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Record Information

Version

5.0

Status

Detected but not Quantified

Creation Date

2021-08-29 23:16:59 UTC

Update Date

2021-09-26 22:48:56 UTC

HMDB ID

HMDB0242330

Secondary Accession Numbers

None

Metabolite Identification

Common Name

(1R,3Z)-3-[(2E)-2-[(1R,3As,7aR)-1-[(2R)-7-hydroxy-6-methylheptan-2-yl]-7a-methyl-2,3,3a,5,6,7-hexahydro-1H-inden-4-ylidene]ethylidene]-4-methylidenecyclohexan-1-ol

Description

(1R,3Z)-3-[(2E)-2-[(1R,3As,7aR)-1-[(2R)-7-hydroxy-6-methylheptan-2-yl]-7a-methyl-2,3,3a,5,6,7-hexahydro-1H-inden-4-ylidene]ethylidene]-4-methylidenecyclohexan-1-ol belongs to the class of organic compounds known as vitamin d and derivatives. Vitamin D and derivatives are compounds containing a secosteroid backbone, usually secoergostane or secocholestane. Based on a literature review very few articles have been published on (1R,3Z)-3-[(2E)-2-[(1R,3As,7aR)-1-[(2R)-7-hydroxy-6-methylheptan-2-yl]-7a-methyl-2,3,3a,5,6,7-hexahydro-1H-inden-4-ylidene]ethylidene]-4-methylidenecyclohexan-1-ol. This compound has been identified in human blood as reported by (PMID: 31557052 ). (1r,3z)-3-[(2e)-2-[(1r,3as,7ar)-1-[(2r)-7-hydroxy-6-methylheptan-2-yl]-7a-methyl-2,3,3a,5,6,7-hexahydro-1h-inden-4-ylidene]ethylidene]-4-methylidenecyclohexan-1-ol is not a naturally occurring metabolite and is only found in those individuals exposed to this compound or its derivatives. Technically (1R,3Z)-3-[(2E)-2-[(1R,3As,7aR)-1-[(2R)-7-hydroxy-6-methylheptan-2-yl]-7a-methyl-2,3,3a,5,6,7-hexahydro-1H-inden-4-ylidene]ethylidene]-4-methylidenecyclohexan-1-ol is part of the human exposome. The exposome can be defined as the collection of all the exposures of an individual in a lifetime and how those exposures relate to health. An individual's exposure begins before birth and includes insults from environmental and occupational sources.

Structure

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


  Mrv1652308302101272D          

 29 31  0  0  0  0            999 V2000
    0.4684    1.6416    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4684    0.8166    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2461    0.4041    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9605    0.8166    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6750    0.4041    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3895    0.8166    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3895    1.6416    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1039    0.4041    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8576    0.7397    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4097    0.1266    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9972   -0.5879    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1902   -0.4164    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6382   -1.0295    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8931   -1.8141    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7001   -1.9856    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2521   -1.3725    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0591   -1.5440    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.3140   -2.3287    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.1210   -2.5002    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.3759   -3.2848    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.1829   -3.4563    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.7349   -2.8432    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.4800   -2.0586    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.6730   -1.8871    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.4181   -1.1025    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.4378   -4.2410    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4056   -0.1614    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1829    0.4041    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8973    0.8166    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  1  0  0  0  0
  6  8  1  0  0  0  0
  8  9  1  0  0  0  0
  9 10  1  0  0  0  0
 10 11  1  0  0  0  0
 11 12  1  0  0  0  0
  8 12  1  0  0  0  0
 12 13  1  0  0  0  0
 13 14  1  0  0  0  0
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 15 16  1  0  0  0  0
 11 16  1  0  0  0  0
 16 17  2  0  0  0  0
 17 18  1  4  0  0  0
 18 19  2  0  0  0  0
 19 20  1  4  0  0  0
 20 21  1  0  0  0  0
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 22 23  1  0  0  0  0
 23 24  1  0  0  0  0
 19 24  1  0  0  0  0
 24 25  2  0  0  0  0
 21 26  1  0  0  0  0
 12 27  1  0  0  0  0
  2 28  1  0  0  0  0
 28 29  1  0  0  0  0
M  END

HMDB0242649
     RDKit          3D
26-Hydroxycholecalciferol
 73 75  0  0  0  0  0  0  0  0999 V2000
    4.7128    1.1894    2.3887 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.4936    0.6314    1.4969 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.4736   -0.4375    1.9517 C   0  0  0  0  0  0  0  0  0  0  0  0
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   -7.2624    1.0922    1.3075 C   0  0  0  0  0  0  0  0  0  0  0  0
   -8.1510   -1.0065    2.1554 C   0  0  0  0  0  0  0  0  0  0  0  0
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    1.1716    0.7380   -4.0887 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7100    1.0002   -2.8145 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4173   -0.8081   -3.1767 H   0  0  0  0  0  0  0  0  0  0  0  0
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    1.9665   -1.1167   -1.0229 H   0  0  0  0  0  0  0  0  0  0  0  0
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   -5.4219   -0.8064    2.3479 H   0  0  0  0  0  0  0  0  0  0  0  0
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   -8.8248   -2.7085    2.7260 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  2  3
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  4  5  1  0
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  5  7  1  0
  7  8  1  0
  8  9  2  3
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 23 24  1  0
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 25 26  1  0
 26 27  1  0
 26 28  1  0
 28 29  1  0
  8  2  1  0
 17 11  1  0
 20 15  1  0
  1 30  1  0
  1 31  1  0
  3 32  1  0
  3 33  1  0
  4 34  1  0
  4 35  1  0
  5 36  1  0
  6 37  1  0
  7 38  1  0
  7 39  1  0
  9 40  1  0
 10 41  1  0
 12 42  1  0
 12 43  1  0
 13 44  1  0
 13 45  1  0
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 27 68  1  0
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 27 70  1  0
 28 71  1  0
 28 72  1  0
 29 73  1  0
M  END


  Mrv1652308302101272D          

 29 31  0  0  0  0            999 V2000
    0.4684    1.6416    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4684    0.8166    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2461    0.4041    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9605    0.8166    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6750    0.4041    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3895    0.8166    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3895    1.6416    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1039    0.4041    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8576    0.7397    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4097    0.1266    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9972   -0.5879    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1902   -0.4164    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6382   -1.0295    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8931   -1.8141    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7001   -1.9856    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2521   -1.3725    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0591   -1.5440    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
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   -6.3759   -3.2848    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.1829   -3.4563    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
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    1.8973    0.8166    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0  0  0  0
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  4  5  1  0  0  0  0
  5  6  1  0  0  0  0
  6  7  1  0  0  0  0
  6  8  1  0  0  0  0
  8  9  1  0  0  0  0
  9 10  1  0  0  0  0
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  8 12  1  0  0  0  0
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 19 20  1  4  0  0  0
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 22 23  1  0  0  0  0
 23 24  1  0  0  0  0
 19 24  1  0  0  0  0
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 21 26  1  0  0  0  0
 12 27  1  0  0  0  0
  2 28  1  0  0  0  0
 28 29  1  0  0  0  0
M  END
> <DATABASE_ID>
HMDB0242330

> <DATABASE_NAME>
hmdb

> <SMILES>
CC(CO)CCCC(C)C1CCC2C(CCCC12C)=CC=C1CC(O)CCC1=C

> <INCHI_IDENTIFIER>
InChI=1S/C27H44O2/c1-19(18-28)7-5-8-21(3)25-14-15-26-22(9-6-16-27(25,26)4)11-12-23-17-24(29)13-10-20(23)2/h11-12,19,21,24-26,28-29H,2,5-10,13-18H2,1,3-4H3

> <INCHI_KEY>
UZHJNFDLHNKRIM-UHFFFAOYSA-N

> <FORMULA>
C27H44O2

> <MOLECULAR_WEIGHT>
400.647

> <EXACT_MASS>
400.334130657

> <JCHEM_ACCEPTOR_COUNT>
2

> <JCHEM_ATOM_COUNT>
73

> <JCHEM_AVERAGE_POLARIZABILITY>
50.02025399522518

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
2

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
3-{2-[1-(7-hydroxy-6-methylheptan-2-yl)-7a-methyl-octahydro-1H-inden-4-ylidene]ethylidene}-4-methylidenecyclohexan-1-ol

> <ALOGPS_LOGP>
6.76

> <JCHEM_LOGP>
5.7667358680000005

> <ALOGPS_LOGS>
-5.29

> <JCHEM_MDDR_LIKE_RULE>
1

> <JCHEM_NUMBER_OF_RINGS>
3

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
18.384341369959035

> <JCHEM_PKA_STRONGEST_ACIDIC>
17.41832287471465

> <JCHEM_PKA_STRONGEST_BASIC>
-1.1792476271775763

> <JCHEM_POLAR_SURFACE_AREA>
40.46

> <JCHEM_REFRACTIVITY>
125.07619999999999

> <JCHEM_ROTATABLE_BOND_COUNT>
7

> <JCHEM_RULE_OF_FIVE>
0

> <ALOGPS_SOLUBILITY>
2.07e-03 g/l

> <JCHEM_TRADITIONAL_IUPAC>
3-{2-[1-(7-hydroxy-6-methylheptan-2-yl)-7a-methyl-hexahydro-1H-inden-4-ylidene]ethylidene}-4-methylidenecyclohexan-1-ol

> <JCHEM_VEBER_RULE>
0

$$$$

HMDB0242649
     RDKit          3D
26-Hydroxycholecalciferol
 73 75  0  0  0  0  0  0  0  0999 V2000
    4.7128    1.1894    2.3887 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.4936    0.6314    1.4969 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.4736   -0.4375    1.9517 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.7442   -0.2783    1.1360 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.5229   -0.0632   -0.3176 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.7558   -0.0644   -0.9577 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.7533    1.2108   -0.5911 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.4359    1.0160    0.1205 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3075    1.1261   -0.5312 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9838    0.9010   -0.0762 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8970    1.0626   -0.8330 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8914    1.4938   -2.2403 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2811    0.3703   -3.0471 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1570    0.0808   -2.5663 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0786   -0.2980   -1.1537 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9375   -1.4598   -1.0770 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5387    0.8077   -0.2828 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5727    0.0756    1.0328 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8789   -0.3773    1.0846 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2427   -0.6939   -0.3854 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5774   -0.1383   -0.6041 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2494   -0.3011   -1.9069 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5109   -0.7910    0.4399 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9185   -0.2673    0.2792 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.7903   -0.9342    1.3220 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.1910   -0.3905    1.1349 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.2624    1.0922    1.3075 C   0  0  0  0  0  0  0  0  0  0  0  0
   -8.1510   -1.0065    2.1554 C   0  0  0  0  0  0  0  0  0  0  0  0
   -8.2137   -2.3747    2.0330 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.7343    0.9186    3.4330 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.0333    1.9700    2.1258 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.6897   -0.3715    3.0207 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.0102   -1.4061    1.7228 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.4156    0.4806    1.5392 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.2868   -1.2626    1.2444 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.8777   -0.8906   -0.7379 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.8132    0.7419   -1.5223 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.5367    1.3194   -1.6780 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.2272    2.1043   -0.1657 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.4025    1.4459   -1.5925 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.8371    0.5389    0.9587 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.8410    1.7247   -2.6962 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.1539    2.3345   -2.2976 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.8918   -0.5479   -2.9727 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.1716    0.7380   -4.0887 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7100    1.0002   -2.8145 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4173   -0.8081   -3.1767 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.6634   -2.1689   -0.2567 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.9665   -1.1167   -1.0229 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.8224   -2.0489   -2.0103 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0873    1.6899   -0.1974 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.2720   -0.7566    1.0773 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.7998    0.8121    1.8308 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0509   -1.2309    1.7397 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4263    0.5587    1.4099 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3311   -1.8299   -0.4464 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5296    0.9709   -0.3804 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6691   -0.2824   -2.8153 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8390   -1.2736   -1.9747 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9836    0.5590   -2.0228 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5641   -1.8843    0.2632 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1106   -0.5563    1.4427 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9955    0.8194    0.4512 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.2918   -0.5876   -0.7064 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.4219   -0.8064    2.3479 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.8155   -2.0222    1.0469 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.5583   -0.6640    0.1331 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.6310    1.4701    2.1285 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.0533    1.6658    0.3966 H   0  0  0  0  0  0  0  0  0  0  0  0
   -8.3221    1.3402    1.5913 H   0  0  0  0  0  0  0  0  0  0  0  0
   -9.1270   -0.4946    1.9933 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.7664   -0.6657    3.1523 H   0  0  0  0  0  0  0  0  0  0  0  0
   -8.8248   -2.7085    2.7260 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  2  3
  2  3  1  0
  3  4  1  0
  4  5  1  0
  5  6  1  0
  5  7  1  0
  7  8  1  0
  8  9  2  3
  9 10  1  0
 10 11  2  3
 11 12  1  0
 12 13  1  0
 13 14  1  0
 14 15  1  0
 15 16  1  0
 15 17  1  0
 17 18  1  0
 18 19  1  0
 19 20  1  0
 20 21  1  0
 21 22  1  0
 21 23  1  0
 23 24  1  0
 24 25  1  0
 25 26  1  0
 26 27  1  0
 26 28  1  0
 28 29  1  0
  8  2  1  0
 17 11  1  0
 20 15  1  0
  1 30  1  0
  1 31  1  0
  3 32  1  0
  3 33  1  0
  4 34  1  0
  4 35  1  0
  5 36  1  0
  6 37  1  0
  7 38  1  0
  7 39  1  0
  9 40  1  0
 10 41  1  0
 12 42  1  0
 12 43  1  0
 13 44  1  0
 13 45  1  0
 14 46  1  0
 14 47  1  0
 16 48  1  0
 16 49  1  0
 16 50  1  0
 17 51  1  0
 18 52  1  0
 18 53  1  0
 19 54  1  0
 19 55  1  0
 20 56  1  0
 21 57  1  0
 22 58  1  0
 22 59  1  0
 22 60  1  0
 23 61  1  0
 23 62  1  0
 24 63  1  0
 24 64  1  0
 25 65  1  0
 25 66  1  0
 26 67  1  0
 27 68  1  0
 27 69  1  0
 27 70  1  0
 28 71  1  0
 28 72  1  0
 29 73  1  0
M  END

HEADER    PROTEIN                                 30-AUG-21   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   30-AUG-21         0                                  
HETATM    1  C   UNK     0       0.874   3.064   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       0.874   1.524   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0      -0.459   0.754   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0      -1.793   1.524   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0      -3.127   0.754   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0      -4.460   1.524   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0      -4.460   3.064   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0      -5.794   0.754   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0      -7.201   1.381   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0      -8.231   0.236   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0      -7.461  -1.097   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0      -5.955  -0.777   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0      -4.925  -1.922   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0      -5.400  -3.386   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0      -6.907  -3.706   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0      -7.937  -2.562   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0      -9.444  -2.882   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0      -9.919  -4.347   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0     -11.426  -4.667   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0     -11.902  -6.132   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0     -13.408  -6.452   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0     -14.439  -5.307   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0     -13.963  -3.843   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0     -12.456  -3.523   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0     -11.980  -2.058   0.000  0.00  0.00           C+0
HETATM   26  O   UNK     0     -13.884  -7.916   0.000  0.00  0.00           O+0
HETATM   27  C   UNK     0      -4.490  -0.301   0.000  0.00  0.00           C+0
HETATM   28  C   UNK     0       2.208   0.754   0.000  0.00  0.00           C+0
HETATM   29  O   UNK     0       3.542   1.524   0.000  0.00  0.00           O+0
CONECT    1    2                                                            
CONECT    2    1    3   28                                                  
CONECT    3    2    4                                                       
CONECT    4    3    5                                                       
CONECT    5    4    6                                                       
CONECT    6    5    7    8                                                  
CONECT    7    6                                                            
CONECT    8    6    9   12                                                  
CONECT    9    8   10                                                       
CONECT   10    9   11                                                       
CONECT   11   10   12   16                                                  
CONECT   12   11    8   13   27                                             
CONECT   13   12   14                                                       
CONECT   14   13   15                                                       
CONECT   15   14   16                                                       
CONECT   16   15   11   17                                                  
CONECT   17   16   18                                                       
CONECT   18   17   19                                                       
CONECT   19   18   20   24                                                  
CONECT   20   19   21                                                       
CONECT   21   20   22   26                                                  
CONECT   22   21   23                                                       
CONECT   23   22   24                                                       
CONECT   24   23   19   25                                                  
CONECT   25   24                                                            
CONECT   26   21                                                            
CONECT   27   12                                                            
CONECT   28    2   29                                                       
CONECT   29   28                                                            
MASTER        0    0    0    0    0    0    0    0   29    0   62    0
END

COMPND    HMDB0242330
HETATM    1  C1  UNL     1       6.529  -2.280   0.680  1.00  0.00           C  
HETATM    2  C2  UNL     1       6.511  -0.960   0.715  1.00  0.00           C  
HETATM    3  C3  UNL     1       7.674  -0.179   1.253  1.00  0.00           C  
HETATM    4  C4  UNL     1       8.072   0.879   0.283  1.00  0.00           C  
HETATM    5  C5  UNL     1       7.071   1.153  -0.799  1.00  0.00           C  
HETATM    6  O1  UNL     1       7.370   2.389  -1.401  1.00  0.00           O  
HETATM    7  C6  UNL     1       5.638   1.157  -0.304  1.00  0.00           C  
HETATM    8  C7  UNL     1       5.372  -0.194   0.237  1.00  0.00           C  
HETATM    9  C8  UNL     1       4.153  -0.741   0.310  1.00  0.00           C  
HETATM   10  C9  UNL     1       2.969  -0.031  -0.149  1.00  0.00           C  
HETATM   11  C10 UNL     1       1.797  -0.603  -0.059  1.00  0.00           C  
HETATM   12  C11 UNL     1       1.665  -1.980   0.511  1.00  0.00           C  
HETATM   13  C12 UNL     1       0.282  -2.470   0.124  1.00  0.00           C  
HETATM   14  C13 UNL     1      -0.823  -1.583   0.714  1.00  0.00           C  
HETATM   15  C14 UNL     1      -0.423  -0.156   0.716  1.00  0.00           C  
HETATM   16  C15 UNL     1       0.359   0.099   2.007  1.00  0.00           C  
HETATM   17  C16 UNL     1       0.526   0.004  -0.485  1.00  0.00           C  
HETATM   18  C17 UNL     1       0.524   1.472  -0.682  1.00  0.00           C  
HETATM   19  C18 UNL     1      -0.992   1.742  -0.698  1.00  0.00           C  
HETATM   20  C19 UNL     1      -1.434   0.873   0.486  1.00  0.00           C  
HETATM   21  C20 UNL     1      -2.862   0.434   0.378  1.00  0.00           C  
HETATM   22  C21 UNL     1      -3.260  -0.236   1.653  1.00  0.00           C  
HETATM   23  C22 UNL     1      -3.688   1.668   0.083  1.00  0.00           C  
HETATM   24  C23 UNL     1      -5.168   1.364  -0.050  1.00  0.00           C  
HETATM   25  C24 UNL     1      -5.464   0.408  -1.141  1.00  0.00           C  
HETATM   26  C25 UNL     1      -6.904   0.061  -1.360  1.00  0.00           C  
HETATM   27  C26 UNL     1      -6.959  -0.924  -2.557  1.00  0.00           C  
HETATM   28  C27 UNL     1      -7.449  -0.714  -0.209  1.00  0.00           C  
HETATM   29  O2  UNL     1      -7.439  -0.112   1.014  1.00  0.00           O  
HETATM   30  H1  UNL     1       7.401  -2.798   1.048  1.00  0.00           H  
HETATM   31  H2  UNL     1       5.695  -2.809   0.294  1.00  0.00           H  
HETATM   32  H3  UNL     1       8.510  -0.875   1.420  1.00  0.00           H  
HETATM   33  H4  UNL     1       7.317   0.252   2.231  1.00  0.00           H  
HETATM   34  H5  UNL     1       9.028   0.585  -0.200  1.00  0.00           H  
HETATM   35  H6  UNL     1       8.307   1.805   0.859  1.00  0.00           H  
HETATM   36  H7  UNL     1       7.129   0.397  -1.610  1.00  0.00           H  
HETATM   37  H8  UNL     1       7.415   3.063  -0.693  1.00  0.00           H  
HETATM   38  H9  UNL     1       5.573   1.884   0.532  1.00  0.00           H  
HETATM   39  H10 UNL     1       5.010   1.420  -1.171  1.00  0.00           H  
HETATM   40  H11 UNL     1       4.018  -1.734   0.716  1.00  0.00           H  
HETATM   41  H12 UNL     1       3.123   0.964  -0.553  1.00  0.00           H  
HETATM   42  H13 UNL     1       1.870  -2.031   1.576  1.00  0.00           H  
HETATM   43  H14 UNL     1       2.369  -2.611  -0.099  1.00  0.00           H  
HETATM   44  H15 UNL     1       0.217  -2.512  -0.971  1.00  0.00           H  
HETATM   45  H16 UNL     1       0.163  -3.488   0.518  1.00  0.00           H  
HETATM   46  H17 UNL     1      -1.719  -1.811   0.110  1.00  0.00           H  
HETATM   47  H18 UNL     1      -0.989  -1.981   1.736  1.00  0.00           H  
HETATM   48  H19 UNL     1       1.422   0.314   1.810  1.00  0.00           H  
HETATM   49  H20 UNL     1      -0.093   0.989   2.492  1.00  0.00           H  
HETATM   50  H21 UNL     1       0.213  -0.740   2.735  1.00  0.00           H  
HETATM   51  H22 UNL     1       0.066  -0.509  -1.341  1.00  0.00           H  
HETATM   52  H23 UNL     1       0.923   2.021   0.170  1.00  0.00           H  
HETATM   53  H24 UNL     1       0.985   1.771  -1.646  1.00  0.00           H  
HETATM   54  H25 UNL     1      -1.368   1.309  -1.637  1.00  0.00           H  
HETATM   55  H26 UNL     1      -1.213   2.797  -0.547  1.00  0.00           H  
HETATM   56  H27 UNL     1      -1.414   1.598   1.356  1.00  0.00           H  
HETATM   57  H28 UNL     1      -3.006  -0.244  -0.517  1.00  0.00           H  
HETATM   58  H29 UNL     1      -3.567  -1.279   1.534  1.00  0.00           H  
HETATM   59  H30 UNL     1      -2.428  -0.194   2.417  1.00  0.00           H  
HETATM   60  H31 UNL     1      -4.109   0.281   2.166  1.00  0.00           H  
HETATM   61  H32 UNL     1      -3.590   2.435   0.872  1.00  0.00           H  
HETATM   62  H33 UNL     1      -3.379   2.132  -0.876  1.00  0.00           H  
HETATM   63  H34 UNL     1      -5.630   1.165   0.931  1.00  0.00           H  
HETATM   64  H35 UNL     1      -5.623   2.353  -0.366  1.00  0.00           H  
HETATM   65  H36 UNL     1      -4.941  -0.580  -1.015  1.00  0.00           H  
HETATM   66  H37 UNL     1      -5.116   0.870  -2.114  1.00  0.00           H  
HETATM   67  H38 UNL     1      -7.525   0.927  -1.645  1.00  0.00           H  
HETATM   68  H39 UNL     1      -6.470  -1.866  -2.233  1.00  0.00           H  
HETATM   69  H40 UNL     1      -8.043  -1.111  -2.705  1.00  0.00           H  
HETATM   70  H41 UNL     1      -6.499  -0.464  -3.444  1.00  0.00           H  
HETATM   71  H42 UNL     1      -8.523  -1.024  -0.396  1.00  0.00           H  
HETATM   72  H43 UNL     1      -6.930  -1.714  -0.100  1.00  0.00           H  
HETATM   73  H44 UNL     1      -8.228   0.503   1.126  1.00  0.00           H  
CONECT    1    2    2   30   31
CONECT    2    3    8
CONECT    3    4   32   33
CONECT    4    5   34   35
CONECT    5    6    7   36
CONECT    6   37
CONECT    7    8   38   39
CONECT    8    9    9
CONECT    9   10   40
CONECT   10   11   11   41
CONECT   11   12   17
CONECT   12   13   42   43
CONECT   13   14   44   45
CONECT   14   15   46   47
CONECT   15   16   17   20
CONECT   16   48   49   50
CONECT   17   18   51
CONECT   18   19   52   53
CONECT   19   20   54   55
CONECT   20   21   56
CONECT   21   22   23   57
CONECT   22   58   59   60
CONECT   23   24   61   62
CONECT   24   25   63   64
CONECT   25   26   65   66
CONECT   26   27   28   67
CONECT   27   68   69   70
CONECT   28   29   71   72
CONECT   29   73
END

HMDB0242649
     RDKit          3D
26-Hydroxycholecalciferol
 73 75  0  0  0  0  0  0  0  0999 V2000
    4.7128    1.1894    2.3887 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.4936    0.6314    1.4969 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.4736   -0.4375    1.9517 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.7442   -0.2783    1.1360 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.5229   -0.0632   -0.3176 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.7558   -0.0644   -0.9577 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.7533    1.2108   -0.5911 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.4359    1.0160    0.1205 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3075    1.1261   -0.5312 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9838    0.9010   -0.0762 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8970    1.0626   -0.8330 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8914    1.4938   -2.2403 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2811    0.3703   -3.0471 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1570    0.0808   -2.5663 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0786   -0.2980   -1.1537 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9375   -1.4598   -1.0770 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5387    0.8077   -0.2828 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5727    0.0756    1.0328 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8789   -0.3773    1.0846 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2427   -0.6939   -0.3854 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5774   -0.1383   -0.6041 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2494   -0.3011   -1.9069 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5109   -0.7910    0.4399 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9185   -0.2673    0.2792 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.7903   -0.9342    1.3220 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.1910   -0.3905    1.1349 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.2624    1.0922    1.3075 C   0  0  0  0  0  0  0  0  0  0  0  0
   -8.1510   -1.0065    2.1554 C   0  0  0  0  0  0  0  0  0  0  0  0
   -8.2137   -2.3747    2.0330 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.7343    0.9186    3.4330 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.0333    1.9700    2.1258 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.6897   -0.3715    3.0207 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.0102   -1.4061    1.7228 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.4156    0.4806    1.5392 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.2868   -1.2626    1.2444 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.8777   -0.8906   -0.7379 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.8132    0.7419   -1.5223 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.5367    1.3194   -1.6780 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.2272    2.1043   -0.1657 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.4025    1.4459   -1.5925 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.8371    0.5389    0.9587 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.8410    1.7247   -2.6962 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.1539    2.3345   -2.2976 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.8918   -0.5479   -2.9727 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.1716    0.7380   -4.0887 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7100    1.0002   -2.8145 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4173   -0.8081   -3.1767 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.6634   -2.1689   -0.2567 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.9665   -1.1167   -1.0229 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.8224   -2.0489   -2.0103 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0873    1.6899   -0.1974 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.2720   -0.7566    1.0773 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.7998    0.8121    1.8308 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0509   -1.2309    1.7397 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4263    0.5587    1.4099 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3311   -1.8299   -0.4464 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5296    0.9709   -0.3804 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6691   -0.2824   -2.8153 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8390   -1.2736   -1.9747 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9836    0.5590   -2.0228 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5641   -1.8843    0.2632 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1106   -0.5563    1.4427 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9955    0.8194    0.4512 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.2918   -0.5876   -0.7064 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.4219   -0.8064    2.3479 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.8155   -2.0222    1.0469 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.5583   -0.6640    0.1331 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.6310    1.4701    2.1285 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.0533    1.6658    0.3966 H   0  0  0  0  0  0  0  0  0  0  0  0
   -8.3221    1.3402    1.5913 H   0  0  0  0  0  0  0  0  0  0  0  0
   -9.1270   -0.4946    1.9933 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.7664   -0.6657    3.1523 H   0  0  0  0  0  0  0  0  0  0  0  0
   -8.8248   -2.7085    2.7260 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  2  3
  2  3  1  0
  3  4  1  0
  4  5  1  0
  5  6  1  0
  5  7  1  0
  7  8  1  0
  8  9  2  3
  9 10  1  0
 10 11  2  3
 11 12  1  0
 12 13  1  0
 13 14  1  0
 14 15  1  0
 15 16  1  0
 15 17  1  0
 17 18  1  0
 18 19  1  0
 19 20  1  0
 20 21  1  0
 21 22  1  0
 21 23  1  0
 23 24  1  0
 24 25  1  0
 25 26  1  0
 26 27  1  0
 26 28  1  0
 28 29  1  0
  8  2  1  0
 17 11  1  0
 20 15  1  0
  1 30  1  0
  1 31  1  0
  3 32  1  0
  3 33  1  0
  4 34  1  0
  4 35  1  0
  5 36  1  0
  6 37  1  0
  7 38  1  0
  7 39  1  0
  9 40  1  0
 10 41  1  0
 12 42  1  0
 12 43  1  0
 13 44  1  0
 13 45  1  0
 14 46  1  0
 14 47  1  0
 16 48  1  0
 16 49  1  0
 16 50  1  0
 17 51  1  0
 18 52  1  0
 18 53  1  0
 19 54  1  0
 19 55  1  0
 20 56  1  0
 21 57  1  0
 22 58  1  0
 22 59  1  0
 22 60  1  0
 23 61  1  0
 23 62  1  0
 24 63  1  0
 24 64  1  0
 25 65  1  0
 25 66  1  0
 26 67  1  0
 27 68  1  0
 27 69  1  0
 27 70  1  0
 28 71  1  0
 28 72  1  0
 29 73  1  0
M  END

View in JSmol View Stereo Labels

Synonyms

Not Available

Chemical Formula

C₂₇H₄₄O₂

Average Molecular Weight

400.647

Monoisotopic Molecular Weight

400.334130657

IUPAC Name

3-{2-[1-(7-hydroxy-6-methylheptan-2-yl)-7a-methyl-octahydro-1H-inden-4-ylidene]ethylidene}-4-methylidenecyclohexan-1-ol

Traditional Name

3-{2-[1-(7-hydroxy-6-methylheptan-2-yl)-7a-methyl-hexahydro-1H-inden-4-ylidene]ethylidene}-4-methylidenecyclohexan-1-ol

CAS Registry Number

Not Available

SMILES

CC(CO)CCCC(C)C1CCC2C(CCCC12C)=CC=C1CC(O)CCC1=C

InChI Identifier

InChI=1S/C27H44O2/c1-19(18-28)7-5-8-21(3)25-14-15-26-22(9-6-16-27(25,26)4)11-12-23-17-24(29)13-10-20(23)2/h11-12,19,21,24-26,28-29H,2,5-10,13-18H2,1,3-4H3

InChI Key

UZHJNFDLHNKRIM-UHFFFAOYSA-N

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as vitamin d and derivatives. Vitamin D and derivatives are compounds containing a secosteroid backbone, usually secoergostane or secocholestane.

Kingdom

Organic compounds

Super Class

Lipids and lipid-like molecules

Class

Steroids and steroid derivatives

Sub Class

Vitamin D and derivatives

Direct Parent

Vitamin D and derivatives

Alternative Parents

Substituents

Triterpenoid
Fatty alcohol
Fatty acyl
Cyclic alcohol
Secondary alcohol
Organic oxygen compound
Hydrocarbon derivative
Primary alcohol
Organooxygen compound
Alcohol
Aliphatic homopolycyclic compound

Molecular Framework

Aliphatic homopolycyclic compounds

External Descriptors

Not Available

Ontology

Physiological effect

Not Available

Disposition

Biological location

Non-excretory biofluid

Biofluid or Excreta

Blood (PMID: 31557052)

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	6.76	ALOGPS
logP	5.77	ChemAxon
logS	-5.3	ALOGPS
pKa (Strongest Acidic)	17.42	ChemAxon
pKa (Strongest Basic)	-1.2	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	2	ChemAxon
Hydrogen Donor Count	2	ChemAxon
Polar Surface Area	40.46 Å²	ChemAxon
Rotatable Bond Count	7	ChemAxon
Refractivity	125.08 m³·mol⁻¹	ChemAxon
Polarizability	50.02 Å³	ChemAxon
Number of Rings	3	ChemAxon
Bioavailability	Yes	ChemAxon
Rule of Five	No	ChemAxon
Ghose Filter	No	ChemAxon
Veber's Rule	No	ChemAxon
MDDR-like Rule	Yes	ChemAxon

Predicted Chromatographic Properties

Predicted Collision Cross Sections

Predictor	Adduct Type	CCS Value (Å²)	Reference
DeepCCS	[M-2H]-	233.483	30932474
DeepCCS	[M+Na]+	208.836	30932474
AllCCS	[M+H]+	206.0	32859911
AllCCS	[M+H-H2O]+	203.8	32859911
AllCCS	[M+NH4]+	208.1	32859911
AllCCS	[M+Na]+	208.7	32859911
AllCCS	[M-H]-	203.6	32859911
AllCCS	[M+Na-2H]-	205.7	32859911
AllCCS	[M+HCOO]-	208.0	32859911

Predicted Kovats Retention Indices

Derivatized

Derivative Name / Structure	SMILES	Kovats RI Value	Column Type	Reference
(1R,3Z)-3-[(2E)-2-[(1R,3As,7aR)-1-[(2R)-7-hydroxy-6-methylheptan-2-yl]-7a-methyl-2,3,3a,5,6,7-hexahydro-1H-inden-4-ylidene]ethylidene]-4-methylidenecyclohexan-1-ol,1TMS,isomer #1	C=C1CCC(O)CC1=CC=C1CCCC2(C)C1CCC2C(C)CCCC(C)CO[Si](C)(C)C	3367.4	Semi standard non polar	33892256
(1R,3Z)-3-[(2E)-2-[(1R,3As,7aR)-1-[(2R)-7-hydroxy-6-methylheptan-2-yl]-7a-methyl-2,3,3a,5,6,7-hexahydro-1H-inden-4-ylidene]ethylidene]-4-methylidenecyclohexan-1-ol,1TMS,isomer #1	C=C1CCC(O)CC1=CC=C1CCCC2(C)C1CCC2C(C)CCCC(C)CO[Si](C)(C)C	3237.2	Standard non polar	33892256
(1R,3Z)-3-[(2E)-2-[(1R,3As,7aR)-1-[(2R)-7-hydroxy-6-methylheptan-2-yl]-7a-methyl-2,3,3a,5,6,7-hexahydro-1H-inden-4-ylidene]ethylidene]-4-methylidenecyclohexan-1-ol,1TMS,isomer #1	C=C1CCC(O)CC1=CC=C1CCCC2(C)C1CCC2C(C)CCCC(C)CO[Si](C)(C)C	3560.9	Standard polar	33892256
(1R,3Z)-3-[(2E)-2-[(1R,3As,7aR)-1-[(2R)-7-hydroxy-6-methylheptan-2-yl]-7a-methyl-2,3,3a,5,6,7-hexahydro-1H-inden-4-ylidene]ethylidene]-4-methylidenecyclohexan-1-ol,1TMS,isomer #2	C=C1CCC(O[Si](C)(C)C)CC1=CC=C1CCCC2(C)C1CCC2C(C)CCCC(C)CO	3378.2	Semi standard non polar	33892256
(1R,3Z)-3-[(2E)-2-[(1R,3As,7aR)-1-[(2R)-7-hydroxy-6-methylheptan-2-yl]-7a-methyl-2,3,3a,5,6,7-hexahydro-1H-inden-4-ylidene]ethylidene]-4-methylidenecyclohexan-1-ol,1TMS,isomer #2	C=C1CCC(O[Si](C)(C)C)CC1=CC=C1CCCC2(C)C1CCC2C(C)CCCC(C)CO	3160.9	Standard non polar	33892256
(1R,3Z)-3-[(2E)-2-[(1R,3As,7aR)-1-[(2R)-7-hydroxy-6-methylheptan-2-yl]-7a-methyl-2,3,3a,5,6,7-hexahydro-1H-inden-4-ylidene]ethylidene]-4-methylidenecyclohexan-1-ol,1TMS,isomer #2	C=C1CCC(O[Si](C)(C)C)CC1=CC=C1CCCC2(C)C1CCC2C(C)CCCC(C)CO	3610.8	Standard polar	33892256
(1R,3Z)-3-[(2E)-2-[(1R,3As,7aR)-1-[(2R)-7-hydroxy-6-methylheptan-2-yl]-7a-methyl-2,3,3a,5,6,7-hexahydro-1H-inden-4-ylidene]ethylidene]-4-methylidenecyclohexan-1-ol,2TMS,isomer #1	C=C1CCC(O[Si](C)(C)C)CC1=CC=C1CCCC2(C)C1CCC2C(C)CCCC(C)CO[Si](C)(C)C	3374.0	Semi standard non polar	33892256
(1R,3Z)-3-[(2E)-2-[(1R,3As,7aR)-1-[(2R)-7-hydroxy-6-methylheptan-2-yl]-7a-methyl-2,3,3a,5,6,7-hexahydro-1H-inden-4-ylidene]ethylidene]-4-methylidenecyclohexan-1-ol,2TMS,isomer #1	C=C1CCC(O[Si](C)(C)C)CC1=CC=C1CCCC2(C)C1CCC2C(C)CCCC(C)CO[Si](C)(C)C	3321.7	Standard non polar	33892256
(1R,3Z)-3-[(2E)-2-[(1R,3As,7aR)-1-[(2R)-7-hydroxy-6-methylheptan-2-yl]-7a-methyl-2,3,3a,5,6,7-hexahydro-1H-inden-4-ylidene]ethylidene]-4-methylidenecyclohexan-1-ol,2TMS,isomer #1	C=C1CCC(O[Si](C)(C)C)CC1=CC=C1CCCC2(C)C1CCC2C(C)CCCC(C)CO[Si](C)(C)C	3527.0	Standard polar	33892256
(1R,3Z)-3-[(2E)-2-[(1R,3As,7aR)-1-[(2R)-7-hydroxy-6-methylheptan-2-yl]-7a-methyl-2,3,3a,5,6,7-hexahydro-1H-inden-4-ylidene]ethylidene]-4-methylidenecyclohexan-1-ol,1TBDMS,isomer #1	C=C1CCC(O)CC1=CC=C1CCCC2(C)C1CCC2C(C)CCCC(C)CO[Si](C)(C)C(C)(C)C	3612.0	Semi standard non polar	33892256
(1R,3Z)-3-[(2E)-2-[(1R,3As,7aR)-1-[(2R)-7-hydroxy-6-methylheptan-2-yl]-7a-methyl-2,3,3a,5,6,7-hexahydro-1H-inden-4-ylidene]ethylidene]-4-methylidenecyclohexan-1-ol,1TBDMS,isomer #1	C=C1CCC(O)CC1=CC=C1CCCC2(C)C1CCC2C(C)CCCC(C)CO[Si](C)(C)C(C)(C)C	3470.6	Standard non polar	33892256
(1R,3Z)-3-[(2E)-2-[(1R,3As,7aR)-1-[(2R)-7-hydroxy-6-methylheptan-2-yl]-7a-methyl-2,3,3a,5,6,7-hexahydro-1H-inden-4-ylidene]ethylidene]-4-methylidenecyclohexan-1-ol,1TBDMS,isomer #1	C=C1CCC(O)CC1=CC=C1CCCC2(C)C1CCC2C(C)CCCC(C)CO[Si](C)(C)C(C)(C)C	3687.9	Standard polar	33892256
(1R,3Z)-3-[(2E)-2-[(1R,3As,7aR)-1-[(2R)-7-hydroxy-6-methylheptan-2-yl]-7a-methyl-2,3,3a,5,6,7-hexahydro-1H-inden-4-ylidene]ethylidene]-4-methylidenecyclohexan-1-ol,1TBDMS,isomer #2	C=C1CCC(O[Si](C)(C)C(C)(C)C)CC1=CC=C1CCCC2(C)C1CCC2C(C)CCCC(C)CO	3610.4	Semi standard non polar	33892256
(1R,3Z)-3-[(2E)-2-[(1R,3As,7aR)-1-[(2R)-7-hydroxy-6-methylheptan-2-yl]-7a-methyl-2,3,3a,5,6,7-hexahydro-1H-inden-4-ylidene]ethylidene]-4-methylidenecyclohexan-1-ol,1TBDMS,isomer #2	C=C1CCC(O[Si](C)(C)C(C)(C)C)CC1=CC=C1CCCC2(C)C1CCC2C(C)CCCC(C)CO	3379.6	Standard non polar	33892256
(1R,3Z)-3-[(2E)-2-[(1R,3As,7aR)-1-[(2R)-7-hydroxy-6-methylheptan-2-yl]-7a-methyl-2,3,3a,5,6,7-hexahydro-1H-inden-4-ylidene]ethylidene]-4-methylidenecyclohexan-1-ol,1TBDMS,isomer #2	C=C1CCC(O[Si](C)(C)C(C)(C)C)CC1=CC=C1CCCC2(C)C1CCC2C(C)CCCC(C)CO	3735.2	Standard polar	33892256
(1R,3Z)-3-[(2E)-2-[(1R,3As,7aR)-1-[(2R)-7-hydroxy-6-methylheptan-2-yl]-7a-methyl-2,3,3a,5,6,7-hexahydro-1H-inden-4-ylidene]ethylidene]-4-methylidenecyclohexan-1-ol,2TBDMS,isomer #1	C=C1CCC(O[Si](C)(C)C(C)(C)C)CC1=CC=C1CCCC2(C)C1CCC2C(C)CCCC(C)CO[Si](C)(C)C(C)(C)C	3848.1	Semi standard non polar	33892256
(1R,3Z)-3-[(2E)-2-[(1R,3As,7aR)-1-[(2R)-7-hydroxy-6-methylheptan-2-yl]-7a-methyl-2,3,3a,5,6,7-hexahydro-1H-inden-4-ylidene]ethylidene]-4-methylidenecyclohexan-1-ol,2TBDMS,isomer #1	C=C1CCC(O[Si](C)(C)C(C)(C)C)CC1=CC=C1CCCC2(C)C1CCC2C(C)CCCC(C)CO[Si](C)(C)C(C)(C)C	3759.4	Standard non polar	33892256
(1R,3Z)-3-[(2E)-2-[(1R,3As,7aR)-1-[(2R)-7-hydroxy-6-methylheptan-2-yl]-7a-methyl-2,3,3a,5,6,7-hexahydro-1H-inden-4-ylidene]ethylidene]-4-methylidenecyclohexan-1-ol,2TBDMS,isomer #1	C=C1CCC(O[Si](C)(C)C(C)(C)C)CC1=CC=C1CCCC2(C)C1CCC2C(C)CCCC(C)CO[Si](C)(C)C(C)(C)C	3704.8	Standard polar	33892256

Spectra

GC-MS Spectra

Spectrum Type	Description	Splash Key	Deposition Date	Source	View
Predicted GC-MS	Predicted GC-MS Spectrum - (1R,3Z)-3-[(2E)-2-[(1R,3As,7aR)-1-[(2R)-7-hydroxy-6-methylheptan-2-yl]-7a-methyl-2,3,3a,5,6,7-hexahydro-1H-inden-4-ylidene]ethylidene]-4-methylidenecyclohexan-1-ol GC-MS (Non-derivatized) - 70eV, Positive	splash10-00ei-1029000000-2d2c8bf2ad53247856f9	2021-09-23	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - (1R,3Z)-3-[(2E)-2-[(1R,3As,7aR)-1-[(2R)-7-hydroxy-6-methylheptan-2-yl]-7a-methyl-2,3,3a,5,6,7-hexahydro-1H-inden-4-ylidene]ethylidene]-4-methylidenecyclohexan-1-ol GC-MS (Non-derivatized) - 70eV, Positive	Not Available	2021-10-12	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - (1R,3Z)-3-[(2E)-2-[(1R,3As,7aR)-1-[(2R)-7-hydroxy-6-methylheptan-2-yl]-7a-methyl-2,3,3a,5,6,7-hexahydro-1H-inden-4-ylidene]ethylidene]-4-methylidenecyclohexan-1-ol 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 - (1R,3Z)-3-[(2E)-2-[(1R,3As,7aR)-1-[(2R)-7-hydroxy-6-methylheptan-2-yl]-7a-methyl-2,3,3a,5,6,7-hexahydro-1H-inden-4-ylidene]ethylidene]-4-methylidenecyclohexan-1-ol 10V, Positive-QTOF	splash10-0ue9-1767900000-93454d814dc05f2be123	2021-10-12	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - (1R,3Z)-3-[(2E)-2-[(1R,3As,7aR)-1-[(2R)-7-hydroxy-6-methylheptan-2-yl]-7a-methyl-2,3,3a,5,6,7-hexahydro-1H-inden-4-ylidene]ethylidene]-4-methylidenecyclohexan-1-ol 20V, Positive-QTOF	splash10-106r-5794100000-0891fb5c9da001d3919b	2021-10-12	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - (1R,3Z)-3-[(2E)-2-[(1R,3As,7aR)-1-[(2R)-7-hydroxy-6-methylheptan-2-yl]-7a-methyl-2,3,3a,5,6,7-hexahydro-1H-inden-4-ylidene]ethylidene]-4-methylidenecyclohexan-1-ol 40V, Positive-QTOF	splash10-0avj-4940000000-a448b3f1f866c8e9a3cf	2021-10-12	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - (1R,3Z)-3-[(2E)-2-[(1R,3As,7aR)-1-[(2R)-7-hydroxy-6-methylheptan-2-yl]-7a-methyl-2,3,3a,5,6,7-hexahydro-1H-inden-4-ylidene]ethylidene]-4-methylidenecyclohexan-1-ol 10V, Negative-QTOF	splash10-0002-0009000000-a0a7f55957a4298ef440	2021-10-12	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - (1R,3Z)-3-[(2E)-2-[(1R,3As,7aR)-1-[(2R)-7-hydroxy-6-methylheptan-2-yl]-7a-methyl-2,3,3a,5,6,7-hexahydro-1H-inden-4-ylidene]ethylidene]-4-methylidenecyclohexan-1-ol 20V, Negative-QTOF	splash10-0f7k-0009000000-14aa41521742d2eaf8ed	2021-10-12	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - (1R,3Z)-3-[(2E)-2-[(1R,3As,7aR)-1-[(2R)-7-hydroxy-6-methylheptan-2-yl]-7a-methyl-2,3,3a,5,6,7-hexahydro-1H-inden-4-ylidene]ethylidene]-4-methylidenecyclohexan-1-ol 40V, Negative-QTOF	splash10-0002-0219000000-9fcd4b68c452a0164a53	2021-10-12	Wishart Lab	View Spectrum

Biological Properties

Cellular Locations

Not Available

Biospecimen Locations

Blood

Tissue Locations

Not Available

Pathways

Not Available

Name	SMPDB/PathBank	KEGG

Normal Concentrations

Biospecimen	Status	Value	Age	Sex	Condition	Reference	Details
Blood	Detected but not Quantified	Not Quantified	Not Specified	Not Specified	Normal	31557052	details

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

Not Available

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

73717601

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

Barupal DK, Fiehn O: Generating the Blood Exposome Database Using a Comprehensive Text Mining and Database Fusion Approach. Environ Health Perspect. 2019 Sep;127(9):97008. doi: 10.1289/EHP4713. Epub 2019 Sep 26. [PubMed:31557052 ]

Showing metabocard for (1R,3Z)-3-[(2E)-2-[(1R,3As,7aR)-1-[(2R)-7-hydroxy-6-methylheptan-2-yl]-7a-methyl-2,3,3a,5,6,7-hexahydro-1H-inden-4-ylidene]ethylidene]-4-methylidenecyclohexan-1-ol (HMDB0242330)

MOL for HMDB0242330 ((1R,3Z)-3-[(2E)-2-[(1R,3As,7aR)-1-[(2R)-7-hydroxy-6-methylheptan-2-yl]-7a-methyl-2,3,3a,5,6,7-hexahydro-1H-inden-4-ylidene]ethylidene]-4-methylidenecyclohexan-1-ol)

3D MOL for HMDB0242330 ((1R,3Z)-3-[(2E)-2-[(1R,3As,7aR)-1-[(2R)-7-hydroxy-6-methylheptan-2-yl]-7a-methyl-2,3,3a,5,6,7-hexahydro-1H-inden-4-ylidene]ethylidene]-4-methylidenecyclohexan-1-ol)

3D SDF for HMDB0242330 ((1R,3Z)-3-[(2E)-2-[(1R,3As,7aR)-1-[(2R)-7-hydroxy-6-methylheptan-2-yl]-7a-methyl-2,3,3a,5,6,7-hexahydro-1H-inden-4-ylidene]ethylidene]-4-methylidenecyclohexan-1-ol)

3D-SDF for HMDB0242330 ((1R,3Z)-3-[(2E)-2-[(1R,3As,7aR)-1-[(2R)-7-hydroxy-6-methylheptan-2-yl]-7a-methyl-2,3,3a,5,6,7-hexahydro-1H-inden-4-ylidene]ethylidene]-4-methylidenecyclohexan-1-ol)

PDB for HMDB0242330 ((1R,3Z)-3-[(2E)-2-[(1R,3As,7aR)-1-[(2R)-7-hydroxy-6-methylheptan-2-yl]-7a-methyl-2,3,3a,5,6,7-hexahydro-1H-inden-4-ylidene]ethylidene]-4-methylidenecyclohexan-1-ol)

3D PDB for HMDB0242330 ((1R,3Z)-3-[(2E)-2-[(1R,3As,7aR)-1-[(2R)-7-hydroxy-6-methylheptan-2-yl]-7a-methyl-2,3,3a,5,6,7-hexahydro-1H-inden-4-ylidene]ethylidene]-4-methylidenecyclohexan-1-ol)

SMILES for HMDB0242330 ((1R,3Z)-3-[(2E)-2-[(1R,3As,7aR)-1-[(2R)-7-hydroxy-6-methylheptan-2-yl]-7a-methyl-2,3,3a,5,6,7-hexahydro-1H-inden-4-ylidene]ethylidene]-4-methylidenecyclohexan-1-ol)

INCHI for HMDB0242330 ((1R,3Z)-3-[(2E)-2-[(1R,3As,7aR)-1-[(2R)-7-hydroxy-6-methylheptan-2-yl]-7a-methyl-2,3,3a,5,6,7-hexahydro-1H-inden-4-ylidene]ethylidene]-4-methylidenecyclohexan-1-ol)

Structure for HMDB0242330 ((1R,3Z)-3-[(2E)-2-[(1R,3As,7aR)-1-[(2R)-7-hydroxy-6-methylheptan-2-yl]-7a-methyl-2,3,3a,5,6,7-hexahydro-1H-inden-4-ylidene]ethylidene]-4-methylidenecyclohexan-1-ol)

3D Structure for HMDB0242330 ((1R,3Z)-3-[(2E)-2-[(1R,3As,7aR)-1-[(2R)-7-hydroxy-6-methylheptan-2-yl]-7a-methyl-2,3,3a,5,6,7-hexahydro-1H-inden-4-ylidene]ethylidene]-4-methylidenecyclohexan-1-ol)

Predicted Collision Cross Sections

Predicted Kovats Retention Indices

Derivatized

GC-MS Spectra

MS/MS Spectra