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Record Information

Version

5.0

Status

Detected but not Quantified

Creation Date

2009-07-25 00:01:52 UTC

Update Date

2022-03-07 02:51:26 UTC

HMDB ID

HMDB0012504

Secondary Accession Numbers

HMDB12504

Metabolite Identification

Common Name

10,11-dihydro-leukotriene B4

Description

10,11-dihydro-leukotriene B4 is the metabolite of lipid omega-oxidation of leukotriene B4 (LTB4). LTB4 is the major metabolite in neutrophil polymorphonuclear leukocytes. Omega-oxidation is the major pathway for the catabolism of leukotriene B4 in human polymorphonuclear leukocytes. Leukotrienes are metabolites of arachidonic acid derived from the action of 5-LO (5-lipoxygenase). The immediate product of 5-LO is LTA4 (leukotriene A4), which is enzymatically converted into either LTB4 (leukotriene B4) by LTA4 hydrolase or LTC4 (leukotriene C4) by LTC4 synthase. The regulation of leukotriene production occurs at various levels, including expression of 5-LO, translocation of 5-LO to the perinuclear region, and phosphorylation to either enhance or inhibit the activity of 5-LO. Biologically active LTB4 is metabolized by omega-oxidation carried out by specific cytochrome P450s (CYP4F) followed by beta-oxidation from the omega-carboxy position and after CoA ester formation (PMID: 7649996 , 17623009 , 2853166 , 6088485 ). Leukotrienes are eicosanoids. The eicosanoids consist of the prostaglandins (PGs), thromboxanes (TXs), leukotrienes (LTs), and lipoxins (LXs). The PGs and TXs are collectively identified as prostanoids. Prostaglandins were originally shown to be synthesized in the prostate gland, thromboxanes from platelets (thrombocytes), and leukotrienes from leukocytes, hence the derivation of their names. All mammalian cells except erythrocytes synthesize eicosanoids. These molecules are extremely potent, able to cause profound physiological effects at very dilute concentrations. All eicosanoids function locally at the site of synthesis, through receptor-mediated G-protein linked signalling pathways.

Structure

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

HMDB0012504
     RDKit          3D
10,11-dihydro-leukotriene B4
 58 57  0  0  0  0  0  0  0  0999 V2000
   -7.8894   -2.2453    0.9140 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.7988   -1.1308    0.9743 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.8468   -0.4822   -0.3436 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.0023    0.6497   -0.6921 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5337    0.5807   -0.7169 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8044    0.2890    0.5152 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9358    1.1363    1.0725 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5959    2.4484    0.5455 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0825    2.4591    0.2499 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.6848    3.6881   -0.2590 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7680    1.4068   -0.7994 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7298    1.4644   -1.0481 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5231    1.1926    0.1522 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3649    0.1525    0.1432 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1758   -0.1675    1.2983 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0165   -1.1677    1.3364 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2026   -2.0464    0.1919 C   0  0  2  0  0  0  0  0  0  0  0  0
    4.7386   -3.2754    0.6514 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.0767   -1.5827   -0.8989 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.4885   -1.2933   -0.5832 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.7485   -0.1846    0.3840 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.2234   -0.0144    0.5672 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.6500    0.8605    1.3363 O   0  0  0  0  0  0  0  0  0  0  0  0
    9.0760   -0.8357   -0.1245 O   0  0  0  0  0  0  0  0  0  0  0  0
   -7.7616   -2.9176    1.7610 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.6663   -2.7962   -0.0360 H   0  0  0  0  0  0  0  0  0  0  0  0
   -8.8888   -1.7706    0.8433 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.8912   -1.6266    1.2936 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.1450   -0.4836    1.8058 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.7725   -1.2644   -1.1693 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.9312   -0.1314   -0.4783 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.3396    0.9695   -1.7452 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.3447    1.5479   -0.0875 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1083    1.4749   -1.2680 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2069   -0.2590   -1.4504 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9215   -0.6780    1.0429 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4260    0.8345    2.0070 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7561    3.2190    1.3457 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0611    2.7944   -0.3606 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5198    2.2350    1.1660 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0355    3.7364   -1.1951 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2737    1.6238   -1.7467 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9864    0.3830   -0.4217 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.9422    2.4980   -1.4171 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.9726    0.7562   -1.8616 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.4652    1.7852    1.0417 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.3898   -0.4251   -0.7534 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.0806    0.4596    2.1852 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.5745   -1.3685    2.2789 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.2022   -2.3390   -0.2684 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.2549   -3.7041   -0.0632 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.0789   -2.4167   -1.6848 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.5891   -0.6902   -1.4079 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.9600   -2.2323   -0.1626 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.0223   -1.0778   -1.5641 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.4013    0.7958   -0.0535 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.3286   -0.3336    1.3800 H   0  0  0  0  0  0  0  0  0  0  0  0
    9.7021   -0.5008   -0.8425 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  1  0
  3  4  1  0
  4  5  1  0
  5  6  1  0
  6  7  2  0
  7  8  1  0
  8  9  1  0
  9 10  1  0
  9 11  1  0
 11 12  1  0
 12 13  1  0
 13 14  2  0
 14 15  1  0
 15 16  2  0
 16 17  1  0
 17 18  1  0
 17 19  1  0
 19 20  1  0
 20 21  1  0
 21 22  1  0
 22 23  2  0
 22 24  1  0
  1 25  1  0
  1 26  1  0
  1 27  1  0
  2 28  1  0
  2 29  1  0
  3 30  1  0
  3 31  1  0
  4 32  1  0
  4 33  1  0
  5 34  1  0
  5 35  1  0
  6 36  1  0
  7 37  1  0
  8 38  1  0
  8 39  1  0
  9 40  1  1
 10 41  1  0
 11 42  1  0
 11 43  1  0
 12 44  1  0
 12 45  1  0
 13 46  1  0
 14 47  1  0
 15 48  1  0
 16 49  1  0
 17 50  1  6
 18 51  1  0
 19 52  1  0
 19 53  1  0
 20 54  1  0
 20 55  1  0
 21 56  1  0
 21 57  1  0
 24 58  1  0
M  END

  Mrv0541 02251208062D          

 24 23  0  0  1  0            999 V2000
   15.5082   -9.6398    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   16.2227  -10.0523    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   16.2227  -10.8773    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   16.9372  -11.2898    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   16.9372  -12.1148    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   17.6516  -12.5273    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   17.6516  -13.3523    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   16.9372  -13.7648    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   16.9372  -14.5899    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   17.6516  -15.0024    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   16.2227  -15.0024    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   15.5082  -14.5899    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   14.7937  -15.0024    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   14.0792  -14.5899    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   13.3647  -15.0024    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   12.6503  -14.5899    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   12.6503  -13.7648    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   11.9358  -13.3523    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   13.3647  -13.3523    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   13.3647  -12.5273    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   14.0792  -12.1148    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   14.0792  -11.2898    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   14.7937  -10.8773    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   13.3647  -10.8773    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0  0  0  0
  2  3  1  0  0  0  0
  3  4  1  0  0  0  0
  4  5  1  0  0  0  0
  5  6  1  0  0  0  0
  6  7  2  0  0  0  0
  7  8  1  0  0  0  0
  8  9  1  0  0  0  0
  9 10  1  6  0  0  0
  9 11  1  0  0  0  0
 11 12  1  0  0  0  0
 12 13  1  0  0  0  0
 13 14  2  0  0  0  0
 14 15  1  0  0  0  0
 15 16  2  0  0  0  0
 16 17  1  0  0  0  0
 17 18  1  6  0  0  0
 17 19  1  0  0  0  0
 19 20  1  0  0  0  0
 20 21  1  0  0  0  0
 21 22  1  0  0  0  0
 22 23  1  0  0  0  0
 22 24  2  0  0  0  0
M  END
> <DATABASE_ID>
HMDB0012504

> <DATABASE_NAME>
hmdb

> <SMILES>
CCCCC\C=C/C[C@H](O)CC\C=C\C=C/[C@H](O)CCCC(O)=O

> <INCHI_IDENTIFIER>
InChI=1S/C20H34O4/c1-2-3-4-5-6-9-13-18(21)14-10-7-8-11-15-19(22)16-12-17-20(23)24/h6-9,11,15,18-19,21-22H,2-5,10,12-14,16-17H2,1H3,(H,23,24)/b8-7+,9-6-,15-11-/t18-,19-/m0/s1

> <INCHI_KEY>
NKUPFHTVILUPKF-RNEQFKNCSA-N

> <FORMULA>
C20H34O4

> <MOLECULAR_WEIGHT>
338.4816

> <EXACT_MASS>
338.245709576

> <JCHEM_ACCEPTOR_COUNT>
4

> <JCHEM_AVERAGE_POLARIZABILITY>
40.21032378935661

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
3

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
(5R,6Z,8E,12R,14Z)-5,12-dihydroxyicosa-6,8,14-trienoic acid

> <ALOGPS_LOGP>
5.84

> <JCHEM_LOGP>
4.331562873666666

> <ALOGPS_LOGS>
-4.46

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
0

> <JCHEM_PHYSIOLOGICAL_CHARGE>
-1

> <JCHEM_PKA>
17.865306559197933

> <JCHEM_PKA_STRONGEST_ACIDIC>
4.584102239638748

> <JCHEM_PKA_STRONGEST_BASIC>
-1.0842007383674774

> <JCHEM_POLAR_SURFACE_AREA>
77.75999999999999

> <JCHEM_REFRACTIVITY>
102.02239999999999

> <JCHEM_ROTATABLE_BOND_COUNT>
15

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
1.18e-02 g/l

> <JCHEM_TRADITIONAL_IUPAC>
(5R,6Z,8E,12R,14Z)-5,12-dihydroxyicosa-6,8,14-trienoic acid

> <JCHEM_VEBER_RULE>
0

$$$$

HMDB0012504
     RDKit          3D
10,11-dihydro-leukotriene B4
 58 57  0  0  0  0  0  0  0  0999 V2000
   -7.8894   -2.2453    0.9140 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.7988   -1.1308    0.9743 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.8468   -0.4822   -0.3436 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.0023    0.6497   -0.6921 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5337    0.5807   -0.7169 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8044    0.2890    0.5152 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9358    1.1363    1.0725 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5959    2.4484    0.5455 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0825    2.4591    0.2499 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.6848    3.6881   -0.2590 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7680    1.4068   -0.7994 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7298    1.4644   -1.0481 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5231    1.1926    0.1522 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3649    0.1525    0.1432 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1758   -0.1675    1.2983 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0165   -1.1677    1.3364 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2026   -2.0464    0.1919 C   0  0  2  0  0  0  0  0  0  0  0  0
    4.7386   -3.2754    0.6514 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.0767   -1.5827   -0.8989 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.4885   -1.2933   -0.5832 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.7485   -0.1846    0.3840 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.2234   -0.0144    0.5672 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.6500    0.8605    1.3363 O   0  0  0  0  0  0  0  0  0  0  0  0
    9.0760   -0.8357   -0.1245 O   0  0  0  0  0  0  0  0  0  0  0  0
   -7.7616   -2.9176    1.7610 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.6663   -2.7962   -0.0360 H   0  0  0  0  0  0  0  0  0  0  0  0
   -8.8888   -1.7706    0.8433 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.8912   -1.6266    1.2936 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.1450   -0.4836    1.8058 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.7725   -1.2644   -1.1693 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.9312   -0.1314   -0.4783 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.3396    0.9695   -1.7452 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.3447    1.5479   -0.0875 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1083    1.4749   -1.2680 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2069   -0.2590   -1.4504 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9215   -0.6780    1.0429 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4260    0.8345    2.0070 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7561    3.2190    1.3457 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0611    2.7944   -0.3606 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5198    2.2350    1.1660 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0355    3.7364   -1.1951 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2737    1.6238   -1.7467 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9864    0.3830   -0.4217 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.9422    2.4980   -1.4171 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.9726    0.7562   -1.8616 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.4652    1.7852    1.0417 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.3898   -0.4251   -0.7534 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.0806    0.4596    2.1852 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.5745   -1.3685    2.2789 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.2022   -2.3390   -0.2684 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.2549   -3.7041   -0.0632 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.0789   -2.4167   -1.6848 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.5891   -0.6902   -1.4079 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.9600   -2.2323   -0.1626 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.0223   -1.0778   -1.5641 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.4013    0.7958   -0.0535 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.3286   -0.3336    1.3800 H   0  0  0  0  0  0  0  0  0  0  0  0
    9.7021   -0.5008   -0.8425 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  1  0
  3  4  1  0
  4  5  1  0
  5  6  1  0
  6  7  2  0
  7  8  1  0
  8  9  1  0
  9 10  1  0
  9 11  1  0
 11 12  1  0
 12 13  1  0
 13 14  2  0
 14 15  1  0
 15 16  2  0
 16 17  1  0
 17 18  1  0
 17 19  1  0
 19 20  1  0
 20 21  1  0
 21 22  1  0
 22 23  2  0
 22 24  1  0
  1 25  1  0
  1 26  1  0
  1 27  1  0
  2 28  1  0
  2 29  1  0
  3 30  1  0
  3 31  1  0
  4 32  1  0
  4 33  1  0
  5 34  1  0
  5 35  1  0
  6 36  1  0
  7 37  1  0
  8 38  1  0
  8 39  1  0
  9 40  1  1
 10 41  1  0
 11 42  1  0
 11 43  1  0
 12 44  1  0
 12 45  1  0
 13 46  1  0
 14 47  1  0
 15 48  1  0
 16 49  1  0
 17 50  1  6
 18 51  1  0
 19 52  1  0
 19 53  1  0
 20 54  1  0
 20 55  1  0
 21 56  1  0
 21 57  1  0
 24 58  1  0
M  END

HEADER    PROTEIN                                 25-FEB-12   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   25-FEB-12         0                                  
HETATM    1  C   UNK     0      28.949 -17.994   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0      30.282 -18.764   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0      30.282 -20.304   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0      31.616 -21.074   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0      31.616 -22.614   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0      32.950 -23.384   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0      32.950 -24.924   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0      31.616 -25.694   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0      31.616 -27.234   0.000  0.00  0.00           C+0
HETATM   10  O   UNK     0      32.950 -28.004   0.000  0.00  0.00           O+0
HETATM   11  C   UNK     0      30.282 -28.004   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0      28.949 -27.234   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0      27.615 -28.004   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0      26.281 -27.234   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0      24.947 -28.004   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0      23.614 -27.234   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0      23.614 -25.694   0.000  0.00  0.00           C+0
HETATM   18  O   UNK     0      22.280 -24.924   0.000  0.00  0.00           O+0
HETATM   19  C   UNK     0      24.947 -24.924   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0      24.947 -23.384   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0      26.281 -22.614   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0      26.281 -21.074   0.000  0.00  0.00           C+0
HETATM   23  O   UNK     0      27.615 -20.304   0.000  0.00  0.00           O+0
HETATM   24  O   UNK     0      24.947 -20.304   0.000  0.00  0.00           O+0
CONECT    1    2                                                            
CONECT    2    1    3                                                       
CONECT    3    2    4                                                       
CONECT    4    3    5                                                       
CONECT    5    4    6                                                       
CONECT    6    5    7                                                       
CONECT    7    6    8                                                       
CONECT    8    7    9                                                       
CONECT    9    8   10   11                                                  
CONECT   10    9                                                            
CONECT   11    9   12                                                       
CONECT   12   11   13                                                       
CONECT   13   12   14                                                       
CONECT   14   13   15                                                       
CONECT   15   14   16                                                       
CONECT   16   15   17                                                       
CONECT   17   16   18   19                                                  
CONECT   18   17                                                            
CONECT   19   17   20                                                       
CONECT   20   19   21                                                       
CONECT   21   20   22                                                       
CONECT   22   21   23   24                                                  
CONECT   23   22                                                            
CONECT   24   22                                                            
MASTER        0    0    0    0    0    0    0    0   24    0   46    0
END

COMPND    HMDB0012504
HETATM    1  C1  UNL     1      -7.889  -2.245   0.914  1.00  0.00           C  
HETATM    2  C2  UNL     1      -6.799  -1.131   0.974  1.00  0.00           C  
HETATM    3  C3  UNL     1      -6.847  -0.482  -0.344  1.00  0.00           C  
HETATM    4  C4  UNL     1      -6.002   0.650  -0.692  1.00  0.00           C  
HETATM    5  C5  UNL     1      -4.534   0.581  -0.717  1.00  0.00           C  
HETATM    6  C6  UNL     1      -3.804   0.289   0.515  1.00  0.00           C  
HETATM    7  C7  UNL     1      -2.936   1.136   1.072  1.00  0.00           C  
HETATM    8  C8  UNL     1      -2.596   2.448   0.545  1.00  0.00           C  
HETATM    9  C9  UNL     1      -1.082   2.459   0.250  1.00  0.00           C  
HETATM   10  O1  UNL     1      -0.685   3.688  -0.259  1.00  0.00           O  
HETATM   11  C10 UNL     1      -0.768   1.407  -0.799  1.00  0.00           C  
HETATM   12  C11 UNL     1       0.730   1.464  -1.048  1.00  0.00           C  
HETATM   13  C12 UNL     1       1.523   1.193   0.152  1.00  0.00           C  
HETATM   14  C13 UNL     1       2.365   0.152   0.143  1.00  0.00           C  
HETATM   15  C14 UNL     1       3.176  -0.168   1.298  1.00  0.00           C  
HETATM   16  C15 UNL     1       4.017  -1.168   1.336  1.00  0.00           C  
HETATM   17  C16 UNL     1       4.203  -2.046   0.192  1.00  0.00           C  
HETATM   18  O2  UNL     1       4.739  -3.275   0.651  1.00  0.00           O  
HETATM   19  C17 UNL     1       5.077  -1.583  -0.899  1.00  0.00           C  
HETATM   20  C18 UNL     1       6.489  -1.293  -0.583  1.00  0.00           C  
HETATM   21  C19 UNL     1       6.749  -0.185   0.384  1.00  0.00           C  
HETATM   22  C20 UNL     1       8.223  -0.014   0.567  1.00  0.00           C  
HETATM   23  O3  UNL     1       8.650   0.861   1.336  1.00  0.00           O  
HETATM   24  O4  UNL     1       9.076  -0.836  -0.125  1.00  0.00           O  
HETATM   25  H1  UNL     1      -7.762  -2.918   1.761  1.00  0.00           H  
HETATM   26  H2  UNL     1      -7.666  -2.796  -0.036  1.00  0.00           H  
HETATM   27  H3  UNL     1      -8.889  -1.771   0.843  1.00  0.00           H  
HETATM   28  H4  UNL     1      -5.891  -1.627   1.294  1.00  0.00           H  
HETATM   29  H5  UNL     1      -7.145  -0.484   1.806  1.00  0.00           H  
HETATM   30  H6  UNL     1      -6.772  -1.264  -1.169  1.00  0.00           H  
HETATM   31  H7  UNL     1      -7.931  -0.131  -0.478  1.00  0.00           H  
HETATM   32  H8  UNL     1      -6.340   0.969  -1.745  1.00  0.00           H  
HETATM   33  H9  UNL     1      -6.345   1.548  -0.088  1.00  0.00           H  
HETATM   34  H10 UNL     1      -4.108   1.475  -1.268  1.00  0.00           H  
HETATM   35  H11 UNL     1      -4.207  -0.259  -1.450  1.00  0.00           H  
HETATM   36  H12 UNL     1      -3.922  -0.678   1.043  1.00  0.00           H  
HETATM   37  H13 UNL     1      -2.426   0.834   2.007  1.00  0.00           H  
HETATM   38  H14 UNL     1      -2.756   3.219   1.346  1.00  0.00           H  
HETATM   39  H15 UNL     1      -3.061   2.794  -0.361  1.00  0.00           H  
HETATM   40  H16 UNL     1      -0.520   2.235   1.166  1.00  0.00           H  
HETATM   41  H17 UNL     1      -1.036   3.736  -1.195  1.00  0.00           H  
HETATM   42  H18 UNL     1      -1.274   1.624  -1.747  1.00  0.00           H  
HETATM   43  H19 UNL     1      -0.986   0.383  -0.422  1.00  0.00           H  
HETATM   44  H20 UNL     1       0.942   2.498  -1.417  1.00  0.00           H  
HETATM   45  H21 UNL     1       0.973   0.756  -1.862  1.00  0.00           H  
HETATM   46  H22 UNL     1       1.465   1.785   1.042  1.00  0.00           H  
HETATM   47  H23 UNL     1       2.390  -0.425  -0.753  1.00  0.00           H  
HETATM   48  H24 UNL     1       3.081   0.460   2.185  1.00  0.00           H  
HETATM   49  H25 UNL     1       4.574  -1.368   2.279  1.00  0.00           H  
HETATM   50  H26 UNL     1       3.202  -2.339  -0.268  1.00  0.00           H  
HETATM   51  H27 UNL     1       5.255  -3.704  -0.063  1.00  0.00           H  
HETATM   52  H28 UNL     1       5.079  -2.417  -1.685  1.00  0.00           H  
HETATM   53  H29 UNL     1       4.589  -0.690  -1.408  1.00  0.00           H  
HETATM   54  H30 UNL     1       6.960  -2.232  -0.163  1.00  0.00           H  
HETATM   55  H31 UNL     1       7.022  -1.078  -1.564  1.00  0.00           H  
HETATM   56  H32 UNL     1       6.401   0.796  -0.053  1.00  0.00           H  
HETATM   57  H33 UNL     1       6.329  -0.334   1.380  1.00  0.00           H  
HETATM   58  H34 UNL     1       9.702  -0.501  -0.843  1.00  0.00           H  
CONECT    1    2   25   26   27
CONECT    2    3   28   29
CONECT    3    4   30   31
CONECT    4    5   32   33
CONECT    5    6   34   35
CONECT    6    7    7   36
CONECT    7    8   37
CONECT    8    9   38   39
CONECT    9   10   11   40
CONECT   10   41
CONECT   11   12   42   43
CONECT   12   13   44   45
CONECT   13   14   14   46
CONECT   14   15   47
CONECT   15   16   16   48
CONECT   16   17   49
CONECT   17   18   19   50
CONECT   18   51
CONECT   19   20   52   53
CONECT   20   21   54   55
CONECT   21   22   56   57
CONECT   22   23   23   24
CONECT   24   58
END

HMDB0012504
     RDKit          3D
10,11-dihydro-leukotriene B4
 58 57  0  0  0  0  0  0  0  0999 V2000
   -7.8894   -2.2453    0.9140 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.7988   -1.1308    0.9743 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.8468   -0.4822   -0.3436 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.0023    0.6497   -0.6921 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5337    0.5807   -0.7169 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8044    0.2890    0.5152 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9358    1.1363    1.0725 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5959    2.4484    0.5455 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0825    2.4591    0.2499 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.6848    3.6881   -0.2590 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7680    1.4068   -0.7994 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7298    1.4644   -1.0481 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5231    1.1926    0.1522 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3649    0.1525    0.1432 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1758   -0.1675    1.2983 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0165   -1.1677    1.3364 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2026   -2.0464    0.1919 C   0  0  2  0  0  0  0  0  0  0  0  0
    4.7386   -3.2754    0.6514 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.0767   -1.5827   -0.8989 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.4885   -1.2933   -0.5832 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.7485   -0.1846    0.3840 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.2234   -0.0144    0.5672 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.6500    0.8605    1.3363 O   0  0  0  0  0  0  0  0  0  0  0  0
    9.0760   -0.8357   -0.1245 O   0  0  0  0  0  0  0  0  0  0  0  0
   -7.7616   -2.9176    1.7610 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.6663   -2.7962   -0.0360 H   0  0  0  0  0  0  0  0  0  0  0  0
   -8.8888   -1.7706    0.8433 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.8912   -1.6266    1.2936 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.1450   -0.4836    1.8058 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.7725   -1.2644   -1.1693 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.9312   -0.1314   -0.4783 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.3396    0.9695   -1.7452 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.3447    1.5479   -0.0875 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1083    1.4749   -1.2680 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2069   -0.2590   -1.4504 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9215   -0.6780    1.0429 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4260    0.8345    2.0070 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7561    3.2190    1.3457 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0611    2.7944   -0.3606 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5198    2.2350    1.1660 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0355    3.7364   -1.1951 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2737    1.6238   -1.7467 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9864    0.3830   -0.4217 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.9422    2.4980   -1.4171 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.9726    0.7562   -1.8616 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.4652    1.7852    1.0417 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.3898   -0.4251   -0.7534 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.0806    0.4596    2.1852 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.5745   -1.3685    2.2789 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.2022   -2.3390   -0.2684 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.2549   -3.7041   -0.0632 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.0789   -2.4167   -1.6848 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.5891   -0.6902   -1.4079 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.9600   -2.2323   -0.1626 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.0223   -1.0778   -1.5641 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.4013    0.7958   -0.0535 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.3286   -0.3336    1.3800 H   0  0  0  0  0  0  0  0  0  0  0  0
    9.7021   -0.5008   -0.8425 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  1  0
  3  4  1  0
  4  5  1  0
  5  6  1  0
  6  7  2  0
  7  8  1  0
  8  9  1  0
  9 10  1  0
  9 11  1  0
 11 12  1  0
 12 13  1  0
 13 14  2  0
 14 15  1  0
 15 16  2  0
 16 17  1  0
 17 18  1  0
 17 19  1  0
 19 20  1  0
 20 21  1  0
 21 22  1  0
 22 23  2  0
 22 24  1  0
  1 25  1  0
  1 26  1  0
  1 27  1  0
  2 28  1  0
  2 29  1  0
  3 30  1  0
  3 31  1  0
  4 32  1  0
  4 33  1  0
  5 34  1  0
  5 35  1  0
  6 36  1  0
  7 37  1  0
  8 38  1  0
  8 39  1  0
  9 40  1  1
 10 41  1  0
 11 42  1  0
 11 43  1  0
 12 44  1  0
 12 45  1  0
 13 46  1  0
 14 47  1  0
 15 48  1  0
 16 49  1  0
 17 50  1  6
 18 51  1  0
 19 52  1  0
 19 53  1  0
 20 54  1  0
 20 55  1  0
 21 56  1  0
 21 57  1  0
 24 58  1  0
M  END

View in JSmol View Stereo Labels

Synonyms

Value	Source
(5S,12R)-Dihydroxy-(6Z,8E,14Z)-eicosa-6,8,14-trienoate	HMDB
(5S,12R)-Dihydroxy-(6Z,8E,14Z)-eicosa-6,8,14-trienoic acid	HMDB
(5S,12R)-Dihydroxy-(6Z,8E,14Z)-eicosatrienoate	HMDB
(5S,12R)-Dihydroxy-(6Z,8E,14Z)-eicosatrienoic acid	HMDB
10,11-dihydro-LTB(,4)	HMDB
DHLTB4	HMDB

Chemical Formula

C₂₀H₃₄O₄

Average Molecular Weight

338.4816

Monoisotopic Molecular Weight

338.245709576

IUPAC Name

(5R,6Z,8E,12R,14Z)-5,12-dihydroxyicosa-6,8,14-trienoic acid

Traditional Name

(5R,6Z,8E,12R,14Z)-5,12-dihydroxyicosa-6,8,14-trienoic acid

CAS Registry Number

Not Available

SMILES

CCCCC\C=C/C[C@H](O)CC\C=C\C=C/[C@H](O)CCCC(O)=O

InChI Identifier

InChI=1S/C20H34O4/c1-2-3-4-5-6-9-13-18(21)14-10-7-8-11-15-19(22)16-12-17-20(23)24/h6-9,11,15,18-19,21-22H,2-5,10,12-14,16-17H2,1H3,(H,23,24)/b8-7+,9-6-,15-11-/t18-,19-/m0/s1

InChI Key

NKUPFHTVILUPKF-RNEQFKNCSA-N

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as hydroxyeicosatrienoic acids. These are eicosanoic acids with an attached hydroxyl group and three CC double bonds.

Kingdom

Organic compounds

Super Class

Lipids and lipid-like molecules

Class

Fatty Acyls

Sub Class

Eicosanoids

Direct Parent

Hydroxyeicosatrienoic acids

Alternative Parents

Substituents

Hydroxyeicosatrienoic acid
Long-chain fatty acid
Hydroxy fatty acid
Fatty acid
Unsaturated fatty acid
Secondary alcohol
Carboxylic acid derivative
Carboxylic acid
Monocarboxylic acid or derivatives
Organic oxide
Organic oxygen compound
Alcohol
Hydrocarbon derivative
Carbonyl group
Organooxygen compound
Aliphatic acyclic compound

Molecular Framework

Aliphatic acyclic compounds

External Descriptors

Not Available

Ontology

Physiological effect

Not Available

Disposition

Biological location

Cellular substructure

Excreta

Biofluid or Excreta

Feces (PMID: 28701177)
Urine (HMDB: HMDB0012504)

Route of exposure

Enteral

Ingestion (HMDB: HMDB0012504)

Source

Endogenous

Endogenous (HMDB: HMDB0012504)

Animal

Animal (HMDB: HMDB0012504)

Exogenous

Food

Food (HMDB: HMDB0012504)

Exogenous (HMDB: HMDB0012504)

Process

Naturally occurring process

Biological process

Chemical reaction

Lipid Peroxidation (HMDB: HMDB0012504)

Biochemical pathway

Metabolic pathway

Fatty Acid Metabolism (HMDB: HMDB0012504)

Lipid metabolism pathway (HMDB: HMDB0012504)

Cellular process

Cell signaling (HMDB: HMDB0012504)

Biochemical process

Lipid transport (HMDB: HMDB0012504)

Role

Biological role

Energy source (HMDB: HMDB0012504)

Industrial application

Manufacturing industry

Material processing agent

Fluid processing agent

Surfactant

Surfactant (HMDB: HMDB0012504)

Physical Properties

State

Solid

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
Water Solubility	0.012 g/L	ALOGPS
logP	5.84	ALOGPS
logP	4.33	ChemAxon
logS	-4.5	ALOGPS
pKa (Strongest Acidic)	4.58	ChemAxon
pKa (Strongest Basic)	-1.1	ChemAxon
Physiological Charge	-1	ChemAxon
Hydrogen Acceptor Count	4	ChemAxon
Hydrogen Donor Count	3	ChemAxon
Polar Surface Area	77.76 Å²	ChemAxon
Rotatable Bond Count	15	ChemAxon
Refractivity	102.02 m³·mol⁻¹	ChemAxon
Polarizability	40.21 Å³	ChemAxon
Number of Rings	0	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
DarkChem	[M+H]+	191.69	31661259
DarkChem	[M-H]-	189.505	31661259
DeepCCS	[M+H]+	198.649	30932474
DeepCCS	[M-H]-	196.291	30932474
DeepCCS	[M-2H]-	229.892	30932474
DeepCCS	[M+Na]+	205.118	30932474
AllCCS	[M+H]+	192.2	32859911
AllCCS	[M+H-H2O]+	189.5	32859911
AllCCS	[M+NH4]+	194.8	32859911
AllCCS	[M+Na]+	195.5	32859911
AllCCS	[M-H]-	189.3	32859911
AllCCS	[M+Na-2H]-	191.2	32859911
AllCCS	[M+HCOO]-	193.5	32859911

Predicted Kovats Retention Indices

Underivatized

Metabolite	SMILES	Kovats RI Value	Column Type	Reference
10,11-dihydro-leukotriene B4	CCCCC\C=C/C[C@H](O)CC\C=C\C=C/[C@H](O)CCCC(O)=O	4404.9	Standard polar	33892256
10,11-dihydro-leukotriene B4	CCCCC\C=C/C[C@H](O)CC\C=C\C=C/[C@H](O)CCCC(O)=O	2601.5	Standard non polar	33892256
10,11-dihydro-leukotriene B4	CCCCC\C=C/C[C@H](O)CC\C=C\C=C/[C@H](O)CCCC(O)=O	2800.6	Semi standard non polar	33892256

Derivatized

Derivative Name / Structure	SMILES	Kovats RI Value	Column Type	Reference
10,11-dihydro-leukotriene B4,1TMS,isomer #1	CCCCC/C=C\C[C@@H](CC/C=C/C=C\[C@H](O)CCCC(=O)O)O[Si](C)(C)C	2902.8	Semi standard non polar	33892256
10,11-dihydro-leukotriene B4,1TMS,isomer #2	CCCCC/C=C\C[C@H](O)CC/C=C/C=C\[C@@H](CCCC(=O)O)O[Si](C)(C)C	2922.9	Semi standard non polar	33892256
10,11-dihydro-leukotriene B4,1TMS,isomer #3	CCCCC/C=C\C[C@H](O)CC/C=C/C=C\[C@H](O)CCCC(=O)O[Si](C)(C)C	2835.4	Semi standard non polar	33892256
10,11-dihydro-leukotriene B4,2TMS,isomer #1	CCCCC/C=C\C[C@@H](CC/C=C/C=C\[C@@H](CCCC(=O)O)O[Si](C)(C)C)O[Si](C)(C)C	2941.0	Semi standard non polar	33892256
10,11-dihydro-leukotriene B4,2TMS,isomer #2	CCCCC/C=C\C[C@@H](CC/C=C/C=C\[C@H](O)CCCC(=O)O[Si](C)(C)C)O[Si](C)(C)C	2882.2	Semi standard non polar	33892256
10,11-dihydro-leukotriene B4,2TMS,isomer #3	CCCCC/C=C\C[C@H](O)CC/C=C/C=C\[C@@H](CCCC(=O)O[Si](C)(C)C)O[Si](C)(C)C	2903.8	Semi standard non polar	33892256
10,11-dihydro-leukotriene B4,3TMS,isomer #1	CCCCC/C=C\C[C@@H](CC/C=C/C=C\[C@@H](CCCC(=O)O[Si](C)(C)C)O[Si](C)(C)C)O[Si](C)(C)C	2888.1	Semi standard non polar	33892256
10,11-dihydro-leukotriene B4,1TBDMS,isomer #1	CCCCC/C=C\C[C@@H](CC/C=C/C=C\[C@H](O)CCCC(=O)O)O[Si](C)(C)C(C)(C)C	3140.8	Semi standard non polar	33892256
10,11-dihydro-leukotriene B4,1TBDMS,isomer #2	CCCCC/C=C\C[C@H](O)CC/C=C/C=C\[C@@H](CCCC(=O)O)O[Si](C)(C)C(C)(C)C	3169.6	Semi standard non polar	33892256
10,11-dihydro-leukotriene B4,1TBDMS,isomer #3	CCCCC/C=C\C[C@H](O)CC/C=C/C=C\[C@H](O)CCCC(=O)O[Si](C)(C)C(C)(C)C	3085.4	Semi standard non polar	33892256
10,11-dihydro-leukotriene B4,2TBDMS,isomer #1	CCCCC/C=C\C[C@@H](CC/C=C/C=C\[C@@H](CCCC(=O)O)O[Si](C)(C)C(C)(C)C)O[Si](C)(C)C(C)(C)C	3421.0	Semi standard non polar	33892256
10,11-dihydro-leukotriene B4,2TBDMS,isomer #2	CCCCC/C=C\C[C@@H](CC/C=C/C=C\[C@H](O)CCCC(=O)O[Si](C)(C)C(C)(C)C)O[Si](C)(C)C(C)(C)C	3356.0	Semi standard non polar	33892256
10,11-dihydro-leukotriene B4,2TBDMS,isomer #3	CCCCC/C=C\C[C@H](O)CC/C=C/C=C\[C@@H](CCCC(=O)O[Si](C)(C)C(C)(C)C)O[Si](C)(C)C(C)(C)C	3380.3	Semi standard non polar	33892256
10,11-dihydro-leukotriene B4,3TBDMS,isomer #1	CCCCC/C=C\C[C@@H](CC/C=C/C=C\[C@@H](CCCC(=O)O[Si](C)(C)C(C)(C)C)O[Si](C)(C)C(C)(C)C)O[Si](C)(C)C(C)(C)C	3642.6	Semi standard non polar	33892256

Spectra

GC-MS Spectra

Spectrum Type	Description	Splash Key	Deposition Date	Source	View
Predicted GC-MS	Predicted GC-MS Spectrum - 10,11-dihydro-leukotriene B4 GC-MS (Non-derivatized) - 70eV, Positive	splash10-00dl-9887000000-690286bf648961968256	2017-09-01	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - 10,11-dihydro-leukotriene B4 GC-MS (3 TMS) - 70eV, Positive	splash10-00bm-9124640000-4783aa18d6e07934d465	2017-10-06	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - 10,11-dihydro-leukotriene B4 GC-MS (Non-derivatized) - 70eV, Positive	Not Available	2021-10-12	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - 10,11-dihydro-leukotriene B4 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 - 10,11-dihydro-leukotriene B4 10V, Positive-QTOF	splash10-0fk9-0019000000-1d1e1cea32208dbe3634	2017-09-01	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 10,11-dihydro-leukotriene B4 20V, Positive-QTOF	splash10-0wb9-5498000000-7741da59bcddc124a6c3	2017-09-01	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 10,11-dihydro-leukotriene B4 40V, Positive-QTOF	splash10-000f-9450000000-de55909d83de13ce9f08	2017-09-01	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 10,11-dihydro-leukotriene B4 10V, Negative-QTOF	splash10-00kr-0019000000-04ba161b7a53e2b655f2	2017-09-01	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 10,11-dihydro-leukotriene B4 20V, Negative-QTOF	splash10-014r-1249000000-dfdb83af077f8dad3009	2017-09-01	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 10,11-dihydro-leukotriene B4 40V, Negative-QTOF	splash10-0a4l-9350000000-7449096257f09b928abe	2017-09-01	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 10,11-dihydro-leukotriene B4 10V, Positive-QTOF	splash10-0uk9-0019000000-f332f84891bf6e914004	2021-09-22	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 10,11-dihydro-leukotriene B4 20V, Positive-QTOF	splash10-0uk9-2239000000-cc673b4c586984efdf86	2021-09-22	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 10,11-dihydro-leukotriene B4 40V, Positive-QTOF	splash10-0aor-9300000000-ae2ee2279a8c0a058750	2021-09-22	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 10,11-dihydro-leukotriene B4 10V, Negative-QTOF	splash10-000i-0009000000-42bc55e4154316e37496	2021-09-22	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 10,11-dihydro-leukotriene B4 20V, Negative-QTOF	splash10-00kr-3349000000-0551b9e6c344eea69236	2021-09-22	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 10,11-dihydro-leukotriene B4 40V, Negative-QTOF	splash10-0k96-8394000000-9132c6710a7579726f96	2021-09-22	Wishart Lab	View Spectrum

Biological Properties

Cellular Locations

Extracellular
Membrane

Biospecimen Locations

Feces

Tissue Locations

Not Available

Pathways

Not Available

Name	SMPDB/PathBank	KEGG

Normal Concentrations

Biospecimen	Status	Value	Age	Sex	Condition	Reference	Details
Feces	Detected but not Quantified	Not Quantified	Infant (0-1 year old)	Both	Normal	28701177	details

Abnormal Concentrations

Biospecimen	Status	Value	Age	Sex	Condition	Reference	Details
Feces	Detected but not Quantified	Not Quantified	Newborn (0-30 days old)	Both	Sepsis	28701177	details

Associated Disorders and Diseases

Disease References

Sepsis
Stewart CJ, Embleton ND, Marrs ECL, Smith DP, Fofanova T, Nelson A, Skeath T, Perry JD, Petrosino JF, Berrington JE, Cummings SP: Longitudinal development of the gut microbiome and metabolome in preterm neonates with late onset sepsis and healthy controls. Microbiome. 2017 Jul 12;5(1):75. doi: 10.1186/s40168-017-0295-1. [PubMed:28701177 ]

Associated OMIM IDs

None

External Links

DrugBank ID

Not Available

Phenol Explorer Compound ID

Not Available

FooDB ID

FDB029106

KNApSAcK ID

Not Available

Chemspider ID

30776625

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

53481449

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

Wheelan P, Murphy RC: Metabolism of 6-trans-isomers of leukotriene B4 in cultured hepatoma cells and in human polymorphonuclear leukocytes. Identification of a delta 6-reductase metabolic pathway. J Biol Chem. 1995 Aug 25;270(34):19845-52. [PubMed:7649996 ]
Murphy RC, Gijon MA: Biosynthesis and metabolism of leukotrienes. Biochem J. 2007 Aug 1;405(3):379-95. [PubMed:17623009 ]
Mita H, Yui Y, Yasueda H, Shida T: Isocratic determination of arachidonic acid 5-lipoxygenase products in human neutrophils by high-performance liquid chromatography. J Chromatogr. 1988 Sep 9;430(2):299-308. [PubMed:2853166 ]
Shak S, Goldstein IM: Omega-oxidation is the major pathway for the catabolism of leukotriene B4 in human polymorphonuclear leukocytes. J Biol Chem. 1984 Aug 25;259(16):10181-7. [PubMed:6088485 ]
Simons K, Toomre D: Lipid rafts and signal transduction. Nat Rev Mol Cell Biol. 2000 Oct;1(1):31-9. [PubMed:11413487 ]
Watson AD: Thematic review series: systems biology approaches to metabolic and cardiovascular disorders. Lipidomics: a global approach to lipid analysis in biological systems. J Lipid Res. 2006 Oct;47(10):2101-11. Epub 2006 Aug 10. [PubMed:16902246 ]
Sethi JK, Vidal-Puig AJ: Thematic review series: adipocyte biology. Adipose tissue function and plasticity orchestrate nutritional adaptation. J Lipid Res. 2007 Jun;48(6):1253-62. Epub 2007 Mar 20. [PubMed:17374880 ]
Lingwood D, Simons K: Lipid rafts as a membrane-organizing principle. Science. 2010 Jan 1;327(5961):46-50. doi: 10.1126/science.1174621. [PubMed:20044567 ]
Gunstone, Frank D., John L. Harwood, and Albert J. Dijkstra (2007). The lipid handbook with CD-ROM. CRC Press.

Showing metabocard for 10,11-dihydro-leukotriene B4 (HMDB0012504)

MOL for HMDB0012504 (10,11-dihydro-leukotriene B4)

3D MOL for HMDB0012504 (10,11-dihydro-leukotriene B4)

3D SDF for HMDB0012504 (10,11-dihydro-leukotriene B4)

3D-SDF for HMDB0012504 (10,11-dihydro-leukotriene B4)

PDB for HMDB0012504 (10,11-dihydro-leukotriene B4)

3D PDB for HMDB0012504 (10,11-dihydro-leukotriene B4)

SMILES for HMDB0012504 (10,11-dihydro-leukotriene B4)

INCHI for HMDB0012504 (10,11-dihydro-leukotriene B4)

Structure for HMDB0012504 (10,11-dihydro-leukotriene B4)

3D Structure for HMDB0012504 (10,11-dihydro-leukotriene B4)

Predicted Collision Cross Sections

Predicted Kovats Retention Indices

Underivatized

Derivatized

GC-MS Spectra

MS/MS Spectra