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Record Information

Version

5.0

Status

Expected but not Quantified

Creation Date

2021-09-23 23:27:49 UTC

Update Date

2021-09-23 23:27:50 UTC

HMDB ID

HMDB0303120

Secondary Accession Numbers

None

Metabolite Identification

Common Name

31-Norlanostenol

Description

31-Norlanostenol belongs to the class of organic compounds known as cholesterols and derivatives. Cholesterols and derivatives are compounds containing a 3-hydroxylated cholestane core. 31-Norlanostenol is an extremely weak basic (essentially neutral) compound (based on its pKa).

Structure

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


  Mrv0541 02241212542D          

 31 34  0  0  0  0            999 V2000
   -2.6334   -1.3632    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3479   -1.7757    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3479   -2.6007    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -2.6334   -3.0132    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9190   -2.6007    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -1.9190   -1.7757    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -1.2045   -1.3632    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2045   -3.0132    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4900   -2.6007    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4900   -1.7757    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4900   -0.1257    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2045   -0.5382    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9389   -0.1257    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.2244   -0.5382    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.2244   -1.3632    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.6533   -1.3632    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6533   -0.5382    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0624   -3.0132    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9190   -0.9507    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2244    0.2868    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6534    1.1118    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9389    0.6993    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.3678    0.6993    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0823    1.1118    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7968    0.6993    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5112    1.1118    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7968   -0.1257    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2244    1.1118    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2244   -2.1882    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6334   -3.8382    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9190   -3.4257    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0  0  0  0
  1  6  1  0  0  0  0
  2  3  1  0  0  0  0
  3  4  1  0  0  0  0
  3 18  1  1  0  0  0
  4  5  1  0  0  0  0
  6  5  1  0  0  0  0
  5  8  1  0  0  0  0
  7  6  1  0  0  0  0
  6 19  1  1  0  0  0
 12  7  1  0  0  0  0
  7 10  2  0  0  0  0
  8  9  1  0  0  0  0
  9 10  1  0  0  0  0
 10 15  1  0  0  0  0
 11 12  1  0  0  0  0
 11 14  1  0  0  0  0
 13 14  1  0  0  0  0
 13 17  1  0  0  0  0
 14 15  1  0  0  0  0
 14 20  1  1  0  0  0
 15 16  1  0  0  0  0
 16 17  1  0  0  0  0
 21 22  1  0  0  0  0
 21 23  1  0  0  0  0
 22 28  1  6  0  0  0
 23 24  1  0  0  0  0
 24 25  1  0  0  0  0
 25 26  1  0  0  0  0
 25 27  1  0  0  0  0
 15 29  1  6  0  0  0
 13 22  1  1  0  0  0
  4 30  1  0  0  0  0
  5 31  1  6  0  0  0
M  END

HMDB0303120
     RDKit          3D
31-Norlanostenol
 80 83  0  0  0  0  0  0  0  0999 V2000
    7.2004    1.4022    0.2824 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.9850    0.1021   -0.4748 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.3329   -0.3259   -1.0297 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.5627   -0.9348    0.5099 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.2890   -0.5523    1.2143 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.1885   -0.3907    0.1997 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8677   -0.0080    0.8888 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.0772    1.2801    1.6060 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8233    0.0048   -0.1782 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.7945   -1.4174   -0.7612 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3336   -1.7988   -0.8810 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3541   -0.4840   -0.8424 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.1430    0.2201   -2.1453 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7618   -0.5249   -0.4107 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3224    0.6414   -0.1060 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4692    1.8411   -0.1538 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0599    1.6203    0.3279 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4218    0.2195    0.2844 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.1281   -0.4766    1.5941 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7644    0.6513    0.2594 C   0  0  1  0  0  0  0  0  0  0  0  0
   -3.8636    0.3188    1.7226 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3447    2.0584    0.0928 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.7146    2.0559   -0.4940 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.5991    0.9553   -0.0016 C   0  0  2  0  0  0  0  0  0  0  0  0
   -7.1133    1.2197    1.2871 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.9796   -0.4036   -0.0975 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.7071   -1.2843   -1.1228 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5637   -0.2455   -0.6251 C   0  0  2  0  0  0  0  0  0  0  0  0
   -3.9300   -1.5622   -0.9490 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5765   -1.7486   -0.2975 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.3599    1.2469    1.3619 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.0910    1.9144   -0.1204 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.3257    2.0612    0.1645 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.3059    0.2288   -1.3150 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.8817   -0.9734   -0.3330 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.1402   -0.9188   -1.9578 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.9101    0.5713   -1.3276 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.4018   -1.1076    1.2166 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.3713   -1.8750   -0.0477 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.0636   -1.3612    1.9485 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.4612    0.3642    1.8232 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.1013   -1.3541   -0.3388 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.4884    0.4433   -0.4833 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.7101   -0.8013    1.6494 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.0600    1.7383    1.2889 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.3310    2.0486    1.3993 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.2205    1.1154    2.7145 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.1024    0.7032   -0.9637 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.2525   -2.1451   -0.0585 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.3398   -1.4731   -1.7078 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.1366   -2.3606   -1.8258 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.0019   -2.4013   -0.0158 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1233    0.3732   -2.6587 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.4469    1.1560   -2.0647 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.4444   -0.4217   -2.8665 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9651    2.6247    0.4610 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5111    2.2390   -1.2027 H   0  0  0  0  0  0  0  0  0  0  0  0
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    0.5827    2.3565   -0.2011 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.7471   -1.3748    1.7564 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9287   -0.8127    1.5864 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.2022    0.2498    2.4536 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5475    1.0187    2.2635 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8933    0.3875    2.2582 H   0  0  0  0  0  0  0  0  0  0  0  0
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   -4.2548    2.6493    1.0208 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.7379    2.0447   -1.6036 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.2035    3.0233   -0.1915 H   0  0  0  0  0  0  0  0  0  0  0  0
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   -6.9299    0.3927    1.8225 H   0  0  0  0  0  0  0  0  0  0  0  0
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   -6.3734   -1.0512   -2.1546 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.6502   -2.3418   -0.8566 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6848    0.2990   -1.6088 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7845   -1.7329   -2.0389 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5608   -2.4300   -0.6000 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0461   -2.5597   -0.8517 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7463   -2.1094    0.7153 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
  7  8  1  0
  7  9  1  0
  9 10  1  0
 10 11  1  0
 11 12  1  0
 12 13  1  6
 12 14  1  0
 14 15  2  0
 15 16  1  0
 16 17  1  0
 17 18  1  0
 18 19  1  1
 15 20  1  0
 20 21  1  1
 20 22  1  0
 22 23  1  0
 23 24  1  0
 24 25  1  0
 24 26  1  0
 26 27  1  0
 26 28  1  0
 28 29  1  0
 29 30  1  0
 18  9  1  0
 28 20  1  0
 18 12  1  0
 30 14  1  0
  1 31  1  0
  1 32  1  0
  1 33  1  0
  2 34  1  0
  3 35  1  0
  3 36  1  0
  3 37  1  0
  4 38  1  0
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  9 48  1  6
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 11 51  1  0
 11 52  1  0
 13 53  1  0
 13 54  1  0
 13 55  1  0
 16 56  1  0
 16 57  1  0
 17 58  1  0
 17 59  1  0
 19 60  1  0
 19 61  1  0
 19 62  1  0
 21 63  1  0
 21 64  1  0
 21 65  1  0
 22 66  1  0
 22 67  1  0
 23 68  1  0
 23 69  1  0
 24 70  1  6
 25 71  1  0
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 27 73  1  0
 27 74  1  0
 27 75  1  0
 28 76  1  6
 29 77  1  0
 29 78  1  0
 30 79  1  0
 30 80  1  0
M  END


  Mrv0541 02241212542D          

 31 34  0  0  0  0            999 V2000
   -2.6334   -1.3632    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3479   -1.7757    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3479   -2.6007    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -2.6334   -3.0132    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9190   -2.6007    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -1.9190   -1.7757    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -1.2045   -1.3632    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2045   -3.0132    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
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   -0.4900   -1.7757    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
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    0.9389    0.6993    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
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    3.0823    1.1118    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
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    0.2244    1.1118    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2244   -2.1882    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6334   -3.8382    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9190   -3.4257    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0  0  0  0
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  2  3  1  0  0  0  0
  3  4  1  0  0  0  0
  3 18  1  1  0  0  0
  4  5  1  0  0  0  0
  6  5  1  0  0  0  0
  5  8  1  0  0  0  0
  7  6  1  0  0  0  0
  6 19  1  1  0  0  0
 12  7  1  0  0  0  0
  7 10  2  0  0  0  0
  8  9  1  0  0  0  0
  9 10  1  0  0  0  0
 10 15  1  0  0  0  0
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 16 17  1  0  0  0  0
 21 22  1  0  0  0  0
 21 23  1  0  0  0  0
 22 28  1  6  0  0  0
 23 24  1  0  0  0  0
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 15 29  1  6  0  0  0
 13 22  1  1  0  0  0
  4 30  1  0  0  0  0
  5 31  1  6  0  0  0
M  END
> <DATABASE_ID>
HMDB0303120

> <DATABASE_NAME>
hmdb

> <SMILES>
[H][C@@]12CCC3=C(CC[C@]4(C)[C@H](CC[C@@]34C)[C@H](C)CCCC(C)C)[C@@]1(C)CC[C@H](O)C2C

> <INCHI_IDENTIFIER>
InChI=1S/C29H50O/c1-19(2)9-8-10-20(3)22-13-17-29(7)25-12-11-23-21(4)26(30)15-16-27(23,5)24(25)14-18-28(22,29)6/h19-23,26,30H,8-18H2,1-7H3/t20-,21?,22-,23+,26+,27+,28-,29+/m1/s1

> <INCHI_KEY>
IXVNEXDHXGHWLS-CNWMGSDUSA-N

> <FORMULA>
C29H50O

> <MOLECULAR_WEIGHT>
414.7067

> <EXACT_MASS>
414.386166222

> <JCHEM_ACCEPTOR_COUNT>
1

> <JCHEM_AVERAGE_POLARIZABILITY>
54.100836498295

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
1

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
(2S,5S,7S,11R,14R,15R)-2,6,11,15-tetramethyl-14-[(2R)-6-methylheptan-2-yl]tetracyclo[8.7.0.0²,⁷.0¹¹,¹⁵]heptadec-1(10)-en-5-ol

> <ALOGPS_LOGP>
7.38

> <JCHEM_LOGP>
7.734251152333331

> <ALOGPS_LOGS>
-6.39

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
4

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA_STRONGEST_ACIDIC>
18.95724607023405

> <JCHEM_PKA_STRONGEST_BASIC>
-1.067900568879626

> <JCHEM_POLAR_SURFACE_AREA>
20.23

> <JCHEM_REFRACTIVITY>
129.29659999999998

> <JCHEM_ROTATABLE_BOND_COUNT>
5

> <JCHEM_RULE_OF_FIVE>
0

> <ALOGPS_SOLUBILITY>
1.67e-04 g/l

> <JCHEM_TRADITIONAL_IUPAC>
(2S,5S,7S,11R,14R,15R)-2,6,11,15-tetramethyl-14-[(2R)-6-methylheptan-2-yl]tetracyclo[8.7.0.0²,⁷.0¹¹,¹⁵]heptadec-1(10)-en-5-ol

> <JCHEM_VEBER_RULE>
1

$$$$

HMDB0303120
     RDKit          3D
31-Norlanostenol
 80 83  0  0  0  0  0  0  0  0999 V2000
    7.2004    1.4022    0.2824 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.9850    0.1021   -0.4748 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.3329   -0.3259   -1.0297 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.5627   -0.9348    0.5099 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.2890   -0.5523    1.2143 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.1885   -0.3907    0.1997 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8677   -0.0080    0.8888 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.0772    1.2801    1.6060 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8233    0.0048   -0.1782 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.7945   -1.4174   -0.7612 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3336   -1.7988   -0.8810 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3541   -0.4840   -0.8424 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.1430    0.2201   -2.1453 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7618   -0.5249   -0.4107 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3224    0.6414   -0.1060 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4692    1.8411   -0.1538 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0599    1.6203    0.3279 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4218    0.2195    0.2844 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.1281   -0.4766    1.5941 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7644    0.6513    0.2594 C   0  0  1  0  0  0  0  0  0  0  0  0
   -3.8636    0.3188    1.7226 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3447    2.0584    0.0928 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.7146    2.0559   -0.4940 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.5991    0.9553   -0.0016 C   0  0  2  0  0  0  0  0  0  0  0  0
   -7.1133    1.2197    1.2871 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.9796   -0.4036   -0.0975 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.7071   -1.2843   -1.1228 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5637   -0.2455   -0.6251 C   0  0  2  0  0  0  0  0  0  0  0  0
   -3.9300   -1.5622   -0.9490 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5765   -1.7486   -0.2975 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.3599    1.2469    1.3619 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.0910    1.9144   -0.1204 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.3257    2.0612    0.1645 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.3059    0.2288   -1.3150 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.8817   -0.9734   -0.3330 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.1402   -0.9188   -1.9578 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.9101    0.5713   -1.3276 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.4018   -1.1076    1.2166 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.3713   -1.8750   -0.0477 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.0636   -1.3612    1.9485 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.4612    0.3642    1.8232 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.1013   -1.3541   -0.3388 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.4884    0.4433   -0.4833 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.7101   -0.8013    1.6494 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.0600    1.7383    1.2889 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.3310    2.0486    1.3993 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.2205    1.1154    2.7145 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.1024    0.7032   -0.9637 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.2525   -2.1451   -0.0585 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.3398   -1.4731   -1.7078 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.1366   -2.3606   -1.8258 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.0019   -2.4013   -0.0158 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1233    0.3732   -2.6587 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.4469    1.1560   -2.0647 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.4444   -0.4217   -2.8665 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9651    2.6247    0.4610 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5111    2.2390   -1.2027 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0507    1.9391    1.4123 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.5827    2.3565   -0.2011 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.7471   -1.3748    1.7564 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9287   -0.8127    1.5864 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.2022    0.2498    2.4536 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5475    1.0187    2.2635 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8933    0.3875    2.2582 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2624   -0.6936    1.9202 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6720    2.5746   -0.6526 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2548    2.6493    1.0208 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.7379    2.0447   -1.6036 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.2035    3.0233   -0.1915 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.5117    0.9535   -0.6656 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.9299    0.3927    1.8225 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.0039   -0.9789    0.8493 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.7764   -0.9856   -1.0729 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.3734   -1.0512   -2.1546 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.6502   -2.3418   -0.8566 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6848    0.2990   -1.6088 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7845   -1.7329   -2.0389 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5608   -2.4300   -0.6000 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0461   -2.5597   -0.8517 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7463   -2.1094    0.7153 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
  7  8  1  0
  7  9  1  0
  9 10  1  0
 10 11  1  0
 11 12  1  0
 12 13  1  6
 12 14  1  0
 14 15  2  0
 15 16  1  0
 16 17  1  0
 17 18  1  0
 18 19  1  1
 15 20  1  0
 20 21  1  1
 20 22  1  0
 22 23  1  0
 23 24  1  0
 24 25  1  0
 24 26  1  0
 26 27  1  0
 26 28  1  0
 28 29  1  0
 29 30  1  0
 18  9  1  0
 28 20  1  0
 18 12  1  0
 30 14  1  0
  1 31  1  0
  1 32  1  0
  1 33  1  0
  2 34  1  0
  3 35  1  0
  3 36  1  0
  3 37  1  0
  4 38  1  0
  4 39  1  0
  5 40  1  0
  5 41  1  0
  6 42  1  0
  6 43  1  0
  7 44  1  1
  8 45  1  0
  8 46  1  0
  8 47  1  0
  9 48  1  6
 10 49  1  0
 10 50  1  0
 11 51  1  0
 11 52  1  0
 13 53  1  0
 13 54  1  0
 13 55  1  0
 16 56  1  0
 16 57  1  0
 17 58  1  0
 17 59  1  0
 19 60  1  0
 19 61  1  0
 19 62  1  0
 21 63  1  0
 21 64  1  0
 21 65  1  0
 22 66  1  0
 22 67  1  0
 23 68  1  0
 23 69  1  0
 24 70  1  6
 25 71  1  0
 26 72  1  0
 27 73  1  0
 27 74  1  0
 27 75  1  0
 28 76  1  6
 29 77  1  0
 29 78  1  0
 30 79  1  0
 30 80  1  0
M  END

HEADER    PROTEIN                                 24-FEB-12   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   24-FEB-12         0                                  
HETATM    1  C   UNK     0      -4.916  -2.545   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0      -6.249  -3.315   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0      -6.249  -4.855   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0      -4.916  -5.625   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0      -3.582  -4.855   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0      -3.582  -3.315   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0      -2.248  -2.545   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0      -2.248  -5.625   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0      -0.915  -4.855   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0      -0.915  -3.315   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0      -0.915  -0.235   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0      -2.248  -1.005   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       1.753  -0.235   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       0.419  -1.005   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       0.419  -2.545   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       3.086  -2.545   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       3.086  -1.005   0.000  0.00  0.00           C+0
HETATM   18  O   UNK     0      -7.583  -5.625   0.000  0.00  0.00           O+0
HETATM   19  C   UNK     0      -3.582  -1.775   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0       0.419   0.535   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0       3.086   2.075   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0       1.753   1.305   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0       4.420   1.305   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0       5.754   2.075   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0       7.087   1.305   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0       8.421   2.075   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0       7.087  -0.235   0.000  0.00  0.00           C+0
HETATM   28  C   UNK     0       0.419   2.075   0.000  0.00  0.00           C+0
HETATM   29  C   UNK     0       0.419  -4.085   0.000  0.00  0.00           C+0
HETATM   30  C   UNK     0      -4.916  -7.165   0.000  0.00  0.00           C+0
HETATM   31  H   UNK     0      -3.582  -6.395   0.000  0.00  0.00           H+0
CONECT    1    2    6                                                       
CONECT    2    1    3                                                       
CONECT    3    2    4   18                                                  
CONECT    4    3    5   30                                                  
CONECT    5    4    6    8   31                                             
CONECT    6    1    5    7   19                                             
CONECT    7    6   12   10                                                  
CONECT    8    5    9                                                       
CONECT    9    8   10                                                       
CONECT   10    7    9   15                                                  
CONECT   11   12   14                                                       
CONECT   12    7   11                                                       
CONECT   13   14   17   22                                                  
CONECT   14   11   13   15   20                                             
CONECT   15   10   14   16   29                                             
CONECT   16   15   17                                                       
CONECT   17   13   16                                                       
CONECT   18    3                                                            
CONECT   19    6                                                            
CONECT   20   14                                                            
CONECT   21   22   23                                                       
CONECT   22   21   28   13                                                  
CONECT   23   21   24                                                       
CONECT   24   23   25                                                       
CONECT   25   24   26   27                                                  
CONECT   26   25                                                            
CONECT   27   25                                                            
CONECT   28   22                                                            
CONECT   29   15                                                            
CONECT   30    4                                                            
CONECT   31    5                                                            
MASTER        0    0    0    0    0    0    0    0   31    0   68    0
END

COMPND    HMDB0303120
HETATM    1  C1  UNL     1       7.200   1.402   0.282  1.00  0.00           C  
HETATM    2  C2  UNL     1       6.985   0.102  -0.475  1.00  0.00           C  
HETATM    3  C3  UNL     1       8.333  -0.326  -1.030  1.00  0.00           C  
HETATM    4  C4  UNL     1       6.563  -0.935   0.510  1.00  0.00           C  
HETATM    5  C5  UNL     1       5.289  -0.552   1.214  1.00  0.00           C  
HETATM    6  C6  UNL     1       4.189  -0.391   0.200  1.00  0.00           C  
HETATM    7  C7  UNL     1       2.868  -0.008   0.889  1.00  0.00           C  
HETATM    8  C8  UNL     1       3.077   1.280   1.606  1.00  0.00           C  
HETATM    9  C9  UNL     1       1.823   0.005  -0.178  1.00  0.00           C  
HETATM   10  C10 UNL     1       1.795  -1.417  -0.761  1.00  0.00           C  
HETATM   11  C11 UNL     1       0.334  -1.799  -0.881  1.00  0.00           C  
HETATM   12  C12 UNL     1      -0.354  -0.484  -0.842  1.00  0.00           C  
HETATM   13  C13 UNL     1      -0.143   0.220  -2.145  1.00  0.00           C  
HETATM   14  C14 UNL     1      -1.762  -0.525  -0.411  1.00  0.00           C  
HETATM   15  C15 UNL     1      -2.322   0.641  -0.106  1.00  0.00           C  
HETATM   16  C16 UNL     1      -1.469   1.841  -0.154  1.00  0.00           C  
HETATM   17  C17 UNL     1      -0.060   1.620   0.328  1.00  0.00           C  
HETATM   18  C18 UNL     1       0.422   0.220   0.284  1.00  0.00           C  
HETATM   19  C19 UNL     1       0.128  -0.477   1.594  1.00  0.00           C  
HETATM   20  C20 UNL     1      -3.764   0.651   0.259  1.00  0.00           C  
HETATM   21  C21 UNL     1      -3.864   0.319   1.723  1.00  0.00           C  
HETATM   22  C22 UNL     1      -4.345   2.058   0.093  1.00  0.00           C  
HETATM   23  C23 UNL     1      -5.715   2.056  -0.494  1.00  0.00           C  
HETATM   24  C24 UNL     1      -6.599   0.955  -0.002  1.00  0.00           C  
HETATM   25  O1  UNL     1      -7.113   1.220   1.287  1.00  0.00           O  
HETATM   26  C25 UNL     1      -5.980  -0.404  -0.097  1.00  0.00           C  
HETATM   27  C26 UNL     1      -6.707  -1.284  -1.123  1.00  0.00           C  
HETATM   28  C27 UNL     1      -4.564  -0.245  -0.625  1.00  0.00           C  
HETATM   29  C28 UNL     1      -3.930  -1.562  -0.949  1.00  0.00           C  
HETATM   30  C29 UNL     1      -2.576  -1.749  -0.297  1.00  0.00           C  
HETATM   31  H1  UNL     1       7.360   1.247   1.362  1.00  0.00           H  
HETATM   32  H2  UNL     1       8.091   1.914  -0.120  1.00  0.00           H  
HETATM   33  H3  UNL     1       6.326   2.061   0.164  1.00  0.00           H  
HETATM   34  H4  UNL     1       6.306   0.229  -1.315  1.00  0.00           H  
HETATM   35  H5  UNL     1       8.882  -0.973  -0.333  1.00  0.00           H  
HETATM   36  H6  UNL     1       8.140  -0.919  -1.958  1.00  0.00           H  
HETATM   37  H7  UNL     1       8.910   0.571  -1.328  1.00  0.00           H  
HETATM   38  H8  UNL     1       7.402  -1.108   1.217  1.00  0.00           H  
HETATM   39  H9  UNL     1       6.371  -1.875  -0.048  1.00  0.00           H  
HETATM   40  H10 UNL     1       5.064  -1.361   1.949  1.00  0.00           H  
HETATM   41  H11 UNL     1       5.461   0.364   1.823  1.00  0.00           H  
HETATM   42  H12 UNL     1       4.101  -1.354  -0.339  1.00  0.00           H  
HETATM   43  H13 UNL     1       4.488   0.443  -0.483  1.00  0.00           H  
HETATM   44  H14 UNL     1       2.710  -0.801   1.649  1.00  0.00           H  
HETATM   45  H15 UNL     1       4.060   1.738   1.289  1.00  0.00           H  
HETATM   46  H16 UNL     1       2.331   2.049   1.399  1.00  0.00           H  
HETATM   47  H17 UNL     1       3.220   1.115   2.715  1.00  0.00           H  
HETATM   48  H18 UNL     1       2.102   0.703  -0.964  1.00  0.00           H  
HETATM   49  H19 UNL     1       2.253  -2.145  -0.058  1.00  0.00           H  
HETATM   50  H20 UNL     1       2.340  -1.473  -1.708  1.00  0.00           H  
HETATM   51  H21 UNL     1       0.137  -2.361  -1.826  1.00  0.00           H  
HETATM   52  H22 UNL     1       0.002  -2.401  -0.016  1.00  0.00           H  
HETATM   53  H23 UNL     1      -1.123   0.373  -2.659  1.00  0.00           H  
HETATM   54  H24 UNL     1       0.447   1.156  -2.065  1.00  0.00           H  
HETATM   55  H25 UNL     1       0.444  -0.422  -2.866  1.00  0.00           H  
HETATM   56  H26 UNL     1      -1.965   2.625   0.461  1.00  0.00           H  
HETATM   57  H27 UNL     1      -1.511   2.239  -1.203  1.00  0.00           H  
HETATM   58  H28 UNL     1      -0.051   1.939   1.412  1.00  0.00           H  
HETATM   59  H29 UNL     1       0.583   2.356  -0.201  1.00  0.00           H  
HETATM   60  H30 UNL     1       0.747  -1.375   1.756  1.00  0.00           H  
HETATM   61  H31 UNL     1      -0.929  -0.813   1.586  1.00  0.00           H  
HETATM   62  H32 UNL     1       0.202   0.250   2.454  1.00  0.00           H  
HETATM   63  H33 UNL     1      -4.548   1.019   2.264  1.00  0.00           H  
HETATM   64  H34 UNL     1      -2.893   0.387   2.258  1.00  0.00           H  
HETATM   65  H35 UNL     1      -4.262  -0.694   1.920  1.00  0.00           H  
HETATM   66  H36 UNL     1      -3.672   2.575  -0.653  1.00  0.00           H  
HETATM   67  H37 UNL     1      -4.255   2.649   1.021  1.00  0.00           H  
HETATM   68  H38 UNL     1      -5.738   2.045  -1.604  1.00  0.00           H  
HETATM   69  H39 UNL     1      -6.203   3.023  -0.191  1.00  0.00           H  
HETATM   70  H40 UNL     1      -7.512   0.954  -0.666  1.00  0.00           H  
HETATM   71  H41 UNL     1      -6.930   0.393   1.823  1.00  0.00           H  
HETATM   72  H42 UNL     1      -6.004  -0.979   0.849  1.00  0.00           H  
HETATM   73  H43 UNL     1      -7.776  -0.986  -1.073  1.00  0.00           H  
HETATM   74  H44 UNL     1      -6.373  -1.051  -2.155  1.00  0.00           H  
HETATM   75  H45 UNL     1      -6.650  -2.342  -0.857  1.00  0.00           H  
HETATM   76  H46 UNL     1      -4.685   0.299  -1.609  1.00  0.00           H  
HETATM   77  H47 UNL     1      -3.784  -1.733  -2.039  1.00  0.00           H  
HETATM   78  H48 UNL     1      -4.561  -2.430  -0.600  1.00  0.00           H  
HETATM   79  H49 UNL     1      -2.046  -2.560  -0.852  1.00  0.00           H  
HETATM   80  H50 UNL     1      -2.746  -2.109   0.715  1.00  0.00           H  
CONECT    1    2   31   32   33
CONECT    2    3    4   34
CONECT    3   35   36   37
CONECT    4    5   38   39
CONECT    5    6   40   41
CONECT    6    7   42   43
CONECT    7    8    9   44
CONECT    8   45   46   47
CONECT    9   10   18   48
CONECT   10   11   49   50
CONECT   11   12   51   52
CONECT   12   13   14   18
CONECT   13   53   54   55
CONECT   14   15   15   30
CONECT   15   16   20
CONECT   16   17   56   57
CONECT   17   18   58   59
CONECT   18   19
CONECT   19   60   61   62
CONECT   20   21   22   28
CONECT   21   63   64   65
CONECT   22   23   66   67
CONECT   23   24   68   69
CONECT   24   25   26   70
CONECT   25   71
CONECT   26   27   28   72
CONECT   27   73   74   75
CONECT   28   29   76
CONECT   29   30   77   78
CONECT   30   79   80
END

HMDB0303120
     RDKit          3D
31-Norlanostenol
 80 83  0  0  0  0  0  0  0  0999 V2000
    7.2004    1.4022    0.2824 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.9850    0.1021   -0.4748 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.3329   -0.3259   -1.0297 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.5627   -0.9348    0.5099 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.2890   -0.5523    1.2143 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.1885   -0.3907    0.1997 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8677   -0.0080    0.8888 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.0772    1.2801    1.6060 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8233    0.0048   -0.1782 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.7945   -1.4174   -0.7612 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3336   -1.7988   -0.8810 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3541   -0.4840   -0.8424 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.1430    0.2201   -2.1453 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7618   -0.5249   -0.4107 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3224    0.6414   -0.1060 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4692    1.8411   -0.1538 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0599    1.6203    0.3279 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4218    0.2195    0.2844 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.1281   -0.4766    1.5941 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7644    0.6513    0.2594 C   0  0  1  0  0  0  0  0  0  0  0  0
   -3.8636    0.3188    1.7226 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3447    2.0584    0.0928 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.7146    2.0559   -0.4940 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.5991    0.9553   -0.0016 C   0  0  2  0  0  0  0  0  0  0  0  0
   -7.1133    1.2197    1.2871 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.9796   -0.4036   -0.0975 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.7071   -1.2843   -1.1228 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5637   -0.2455   -0.6251 C   0  0  2  0  0  0  0  0  0  0  0  0
   -3.9300   -1.5622   -0.9490 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5765   -1.7486   -0.2975 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.3599    1.2469    1.3619 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.0910    1.9144   -0.1204 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.3257    2.0612    0.1645 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.3059    0.2288   -1.3150 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.8817   -0.9734   -0.3330 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.1402   -0.9188   -1.9578 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.9101    0.5713   -1.3276 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.4018   -1.1076    1.2166 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.3713   -1.8750   -0.0477 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.0636   -1.3612    1.9485 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.4612    0.3642    1.8232 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.1013   -1.3541   -0.3388 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.4884    0.4433   -0.4833 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.7101   -0.8013    1.6494 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.0600    1.7383    1.2889 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.3310    2.0486    1.3993 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.2205    1.1154    2.7145 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.1024    0.7032   -0.9637 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.2525   -2.1451   -0.0585 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.3398   -1.4731   -1.7078 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.1366   -2.3606   -1.8258 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.0019   -2.4013   -0.0158 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1233    0.3732   -2.6587 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.4469    1.1560   -2.0647 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.4444   -0.4217   -2.8665 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9651    2.6247    0.4610 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5111    2.2390   -1.2027 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0507    1.9391    1.4123 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.5827    2.3565   -0.2011 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.7471   -1.3748    1.7564 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9287   -0.8127    1.5864 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.2022    0.2498    2.4536 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5475    1.0187    2.2635 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8933    0.3875    2.2582 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2624   -0.6936    1.9202 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6720    2.5746   -0.6526 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2548    2.6493    1.0208 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.7379    2.0447   -1.6036 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.2035    3.0233   -0.1915 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.5117    0.9535   -0.6656 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.9299    0.3927    1.8225 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.0039   -0.9789    0.8493 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.7764   -0.9856   -1.0729 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.3734   -1.0512   -2.1546 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.6502   -2.3418   -0.8566 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6848    0.2990   -1.6088 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7845   -1.7329   -2.0389 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5608   -2.4300   -0.6000 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0461   -2.5597   -0.8517 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7463   -2.1094    0.7153 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
  7  8  1  0
  7  9  1  0
  9 10  1  0
 10 11  1  0
 11 12  1  0
 12 13  1  6
 12 14  1  0
 14 15  2  0
 15 16  1  0
 16 17  1  0
 17 18  1  0
 18 19  1  1
 15 20  1  0
 20 21  1  1
 20 22  1  0
 22 23  1  0
 23 24  1  0
 24 25  1  0
 24 26  1  0
 26 27  1  0
 26 28  1  0
 28 29  1  0
 29 30  1  0
 18  9  1  0
 28 20  1  0
 18 12  1  0
 30 14  1  0
  1 31  1  0
  1 32  1  0
  1 33  1  0
  2 34  1  0
  3 35  1  0
  3 36  1  0
  3 37  1  0
  4 38  1  0
  4 39  1  0
  5 40  1  0
  5 41  1  0
  6 42  1  0
  6 43  1  0
  7 44  1  1
  8 45  1  0
  8 46  1  0
  8 47  1  0
  9 48  1  6
 10 49  1  0
 10 50  1  0
 11 51  1  0
 11 52  1  0
 13 53  1  0
 13 54  1  0
 13 55  1  0
 16 56  1  0
 16 57  1  0
 17 58  1  0
 17 59  1  0
 19 60  1  0
 19 61  1  0
 19 62  1  0
 21 63  1  0
 21 64  1  0
 21 65  1  0
 22 66  1  0
 22 67  1  0
 23 68  1  0
 23 69  1  0
 24 70  1  6
 25 71  1  0
 26 72  1  0
 27 73  1  0
 27 74  1  0
 27 75  1  0
 28 76  1  6
 29 77  1  0
 29 78  1  0
 30 79  1  0
 30 80  1  0
M  END

View in JSmol View Stereo Labels

Synonyms

Not Available

Chemical Formula

C₂₉H₅₀O

Average Molecular Weight

414.7067

Monoisotopic Molecular Weight

414.386166222

IUPAC Name

(2S,5S,7S,11R,14R,15R)-2,6,11,15-tetramethyl-14-[(2R)-6-methylheptan-2-yl]tetracyclo[8.7.0.0²,⁷.0¹¹,¹⁵]heptadec-1(10)-en-5-ol

Traditional Name

(2S,5S,7S,11R,14R,15R)-2,6,11,15-tetramethyl-14-[(2R)-6-methylheptan-2-yl]tetracyclo[8.7.0.0²,⁷.0¹¹,¹⁵]heptadec-1(10)-en-5-ol

CAS Registry Number

Not Available

SMILES

[H][C@@]12CCC3=C(CC[C@]4(C)[C@H](CC[C@@]34C)[C@H](C)CCCC(C)C)[C@@]1(C)CC[C@H](O)C2C

InChI Identifier

InChI=1S/C29H50O/c1-19(2)9-8-10-20(3)22-13-17-29(7)25-12-11-23-21(4)26(30)15-16-27(23,5)24(25)14-18-28(22,29)6/h19-23,26,30H,8-18H2,1-7H3/t20-,21?,22-,23+,26+,27+,28-,29+/m1/s1

InChI Key

IXVNEXDHXGHWLS-CNWMGSDUSA-N

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as cholesterols and derivatives. Cholesterols and derivatives are compounds containing a 3-hydroxylated cholestane core.

Kingdom

Organic compounds

Super Class

Lipids and lipid-like molecules

Class

Steroids and steroid derivatives

Sub Class

Cholestane steroids

Direct Parent

Cholesterols and derivatives

Alternative Parents

Substituents

Cholesterol-skeleton
14-alpha-methylsteroid
3-beta-hydroxysteroid
Hydroxysteroid
3-hydroxysteroid
Cyclic alcohol
Secondary alcohol
Organic oxygen compound
Hydrocarbon derivative
Organooxygen compound
Alcohol
Aliphatic homopolycyclic compound

Molecular Framework

Aliphatic homopolycyclic compounds

External Descriptors

Not Available

Ontology

Not Available

Onion-family vegetable

Garden onion (FooDB: FOOD00006)

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	7.38	ALOGPS
logP	7.73	ChemAxon
logS	-6.4	ALOGPS
pKa (Strongest Acidic)	18.96	ChemAxon
pKa (Strongest Basic)	-1.1	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	1	ChemAxon
Hydrogen Donor Count	1	ChemAxon
Polar Surface Area	20.23 Å²	ChemAxon
Rotatable Bond Count	5	ChemAxon
Refractivity	129.3 m³·mol⁻¹	ChemAxon
Polarizability	54.1 Å³	ChemAxon
Number of Rings	4	ChemAxon
Bioavailability	Yes	ChemAxon
Rule of Five	No	ChemAxon
Ghose Filter	No	ChemAxon
Veber's Rule	Yes	ChemAxon
MDDR-like Rule	No	ChemAxon

Predicted Chromatographic Properties

Predicted Collision Cross Sections

Predictor	Adduct Type	CCS Value (Å²)	Reference
AllCCS	[M+H]+	210.715	32859911
AllCCS	[M+H-H2O]+	208.812	32859911
AllCCS	[M+Na]+	212.964	32859911
AllCCS	[M+NH4]+	212.464	32859911
AllCCS	[M-H]-	206.613	32859911
AllCCS	[M+Na-2H]-	208.861	32859911
AllCCS	[M+HCOO]-	211.488	32859911
DeepCCS	[M-2H]-	249.859	30932474
DeepCCS	[M+Na]+	224.882	30932474

Predicted Kovats Retention Indices

Not Available

Spectra

MS/MS Spectra

Spectrum Type	Description	Splash Key	Deposition Date	Source	View
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 31-Norlanostenol 10V, Positive-QTOF	splash10-00kb-0009500000-58e1303b1253c6673ef2	2016-06-03	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 31-Norlanostenol 20V, Positive-QTOF	splash10-05vt-3139100000-655683d8c5aea1ada3c4	2016-06-03	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 31-Norlanostenol 40V, Positive-QTOF	splash10-0a70-6149000000-7b2515984545b9b13020	2016-06-03	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 31-Norlanostenol 10V, Negative-QTOF	splash10-03di-0001900000-3e66f6639366c8e0915e	2016-08-04	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 31-Norlanostenol 20V, Negative-QTOF	splash10-03di-0004900000-ccb3e9b864ecfd204f22	2016-08-04	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 31-Norlanostenol 40V, Negative-QTOF	splash10-000t-1009000000-95bb4444e1a35a9d5790	2016-08-04	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 31-Norlanostenol 10V, Positive-QTOF	splash10-014j-9117400000-e35471d5fffa61acfe50	2021-10-21	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 31-Norlanostenol 20V, Positive-QTOF	splash10-0a4i-9121000000-24b304037f51752a0354	2021-10-21	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 31-Norlanostenol 40V, Positive-QTOF	splash10-0a4i-7930000000-39373f8452331a2dbf40	2021-10-21	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 31-Norlanostenol 10V, Negative-QTOF	splash10-03di-0000900000-eda302082c5114b2ab3a	2021-10-21	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 31-Norlanostenol 20V, Negative-QTOF	splash10-03di-0000900000-eda302082c5114b2ab3a	2021-10-21	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 31-Norlanostenol 40V, Negative-QTOF	splash10-03di-0005900000-d14e9f77b9ce6285e4a2	2021-10-21	Wishart Lab	View Spectrum

Biological Properties

Cellular Locations

Not Available

Biospecimen Locations

Not Available

Tissue Locations

Not Available

Pathways

Not Available

Name	SMPDB/PathBank	KEGG

Normal Concentrations

Not Available

Abnormal Concentrations

Not Available

Associated Disorders and Diseases

Disease References

None

Associated OMIM IDs

None

External Links

DrugBank ID

Not Available

Phenol Explorer Compound ID

Not Available

FooDB ID

FDB007846

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

Not Available

PDB ID

Not Available

ChEBI ID

Not Available

Food Biomarker Ontology

Not Available

VMH ID

Not Available

MarkerDB ID

Not Available

Good Scents ID

Not Available

References

Synthesis Reference

Not Available

Material Safety Data Sheet (MSDS)

Not Available

General References

Not Available

Showing metabocard for 31-Norlanostenol (HMDB0303120)

MOL for HMDB0303120 (31-Norlanostenol)

3D MOL for HMDB0303120 (31-Norlanostenol)

3D SDF for HMDB0303120 (31-Norlanostenol)

3D-SDF for HMDB0303120 (31-Norlanostenol)

PDB for HMDB0303120 (31-Norlanostenol)

3D PDB for HMDB0303120 (31-Norlanostenol)

SMILES for HMDB0303120 (31-Norlanostenol)

INCHI for HMDB0303120 (31-Norlanostenol)

Structure for HMDB0303120 (31-Norlanostenol)

3D Structure for HMDB0303120 (31-Norlanostenol)

Predicted Collision Cross Sections

Predicted Kovats Retention Indices

MS/MS Spectra