NP-MRD: Showing NP-Card for (1r,3as,3br,9as,9bs,11as)-9a,11a-dimethyl-1-(6-methylhepta-2,4,6-trien-2-yl)-tetradecahydro-1h-cyclopenta[a]phenanthrene (NP0237693)

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Record Information

Version

2.0

Created at

2022-09-06 20:54:47 UTC

Updated at

2022-09-06 20:54:47 UTC

NP-MRD ID

NP0237693

Secondary Accession Numbers

None

Natural Product Identification

Common Name

(1r,3as,3br,9as,9bs,11as)-9a,11a-dimethyl-1-(6-methylhepta-2,4,6-trien-2-yl)-tetradecahydro-1h-cyclopenta[a]phenanthrene

Description

Cholestatriene belongs to the class of organic compounds known as cholestane steroids. These are steroids with a structure containing the 27-carbon cholestane skeleton. (1r,3as,3br,9as,9bs,11as)-9a,11a-dimethyl-1-(6-methylhepta-2,4,6-trien-2-yl)-tetradecahydro-1h-cyclopenta[a]phenanthrene is found in Aulacomya atra. (1r,3as,3br,9as,9bs,11as)-9a,11a-dimethyl-1-(6-methylhepta-2,4,6-trien-2-yl)-tetradecahydro-1h-cyclopenta[a]phenanthrene was first documented in 2003 (PMID: 12951275). Based on a literature review a small amount of articles have been published on Cholestatriene (PMID: 16377021) (PMID: 15863958).

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652309062222542D          

 27 30  0  0  1  0            999 V2000
   -0.9025   -4.1049    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0853   -4.2178    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2256   -4.9820    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4211   -3.5665    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2383   -3.6793    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7447   -3.0280    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5619   -3.1408    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8728   -3.9050    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0683   -2.4895    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.8390   -1.6970    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5218   -1.2340    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.1731   -1.7404    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    4.9853   -1.5952    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    5.2655   -0.8192    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.0777   -0.6740    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.6095   -1.3047    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.4216   -1.1595    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.9534   -1.7902    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.6731   -2.5662    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.8610   -2.7114    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.3292   -2.0807    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    6.0489   -2.8566    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.5171   -2.2259    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    5.2368   -3.0018    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.4247   -3.1470    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8928   -2.5163    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    3.5330   -3.2587    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  2  0  0  0  0
  2  3  1  0  0  0  0
  4  2  1  4  0  0  0
  4  5  2  0  0  0  0
  6  5  1  4  0  0  0
  6  7  2  0  0  0  0
  7  8  1  0  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
 15 16  1  0  0  0  0
 16 17  1  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
 20 21  1  0  0  0  0
 16 21  1  0  0  0  0
 21 22  1  1  0  0  0
 21 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
  9 26  1  0  0  0  0
 12 26  1  0  0  0  0
 26 27  1  1  0  0  0
M  END

     RDKit          3D

 69 72  0  0  0  0  0  0  0  0999 V2000
    7.7498   -2.0316   -0.2385 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.9545   -1.1826    0.2148 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.1131   -0.9361    1.6409 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.0921   -0.2611    0.7075 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.8653    0.0008    0.0812 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0333    0.9859    0.6670 C   0  0  0  0  0  0  0  0  0  0  0  0
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    2.3983    2.5645    1.3610 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8790    1.1265   -0.6339 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.2794   -0.1926   -1.3284 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9862   -0.7909   -1.8812 C   0  0  0  0  0  0  0  0  0  0  0  0
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   -1.2974   -0.5650   -0.8585 C   0  0  2  0  0  0  0  0  0  0  0  0
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   -4.7034    1.0022   -0.9037 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5932    0.1978   -0.2045 C   0  0  1  0  0  0  0  0  0  0  0  0
   -3.6199    0.7226    1.2400 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3262    0.5814   -0.8706 C   0  0  1  0  0  0  0  0  0  0  0  0
   -1.7416    1.8605   -0.4344 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4056    1.8376    0.2472 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5266    0.7381   -0.1430 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.7007   -0.3201    0.9183 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.4865   -2.5610   -1.2294 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.7060   -2.4431    0.0855 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.9950   -1.1540    1.1130 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.6097   -1.6794    2.1991 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.8812    0.0680    1.8099 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.1873    0.3738    1.5774 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.7347   -0.5975   -0.7919 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.4923    1.4775    1.5993 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.2589    2.8438    2.0520 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.6293    2.1210    1.9821 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.1736    3.4944    0.8338 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.8394    1.9253   -1.4152 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.5467   -0.8601   -0.4944 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.0068   -0.0197   -2.1106 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.0693   -0.7223   -2.9978 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.8895   -1.8654   -1.6424 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2953    0.9393   -2.0802 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2332   -0.8805    0.1952 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2630   -1.3853   -2.6579 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1483   -2.4636   -1.7769 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4829   -2.7312    0.0908 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5148   -3.0365   -1.3132 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2629   -1.5468    0.7801 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.5210   -2.5464   -0.8711 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.1941   -1.2510   -2.1054 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.3342   -0.8523   -0.9115 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.5317   -1.0848    0.6667 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.9935    1.1235    0.8181 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.7933    1.3292   -0.7729 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7733    0.7370   -1.9728 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4350    2.0670   -0.8508 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6426    0.6660    1.7219 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2975    0.0256    1.8164 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0927    1.7187    1.3134 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5752    0.6591   -1.9783 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4636    2.3564    0.2710 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6650    2.5999   -1.2879 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5617    1.7614    1.3431 H   0  0  0  0  0  0  0  0  0  0  0  0
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  3  2  1  0
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 26  9  1  0
 26 12  1  0
 23 13  1  0
 21 16  1  0
  3 30  1  0
  3 31  1  0
  3 32  1  0
  1 28  1  0
  1 29  1  0
  4 33  1  0
  5 34  1  0
  6 35  1  0
  8 36  1  0
  8 37  1  0
  8 38  1  0
  9 39  1  6
 10 40  1  0
 10 41  1  0
 11 42  1  0
 11 43  1  0
 12 44  1  6
 13 45  1  1
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 16 50  1  1
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 20 57  1  0
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 22 59  1  0
 22 60  1  0
 22 61  1  0
 23 62  1  6
 24 63  1  0
 24 64  1  0
 25 65  1  0
 25 66  1  0
 27 67  1  0
 27 68  1  0
 27 69  1  0
M  END


  Mrv1652309062222542D          

 27 30  0  0  1  0            999 V2000
   -0.9025   -4.1049    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0853   -4.2178    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2256   -4.9820    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4211   -3.5665    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2383   -3.6793    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7447   -3.0280    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5619   -3.1408    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8728   -3.9050    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0683   -2.4895    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
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    7.6731   -2.5662    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
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    6.3292   -2.0807    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
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    5.2368   -3.0018    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.4247   -3.1470    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8928   -2.5163    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    3.5330   -3.2587    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  2  0  0  0  0
  2  3  1  0  0  0  0
  4  2  1  4  0  0  0
  4  5  2  0  0  0  0
  6  5  1  4  0  0  0
  6  7  2  0  0  0  0
  7  8  1  0  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
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 15 16  1  0  0  0  0
 16 17  1  0  0  0  0
 17 18  1  0  0  0  0
 18 19  1  0  0  0  0
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 21 23  1  0  0  0  0
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 26 27  1  1  0  0  0
M  END
> <DATABASE_ID>
NP0237693

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CC(=C)C=CC=C(C)[C@H]1CC[C@H]2[C@@H]3CCC4CCCC[C@]4(C)[C@H]3CC[C@]12C

> <INCHI_IDENTIFIER>
InChI=1S/C27H42/c1-19(2)9-8-10-20(3)23-14-15-24-22-13-12-21-11-6-7-17-26(21,4)25(22)16-18-27(23,24)5/h8-10,21-25H,1,6-7,11-18H2,2-5H3/t21?,22-,23+,24-,25-,26-,27+/m0/s1

> <INCHI_KEY>
BJBPZEABVXLYLJ-LZHGKROGSA-N

> <FORMULA>
C27H42

> <MOLECULAR_WEIGHT>
366.633

> <EXACT_MASS>
366.328651352

> <JCHEM_ACCEPTOR_COUNT>
0

> <JCHEM_ATOM_COUNT>
69

> <JCHEM_AVERAGE_POLARIZABILITY>
47.456028532384245

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
0

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
(1S,2S,10R,11S,14R,15S)-2,15-dimethyl-14-(6-methylhepta-2,4,6-trien-2-yl)tetracyclo[8.7.0.0^{2,7}.0^{11,15}]heptadecane

> <JCHEM_LOGP>
7.7900400900000015

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
4

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_POLAR_SURFACE_AREA>
0.0

> <JCHEM_REFRACTIVITY>
119.84109999999997

> <JCHEM_ROTATABLE_BOND_COUNT>
3

> <JCHEM_RULE_OF_FIVE>
0

> <JCHEM_TRADITIONAL_IUPAC>
(1S,2S,10R,11S,14R,15S)-2,15-dimethyl-14-(6-methylhepta-2,4,6-trien-2-yl)tetracyclo[8.7.0.0^{2,7}.0^{11,15}]heptadecane

> <JCHEM_VEBER_RULE>
1

$$$$

HEADER    PROTEIN                                 06-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   06-SEP-22         0                                  
HETATM    1  C   UNK     0      -1.685  -7.663   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0      -0.159  -7.873   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       0.421  -9.300   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       0.786  -6.657   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       2.312  -6.868   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       3.257  -5.652   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       4.782  -5.863   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       5.363  -7.289   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       5.727  -4.647   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       5.299  -3.168   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       6.574  -2.304   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       7.790  -3.249   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       9.306  -2.978   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       9.829  -1.529   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0      11.345  -1.258   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0      12.338  -2.436   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0      13.854  -2.164   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0      14.846  -3.342   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0      14.323  -4.790   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0      12.807  -5.061   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0      11.814  -3.884   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0      11.291  -5.332   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0      10.299  -4.155   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0       9.775  -5.603   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0       8.259  -5.874   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0       7.267  -4.697   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0       6.595  -6.083   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   21                                                  
CONECT   17   16   18                                                       
CONECT   18   17   19                                                       
CONECT   19   18   20                                                       
CONECT   20   19   21                                                       
CONECT   21   20   16   22   23                                             
CONECT   22   21                                                            
CONECT   23   21   13   24                                                  
CONECT   24   23   25                                                       
CONECT   25   24   26                                                       
CONECT   26   25    9   12   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

C₂₇H₄₂

Average Mass

366.6330 Da

Monoisotopic Mass

366.32865 Da

IUPAC Name

Not Available

Traditional Name

Not Available

CAS Registry Number

Not Available

SMILES

CC(=C)C=CC=C(C)[C@H]1CC[C@H]2[C@@H]3CCC4CCCC[C@]4(C)[C@H]3CC[C@]12C

InChI Identifier

InChI=1S/C27H42/c1-19(2)9-8-10-20(3)23-14-15-24-22-13-12-21-11-6-7-17-26(21,4)25(22)16-18-27(23,24)5/h8-10,21-25H,1,6-7,11-18H2,2-5H3/t21?,22-,23+,24-,25-,26-,27+/m0/s1

InChI Key

BJBPZEABVXLYLJ-LZHGKROGSA-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
Aulacomya atra	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as cholestane steroids. These are steroids with a structure containing the 27-carbon cholestane skeleton.

Kingdom

Organic compounds

Super Class

Lipids and lipid-like molecules

Class

Steroids and steroid derivatives

Sub Class

Cholestane steroids

Direct Parent

Cholestane steroids

Alternative Parents

Substituents

Cholestane-skeleton
Branched unsaturated hydrocarbon
Polycyclic hydrocarbon
Cyclic olefin
Unsaturated aliphatic hydrocarbon
Unsaturated hydrocarbon
Olefin
Hydrocarbon
Aliphatic homopolycyclic compound

Molecular Framework

Aliphatic homopolycyclic compounds

External Descriptors

Not Available

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

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

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

129634134

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

King AJ, Priesbe TJ: Concerns about methodology and use of 3,5,7-cholestatriene as a marker of oxidative stress Response to "Relationship between carotid atherosclerosis and erythrocyte membrane cholesterol oxidation products in type 2 diabetic patients". Diabetes Res Clin Pract. 2006 Jun;72(3):331-4. doi: 10.1016/j.diabres.2005.11.003. Epub 2005 Dec 27. [PubMed:16377021 ]
Miwa S, Watada H, Omura C, Takayanagi N, Nishiyama K, Tanaka Y, Onuma T, Kawamori R: Anti-oxidative effect of fluvastatin in hyperlipidemic type 2 diabetic patients. Endocr J. 2005 Apr;52(2):259-64. doi: 10.1507/endocrj.52.259. [PubMed:15863958 ]
Miwa S, Inouye M, Ohmura C, Mitsuhashi N, Onuma T, Kawamori R: Relationship between carotid atherosclerosis and erythrocyte membrane cholesterol oxidation products in type 2 diabetic patients. Diabetes Res Clin Pract. 2003 Aug;61(2):81-8. doi: 10.1016/s0168-8227(03)00108-6. [PubMed:12951275 ]
LOTUS database [Link]

Showing NP-Card for (1r,3as,3br,9as,9bs,11as)-9a,11a-dimethyl-1-(6-methylhepta-2,4,6-trien-2-yl)-tetradecahydro-1h-cyclopenta[a]phenanthrene (NP0237693)

MOL for NP0237693 ((1r,3as,3br,9as,9bs,11as)-9a,11a-dimethyl-1-(6-methylhepta-2,4,6-trien-2-yl)-tetradecahydro-1h-cyclopenta[a]phenanthrene)

3D MOL for NP0237693 ((1r,3as,3br,9as,9bs,11as)-9a,11a-dimethyl-1-(6-methylhepta-2,4,6-trien-2-yl)-tetradecahydro-1h-cyclopenta[a]phenanthrene)

3D SDF for NP0237693 ((1r,3as,3br,9as,9bs,11as)-9a,11a-dimethyl-1-(6-methylhepta-2,4,6-trien-2-yl)-tetradecahydro-1h-cyclopenta[a]phenanthrene)

3D-SDF for NP0237693 ((1r,3as,3br,9as,9bs,11as)-9a,11a-dimethyl-1-(6-methylhepta-2,4,6-trien-2-yl)-tetradecahydro-1h-cyclopenta[a]phenanthrene)

PDB for NP0237693 ((1r,3as,3br,9as,9bs,11as)-9a,11a-dimethyl-1-(6-methylhepta-2,4,6-trien-2-yl)-tetradecahydro-1h-cyclopenta[a]phenanthrene)

3D PDB for NP0237693 ((1r,3as,3br,9as,9bs,11as)-9a,11a-dimethyl-1-(6-methylhepta-2,4,6-trien-2-yl)-tetradecahydro-1h-cyclopenta[a]phenanthrene)

SMILES for NP0237693 ((1r,3as,3br,9as,9bs,11as)-9a,11a-dimethyl-1-(6-methylhepta-2,4,6-trien-2-yl)-tetradecahydro-1h-cyclopenta[a]phenanthrene)

INCHI for NP0237693 ((1r,3as,3br,9as,9bs,11as)-9a,11a-dimethyl-1-(6-methylhepta-2,4,6-trien-2-yl)-tetradecahydro-1h-cyclopenta[a]phenanthrene)

Structure for NP0237693 ((1r,3as,3br,9as,9bs,11as)-9a,11a-dimethyl-1-(6-methylhepta-2,4,6-trien-2-yl)-tetradecahydro-1h-cyclopenta[a]phenanthrene)

3D Structure for NP0237693 ((1r,3as,3br,9as,9bs,11as)-9a,11a-dimethyl-1-(6-methylhepta-2,4,6-trien-2-yl)-tetradecahydro-1h-cyclopenta[a]phenanthrene)