.197  -0.560  1.00  0.00           O  
HETATM   22  O3  UNL     1       8.588  -1.739  -1.700  1.00  0.00           O  
HETATM   23  C20 UNL     1      -2.667   0.392  -2.137  1.00  0.00           C  
HETATM   24  O4  UNL     1      -1.999   1.269  -2.651  1.00  0.00           O  
HETATM   25  C21 UNL     1      -4.136   0.284  -2.317  1.00  0.00           C  
HETATM   26  C22 UNL     1      -4.471  -1.119  -1.773  1.00  0.00           C  
HETATM   27  O5  UNL     1      -4.177  -2.011  -2.783  1.00  0.00           O  
HETATM   28  H1  UNL     1      -7.408   0.077  -0.682  1.00  0.00           H  
HETATM   29  H2  UNL     1      -7.371   1.856  -0.738  1.00  0.00           H  
HETATM   30  H3  UNL     1      -8.490   1.060   0.449  1.00  0.00           H  
HETATM   31  H4  UNL     1      -5.543   1.457   0.521  1.00  0.00           H  
HETATM   32  H5  UNL     1      -6.790   1.482   1.868  1.00  0.00           H  
HETATM   33  H6  UNL     1      -7.037  -1.039   1.786  1.00  0.00           H  
HETATM   34  H7  UNL     1      -5.031  -2.167   1.468  1.00  0.00           H  
HETATM   35  H8  UNL     1      -3.026  -0.783   1.326  1.00  0.00           H  
HETATM   36  H9  UNL     1      -3.798   0.552   0.488  1.00  0.00           H  
HETATM   37  H10 UNL     1      -3.331  -2.332  -0.364  1.00  0.00           H  
HETATM   38  H11 UNL     1      -1.784  -1.528  -1.909  1.00  0.00           H  
HETATM   39  H12 UNL     1      -0.865  -1.134   0.401  1.00  0.00           H  
HETATM   40  H13 UNL     1      -1.065   1.692  -0.647  1.00  0.00           H  
HETATM   41  H14 UNL     1       0.783   2.155   0.795  1.00  0.00           H  
HETATM   42  H15 UNL     1       0.058   1.944   2.846  1.00  0.00           H  
HETATM   43  H16 UNL     1       0.798  -0.833   1.550  1.00  0.00           H  
HETATM   44  H17 UNL     1       1.738  -0.124   0.214  1.00  0.00           H  
HETATM   45  H18 UNL     1       1.946   0.635   3.241  1.00  0.00           H  
HETATM   46  H19 UNL     1       4.242   0.854   2.856  1.00  0.00           H  
HETATM   47  H20 UNL     1       4.734   1.311   0.392  1.00  0.00           H  
HETATM   48  H21 UNL     1       3.548   0.092  -0.119  1.00  0.00           H  
HETATM   49  H22 UNL     1       4.912  -1.734   1.091  1.00  0.00           H  
HETATM   50  H23 UNL     1       7.206  -1.432   0.648  1.00  0.00           H  
HETATM   51  H24 UNL     1       7.998   0.871   0.856  1.00  0.00           H  
HETATM   52  H25 UNL     1       6.510   1.572   0.121  1.00  0.00           H  
HETATM   53  H26 UNL     1       7.038   0.282  -1.980  1.00  0.00           H  
HETATM   54  H27 UNL     1       8.233   1.533  -1.432  1.00  0.00           H  
HETATM   55  H28 UNL     1       9.353  -2.409  -1.841  1.00  0.00           H  
HETATM   56  H29 UNL     1      -4.708   0.987  -1.676  1.00  0.00           H  
HETATM   57  H30 UNL     1      -4.450   0.371  -3.368  1.00  0.00           H  
HETATM   58  H31 UNL     1      -5.506  -1.180  -1.424  1.00  0.00           H  
HETATM   59  H32 UNL     1      -4.092  -2.935  -2.413  1.00  0.00           H  
CONECT    1    2   28   29   30
CONECT    2    3   31   32
CONECT    3    4    4   33
CONECT    4    5   34
CONECT    5    6   35   36
CONECT    6    7   26   37
CONECT    7    8   23   38
CONECT    8    9    9   39
CONECT    9   10   40
CONECT   10   11   12   41
CONECT   11   42
CONECT   12   13   43   44
CONECT   13   14   14   45
CONECT   14   15   46
CONECT   15   16   47   48
CONECT   16   17   17   49
CONECT   17   18   50
CONECT   18   19   51   52
CONECT   19   20   53   54
CONECT   20   21   21   22
CONECT   22   55
CONECT   23   24   24   25
CONECT   25   26   56   57
CONECT   26   27   58
CONECT   27   59
END

HMDB0062276
     RDKit          3D
10-Hydroxy-E4-neuroprostane
 59 59  0  0  0  0  0  0  0  0999 V2000
   -7.5036    0.9880   -0.0564 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.3687    0.9416    0.9818 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.1973   -0.4640    1.3428 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0733   -1.0975    1.1645 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8613   -0.5178    0.5982 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4548   -1.2716   -0.6694 C   0  0  2  0  0  0  0  0  0  0  0  0
   -2.2162   -0.6988   -1.2739 C   0  0  2  0  0  0  0  0  0  0  0  0
   -1.2175   -0.3249   -0.2400 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7377    0.8597   -0.0381 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2676    1.2020    1.0115 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.3941    1.3495    2.2273 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.3043    0.1033    1.1748 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2883    0.4574    2.2123 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5799    0.5849    2.0170 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2330    0.3860    0.7018 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.2313   -0.7071    0.7973 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.5168   -0.5727    0.5575 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.1201    0.6949    0.1621 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.7889    0.5515   -1.2246 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.8392   -0.4964   -1.1407 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.9138   -0.1971   -0.5597 O   0  0  0  0  0  0  0  0  0  0  0  0
    8.5876   -1.7390   -1.6997 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6673    0.3922   -2.1366 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9991    1.2693   -2.6511 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1359    0.2839   -2.3166 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4709   -1.1186   -1.7725 C   0  0  1  0  0  0  0  0  0  0  0  0
   -4.1767   -2.0109   -2.7828 O   0  0  0  0  0  0  0  0  0  0  0  0
   -7.4083    0.0766   -0.6820 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.3708    1.8558   -0.7380 H   0  0  0  0  0  0  0  0  0  0  0  0
   -8.4895    1.0600    0.4491 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.5431    1.4570    0.5207 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.7904    1.4819    1.8679 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.0371   -1.0386    1.7863 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0314   -2.1669    1.4682 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0263   -0.7826    1.3257 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7983    0.5523    0.4884 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3307   -2.3324   -0.3642 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7839   -1.5283   -1.9092 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8648   -1.1344    0.4015 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0649    1.6921   -0.6475 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.7830    2.1553    0.7949 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.0582    1.9441    2.8457 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.7980   -0.8327    1.5503 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.7383   -0.1238    0.2140 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.9458    0.6348    3.2408 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.2419    0.8536    2.8559 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.7341    1.3108    0.3915 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.5478    0.0924   -0.1189 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.9123   -1.7344    1.0907 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.2063   -1.4322    0.6475 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.9984    0.8713    0.8555 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.5104    1.5723    0.1208 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.0380    0.2820   -1.9798 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.2326    1.5335   -1.4316 H   0  0  0  0  0  0  0  0  0  0  0  0
    9.3530   -2.4093   -1.8408 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7075    0.9874   -1.6759 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4495    0.3707   -3.3682 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.5062   -1.1801   -1.4239 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0918   -2.9354   -2.4127 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  2  0
  9 10  1  0
 10 11  1  0
 10 12  1  0
 12 13  1  0
 13 14  2  0
 14 15  1  0
 15 16  1  0
 16 17  2  0
 17 18  1  0
 18 19  1  0
 19 20  1  0
 20 21  2  0
 20 22  1  0
  7 23  1  0
 23 24  2  0
 23 25  1  0
 25 26  1  0
 26 27  1  0
 26  6  1  0
  1 28  1  0
  1 29  1  0
  1 30  1  0
  2 31  1  0
  2 32  1  0
  3 33  1  0
  4 34  1  0
  5 35  1  0
  5 36  1  0
  6 37  1  1
  7 38  1  6
  8 39  1  0
  9 40  1  0
 10 41  1  6
 11 42  1  0
 12 43  1  0
 12 44  1  0
 13 45  1  0
 14 46  1  0
 15 47  1  0
 15 48  1  0
 16 49  1  0
 17 50  1  0
 18 51  1  0
 18 52  1  0
 19 53  1  0
 19 54  1  0
 22 55  1  0
 25 56  1  0
 25 57  1  0
 26 58  1  1
 27 59  1  0
M  END

View in JSmol View Stereo Labels

Synonyms

Value	Source
10-e4-NeuroP	HMDB
10H-e4np	HMDB

Chemical Formula

C₂₂H₃₂O₅

Average Molecular Weight

376.493

Monoisotopic Molecular Weight

376.22497413

IUPAC Name

(4Z,7Z,10S,11E)-10-hydroxy-12-[(1S,2R,3R)-3-hydroxy-5-oxo-2-[(2Z)-pent-2-en-1-yl]cyclopentyl]dodeca-4,7,11-trienoic acid

Traditional Name

(4Z,7Z,10S,11E)-10-hydroxy-12-[(1S,2R,3R)-3-hydroxy-5-oxo-2-[(2Z)-pent-2-en-1-yl]cyclopentyl]dodeca-4,7,11-trienoic acid

CAS Registry Number

Not Available

SMILES

CC\C=C/C[C@H]1[C@H](O)CC(=O)[C@H]1\C=C\[C@@H](O)C\C=C/C\C=C/CCC(O)=O

InChI Identifier

InChI=1S/C22H32O5/c1-2-3-8-12-18-19(21(25)16-20(18)24)15-14-17(23)11-9-6-4-5-7-10-13-22(26)27/h3,5-9,14-15,17-20,23-24H,2,4,10-13,16H2,1H3,(H,26,27)/b7-5-,8-3-,9-6-,15-14+/t17-,18+,19-,20+/m0/s1

InChI Key

IFQRUHXGXJVRNV-ZNQQBSSQSA-N

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as long-chain fatty acids. These are fatty acids with an aliphatic tail that contains between 13 and 21 carbon atoms.

Kingdom

Organic compounds

Super Class

Lipids and lipid-like molecules

Class

Fatty Acyls

Sub Class

Fatty acids and conjugates

Direct Parent

Long-chain fatty acids

Alternative Parents

Substituents

Long-chain fatty acid
Hydroxy fatty acid
Unsaturated fatty acid
Cyclopentanol
Cyclic alcohol
Cyclic ketone
Secondary alcohol
Ketone
Monocarboxylic acid or derivatives
Carboxylic acid
Carboxylic acid derivative
Organic oxygen compound
Organic oxide
Hydrocarbon derivative
Organooxygen compound
Carbonyl group
Alcohol
Aliphatic homomonocyclic compound

Molecular Framework

Aliphatic homomonocyclic compounds

External Descriptors

Not Available

Ontology

Not Available

Exogenous (HMDB: HMDB0062276)

Process

Not Available

Role

Not Available

Physical Properties

State

Not Available

Experimental Molecular Properties

Property	Value	Reference
Melting Point	Not Available	Not Available
Boiling Point	Not Available	Not Available
Water Solubility	Not Available	Not Available
LogP	Not Available	Not Available

Experimental Chromatographic Properties

Not Available

Predicted Molecular Properties

Property	Value	Source
logP	3.53	ALOGPS
logP	3.39	ChemAxon
logS	-4.2	ALOGPS
pKa (Strongest Acidic)	4.82	ChemAxon
pKa (Strongest Basic)	-1.6	ChemAxon
Physiological Charge	-1	ChemAxon
Hydrogen Acceptor Count	5	ChemAxon
Hydrogen Donor Count	3	ChemAxon
Polar Surface Area	94.83 Å²	ChemAxon
Rotatable Bond Count	12	ChemAxon
Refractivity	110.87 m³·mol⁻¹	ChemAxon
Polarizability	42.23 Å³	ChemAxon
Number of Rings	1	ChemAxon
Bioavailability	Yes	ChemAxon
Rule of Five	Yes	ChemAxon
Ghose Filter	Yes	ChemAxon
Veber's Rule	No	ChemAxon
MDDR-like Rule	No	ChemAxon

Predicted Chromatographic Properties

Predicted Collision Cross Sections

Predictor	Adduct Type	CCS Value (Å²)	Reference
DeepCCS	[M+H]+	202.846	30932474
DeepCCS	[M-H]-	200.45	30932474
DeepCCS	[M-2H]-	233.416	30932474
DeepCCS	[M+Na]+	208.758	30932474
AllCCS	[M+H]+	200.1	32859911
AllCCS	[M+H-H2O]+	197.5	32859911
AllCCS	[M+NH4]+	202.4	32859911
AllCCS	[M+Na]+	203.1	32859911
AllCCS	[M-H]-	196.7	32859911
AllCCS	[M+Na-2H]-	198.4	32859911
AllCCS	[M+HCOO]-	200.5	32859911

Predicted Kovats Retention Indices

Underivatized

Metabolite	SMILES	Kovats RI Value	Column Type	Reference
10-Hydroxy-E4-neuroprostane	CC\C=C/C[C@H]1[C@H](O)CC(=O)[C@H]1\C=C\[C@@H](O)C\C=C/C\C=C/CCC(O)=O	4750.1	Standard polar	33892256
10-Hydroxy-E4-neuroprostane	CC\C=C/C[C@H]1[C@H](O)CC(=O)[C@H]1\C=C\[C@@H](O)C\C=C/C\C=C/CCC(O)=O	2834.0	Standard non polar	33892256
10-Hydroxy-E4-neuroprostane	CC\C=C/C[C@H]1[C@H](O)CC(=O)[C@H]1\C=C\[C@@H](O)C\C=C/C\C=C/CCC(O)=O	3128.3	Semi standard non polar	33892256

Derivatized

Derivative Name / Structure	SMILES	Kovats RI Value	Column Type	Reference
10-Hydroxy-E4-neuroprostane,1TMS,isomer #1	CC/C=C\C[C@@H]1[C@H](/C=C/[C@@H](O)C/C=C\C/C=C\CCC(=O)O)C(=O)C[C@H]1O[Si](C)(C)C	3059.1	Semi standard non polar	33892256
10-Hydroxy-E4-neuroprostane,1TMS,isomer #2	CC/C=C\C[C@@H]1[C@H](/C=C/[C@H](C/C=C\C/C=C\CCC(=O)O)O[Si](C)(C)C)C(=O)C[C@H]1O	3146.5	Semi standard non polar	33892256
10-Hydroxy-E4-neuroprostane,1TMS,isomer #3	CC/C=C\C[C@@H]1[C@H](/C=C/[C@@H](O)C/C=C\C/C=C\CCC(=O)O[Si](C)(C)C)C(=O)C[C@H]1O	3013.2	Semi standard non polar	33892256
10-Hydroxy-E4-neuroprostane,1TMS,isomer #4	CC/C=C\C[C@@H]1C(/C=C/[C@@H](O)C/C=C\C/C=C\CCC(=O)O)=C(O[Si](C)(C)C)C[C@H]1O	3070.0	Semi standard non polar	33892256
10-Hydroxy-E4-neuroprostane,1TMS,isomer #5	CC/C=C\C[C@H]1[C@H](O)C=C(O[Si](C)(C)C)[C@H]1/C=C/[C@@H](O)C/C=C\C/C=C\CCC(=O)O	2980.3	Semi standard non polar	33892256
10-Hydroxy-E4-neuroprostane,2TMS,isomer #1	CC/C=C\C[C@@H]1[C@H](/C=C/[C@H](C/C=C\C/C=C\CCC(=O)O)O[Si](C)(C)C)C(=O)C[C@H]1O[Si](C)(C)C	3045.1	Semi standard non polar	33892256
10-Hydroxy-E4-neuroprostane,2TMS,isomer #2	CC/C=C\C[C@@H]1[C@H](/C=C/[C@@H](O)C/C=C\C/C=C\CCC(=O)O[Si](C)(C)C)C(=O)C[C@H]1O[Si](C)(C)C	2995.7	Semi standard non polar	33892256
10-Hydroxy-E4-neuroprostane,2TMS,isomer #3	CC/C=C\C[C@@H]1C(/C=C/[C@@H](O)C/C=C\C/C=C\CCC(=O)O)=C(O[Si](C)(C)C)C[C@H]1O[Si](C)(C)C	3056.9	Semi standard non polar	33892256
10-Hydroxy-E4-neuroprostane,2TMS,isomer #4	CC/C=C\C[C@H]1[C@H](O[Si](C)(C)C)C=C(O[Si](C)(C)C)[C@H]1/C=C/[C@@H](O)C/C=C\C/C=C\CCC(=O)O	3008.5	Semi standard non polar	33892256
10-Hydroxy-E4-neuroprostane,2TMS,isomer #5	CC/C=C\C[C@@H]1[C@H](/C=C/[C@H](C/C=C\C/C=C\CCC(=O)O[Si](C)(C)C)O[Si](C)(C)C)C(=O)C[C@H]1O	3034.5	Semi standard non polar	33892256
10-Hydroxy-E4-neuroprostane,2TMS,isomer #6	CC/C=C\C[C@@H]1C(/C=C/[C@H](C/C=C\C/C=C\CCC(=O)O)O[Si](C)(C)C)=C(O[Si](C)(C)C)C[C@H]1O	3140.3	Semi standard non polar	33892256
10-Hydroxy-E4-neuroprostane,2TMS,isomer #7	CC/C=C\C[C@H]1[C@H](O)C=C(O[Si](C)(C)C)[C@H]1/C=C/[C@H](C/C=C\C/C=C\CCC(=O)O)O[Si](C)(C)C	3008.0	Semi standard non polar	33892256
10-Hydroxy-E4-neuroprostane,2TMS,isomer #8	CC/C=C\C[C@@H]1C(/C=C/[C@@H](O)C/C=C\C/C=C\CCC(=O)O[Si](C)(C)C)=C(O[Si](C)(C)C)C[C@H]1O	3047.5	Semi standard non polar	33892256
10-Hydroxy-E4-neuroprostane,2TMS,isomer #9	CC/C=C\C[C@H]1[C@H](O)C=C(O[Si](C)(C)C)[C@H]1/C=C/[C@@H](O)C/C=C\C/C=C\CCC(=O)O[Si](C)(C)C	2958.9	Semi standard non polar	33892256
10-Hydroxy-E4-neuroprostane,3TMS,isomer #1	CC/C=C\C[C@@H]1[C@H](/C=C/[C@H](C/C=C\C/C=C\CCC(=O)O[Si](C)(C)C)O[Si](C)(C)C)C(=O)C[C@H]1O[Si](C)(C)C	2975.0	Semi standard non polar	33892256
10-Hydroxy-E4-neuroprostane,3TMS,isomer #2	CC/C=C\C[C@@H]1C(/C=C/[C@H](C/C=C\C/C=C\CCC(=O)O)O[Si](C)(C)C)=C(O[Si](C)(C)C)C[C@H]1O[Si](C)(C)C	3056.3	Semi standard non polar	33892256
10-Hydroxy-E4-neuroprostane,3TMS,isomer #3	CC/C=C\C[C@H]1[C@H](O[Si](C)(C)C)C=C(O[Si](C)(C)C)[C@H]1/C=C/[C@H](C/C=C\C/C=C\CCC(=O)O)O[Si](C)(C)C	3000.3	Semi standard non polar	33892256
10-Hydroxy-E4-neuroprostane,3TMS,isomer #4	CC/C=C\C[C@@H]1C(/C=C/[C@@H](O)C/C=C\C/C=C\CCC(=O)O[Si](C)(C)C)=C(O[Si](C)(C)C)C[C@H]1O[Si](C)(C)C	3021.8	Semi standard non polar	33892256
10-Hydroxy-E4-neuroprostane,3TMS,isomer #5	CC/C=C\C[C@H]1[C@H](O[Si](C)(C)C)C=C(O[Si](C)(C)C)[C@H]1/C=C/[C@@H](O)C/C=C\C/C=C\CCC(=O)O[Si](C)(C)C	2972.9	Semi standard non polar	33892256
10-Hydroxy-E4-neuroprostane,3TMS,isomer #6	CC/C=C\C[C@@H]1C(/C=C/[C@H](C/C=C\C/C=C\CCC(=O)O[Si](C)(C)C)O[Si](C)(C)C)=C(O[Si](C)(C)C)C[C@H]1O	3071.9	Semi standard non polar	33892256
10-Hydroxy-E4-neuroprostane,3TMS,isomer #7	CC/C=C\C[C@H]1[C@H](O)C=C(O[Si](C)(C)C)[C@H]1/C=C/[C@H](C/C=C\C/C=C\CCC(=O)O[Si](C)(C)C)O[Si](C)(C)C	2965.9	Semi standard non polar	33892256
10-Hydroxy-E4-neuroprostane,4TMS,isomer #1	CC/C=C\C[C@@H]1C(/C=C/[C@H](C/C=C\C/C=C\CCC(=O)O[Si](C)(C)C)O[Si](C)(C)C)=C(O[Si](C)(C)C)C[C@H]1O[Si](C)(C)C	3018.6	Semi standard non polar	33892256
10-Hydroxy-E4-neuroprostane,4TMS,isomer #1	CC/C=C\C[C@@H]1C(/C=C/[C@H](C/C=C\C/C=C\CCC(=O)O[Si](C)(C)C)O[Si](C)(C)C)=C(O[Si](C)(C)C)C[C@H]1O[Si](C)(C)C	2961.4	Standard non polar	33892256
10-Hydroxy-E4-neuroprostane,4TMS,isomer #1	CC/C=C\C[C@@H]1C(/C=C/[C@H](C/C=C\C/C=C\CCC(=O)O[Si](C)(C)C)O[Si](C)(C)C)=C(O[Si](C)(C)C)C[C@H]1O[Si](C)(C)C	3035.9	Standard polar	33892256
10-Hydroxy-E4-neuroprostane,4TMS,isomer #2	CC/C=C\C[C@H]1[C@H](O[Si](C)(C)C)C=C(O[Si](C)(C)C)[C@H]1/C=C/[C@H](C/C=C\C/C=C\CCC(=O)O[Si](C)(C)C)O[Si](C)(C)C	3001.9	Semi standard non polar	33892256
10-Hydroxy-E4-neuroprostane,4TMS,isomer #2	CC/C=C\C[C@H]1[C@H](O[Si](C)(C)C)C=C(O[Si](C)(C)C)[C@H]1/C=C/[C@H](C/C=C\C/C=C\CCC(=O)O[Si](C)(C)C)O[Si](C)(C)C	2790.1	Standard non polar	33892256
10-Hydroxy-E4-neuroprostane,4TMS,isomer #2	CC/C=C\C[C@H]1[C@H](O[Si](C)(C)C)C=C(O[Si](C)(C)C)[C@H]1/C=C/[C@H](C/C=C\C/C=C\CCC(=O)O[Si](C)(C)C)O[Si](C)(C)C	3032.8	Standard polar	33892256
10-Hydroxy-E4-neuroprostane,1TBDMS,isomer #1	CC/C=C\C[C@@H]1[C@H](/C=C/[C@@H](O)C/C=C\C/C=C\CCC(=O)O)C(=O)C[C@H]1O[Si](C)(C)C(C)(C)C	3274.2	Semi standard non polar	33892256
10-Hydroxy-E4-neuroprostane,1TBDMS,isomer #2	CC/C=C\C[C@@H]1[C@H](/C=C/[C@H](C/C=C\C/C=C\CCC(=O)O)O[Si](C)(C)C(C)(C)C)C(=O)C[C@H]1O	3374.1	Semi standard non polar	33892256
10-Hydroxy-E4-neuroprostane,1TBDMS,isomer #3	CC/C=C\C[C@@H]1[C@H](/C=C/[C@@H](O)C/C=C\C/C=C\CCC(=O)O[Si](C)(C)C(C)(C)C)C(=O)C[C@H]1O	3269.9	Semi standard non polar	33892256
10-Hydroxy-E4-neuroprostane,1TBDMS,isomer #4	CC/C=C\C[C@@H]1C(/C=C/[C@@H](O)C/C=C\C/C=C\CCC(=O)O)=C(O[Si](C)(C)C(C)(C)C)C[C@H]1O	3318.8	Semi standard non polar	33892256
10-Hydroxy-E4-neuroprostane,1TBDMS,isomer #5	CC/C=C\C[C@H]1[C@H](O)C=C(O[Si](C)(C)C(C)(C)C)[C@H]1/C=C/[C@@H](O)C/C=C\C/C=C\CCC(=O)O	3242.2	Semi standard non polar	33892256
10-Hydroxy-E4-neuroprostane,2TBDMS,isomer #1	CC/C=C\C[C@@H]1[C@H](/C=C/[C@H](C/C=C\C/C=C\CCC(=O)O)O[Si](C)(C)C(C)(C)C)C(=O)C[C@H]1O[Si](C)(C)C(C)(C)C	3487.8	Semi standard non polar	33892256
10-Hydroxy-E4-neuroprostane,2TBDMS,isomer #2	CC/C=C\C[C@@H]1[C@H](/C=C/[C@@H](O)C/C=C\C/C=C\CCC(=O)O[Si](C)(C)C(C)(C)C)C(=O)C[C@H]1O[Si](C)(C)C(C)(C)C	3450.7	Semi standard non polar	33892256
10-Hydroxy-E4-neuroprostane,2TBDMS,isomer #3	CC/C=C\C[C@@H]1C(/C=C/[C@@H](O)C/C=C\C/C=C\CCC(=O)O)=C(O[Si](C)(C)C(C)(C)C)C[C@H]1O[Si](C)(C)C(C)(C)C	3493.6	Semi standard non polar	33892256
10-Hydroxy-E4-neuroprostane,2TBDMS,isomer #4	CC/C=C\C[C@H]1[C@H](O[Si](C)(C)C(C)(C)C)C=C(O[Si](C)(C)C(C)(C)C)[C@H]1/C=C/[C@@H](O)C/C=C\C/C=C\CCC(=O)O	3467.6	Semi standard non polar	33892256
10-Hydroxy-E4-neuroprostane,2TBDMS,isomer #5	CC/C=C\C[C@@H]1[C@H](/C=C/[C@H](C/C=C\C/C=C\CCC(=O)O[Si](C)(C)C(C)(C)C)O[Si](C)(C)C(C)(C)C)C(=O)C[C@H]1O	3505.9	Semi standard non polar	33892256
10-Hydroxy-E4-neuroprostane,2TBDMS,isomer #6	CC/C=C\C[C@@H]1C(/C=C/[C@H](C/C=C\C/C=C\CCC(=O)O)O[Si](C)(C)C(C)(C)C)=C(O[Si](C)(C)C(C)(C)C)C[C@H]1O	3564.0	Semi standard non polar	33892256
10-Hydroxy-E4-neuroprostane,2TBDMS,isomer #7	CC/C=C\C[C@H]1[C@H](O)C=C(O[Si](C)(C)C(C)(C)C)[C@H]1/C=C/[C@H](C/C=C\C/C=C\CCC(=O)O)O[Si](C)(C)C(C)(C)C	3490.9	Semi standard non polar	33892256
10-Hydroxy-E4-neuroprostane,2TBDMS,isomer #8	CC/C=C\C[C@@H]1C(/C=C/[C@@H](O)C/C=C\C/C=C\CCC(=O)O[Si](C)(C)C(C)(C)C)=C(O[Si](C)(C)C(C)(C)C)C[C@H]1O	3505.7	Semi standard non polar	33892256
10-Hydroxy-E4-neuroprostane,2TBDMS,isomer #9	CC/C=C\C[C@H]1[C@H](O)C=C(O[Si](C)(C)C(C)(C)C)[C@H]1/C=C/[C@@H](O)C/C=C\C/C=C\CCC(=O)O[Si](C)(C)C(C)(C)C	3442.3	Semi standard non polar	33892256
10-Hydroxy-E4-neuroprostane,3TBDMS,isomer #1	CC/C=C\C[C@@H]1[C@H](/C=C/[C@H](C/C=C\C/C=C\CCC(=O)O[Si](C)(C)C(C)(C)C)O[Si](C)(C)C(C)(C)C)C(=O)C[C@H]1O[Si](C)(C)C(C)(C)C	3687.9	Semi standard non polar	33892256
10-Hydroxy-E4-neuroprostane,3TBDMS,isomer #2	CC/C=C\C[C@@H]1C(/C=C/[C@H](C/C=C\C/C=C\CCC(=O)O)O[Si](C)(C)C(C)(C)C)=C(O[Si](C)(C)C(C)(C)C)C[C@H]1O[Si](C)(C)C(C)(C)C	3698.2	Semi standard non polar	33892256
10-Hydroxy-E4-neuroprostane,3TBDMS,isomer #3	CC/C=C\C[C@H]1[C@H](O[Si](C)(C)C(C)(C)C)C=C(O[Si](C)(C)C(C)(C)C)[C@H]1/C=C/[C@H](C/C=C\C/C=C\CCC(=O)O)O[Si](C)(C)C(C)(C)C	3691.6	Semi standard non polar	33892256
10-Hydroxy-E4-neuroprostane,3TBDMS,isomer #4	CC/C=C\C[C@@H]1C(/C=C/[C@@H](O)C/C=C\C/C=C\CCC(=O)O[Si](C)(C)C(C)(C)C)=C(O[Si](C)(C)C(C)(C)C)C[C@H]1O[Si](C)(C)C(C)(C)C	3686.6	Semi standard non polar	33892256
10-Hydroxy-E4-neuroprostane,3TBDMS,isomer #5	CC/C=C\C[C@H]1[C@H](O[Si](C)(C)C(C)(C)C)C=C(O[Si](C)(C)C(C)(C)C)[C@H]1/C=C/[C@@H](O)C/C=C\C/C=C\CCC(=O)O[Si](C)(C)C(C)(C)C	3675.5	Semi standard non polar	33892256
10-Hydroxy-E4-neuroprostane,3TBDMS,isomer #6	CC/C=C\C[C@@H]1C(/C=C/[C@H](C/C=C\C/C=C\CCC(=O)O[Si](C)(C)C(C)(C)C)O[Si](C)(C)C(C)(C)C)=C(O[Si](C)(C)C(C)(C)C)C[C@H]1O	3735.2	Semi standard non polar	33892256
10-Hydroxy-E4-neuroprostane,3TBDMS,isomer #7	CC/C=C\C[C@H]1[C@H](O)C=C(O[Si](C)(C)C(C)(C)C)[C@H]1/C=C/[C@H](C/C=C\C/C=C\CCC(=O)O[Si](C)(C)C(C)(C)C)O[Si](C)(C)C(C)(C)C	3686.8	Semi standard non polar	33892256
10-Hydroxy-E4-neuroprostane,4TBDMS,isomer #1	CC/C=C\C[C@@H]1C(/C=C/[C@H](C/C=C\C/C=C\CCC(=O)O[Si](C)(C)C(C)(C)C)O[Si](C)(C)C(C)(C)C)=C(O[Si](C)(C)C(C)(C)C)C[C@H]1O[Si](C)(C)C(C)(C)C	3854.8	Semi standard non polar	33892256
10-Hydroxy-E4-neuroprostane,4TBDMS,isomer #1	CC/C=C\C[C@@H]1C(/C=C/[C@H](C/C=C\C/C=C\CCC(=O)O[Si](C)(C)C(C)(C)C)O[Si](C)(C)C(C)(C)C)=C(O[Si](C)(C)C(C)(C)C)C[C@H]1O[Si](C)(C)C(C)(C)C	3574.5	Standard non polar	33892256
10-Hydroxy-E4-neuroprostane,4TBDMS,isomer #1	CC/C=C\C[C@@H]1C(/C=C/[C@H](C/C=C\C/C=C\CCC(=O)O[Si](C)(C)C(C)(C)C)O[Si](C)(C)C(C)(C)C)=C(O[Si](C)(C)C(C)(C)C)C[C@H]1O[Si](C)(C)C(C)(C)C	3256.0	Standard polar	33892256
10-Hydroxy-E4-neuroprostane,4TBDMS,isomer #2	CC/C=C\C[C@H]1[C@H](O[Si](C)(C)C(C)(C)C)C=C(O[Si](C)(C)C(C)(C)C)[C@H]1/C=C/[C@H](C/C=C\C/C=C\CCC(=O)O[Si](C)(C)C(C)(C)C)O[Si](C)(C)C(C)(C)C	3880.7	Semi standard non polar	33892256
10-Hydroxy-E4-neuroprostane,4TBDMS,isomer #2	CC/C=C\C[C@H]1[C@H](O[Si](C)(C)C(C)(C)C)C=C(O[Si](C)(C)C(C)(C)C)[C@H]1/C=C/[C@H](C/C=C\C/C=C\CCC(=O)O[Si](C)(C)C(C)(C)C)O[Si](C)(C)C(C)(C)C	3339.2	Standard non polar	33892256
10-Hydroxy-E4-neuroprostane,4TBDMS,isomer #2	CC/C=C\C[C@H]1[C@H](O[Si](C)(C)C(C)(C)C)C=C(O[Si](C)(C)C(C)(C)C)[C@H]1/C=C/[C@H](C/C=C\C/C=C\CCC(=O)O[Si](C)(C)C(C)(C)C)O[Si](C)(C)C(C)(C)C	3255.4	Standard polar	33892256

Spectra

GC-MS Spectra

Spectrum Type	Description	Splash Key	Deposition Date	Source	View
Predicted GC-MS	Predicted GC-MS Spectrum - 10-Hydroxy-E4-neuroprostane GC-MS (Non-derivatized) - 70eV, Positive	Not Available	2021-10-12	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - 10-Hydroxy-E4-neuroprostane GC-MS (Non-derivatized) - 70eV, Positive	Not Available	2021-10-12	Wishart Lab	View Spectrum

MS/MS Spectra

Spectrum Type	Description	Splash Key	Deposition Date	Source	View
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 10-Hydroxy-E4-neuroprostane 10V, Positive-QTOF	splash10-0a4l-0009000000-58e1a16fd1f1d6f40fc2	2019-02-22	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 10-Hydroxy-E4-neuroprostane 20V, Positive-QTOF	splash10-0btc-2529000000-582891e4e64fabc80e0e	2019-02-22	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 10-Hydroxy-E4-neuroprostane 40V, Positive-QTOF	splash10-0553-9530000000-000c6ad6c5600db90f15	2019-02-22	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 10-Hydroxy-E4-neuroprostane 10V, Negative-QTOF	splash10-056r-0009000000-b07646a700a3a0cd1f73	2019-02-23	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 10-Hydroxy-E4-neuroprostane 20V, Negative-QTOF	splash10-0a4i-0109000000-9c7282b7fa9d2ddeb3bd	2019-02-23	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 10-Hydroxy-E4-neuroprostane 40V, Negative-QTOF	splash10-0a4i-9422000000-7d1fd6a8710037817079	2019-02-23	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 10-Hydroxy-E4-neuroprostane 10V, Positive-QTOF	splash10-0a4l-0009000000-6e17a6c8b54a85431d2f	2021-09-23	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 10-Hydroxy-E4-neuroprostane 20V, Positive-QTOF	splash10-0a5c-1129000000-04e8ce605c48b9ee9417	2021-09-23	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 10-Hydroxy-E4-neuroprostane 40V, Positive-QTOF	splash10-05ru-9710000000-c12a9f5d97752cf876c3	2021-09-23	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 10-Hydroxy-E4-neuroprostane 10V, Negative-QTOF	splash10-004i-0009000000-f9dd12543dc44d5d21a6	2021-09-25	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 10-Hydroxy-E4-neuroprostane 20V, Negative-QTOF	splash10-0a4i-1009000000-35e15ef8269c4d064d1b	2021-09-25	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 10-Hydroxy-E4-neuroprostane 40V, Negative-QTOF	splash10-00n3-5915000000-710d75a327de2a9dea89	2021-09-25	Wishart Lab	View Spectrum

Biological Properties

Cellular Locations

Not Available

Biospecimen Locations

Not Available

Tissue Locations

Not Available

Pathways

Not Available

Name	SMPDB/PathBank	KEGG

Normal Concentrations

Not Available

Abnormal Concentrations

Not Available

Associated Disorders and Diseases

Disease References

None

Associated OMIM IDs

None

External Links

DrugBank ID

Not Available

Phenol Explorer Compound ID

Not Available

FooDB ID

Not Available

KNApSAcK ID

Not Available

Chemspider ID

74857869

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

131840634

PDB ID

Not Available

ChEBI ID

Not Available

Food Biomarker Ontology

Not Available

VMH ID

Not Available

MarkerDB ID

Not Available

Good Scents ID

Not Available

References

Synthesis Reference

Not Available

Material Safety Data Sheet (MSDS)

Not Available

General References

Not Available

Showing metabocard for 10-Hydroxy-E4-neuroprostane (HMDB0062276)

MOL for HMDB0062276 (10-Hydroxy-E4-neuroprostane)

3D MOL for HMDB0062276 (10-Hydroxy-E4-neuroprostane)

3D SDF for HMDB0062276 (10-Hydroxy-E4-neuroprostane)

3D-SDF for HMDB0062276 (10-Hydroxy-E4-neuroprostane)

PDB for HMDB0062276 (10-Hydroxy-E4-neuroprostane)

3D PDB for HMDB0062276 (10-Hydroxy-E4-neuroprostane)

SMILES for HMDB0062276 (10-Hydroxy-E4-neuroprostane)

INCHI for HMDB0062276 (10-Hydroxy-E4-neuroprostane)

Structure for HMDB0062276 (10-Hydroxy-E4-neuroprostane)

3D Structure for HMDB0062276 (10-Hydroxy-E4-neuroprostane)

Predicted Collision Cross Sections

Predicted Kovats Retention Indices

Underivatized

Derivatized

GC-MS Spectra

MS/MS Spectra