NP-MRD: Showing NP-Card for (1r,3as,3br,5as,7s,9as,9br,11ar)-11a-methyl-1-[(2r)-6-methylheptan-2-yl]-hexadecahydrocyclopenta[a]phenanthren-7-ol (NP0323860)

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Record Information

Version

2.0

Created at

2022-09-12 03:33:35 UTC

Updated at

2022-09-12 03:33:35 UTC

NP-MRD ID

NP0323860

Secondary Accession Numbers

None

Natural Product Identification

Common Name

(1r,3as,3br,5as,7s,9as,9br,11ar)-11a-methyl-1-[(2r)-6-methylheptan-2-yl]-hexadecahydrocyclopenta[a]phenanthren-7-ol

Description

19-Norcholestanol belongs to the class of organic compounds known as cholesterols and derivatives. Cholesterols and derivatives are compounds containing a 3-hydroxylated cholestane core. Thus, 19-norcholestanol is considered to be a sterol. (1r,3as,3br,5as,7s,9as,9br,11ar)-11a-methyl-1-[(2r)-6-methylheptan-2-yl]-hexadecahydrocyclopenta[a]phenanthren-7-ol is found in Axinella polypoides. Based on a literature review very few articles have been published on 19-norcholestanol.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652309122205332D          

 27 30  0  0  1  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
   10.5683   -2.5011    0.0000 C   0  0  1  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  1  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  1  0  0  0  0  0  0  0  0  0
   13.3955   -1.9826    0.0000 C   0  0  2  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  1  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  1  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  2  0  0  0  0  0  0  0  0  0
   13.6504   -2.7673    0.0000 C   0  0  1  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  2  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
  7  8  1  6  0  0  0
  9  7  1  1  0  0  0
  9 10  1  0  0  0  0
 10 11  1  0  0  0  0
 12 11  1  1  0  0  0
 12 13  1  0  0  0  0
 13 14  1  6  0  0  0
 14 15  1  0  0  0  0
 16 15  1  1  0  0  0
 16 17  1  0  0  0  0
 17 18  1  0  0  0  0
 18 19  1  1  0  0  0
 18 20  1  0  0  0  0
 20 21  1  0  0  0  0
 22 21  1  6  0  0  0
 16 22  1  0  0  0  0
 22 23  1  0  0  0  0
 13 23  1  0  0  0  0
 23 24  1  1  0  0  0
 24 25  1  0  0  0  0
 25 26  1  0  0  0  0
 12 26  1  0  0  0  0
  9 26  1  0  0  0  0
 26 27  1  1  0  0  0
M  END

     RDKit          3D

 73 76  0  0  0  0  0  0  0  0999 V2000
    7.9439   -0.0537    0.7716 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.0234   -1.2280    0.6933 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.1221   -1.9497   -0.6109 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.5609   -0.8100    0.9941 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0982    0.1986    0.0238 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7488    0.7356    0.2240 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5627   -0.1628    0.1844 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.5751   -1.1761    1.2412 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3494    0.7156    0.0941 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.4726    1.5130   -1.1914 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1033    1.3958   -1.8840 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7672    1.1157   -0.7490 C   0  0  1  0  0  0  0  0  0  0  0  0
   -2.0910    0.4961   -1.0121 C   0  0  2  0  0  0  0  0  0  0  0  0
   -2.9112    1.0984   -2.0949 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2099    0.2941   -2.1689 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9494    0.3287   -0.8796 C   0  0  1  0  0  0  0  0  0  0  0  0
   -6.1104   -0.6398   -0.9442 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.9511   -0.4090    0.2896 C   0  0  1  0  0  0  0  0  0  0  0  0
   -7.2118   -1.5800    0.9894 O   0  0  0  0  0  0  0  0  0  0  0  0
   -6.3669    0.5930    1.2298 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9128    0.3522    1.5470 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1204   -0.0643    0.3248 C   0  0  2  0  0  0  0  0  0  0  0  0
   -2.8538    0.7453    0.3002 C   0  0  1  0  0  0  0  0  0  0  0  0
   -1.9902    0.6306    1.4941 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6908   -0.0479    1.3566 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0287    0.0621    0.0493 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.0005   -1.2628   -0.6907 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.2618    0.2753   -0.2481 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.4818    0.8356    1.2463 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.8735   -0.2593    1.3494 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.2845   -1.9296    1.5111 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.6296   -2.9410   -0.5304 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.1510   -2.1267   -1.1018 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.7627   -1.3625   -1.3269 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.0234   -1.7841    0.8602 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.5572   -0.4545    2.0157 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.1518   -0.2140   -1.0296 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.8564    1.0539   -0.0162 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.6876    1.3313    1.2190 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.6215    1.6114   -0.5081 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.6225   -0.6468   -0.8614 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.2544   -1.0112    2.0981 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.5678   -1.3392    1.7271 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.7989   -2.1770    0.8154 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.3770    1.3884    0.9854 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.6152    2.5807   -0.9327 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.2627    1.1117   -1.8652 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.1158    0.6817   -2.7027 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1352    2.3988   -2.3456 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8288    2.0049   -0.0902 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0875   -0.5973   -1.1388 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1476    2.1646   -1.9557 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3945    0.9009   -3.0696 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8308    0.8075   -2.9315 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9617   -0.7307   -2.5162 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.3832    1.3394   -0.7489 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.6805   -0.5723   -1.8821 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.6636   -1.6702   -0.8225 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.9244    0.0213   -0.0811 H   0  0  0  0  0  0  0  0  0  0  0  0
   -8.0960   -1.4231    1.4521 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.9195    0.5019    2.1977 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.5503    1.6460    0.8959 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5186    1.3157    1.9603 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7871   -0.3846    2.3802 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9652   -1.1411    0.3659 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1885    1.8223    0.2057 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5916    0.0751    2.2784 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8397    1.6394    1.9870 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0047    0.3787    2.1473 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8076   -1.1193    1.6191 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8052   -1.9315   -0.2680 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.9276   -1.8295   -0.6282 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2256   -1.1315   -1.7676 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
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 11 12  1  0
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 18 19  1  0
 18 20  1  0
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 21 22  1  0
 22 23  1  0
 23 24  1  0
 24 25  1  0
 25 26  1  0
 26 27  1  6
 26  9  1  0
 26 12  1  0
 23 13  1  0
 22 16  1  0
  1 28  1  0
  1 29  1  0
  1 30  1  0
  2 31  1  0
  3 32  1  0
  3 33  1  0
  3 34  1  0
  4 35  1  0
  4 36  1  0
  5 37  1  0
  5 38  1  0
  6 39  1  0
  6 40  1  0
  7 41  1  6
  8 42  1  0
  8 43  1  0
  8 44  1  0
  9 45  1  1
 10 46  1  0
 10 47  1  0
 11 48  1  0
 11 49  1  0
 12 50  1  1
 13 51  1  6
 14 52  1  0
 14 53  1  0
 15 54  1  0
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 16 56  1  1
 17 57  1  0
 17 58  1  0
 18 59  1  6
 19 60  1  0
 20 61  1  0
 20 62  1  0
 21 63  1  0
 21 64  1  0
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 23 66  1  6
 24 67  1  0
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 25 69  1  0
 25 70  1  0
 27 71  1  0
 27 72  1  0
 27 73  1  0
M  END


  Mrv1652309122205332D          

 27 30  0  0  1  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
   10.5683   -2.5011    0.0000 C   0  0  1  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  1  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  1  0  0  0  0  0  0  0  0  0
   13.3955   -1.9826    0.0000 C   0  0  2  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  1  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  1  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  2  0  0  0  0  0  0  0  0  0
   13.6504   -2.7673    0.0000 C   0  0  1  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  2  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
  7  8  1  6  0  0  0
  9  7  1  1  0  0  0
  9 10  1  0  0  0  0
 10 11  1  0  0  0  0
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  9 26  1  0  0  0  0
 26 27  1  1  0  0  0
M  END
> <DATABASE_ID>
NP0323860

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CC(C)CCC[C@@H](C)[C@H]1CC[C@H]2[C@@H]3CC[C@H]4C[C@@H](O)CC[C@@H]4[C@H]3CC[C@]12C

> <INCHI_IDENTIFIER>
InChI=1S/C26H46O/c1-17(2)6-5-7-18(3)24-12-13-25-23-10-8-19-16-20(27)9-11-21(19)22(23)14-15-26(24,25)4/h17-25,27H,5-16H2,1-4H3/t18-,19+,20+,21+,22-,23-,24-,25+,26-/m1/s1

> <INCHI_KEY>
YPUSVPPKDFWEHB-PDCPANKYSA-N

> <FORMULA>
C26H46O

> <MOLECULAR_WEIGHT>
374.653

> <EXACT_MASS>
374.354866101

> <JCHEM_ACCEPTOR_COUNT>
1

> <JCHEM_ATOM_COUNT>
73

> <JCHEM_AVERAGE_POLARIZABILITY>
49.46555915132265

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
1

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
(1R,2S,5S,7S,10R,11S,14R,15R)-15-methyl-14-[(2R)-6-methylheptan-2-yl]tetracyclo[8.7.0.0^{2,7}.0^{11,15}]heptadecan-5-ol

> <JCHEM_LOGP>
7.218421392000001

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
4

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA_STRONGEST_ACIDIC>
18.309468849650695

> <JCHEM_PKA_STRONGEST_BASIC>
-1.351238325162786

> <JCHEM_POLAR_SURFACE_AREA>
20.23

> <JCHEM_REFRACTIVITY>
115.29139999999997

> <JCHEM_ROTATABLE_BOND_COUNT>
5

> <JCHEM_RULE_OF_FIVE>
0

> <JCHEM_TRADITIONAL_IUPAC>
(1R,2S,5S,7S,10R,11S,14R,15R)-15-methyl-14-[(2R)-6-methylheptan-2-yl]tetracyclo[8.7.0.0^{2,7}.0^{11,15}]heptadecan-5-ol

> <JCHEM_VEBER_RULE>
1

$$$$

HEADER    PROTEIN                                 12-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   12-SEP-22         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  C   UNK     0      19.728  -4.669   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0      19.728  -6.209   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0      21.061  -3.899   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0      21.222  -2.367   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0      22.729  -2.047   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0      23.499  -3.381   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0      25.005  -3.701   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0      26.035  -2.556   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0      27.542  -2.877   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0      28.018  -4.341   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0      29.524  -4.661   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0      30.000  -6.126   0.000  0.00  0.00           C+0
HETATM   19  O   UNK     0      31.506  -6.446   0.000  0.00  0.00           O+0
HETATM   20  C   UNK     0      28.969  -7.271   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0      27.463  -6.950   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0      26.987  -5.486   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0      25.481  -5.166   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0      24.450  -6.310   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0      22.944  -5.990   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0      22.468  -4.525   0.000  0.00  0.00           C+0
HETATM   27  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                                                       
CONECT    7    6    8    9                                                  
CONECT    8    7                                                            
CONECT    9    7   10   26                                                  
CONECT   10    9   11                                                       
CONECT   11   10   12                                                       
CONECT   12   11   13   26                                                  
CONECT   13   12   14   23                                                  
CONECT   14   13   15                                                       
CONECT   15   14   16                                                       
CONECT   16   15   17   22                                                  
CONECT   17   16   18                                                       
CONECT   18   17   19   20                                                  
CONECT   19   18                                                            
CONECT   20   18   21                                                       
CONECT   21   20   22                                                       
CONECT   22   21   16   23                                                  
CONECT   23   22   13   24                                                  
CONECT   24   23   25                                                       
CONECT   25   24   26                                                       
CONECT   26   25   12    9   27                                             
CONECT   27   26                                                            
MASTER        0    0    0    0    0    0    0    0   27    0   60    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₂₆H₄₆O

Average Mass

374.6530 Da

Monoisotopic Mass

374.35487 Da

IUPAC Name

(1R,2S,5S,7S,10R,11S,14R,15R)-15-methyl-14-[(2R)-6-methylheptan-2-yl]tetracyclo[8.7.0.0^{2,7}.0^{11,15}]heptadecan-5-ol

Traditional Name

(1R,2S,5S,7S,10R,11S,14R,15R)-15-methyl-14-[(2R)-6-methylheptan-2-yl]tetracyclo[8.7.0.0^{2,7}.0^{11,15}]heptadecan-5-ol

CAS Registry Number

Not Available

SMILES

CC(C)CCC[C@@H](C)[C@H]1CC[C@H]2[C@@H]3CC[C@H]4C[C@@H](O)CC[C@@H]4[C@H]3CC[C@]12C

InChI Identifier

InChI=1S/C26H46O/c1-17(2)6-5-7-18(3)24-12-13-25-23-10-8-19-16-20(27)9-11-21(19)22(23)14-15-26(24,25)4/h17-25,27H,5-16H2,1-4H3/t18-,19+,20+,21+,22-,23-,24-,25+,26-/m1/s1

InChI Key

YPUSVPPKDFWEHB-PDCPANKYSA-N

Experimental Spectra

Not Available

Predicted Spectra

Spectrum Type	Description	Depositor ID	Depositor Organization	Depositor	Deposition Date	View
1D NMR	¹³C NMR Spectrum (1D, 25 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 100 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 252 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 1000 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 50 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 200 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 75 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 300 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 101 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 400 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 126 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 500 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 151 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 600 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 176 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 700 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 201 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 800 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 226 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 900 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum

Chemical Shift Submissions

Not Available

Species

Species of Origin

Species Name	Source	Reference
Axinella polypoides	LOTUS Database	35616633

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
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

Cholesterol and derivatives (LMST01010291 )

Physical Properties

State

Not Available

Experimental 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

Predicted Properties

Property	Value	Source
logP	7.22	ChemAxon
pKa (Strongest Acidic)	18.31	ChemAxon
pKa (Strongest Basic)	-1.4	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	115.29 m³·mol⁻¹	ChemAxon
Polarizability	49.47 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

External Links

HMDB ID

Not Available

DrugBank ID

Not Available

Phenol Explorer Compound ID

Not Available

FoodDB ID

Not Available

KNApSAcK ID

Not Available

Chemspider ID

9637822

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

11462982

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for (1r,3as,3br,5as,7s,9as,9br,11ar)-11a-methyl-1-[(2r)-6-methylheptan-2-yl]-hexadecahydrocyclopenta[a]phenanthren-7-ol (NP0323860)

MOL for NP0323860 ((1r,3as,3br,5as,7s,9as,9br,11ar)-11a-methyl-1-[(2r)-6-methylheptan-2-yl]-hexadecahydrocyclopenta[a]phenanthren-7-ol)

3D MOL for NP0323860 ((1r,3as,3br,5as,7s,9as,9br,11ar)-11a-methyl-1-[(2r)-6-methylheptan-2-yl]-hexadecahydrocyclopenta[a]phenanthren-7-ol)

3D SDF for NP0323860 ((1r,3as,3br,5as,7s,9as,9br,11ar)-11a-methyl-1-[(2r)-6-methylheptan-2-yl]-hexadecahydrocyclopenta[a]phenanthren-7-ol)

3D-SDF for NP0323860 ((1r,3as,3br,5as,7s,9as,9br,11ar)-11a-methyl-1-[(2r)-6-methylheptan-2-yl]-hexadecahydrocyclopenta[a]phenanthren-7-ol)

PDB for NP0323860 ((1r,3as,3br,5as,7s,9as,9br,11ar)-11a-methyl-1-[(2r)-6-methylheptan-2-yl]-hexadecahydrocyclopenta[a]phenanthren-7-ol)

3D PDB for NP0323860 ((1r,3as,3br,5as,7s,9as,9br,11ar)-11a-methyl-1-[(2r)-6-methylheptan-2-yl]-hexadecahydrocyclopenta[a]phenanthren-7-ol)

SMILES for NP0323860 ((1r,3as,3br,5as,7s,9as,9br,11ar)-11a-methyl-1-[(2r)-6-methylheptan-2-yl]-hexadecahydrocyclopenta[a]phenanthren-7-ol)

INCHI for NP0323860 ((1r,3as,3br,5as,7s,9as,9br,11ar)-11a-methyl-1-[(2r)-6-methylheptan-2-yl]-hexadecahydrocyclopenta[a]phenanthren-7-ol)

Structure for NP0323860 ((1r,3as,3br,5as,7s,9as,9br,11ar)-11a-methyl-1-[(2r)-6-methylheptan-2-yl]-hexadecahydrocyclopenta[a]phenanthren-7-ol)

3D Structure for NP0323860 ((1r,3as,3br,5as,7s,9as,9br,11ar)-11a-methyl-1-[(2r)-6-methylheptan-2-yl]-hexadecahydrocyclopenta[a]phenanthren-7-ol)