Jump To Section:

Identification Taxonomy Ontology Physical properties Spectra Biological properties Concentrations Links References XML

Record Information

Version

5.0

Status

Detected but not Quantified

Creation Date

2021-08-31 19:01:46 UTC

Update Date

2021-09-26 22:48:58 UTC

HMDB ID

HMDB0242501

Secondary Accession Numbers

None

Metabolite Identification

Common Name

(22S)-22-Hydroxycholesterol

Description

(22S)-22-Hydroxycholesterol, also known as cholest-5-ene-3beta,22-diol or 22(R)OH cholesterol, belongs to the class of organic compounds known as dihydroxy bile acids, alcohols and derivatives. Dihydroxy bile acids, alcohols and derivatives are compounds containing or derived from a bile acid or alcohol, and which bears exactly two carboxylic acid groups. Based on a literature review very few articles have been published on (22S)-22-Hydroxycholesterol. This compound has been identified in human blood as reported by (PMID: 31557052 ). (22s)-22-hydroxycholesterol is not a naturally occurring metabolite and is only found in those individuals exposed to this compound or its derivatives. Technically (22S)-22-Hydroxycholesterol 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


  Mrv1533004161505542D          

 29 32  0  0  0  0            999 V2000
    6.9960   -2.0886    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.7104   -2.5011    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.7104   -3.3261    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.4249   -2.0886    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.1394   -2.5011    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.8538   -2.0886    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.8538   -1.2636    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   10.5683   -2.5011    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.5683   -3.3261    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   11.2828   -2.0886    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   11.3690   -1.2682    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   12.1760   -1.0966    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   12.5885   -1.8111    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   13.3955   -1.9826    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   13.9475   -1.3695    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   14.7545   -1.5411    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   15.0094   -2.3257    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   15.8164   -2.4972    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   16.0713   -3.2818    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   16.8783   -3.4534    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   15.5193   -3.8949    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   14.7123   -3.7234    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   14.4574   -2.9388    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   13.9053   -3.5519    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   13.6504   -2.7673    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   13.0984   -3.3803    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   12.2914   -3.2088    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   12.0365   -2.4242    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   11.4234   -2.9762    0.0000 C   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
  2  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
  8 10  1  0  0  0  0
 10 11  1  0  0  0  0
 11 12  1  0  0  0  0
 12 13  1  0  0  0  0
 13 14  1  0  0  0  0
 14 15  1  0  0  0  0
 15 16  1  0  0  0  0
 16 17  2  0  0  0  0
 17 18  1  0  0  0  0
 18 19  1  0  0  0  0
 19 20  1  0  0  0  0
 19 21  1  0  0  0  0
 21 22  1  0  0  0  0
 22 23  1  0  0  0  0
 17 23  1  0  0  0  0
 23 24  1  0  0  0  0
 23 25  1  0  0  0  0
 14 25  1  0  0  0  0
 25 26  1  0  0  0  0
 26 27  1  0  0  0  0
 27 28  1  0  0  0  0
 10 28  1  0  0  0  0
 13 28  1  0  0  0  0
 28 29  1  0  0  0  0
M  END

HMDB0260193
     RDKit          3D
(8S,9S,10R,13S,14S,17R)-17-((2S,3R)-3-Hydroxy-6-methylheptan-2-yl)-10,13-dime...
 75 78  0  0  0  0  0  0  0  0999 V2000
    6.1406    2.3725   -1.0756 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.7003    1.3449   -0.1227 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.8495    0.6431   -0.8210 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.6334    0.2551    0.1048 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.4236    0.8697    0.6794 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2652    0.0009    1.0398 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7638   -0.9021    2.0179 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.5774   -0.6813   -0.0600 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5131   -1.6472   -0.7507 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2817   -1.3183    0.1557 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6994   -1.9366   -1.0959 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6117   -2.5006   -0.5603 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9518   -1.5903    0.5767 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3587   -1.1002    0.5578 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2063   -1.6902    1.6585 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5602   -1.0859    1.5678 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8410    0.0280    0.9153 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.2666    0.4937    0.9293 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.6612    0.8083   -0.4812 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.8611    0.1028   -0.7310 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.6660    0.3240   -1.4933 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2772    0.8361   -1.2831 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8671    0.8571    0.1698 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9693    2.2876    0.7180 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4830    0.3903    0.4260 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5262    0.7566   -0.7200 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1574    0.7281   -0.0568 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1267   -0.5380    0.6781 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3087   -0.2637    2.1780 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.9256    2.8034   -1.7474 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.7352    3.2522   -0.5118 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.3742    1.9375   -1.7482 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.0174    1.7870    0.8450 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.4477    1.3325   -1.4381 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.3738   -0.0749   -1.5458 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.4456    0.0263   -0.1375 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.1281   -0.4893    0.7263 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.4331   -0.0762   -0.9583 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.6641    1.5982    1.5102 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.0152    1.5730   -0.1290 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.6083    0.6595    1.6600 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.6245   -1.2742    1.8130 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.4009    0.1154   -0.8603 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.4024   -1.8842   -0.1072 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.7175   -1.4524   -1.7917 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.9851   -2.6569   -0.7444 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.3893   -2.1979    0.8663 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.5057   -1.1032   -1.8114 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.2950   -2.6800   -1.5997 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3857   -2.5450   -1.3484 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4093   -3.5493   -0.2589 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8593   -2.2274    1.5089 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8130   -1.5125   -0.3969 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8383   -1.4884    2.6731 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2990   -2.7740    1.4372 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.3615   -1.6287    2.0913 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.9320   -0.2456    1.4152 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.3561    1.4212    1.5684 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.8707    1.8946   -0.6220 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.8342   -0.7602   -0.2394 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.0308    0.6720   -2.4954 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.6764   -0.7872   -1.4621 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1818    1.8751   -1.6883 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5938    0.2005   -1.8574 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1255    2.8942    0.3132 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7835    2.2168    1.8141 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9188    2.7612    0.4708 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1147    0.8473    1.3664 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7131    1.7988   -1.0473 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5924    0.0292   -1.5499 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2275    1.5567    0.6947 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.5639    0.9726   -0.8631 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.3762    0.8152    2.4032 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6263   -0.5868    2.7312 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.0963   -0.8904    2.6290 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  1  0
  2  4  1  0
  4  5  1  0
  5  6  1  0
  6  7  1  0
  6  8  1  0
  8  9  1  0
  8 10  1  0
 10 11  1  0
 11 12  1  0
 12 13  1  0
 13 14  1  0
 14 15  1  0
 15 16  1  0
 16 17  2  0
 17 18  1  0
 18 19  1  0
 19 20  1  0
 19 21  1  0
 21 22  1  0
 22 23  1  0
 23 24  1  0
 23 25  1  0
 25 26  1  0
 26 27  1  0
 27 28  1  0
 28 29  1  0
 28 10  1  0
 28 13  1  0
 25 14  1  0
 23 17  1  0
  1 30  1  0
  1 31  1  0
  1 32  1  0
  2 33  1  0
  3 34  1  0
  3 35  1  0
  3 36  1  0
  4 37  1  0
  4 38  1  0
  5 39  1  0
  5 40  1  0
  6 41  1  0
  7 42  1  0
  8 43  1  0
  9 44  1  0
  9 45  1  0
  9 46  1  0
 10 47  1  0
 11 48  1  0
 11 49  1  0
 12 50  1  0
 12 51  1  0
 13 52  1  0
 14 53  1  0
 15 54  1  0
 15 55  1  0
 16 56  1  0
 18 57  1  0
 18 58  1  0
 19 59  1  0
 20 60  1  0
 21 61  1  0
 21 62  1  0
 22 63  1  0
 22 64  1  0
 24 65  1  0
 24 66  1  0
 24 67  1  0
 25 68  1  0
 26 69  1  0
 26 70  1  0
 27 71  1  0
 27 72  1  0
 29 73  1  0
 29 74  1  0
 29 75  1  0
M  END


  Mrv1533004161505542D          

 29 32  0  0  0  0            999 V2000
    6.9960   -2.0886    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.7104   -2.5011    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.7104   -3.3261    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.4249   -2.0886    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.1394   -2.5011    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.8538   -2.0886    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.8538   -1.2636    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   10.5683   -2.5011    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.5683   -3.3261    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   11.2828   -2.0886    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   11.3690   -1.2682    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   12.1760   -1.0966    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   12.5885   -1.8111    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   13.3955   -1.9826    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   13.9475   -1.3695    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   14.7545   -1.5411    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   15.0094   -2.3257    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   15.8164   -2.4972    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   16.0713   -3.2818    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   16.8783   -3.4534    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   15.5193   -3.8949    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   14.7123   -3.7234    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   14.4574   -2.9388    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   13.9053   -3.5519    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   13.6504   -2.7673    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   13.0984   -3.3803    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   12.2914   -3.2088    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   12.0365   -2.4242    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   11.4234   -2.9762    0.0000 C   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
  2  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
  8 10  1  0  0  0  0
 10 11  1  0  0  0  0
 11 12  1  0  0  0  0
 12 13  1  0  0  0  0
 13 14  1  0  0  0  0
 14 15  1  0  0  0  0
 15 16  1  0  0  0  0
 16 17  2  0  0  0  0
 17 18  1  0  0  0  0
 18 19  1  0  0  0  0
 19 20  1  0  0  0  0
 19 21  1  0  0  0  0
 21 22  1  0  0  0  0
 22 23  1  0  0  0  0
 17 23  1  0  0  0  0
 23 24  1  0  0  0  0
 23 25  1  0  0  0  0
 14 25  1  0  0  0  0
 25 26  1  0  0  0  0
 26 27  1  0  0  0  0
 27 28  1  0  0  0  0
 10 28  1  0  0  0  0
 13 28  1  0  0  0  0
 28 29  1  0  0  0  0
M  END
> <DATABASE_ID>
HMDB0242501

> <DATABASE_NAME>
hmdb

> <SMILES>
CC(C)CCC(O)C(C)C1CCC2C3CC=C4CC(O)CCC4(C)C3CCC12C

> <INCHI_IDENTIFIER>
InChI=1S/C27H46O2/c1-17(2)6-11-25(29)18(3)22-9-10-23-21-8-7-19-16-20(28)12-14-26(19,4)24(21)13-15-27(22,23)5/h7,17-18,20-25,28-29H,6,8-16H2,1-5H3

> <INCHI_KEY>
RZPAXNJLEKLXNO-UHFFFAOYSA-N

> <FORMULA>
C27H46O2

> <MOLECULAR_WEIGHT>
402.663

> <EXACT_MASS>
402.349780721

> <JCHEM_ACCEPTOR_COUNT>
2

> <JCHEM_ATOM_COUNT>
75

> <JCHEM_AVERAGE_POLARIZABILITY>
50.64136226528891

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
2

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
14-(3-hydroxy-6-methylheptan-2-yl)-2,15-dimethyltetracyclo[8.7.0.0²,⁷.0¹¹,¹⁵]heptadec-7-en-5-ol

> <ALOGPS_LOGP>
5.69

> <JCHEM_LOGP>
5.804124233666668

> <ALOGPS_LOGS>
-5.79

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
4

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
19.477856532809838

> <JCHEM_PKA_STRONGEST_ACIDIC>
18.20428950550382

> <JCHEM_PKA_STRONGEST_BASIC>
-0.7338943961064351

> <JCHEM_POLAR_SURFACE_AREA>
40.46

> <JCHEM_REFRACTIVITY>
122.20899999999996

> <JCHEM_ROTATABLE_BOND_COUNT>
5

> <JCHEM_RULE_OF_FIVE>
0

> <ALOGPS_SOLUBILITY>
6.53e-04 g/l

> <JCHEM_TRADITIONAL_IUPAC>
14-(3-hydroxy-6-methylheptan-2-yl)-2,15-dimethyltetracyclo[8.7.0.0²,⁷.0¹¹,¹⁵]heptadec-7-en-5-ol

> <JCHEM_VEBER_RULE>
0

$$$$

HMDB0260193
     RDKit          3D
(8S,9S,10R,13S,14S,17R)-17-((2S,3R)-3-Hydroxy-6-methylheptan-2-yl)-10,13-dime...
 75 78  0  0  0  0  0  0  0  0999 V2000
    6.1406    2.3725   -1.0756 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.7003    1.3449   -0.1227 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.8495    0.6431   -0.8210 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.6334    0.2551    0.1048 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.4236    0.8697    0.6794 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2652    0.0009    1.0398 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7638   -0.9021    2.0179 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.5774   -0.6813   -0.0600 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5131   -1.6472   -0.7507 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2817   -1.3183    0.1557 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6994   -1.9366   -1.0959 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6117   -2.5006   -0.5603 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9518   -1.5903    0.5767 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3587   -1.1002    0.5578 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2063   -1.6902    1.6585 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5602   -1.0859    1.5678 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8410    0.0280    0.9153 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.2666    0.4937    0.9293 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.6612    0.8083   -0.4812 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.8611    0.1028   -0.7310 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.6660    0.3240   -1.4933 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2772    0.8361   -1.2831 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8671    0.8571    0.1698 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9693    2.2876    0.7180 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4830    0.3903    0.4260 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5262    0.7566   -0.7200 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1574    0.7281   -0.0568 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1267   -0.5380    0.6781 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3087   -0.2637    2.1780 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.9256    2.8034   -1.7474 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.7352    3.2522   -0.5118 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.3742    1.9375   -1.7482 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.0174    1.7870    0.8450 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.4477    1.3325   -1.4381 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.3738   -0.0749   -1.5458 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.4456    0.0263   -0.1375 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.1281   -0.4893    0.7263 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.4331   -0.0762   -0.9583 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.6641    1.5982    1.5102 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.0152    1.5730   -0.1290 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.6083    0.6595    1.6600 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.6245   -1.2742    1.8130 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.4009    0.1154   -0.8603 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.4024   -1.8842   -0.1072 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.7175   -1.4524   -1.7917 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.9851   -2.6569   -0.7444 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.3893   -2.1979    0.8663 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.5057   -1.1032   -1.8114 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.2950   -2.6800   -1.5997 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3857   -2.5450   -1.3484 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4093   -3.5493   -0.2589 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8593   -2.2274    1.5089 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8130   -1.5125   -0.3969 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8383   -1.4884    2.6731 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2990   -2.7740    1.4372 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.3615   -1.6287    2.0913 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.9320   -0.2456    1.4152 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.3561    1.4212    1.5684 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.8707    1.8946   -0.6220 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.8342   -0.7602   -0.2394 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.0308    0.6720   -2.4954 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.6764   -0.7872   -1.4621 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1818    1.8751   -1.6883 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5938    0.2005   -1.8574 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1255    2.8942    0.3132 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7835    2.2168    1.8141 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9188    2.7612    0.4708 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1147    0.8473    1.3664 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7131    1.7988   -1.0473 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5924    0.0292   -1.5499 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2275    1.5567    0.6947 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.5639    0.9726   -0.8631 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.3762    0.8152    2.4032 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6263   -0.5868    2.7312 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.0963   -0.8904    2.6290 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  1  0
  2  4  1  0
  4  5  1  0
  5  6  1  0
  6  7  1  0
  6  8  1  0
  8  9  1  0
  8 10  1  0
 10 11  1  0
 11 12  1  0
 12 13  1  0
 13 14  1  0
 14 15  1  0
 15 16  1  0
 16 17  2  0
 17 18  1  0
 18 19  1  0
 19 20  1  0
 19 21  1  0
 21 22  1  0
 22 23  1  0
 23 24  1  0
 23 25  1  0
 25 26  1  0
 26 27  1  0
 27 28  1  0
 28 29  1  0
 28 10  1  0
 28 13  1  0
 25 14  1  0
 23 17  1  0
  1 30  1  0
  1 31  1  0
  1 32  1  0
  2 33  1  0
  3 34  1  0
  3 35  1  0
  3 36  1  0
  4 37  1  0
  4 38  1  0
  5 39  1  0
  5 40  1  0
  6 41  1  0
  7 42  1  0
  8 43  1  0
  9 44  1  0
  9 45  1  0
  9 46  1  0
 10 47  1  0
 11 48  1  0
 11 49  1  0
 12 50  1  0
 12 51  1  0
 13 52  1  0
 14 53  1  0
 15 54  1  0
 15 55  1  0
 16 56  1  0
 18 57  1  0
 18 58  1  0
 19 59  1  0
 20 60  1  0
 21 61  1  0
 21 62  1  0
 22 63  1  0
 22 64  1  0
 24 65  1  0
 24 66  1  0
 24 67  1  0
 25 68  1  0
 26 69  1  0
 26 70  1  0
 27 71  1  0
 27 72  1  0
 29 73  1  0
 29 74  1  0
 29 75  1  0
M  END

HEADER    PROTEIN                                 16-APR-15   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   16-APR-15         0                                  
HETATM    1  C   UNK     0      13.059  -3.899   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0      14.393  -4.669   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0      14.393  -6.209   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0      15.726  -3.899   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0      17.060  -4.669   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0      18.394  -3.899   0.000  0.00  0.00           C+0
HETATM    7  O   UNK     0      18.394  -2.359   0.000  0.00  0.00           O+0
HETATM    8  C   UNK     0      19.728  -4.669   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0      19.728  -6.209   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0      21.061  -3.899   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0      21.222  -2.367   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0      22.729  -2.047   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0      23.499  -3.381   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0      25.005  -3.701   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0      26.035  -2.556   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0      27.542  -2.877   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0      28.018  -4.341   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0      29.524  -4.661   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0      30.000  -6.126   0.000  0.00  0.00           C+0
HETATM   20  O   UNK     0      31.506  -6.446   0.000  0.00  0.00           O+0
HETATM   21  C   UNK     0      28.969  -7.271   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0      27.463  -6.950   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0      26.987  -5.486   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0      25.957  -6.630   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0      25.481  -5.166   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0      24.450  -6.310   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0      22.944  -5.990   0.000  0.00  0.00           C+0
HETATM   28  C   UNK     0      22.468  -4.525   0.000  0.00  0.00           C+0
HETATM   29  C   UNK     0      21.324  -5.556   0.000  0.00  0.00           C+0
CONECT    1    2                                                            
CONECT    2    1    3    4                                                  
CONECT    3    2                                                            
CONECT    4    2    5                                                       
CONECT    5    4    6                                                       
CONECT    6    5    7    8                                                  
CONECT    7    6                                                            
CONECT    8    6    9   10                                                  
CONECT    9    8                                                            
CONECT   10    8   11   28                                                  
CONECT   11   10   12                                                       
CONECT   12   11   13                                                       
CONECT   13   12   14   28                                                  
CONECT   14   13   15   25                                                  
CONECT   15   14   16                                                       
CONECT   16   15   17                                                       
CONECT   17   16   18   23                                                  
CONECT   18   17   19                                                       
CONECT   19   18   20   21                                                  
CONECT   20   19                                                            
CONECT   21   19   22                                                       
CONECT   22   21   23                                                       
CONECT   23   22   17   24   25                                             
CONECT   24   23                                                            
CONECT   25   23   14   26                                                  
CONECT   26   25   27                                                       
CONECT   27   26   28                                                       
CONECT   28   27   10   13   29                                             
CONECT   29   28                                                            
MASTER        0    0    0    0    0    0    0    0   29    0   64    0
END

COMPND    HMDB0260193
HETATM    1  C1  UNL     1       6.141   2.373  -1.076  1.00  0.00           C  
HETATM    2  C2  UNL     1       6.700   1.345  -0.123  1.00  0.00           C  
HETATM    3  C3  UNL     1       7.849   0.643  -0.821  1.00  0.00           C  
HETATM    4  C4  UNL     1       5.633   0.255   0.105  1.00  0.00           C  
HETATM    5  C5  UNL     1       4.424   0.870   0.679  1.00  0.00           C  
HETATM    6  C6  UNL     1       3.265   0.001   1.040  1.00  0.00           C  
HETATM    7  O1  UNL     1       3.764  -0.902   2.018  1.00  0.00           O  
HETATM    8  C7  UNL     1       2.577  -0.681  -0.060  1.00  0.00           C  
HETATM    9  C8  UNL     1       3.513  -1.647  -0.751  1.00  0.00           C  
HETATM   10  C9  UNL     1       1.282  -1.318   0.156  1.00  0.00           C  
HETATM   11  C10 UNL     1       0.699  -1.937  -1.096  1.00  0.00           C  
HETATM   12  C11 UNL     1      -0.612  -2.501  -0.560  1.00  0.00           C  
HETATM   13  C12 UNL     1      -0.952  -1.590   0.577  1.00  0.00           C  
HETATM   14  C13 UNL     1      -2.359  -1.100   0.558  1.00  0.00           C  
HETATM   15  C14 UNL     1      -3.206  -1.690   1.659  1.00  0.00           C  
HETATM   16  C15 UNL     1      -4.560  -1.086   1.568  1.00  0.00           C  
HETATM   17  C16 UNL     1      -4.841   0.028   0.915  1.00  0.00           C  
HETATM   18  C17 UNL     1      -6.267   0.494   0.929  1.00  0.00           C  
HETATM   19  C18 UNL     1      -6.661   0.808  -0.481  1.00  0.00           C  
HETATM   20  O2  UNL     1      -7.861   0.103  -0.731  1.00  0.00           O  
HETATM   21  C19 UNL     1      -5.666   0.324  -1.493  1.00  0.00           C  
HETATM   22  C20 UNL     1      -4.277   0.836  -1.283  1.00  0.00           C  
HETATM   23  C21 UNL     1      -3.867   0.857   0.170  1.00  0.00           C  
HETATM   24  C22 UNL     1      -3.969   2.288   0.718  1.00  0.00           C  
HETATM   25  C23 UNL     1      -2.483   0.390   0.426  1.00  0.00           C  
HETATM   26  C24 UNL     1      -1.526   0.757  -0.720  1.00  0.00           C  
HETATM   27  C25 UNL     1      -0.157   0.728  -0.057  1.00  0.00           C  
HETATM   28  C26 UNL     1       0.127  -0.538   0.678  1.00  0.00           C  
HETATM   29  C27 UNL     1       0.309  -0.264   2.178  1.00  0.00           C  
HETATM   30  H1  UNL     1       6.926   2.803  -1.747  1.00  0.00           H  
HETATM   31  H2  UNL     1       5.735   3.252  -0.512  1.00  0.00           H  
HETATM   32  H3  UNL     1       5.374   1.937  -1.748  1.00  0.00           H  
HETATM   33  H4  UNL     1       7.017   1.787   0.845  1.00  0.00           H  
HETATM   34  H5  UNL     1       8.448   1.333  -1.438  1.00  0.00           H  
HETATM   35  H6  UNL     1       7.374  -0.075  -1.546  1.00  0.00           H  
HETATM   36  H7  UNL     1       8.446   0.026  -0.138  1.00  0.00           H  
HETATM   37  H8  UNL     1       6.128  -0.489   0.726  1.00  0.00           H  
HETATM   38  H9  UNL     1       5.433  -0.076  -0.958  1.00  0.00           H  
HETATM   39  H10 UNL     1       4.664   1.598   1.510  1.00  0.00           H  
HETATM   40  H11 UNL     1       4.015   1.573  -0.129  1.00  0.00           H  
HETATM   41  H12 UNL     1       2.608   0.660   1.660  1.00  0.00           H  
HETATM   42  H13 UNL     1       4.624  -1.274   1.813  1.00  0.00           H  
HETATM   43  H14 UNL     1       2.401   0.115  -0.860  1.00  0.00           H  
HETATM   44  H15 UNL     1       4.402  -1.884  -0.107  1.00  0.00           H  
HETATM   45  H16 UNL     1       3.718  -1.452  -1.792  1.00  0.00           H  
HETATM   46  H17 UNL     1       2.985  -2.657  -0.744  1.00  0.00           H  
HETATM   47  H18 UNL     1       1.389  -2.198   0.866  1.00  0.00           H  
HETATM   48  H19 UNL     1       0.506  -1.103  -1.811  1.00  0.00           H  
HETATM   49  H20 UNL     1       1.295  -2.680  -1.600  1.00  0.00           H  
HETATM   50  H21 UNL     1      -1.386  -2.545  -1.348  1.00  0.00           H  
HETATM   51  H22 UNL     1      -0.409  -3.549  -0.259  1.00  0.00           H  
HETATM   52  H23 UNL     1      -0.859  -2.227   1.509  1.00  0.00           H  
HETATM   53  H24 UNL     1      -2.813  -1.513  -0.397  1.00  0.00           H  
HETATM   54  H25 UNL     1      -2.838  -1.488   2.673  1.00  0.00           H  
HETATM   55  H26 UNL     1      -3.299  -2.774   1.437  1.00  0.00           H  
HETATM   56  H27 UNL     1      -5.362  -1.629   2.091  1.00  0.00           H  
HETATM   57  H28 UNL     1      -6.932  -0.246   1.415  1.00  0.00           H  
HETATM   58  H29 UNL     1      -6.356   1.421   1.568  1.00  0.00           H  
HETATM   59  H30 UNL     1      -6.871   1.895  -0.622  1.00  0.00           H  
HETATM   60  H31 UNL     1      -7.834  -0.760  -0.239  1.00  0.00           H  
HETATM   61  H32 UNL     1      -6.031   0.672  -2.495  1.00  0.00           H  
HETATM   62  H33 UNL     1      -5.676  -0.787  -1.462  1.00  0.00           H  
HETATM   63  H34 UNL     1      -4.182   1.875  -1.688  1.00  0.00           H  
HETATM   64  H35 UNL     1      -3.594   0.200  -1.857  1.00  0.00           H  
HETATM   65  H36 UNL     1      -3.126   2.894   0.313  1.00  0.00           H  
HETATM   66  H37 UNL     1      -3.783   2.217   1.814  1.00  0.00           H  
HETATM   67  H38 UNL     1      -4.919   2.761   0.471  1.00  0.00           H  
HETATM   68  H39 UNL     1      -2.115   0.847   1.366  1.00  0.00           H  
HETATM   69  H40 UNL     1      -1.713   1.799  -1.047  1.00  0.00           H  
HETATM   70  H41 UNL     1      -1.592   0.029  -1.550  1.00  0.00           H  
HETATM   71  H42 UNL     1      -0.227   1.557   0.695  1.00  0.00           H  
HETATM   72  H43 UNL     1       0.564   0.973  -0.863  1.00  0.00           H  
HETATM   73  H44 UNL     1       0.376   0.815   2.403  1.00  0.00           H  
HETATM   74  H45 UNL     1      -0.626  -0.587   2.731  1.00  0.00           H  
HETATM   75  H46 UNL     1       1.096  -0.890   2.629  1.00  0.00           H  
CONECT    1    2   30   31   32
CONECT    2    3    4   33
CONECT    3   34   35   36
CONECT    4    5   37   38
CONECT    5    6   39   40
CONECT    6    7    8   41
CONECT    7   42
CONECT    8    9   10   43
CONECT    9   44   45   46
CONECT   10   11   28   47
CONECT   11   12   48   49
CONECT   12   13   50   51
CONECT   13   14   28   52
CONECT   14   15   25   53
CONECT   15   16   54   55
CONECT   16   17   17   56
CONECT   17   18   23
CONECT   18   19   57   58
CONECT   19   20   21   59
CONECT   20   60
CONECT   21   22   61   62
CONECT   22   23   63   64
CONECT   23   24   25
CONECT   24   65   66   67
CONECT   25   26   68
CONECT   26   27   69   70
CONECT   27   28   71   72
CONECT   28   29
CONECT   29   73   74   75
END

HMDB0260193
     RDKit          3D
(8S,9S,10R,13S,14S,17R)-17-((2S,3R)-3-Hydroxy-6-methylheptan-2-yl)-10,13-dime...
 75 78  0  0  0  0  0  0  0  0999 V2000
    6.1406    2.3725   -1.0756 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.7003    1.3449   -0.1227 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.8495    0.6431   -0.8210 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.6334    0.2551    0.1048 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.4236    0.8697    0.6794 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2652    0.0009    1.0398 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7638   -0.9021    2.0179 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.5774   -0.6813   -0.0600 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5131   -1.6472   -0.7507 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2817   -1.3183    0.1557 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6994   -1.9366   -1.0959 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6117   -2.5006   -0.5603 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9518   -1.5903    0.5767 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3587   -1.1002    0.5578 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2063   -1.6902    1.6585 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5602   -1.0859    1.5678 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8410    0.0280    0.9153 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.2666    0.4937    0.9293 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.6612    0.8083   -0.4812 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.8611    0.1028   -0.7310 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.6660    0.3240   -1.4933 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2772    0.8361   -1.2831 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8671    0.8571    0.1698 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9693    2.2876    0.7180 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4830    0.3903    0.4260 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5262    0.7566   -0.7200 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1574    0.7281   -0.0568 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1267   -0.5380    0.6781 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3087   -0.2637    2.1780 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.9256    2.8034   -1.7474 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.7352    3.2522   -0.5118 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.3742    1.9375   -1.7482 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.0174    1.7870    0.8450 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.4477    1.3325   -1.4381 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.3738   -0.0749   -1.5458 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.4456    0.0263   -0.1375 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.1281   -0.4893    0.7263 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.4331   -0.0762   -0.9583 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.6641    1.5982    1.5102 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.0152    1.5730   -0.1290 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.6083    0.6595    1.6600 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.6245   -1.2742    1.8130 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.4009    0.1154   -0.8603 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.4024   -1.8842   -0.1072 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.7175   -1.4524   -1.7917 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.9851   -2.6569   -0.7444 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.3893   -2.1979    0.8663 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.5057   -1.1032   -1.8114 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.2950   -2.6800   -1.5997 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3857   -2.5450   -1.3484 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4093   -3.5493   -0.2589 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8593   -2.2274    1.5089 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8130   -1.5125   -0.3969 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8383   -1.4884    2.6731 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2990   -2.7740    1.4372 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.3615   -1.6287    2.0913 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.9320   -0.2456    1.4152 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.3561    1.4212    1.5684 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.8707    1.8946   -0.6220 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.8342   -0.7602   -0.2394 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.0308    0.6720   -2.4954 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.6764   -0.7872   -1.4621 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1818    1.8751   -1.6883 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5938    0.2005   -1.8574 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1255    2.8942    0.3132 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7835    2.2168    1.8141 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9188    2.7612    0.4708 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1147    0.8473    1.3664 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7131    1.7988   -1.0473 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5924    0.0292   -1.5499 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2275    1.5567    0.6947 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.5639    0.9726   -0.8631 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.3762    0.8152    2.4032 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6263   -0.5868    2.7312 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.0963   -0.8904    2.6290 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  1  0
  2  4  1  0
  4  5  1  0
  5  6  1  0
  6  7  1  0
  6  8  1  0
  8  9  1  0
  8 10  1  0
 10 11  1  0
 11 12  1  0
 12 13  1  0
 13 14  1  0
 14 15  1  0
 15 16  1  0
 16 17  2  0
 17 18  1  0
 18 19  1  0
 19 20  1  0
 19 21  1  0
 21 22  1  0
 22 23  1  0
 23 24  1  0
 23 25  1  0
 25 26  1  0
 26 27  1  0
 27 28  1  0
 28 29  1  0
 28 10  1  0
 28 13  1  0
 25 14  1  0
 23 17  1  0
  1 30  1  0
  1 31  1  0
  1 32  1  0
  2 33  1  0
  3 34  1  0
  3 35  1  0
  3 36  1  0
  4 37  1  0
  4 38  1  0
  5 39  1  0
  5 40  1  0
  6 41  1  0
  7 42  1  0
  8 43  1  0
  9 44  1  0
  9 45  1  0
  9 46  1  0
 10 47  1  0
 11 48  1  0
 11 49  1  0
 12 50  1  0
 12 51  1  0
 13 52  1  0
 14 53  1  0
 15 54  1  0
 15 55  1  0
 16 56  1  0
 18 57  1  0
 18 58  1  0
 19 59  1  0
 20 60  1  0
 21 61  1  0
 21 62  1  0
 22 63  1  0
 22 64  1  0
 24 65  1  0
 24 66  1  0
 24 67  1  0
 25 68  1  0
 26 69  1  0
 26 70  1  0
 27 71  1  0
 27 72  1  0
 29 73  1  0
 29 74  1  0
 29 75  1  0
M  END

View in JSmol View Stereo Labels

Synonyms

Value	Source
22-Hydroxycholesterol	HMDB
22-Hydroxycholesterol, (3beta,20R,22R)-isomer	HMDB
22-Hydroxycholesterol, (3beta,22R)-isomer	HMDB
22-Hydroxycholesterol, (3beta,22S)-isomer	HMDB
22S-Hydroxycholesterol	HMDB
Cholest-5-ene-3beta,22-diol	HMDB
(22R)-22-Hydroxycholesterol	HMDB
22(R)OH Cholesterol	HMDB
22R-Hydroxycholesterol	HMDB
22-Hydroxycholesterol, (3beta,20R,22S)-isomer	HMDB

Chemical Formula

C₂₇H₄₆O₂

Average Molecular Weight

402.663

Monoisotopic Molecular Weight

402.349780721

IUPAC Name

14-(3-hydroxy-6-methylheptan-2-yl)-2,15-dimethyltetracyclo[8.7.0.0²,⁷.0¹¹,¹⁵]heptadec-7-en-5-ol

Traditional Name

14-(3-hydroxy-6-methylheptan-2-yl)-2,15-dimethyltetracyclo[8.7.0.0²,⁷.0¹¹,¹⁵]heptadec-7-en-5-ol

CAS Registry Number

Not Available

SMILES

CC(C)CCC(O)C(C)C1CCC2C3CC=C4CC(O)CCC4(C)C3CCC12C

InChI Identifier

InChI=1S/C27H46O2/c1-17(2)6-11-25(29)18(3)22-9-10-23-21-8-7-19-16-20(28)12-14-26(19,4)24(21)13-15-27(22,23)5/h7,17-18,20-25,28-29H,6,8-16H2,1-5H3

InChI Key

RZPAXNJLEKLXNO-UHFFFAOYSA-N

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as dihydroxy bile acids, alcohols and derivatives. Dihydroxy bile acids, alcohols and derivatives are compounds containing or derived from a bile acid or alcohol, and which bears exactly two carboxylic acid groups.

Kingdom

Organic compounds

Super Class

Lipids and lipid-like molecules

Class

Steroids and steroid derivatives

Sub Class

Bile acids, alcohols and derivatives

Direct Parent

Dihydroxy bile acids, alcohols and derivatives

Alternative Parents

Substituents

Cholesterol
Cholesterol-skeleton
Cholestane-skeleton
Dihydroxy bile acid, alcohol, or derivatives
22-hydroxysteroid
Hydroxysteroid
3-hydroxy-delta-5-steroid
3-hydroxysteroid
Delta-5-steroid
Cyclic alcohol
Secondary alcohol
Organooxygen compound
Hydrocarbon derivative
Organic oxygen compound
Alcohol
Aliphatic homopolycyclic compound

Molecular Framework

Aliphatic homopolycyclic compounds

External Descriptors

a small molecule (CPD-7189 )

Ontology

Physiological effect

Not Available

Disposition

Biological location

Non-excretory biofluid

Biofluid or Excreta

Blood (PMID: 31557052)

Source

Exogenous

Exogenous (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	5.69	ALOGPS
logP	5.8	ChemAxon
logS	-5.8	ALOGPS
pKa (Strongest Acidic)	18.2	ChemAxon
pKa (Strongest Basic)	-0.73	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	5	ChemAxon
Refractivity	122.21 m³·mol⁻¹	ChemAxon
Polarizability	50.64 Å³	ChemAxon
Number of Rings	4	ChemAxon
Bioavailability	Yes	ChemAxon
Rule of Five	No	ChemAxon
Ghose Filter	No	ChemAxon
Veber's Rule	No	ChemAxon
MDDR-like Rule	No	ChemAxon

Predicted Chromatographic Properties

Predicted Collision Cross Sections

Predictor	Adduct Type	CCS Value (Å²)	Reference
DeepCCS	[M-2H]-	234.624	30932474
DeepCCS	[M+Na]+	209.976	30932474
AllCCS	[M+H]+	206.5	32859911
AllCCS	[M+H-H2O]+	204.4	32859911
AllCCS	[M+NH4]+	208.4	32859911
AllCCS	[M+Na]+	209.0	32859911
AllCCS	[M-H]-	203.4	32859911
AllCCS	[M+Na-2H]-	205.3	32859911
AllCCS	[M+HCOO]-	207.6	32859911

Predicted Retention Times

Underivatized

Chromatographic Method	Retention Time	Reference
Predicted by Siyang on May 30, 2022	21.4378 minutes	33406817
Predicted by Siyang using ReTip algorithm on June 8, 2022	2.55 minutes	32390414

Predicted Kovats Retention Indices

Derivatized

Derivative Name / Structure	SMILES	Kovats RI Value	Column Type	Reference
(22S)-22-Hydroxycholesterol,1TMS,isomer #1	CC(C)CCC(O[Si](C)(C)C)C(C)C1CCC2C3CC=C4CC(O)CCC4(C)C3CCC12C	3333.1	Semi standard non polar	33892256
(22S)-22-Hydroxycholesterol,1TMS,isomer #1	CC(C)CCC(O[Si](C)(C)C)C(C)C1CCC2C3CC=C4CC(O)CCC4(C)C3CCC12C	3179.7	Standard non polar	33892256
(22S)-22-Hydroxycholesterol,1TMS,isomer #1	CC(C)CCC(O[Si](C)(C)C)C(C)C1CCC2C3CC=C4CC(O)CCC4(C)C3CCC12C	3552.5	Standard polar	33892256
(22S)-22-Hydroxycholesterol,1TMS,isomer #2	CC(C)CCC(O)C(C)C1CCC2C3CC=C4CC(O[Si](C)(C)C)CCC4(C)C3CCC12C	3364.1	Semi standard non polar	33892256
(22S)-22-Hydroxycholesterol,1TMS,isomer #2	CC(C)CCC(O)C(C)C1CCC2C3CC=C4CC(O[Si](C)(C)C)CCC4(C)C3CCC12C	3200.0	Standard non polar	33892256
(22S)-22-Hydroxycholesterol,1TMS,isomer #2	CC(C)CCC(O)C(C)C1CCC2C3CC=C4CC(O[Si](C)(C)C)CCC4(C)C3CCC12C	3606.5	Standard polar	33892256
(22S)-22-Hydroxycholesterol,2TMS,isomer #1	CC(C)CCC(O[Si](C)(C)C)C(C)C1CCC2C3CC=C4CC(O[Si](C)(C)C)CCC4(C)C3CCC12C	3304.9	Semi standard non polar	33892256
(22S)-22-Hydroxycholesterol,2TMS,isomer #1	CC(C)CCC(O[Si](C)(C)C)C(C)C1CCC2C3CC=C4CC(O[Si](C)(C)C)CCC4(C)C3CCC12C	3295.3	Standard non polar	33892256
(22S)-22-Hydroxycholesterol,2TMS,isomer #1	CC(C)CCC(O[Si](C)(C)C)C(C)C1CCC2C3CC=C4CC(O[Si](C)(C)C)CCC4(C)C3CCC12C	3554.6	Standard polar	33892256
(22S)-22-Hydroxycholesterol,1TBDMS,isomer #1	CC(C)CCC(O[Si](C)(C)C(C)(C)C)C(C)C1CCC2C3CC=C4CC(O)CCC4(C)C3CCC12C	3572.5	Semi standard non polar	33892256
(22S)-22-Hydroxycholesterol,1TBDMS,isomer #1	CC(C)CCC(O[Si](C)(C)C(C)(C)C)C(C)C1CCC2C3CC=C4CC(O)CCC4(C)C3CCC12C	3518.8	Standard non polar	33892256
(22S)-22-Hydroxycholesterol,1TBDMS,isomer #1	CC(C)CCC(O[Si](C)(C)C(C)(C)C)C(C)C1CCC2C3CC=C4CC(O)CCC4(C)C3CCC12C	3687.3	Standard polar	33892256
(22S)-22-Hydroxycholesterol,1TBDMS,isomer #2	CC(C)CCC(O)C(C)C1CCC2C3CC=C4CC(O[Si](C)(C)C(C)(C)C)CCC4(C)C3CCC12C	3584.1	Semi standard non polar	33892256
(22S)-22-Hydroxycholesterol,1TBDMS,isomer #2	CC(C)CCC(O)C(C)C1CCC2C3CC=C4CC(O[Si](C)(C)C(C)(C)C)CCC4(C)C3CCC12C	3480.0	Standard non polar	33892256
(22S)-22-Hydroxycholesterol,1TBDMS,isomer #2	CC(C)CCC(O)C(C)C1CCC2C3CC=C4CC(O[Si](C)(C)C(C)(C)C)CCC4(C)C3CCC12C	3741.8	Standard polar	33892256
(22S)-22-Hydroxycholesterol,2TBDMS,isomer #1	CC(C)CCC(O[Si](C)(C)C(C)(C)C)C(C)C1CCC2C3CC=C4CC(O[Si](C)(C)C(C)(C)C)CCC4(C)C3CCC12C	3773.4	Semi standard non polar	33892256
(22S)-22-Hydroxycholesterol,2TBDMS,isomer #1	CC(C)CCC(O[Si](C)(C)C(C)(C)C)C(C)C1CCC2C3CC=C4CC(O[Si](C)(C)C(C)(C)C)CCC4(C)C3CCC12C	3815.0	Standard non polar	33892256
(22S)-22-Hydroxycholesterol,2TBDMS,isomer #1	CC(C)CCC(O[Si](C)(C)C(C)(C)C)C(C)C1CCC2C3CC=C4CC(O[Si](C)(C)C(C)(C)C)CCC4(C)C3CCC12C	3762.7	Standard polar	33892256

Spectra

GC-MS Spectra

Spectrum Type	Description	Splash Key	Deposition Date	Source	View
Predicted GC-MS	Predicted GC-MS Spectrum - (22S)-22-Hydroxycholesterol GC-MS (Non-derivatized) - 70eV, Positive	splash10-00dr-1009000000-7ac86c0504167671b58c	2021-09-23	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - (22S)-22-Hydroxycholesterol GC-MS (Non-derivatized) - 70eV, Positive	Not Available	2021-10-12	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - (22S)-22-Hydroxycholesterol GC-MS (Non-derivatized) - 70eV, Positive	Not Available	2021-10-12	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - (22S)-22-Hydroxycholesterol GC-MS (Non-derivatized) - 70eV, Positive	Not Available	2021-10-12	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - (22S)-22-Hydroxycholesterol 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 - (22S)-22-Hydroxycholesterol 10V, Negative-QTOF	splash10-0udi-0002900000-00b12c268e0a541a2976	2021-10-12	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - (22S)-22-Hydroxycholesterol 20V, Negative-QTOF	splash10-0udi-0003900000-7ec2203e64319bfb73fe	2021-10-12	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - (22S)-22-Hydroxycholesterol 40V, Negative-QTOF	splash10-0gc0-0019100000-594c36ee5dd666b9ff6b	2021-10-12	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - (22S)-22-Hydroxycholesterol 10V, Positive-QTOF	splash10-0uy0-1109400000-8e5bf434532dddff03cc	2021-10-12	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - (22S)-22-Hydroxycholesterol 20V, Positive-QTOF	splash10-0cei-9438000000-90e282f724a5636df22a	2021-10-12	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - (22S)-22-Hydroxycholesterol 40V, Positive-QTOF	splash10-0a4i-5920000000-ef3f91102573a624e81e	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

2713669

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

3472316

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 (22S)-22-Hydroxycholesterol (HMDB0242501)

MOL for HMDB0242501 ((22S)-22-Hydroxycholesterol)

3D MOL for HMDB0242501 ((22S)-22-Hydroxycholesterol)

3D SDF for HMDB0242501 ((22S)-22-Hydroxycholesterol)

3D-SDF for HMDB0242501 ((22S)-22-Hydroxycholesterol)

PDB for HMDB0242501 ((22S)-22-Hydroxycholesterol)

3D PDB for HMDB0242501 ((22S)-22-Hydroxycholesterol)

SMILES for HMDB0242501 ((22S)-22-Hydroxycholesterol)

INCHI for HMDB0242501 ((22S)-22-Hydroxycholesterol)

Structure for HMDB0242501 ((22S)-22-Hydroxycholesterol)

3D Structure for HMDB0242501 ((22S)-22-Hydroxycholesterol)

Predicted Collision Cross Sections

Predicted Retention Times

Underivatized

Predicted Kovats Retention Indices

Derivatized

GC-MS Spectra

MS/MS Spectra