NP-MRD: Showing NP-Card for (1s,3br,4r,9ar,11as)-4-hydroxy-1-(3-hydroxy-2-oxopropyl)-3b,6,6,9a,11a-pentamethyl-1h,2h,3ah,4h,5h,5ah,9bh,10h,11h-cyclopenta[a]phenanthrene-3,7-dione (NP0161383)

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Record Information

Version

2.0

Created at

2022-09-02 19:32:23 UTC

Updated at

2022-09-02 19:32:23 UTC

NP-MRD ID

NP0161383

Secondary Accession Numbers

None

Natural Product Identification

Common Name

(1s,3br,4r,9ar,11as)-4-hydroxy-1-(3-hydroxy-2-oxopropyl)-3b,6,6,9a,11a-pentamethyl-1h,2h,3ah,4h,5h,5ah,9bh,10h,11h-cyclopenta[a]phenanthrene-3,7-dione

Description

(2R,9R,10R,14S,15S)-9-hydroxy-14-(3-hydroxy-2-oxopropyl)-2,6,6,10,15-pentamethyltetracyclo[8.7.0.0²,⁷.0¹¹,¹⁵]Heptadec-3-ene-5,12-dione belongs to the class of organic compounds known as androgens and derivatives. These are 3-hydroxylated C19 steroid hormones. They are known to favor the development of masculine characteristics. They also show profound effects on scalp and body hair in humans. Based on a literature review very few articles have been published on (2R,9R,10R,14S,15S)-9-hydroxy-14-(3-hydroxy-2-oxopropyl)-2,6,6,10,15-pentamethyltetracyclo[8.7.0.0²,⁷.0¹¹,¹⁵]Heptadec-3-ene-5,12-dione.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652309022221322D          

 30 33  0  0  1  0            999 V2000
    1.8641    0.3651    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5776   -0.0491    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8616    0.7255    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0458   -0.6798    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2336   -0.5346    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.3261   -1.4557    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1382   -1.6009    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6700   -0.9702    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.9503   -1.7461    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3897   -0.1943    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9215    0.4364    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7336    0.2912    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    5.2655    0.9219    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.0139   -0.4847    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    5.5458    0.1460    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.8261   -0.6299    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.4774   -0.1236    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.4506    0.7010    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.1602   -0.5866    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.9309   -1.3791    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    7.4373   -2.0304    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.2545   -1.9175    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.5654   -1.1534    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    8.7609   -2.5689    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.5781   -2.4560    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.1064   -1.4059    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    6.4662   -2.1482    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.5745   -2.0366    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7624   -1.8914    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.4821   -1.1154    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  2  0  0  0  0
  4  6  1  0  0  0  0
  6  7  2  0  0  0  0
  7  8  1  0  0  0  0
  8  9  1  6  0  0  0
  8 10  1  0  0  0  0
  2 10  1  0  0  0  0
 10 11  1  0  0  0  0
 11 12  1  0  0  0  0
 12 13  1  1  0  0  0
 12 14  1  0  0  0  0
 14 15  1  6  0  0  0
 14 16  1  0  0  0  0
 16 17  1  0  0  0  0
 17 18  2  0  0  0  0
 17 19  1  0  0  0  0
 19 20  1  0  0  0  0
 20 21  1  1  0  0  0
 21 22  1  0  0  0  0
 22 23  2  0  0  0  0
 22 24  1  0  0  0  0
 24 25  1  0  0  0  0
 20 26  1  0  0  0  0
 16 26  1  0  0  0  0
 26 27  1  1  0  0  0
 26 28  1  0  0  0  0
 28 29  1  0  0  0  0
 29 30  1  0  0  0  0
  8 30  1  0  0  0  0
 14 30  1  0  0  0  0
M  END

     RDKit          3D

 66 69  0  0  0  0  0  0  0  0999 V2000
   -5.1466   -0.8293   -0.1304 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3217    0.2866    0.3532 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0197    1.5986   -0.0442 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2135    0.3873    1.8597 C   0  0  0  0  0  0  0  0  0  0  0  0
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   -1.7831    0.0240    1.8855 C   0  0  0  0  0  0  0  0  0  0  0  0
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   -0.7808   -0.9301   -0.2444 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.2429   -1.6069    0.5990 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6541   -1.4499    0.1596 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0708   -0.0091   -0.1075 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.3951    0.5877    1.2346 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1461   -0.0785   -1.1163 C   0  0  2  0  0  0  0  0  0  0  0  0
    4.5193   -0.4188   -0.7096 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.2651    0.4381    0.1792 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.9210    1.5527    0.4824 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.5626   -0.0277    0.8013 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.8059   -1.3229    0.3505 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.0608    1.2568   -1.8343 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6194    1.5764   -1.7637 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1108    2.3871   -2.5529 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.9525    0.8227   -0.6785 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.2149    0.0713   -1.2070 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.2294   -0.5881   -2.5224 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2607    1.0657   -1.6869 C   0  0  2  0  0  0  0  0  0  0  0  0
   -1.2619    2.1827   -0.8585 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6620    0.4223   -1.5770 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9208    0.3817   -0.1236 C   0  0  1  0  0  0  0  0  0  0  0  0
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   -5.9552   -0.4733   -0.8385 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5922   -1.5813   -0.7471 H   0  0  0  0  0  0  0  0  0  0  0  0
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   -4.3921    2.4668    0.1751 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8203    0.9212    3.4725 H   0  0  0  0  0  0  0  0  0  0  0  0
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   -3.5385   -1.8994    1.3915 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8674   -2.3990    1.5837 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5549   -2.5981   -0.0217 H   0  0  0  0  0  0  0  0  0  0  0  0
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    0.0661   -2.7381    0.5902 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.2086   -1.3854    1.6817 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.3015   -1.7892    1.0297 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.9833   -2.1469   -0.6475 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.4130    1.6745    1.2705 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.1989    0.0668    1.7889 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.4717    0.3154    1.8736 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.8369   -0.8621   -1.8708 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.5101   -1.4974   -0.3198 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.1629   -0.5634   -1.6474 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.3651    0.6747    0.5132 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.4584   -0.0758    1.9015 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.4416   -1.2889   -0.4307 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.7076    2.0265   -1.4244 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.3448    1.0677   -2.9091 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.5800    1.6072    0.0440 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.4997   -1.6416   -2.4039 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.9702    0.0415   -3.0468 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6386   -0.6267   -3.2550 H   0  0  0  0  0  0  0  0  0  0  0  0
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   -1.7316    2.9518   -1.2644 H   0  0  0  0  0  0  0  0  0  0  0  0
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 15 50  1  6
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 19 53  1  0
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M  END


  Mrv1652309022221322D          

 30 33  0  0  1  0            999 V2000
    1.8641    0.3651    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5776   -0.0491    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8616    0.7255    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0458   -0.6798    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2336   -0.5346    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.3261   -1.4557    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1382   -1.6009    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6700   -0.9702    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.9503   -1.7461    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
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    3.9215    0.4364    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7336    0.2912    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    5.2655    0.9219    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
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    6.9309   -1.3791    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    7.4373   -2.0304    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.2545   -1.9175    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.5654   -1.1534    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
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    9.5781   -2.4560    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.1064   -1.4059    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    6.4662   -2.1482    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
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    4.4821   -1.1154    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
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  4  5  2  0  0  0  0
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 14 30  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0161383

> <DATABASE_NAME>
NP-MRD

> <SMILES>
C[C@@]12CCC3[C@@]4(C)C=CC(=O)C(C)(C)C4C[C@@H](O)[C@@]3(C)C1C(=O)C[C@H]2CC(=O)CO

> <INCHI_IDENTIFIER>
InChI=1S/C25H36O5/c1-22(2)18-12-20(30)25(5)17(24(18,4)9-7-19(22)29)6-8-23(3)14(10-15(27)13-26)11-16(28)21(23)25/h7,9,14,17-18,20-21,26,30H,6,8,10-13H2,1-5H3/t14-,17?,18?,20-,21?,23+,24-,25+/m1/s1

> <INCHI_KEY>
HGMJKTQTXZQERC-CVLJXKBESA-N

> <FORMULA>
C25H36O5

> <MOLECULAR_WEIGHT>
416.558

> <EXACT_MASS>
416.256274259

> <JCHEM_ACCEPTOR_COUNT>
5

> <JCHEM_ATOM_COUNT>
66

> <JCHEM_AVERAGE_POLARIZABILITY>
46.135988330479

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
2

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
(2R,9R,10R,14S,15S)-9-hydroxy-14-(3-hydroxy-2-oxopropyl)-2,6,6,10,15-pentamethyltetracyclo[8.7.0.0^{2,7}.0^{11,15}]heptadec-3-ene-5,12-dione

> <ALOGPS_LOGP>
2.96

> <JCHEM_LOGP>
2.808601752333332

> <ALOGPS_LOGS>
-4.29

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
4

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
14.72950449253652

> <JCHEM_PKA_STRONGEST_ACIDIC>
13.808489368886782

> <JCHEM_PKA_STRONGEST_BASIC>
-2.945538851938072

> <JCHEM_POLAR_SURFACE_AREA>
91.67

> <JCHEM_REFRACTIVITY>
114.98259999999996

> <JCHEM_ROTATABLE_BOND_COUNT>
3

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
2.15e-02 g/l

> <JCHEM_TRADITIONAL_IUPAC>
(2R,9R,10R,14S,15S)-9-hydroxy-14-(3-hydroxy-2-oxopropyl)-2,6,6,10,15-pentamethyltetracyclo[8.7.0.0^{2,7}.0^{11,15}]heptadec-3-ene-5,12-dione

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 02-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   02-SEP-22         0                                  
HETATM    1  C   UNK     0       3.480   0.682   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       4.811  -0.092   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       5.342   1.354   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       3.819  -1.269   0.000  0.00  0.00           C+0
HETATM    5  O   UNK     0       2.303  -0.998   0.000  0.00  0.00           O+0
HETATM    6  C   UNK     0       4.342  -2.717   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       5.858  -2.988   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       6.851  -1.811   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       7.374  -3.259   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       6.327  -0.363   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       7.320   0.815   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       8.836   0.544   0.000  0.00  0.00           C+0
HETATM   13  O   UNK     0       9.829   1.721   0.000  0.00  0.00           O+0
HETATM   14  C   UNK     0       9.359  -0.905   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0      10.352   0.273   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0      10.875  -1.176   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0      12.091  -0.231   0.000  0.00  0.00           C+0
HETATM   18  O   UNK     0      12.041   1.308   0.000  0.00  0.00           O+0
HETATM   19  C   UNK     0      13.366  -1.095   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0      12.938  -2.574   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0      13.883  -3.790   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0      15.408  -3.579   0.000  0.00  0.00           C+0
HETATM   23  O   UNK     0      15.989  -2.153   0.000  0.00  0.00           O+0
HETATM   24  C   UNK     0      16.354  -4.795   0.000  0.00  0.00           C+0
HETATM   25  O   UNK     0      17.879  -4.585   0.000  0.00  0.00           O+0
HETATM   26  C   UNK     0      11.399  -2.624   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0      12.070  -4.010   0.000  0.00  0.00           C+0
HETATM   28  C   UNK     0      10.406  -3.802   0.000  0.00  0.00           C+0
HETATM   29  C   UNK     0       8.890  -3.531   0.000  0.00  0.00           C+0
HETATM   30  C   UNK     0       8.367  -2.082   0.000  0.00  0.00           C+0
CONECT    1    2                                                            
CONECT    2    1    3    4   10                                             
CONECT    3    2                                                            
CONECT    4    2    5    6                                                  
CONECT    5    4                                                            
CONECT    6    4    7                                                       
CONECT    7    6    8                                                       
CONECT    8    7    9   10   30                                             
CONECT    9    8                                                            
CONECT   10    8    2   11                                                  
CONECT   11   10   12                                                       
CONECT   12   11   13   14                                                  
CONECT   13   12                                                            
CONECT   14   12   15   16   30                                             
CONECT   15   14                                                            
CONECT   16   14   17   26                                                  
CONECT   17   16   18   19                                                  
CONECT   18   17                                                            
CONECT   19   17   20                                                       
CONECT   20   19   21   26                                                  
CONECT   21   20   22                                                       
CONECT   22   21   23   24                                                  
CONECT   23   22                                                            
CONECT   24   22   25                                                       
CONECT   25   24                                                            
CONECT   26   20   16   27   28                                             
CONECT   27   26                                                            
CONECT   28   26   29                                                       
CONECT   29   28   30                                                       
CONECT   30   29    8   14                                                  
MASTER        0    0    0    0    0    0    0    0   30    0   66    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₂₅H₃₆O₅

Average Mass

416.5580 Da

Monoisotopic Mass

416.25627 Da

IUPAC Name

(2R,9R,10R,14S,15S)-9-hydroxy-14-(3-hydroxy-2-oxopropyl)-2,6,6,10,15-pentamethyltetracyclo[8.7.0.0^{2,7}.0^{11,15}]heptadec-3-ene-5,12-dione

Traditional Name

(2R,9R,10R,14S,15S)-9-hydroxy-14-(3-hydroxy-2-oxopropyl)-2,6,6,10,15-pentamethyltetracyclo[8.7.0.0^{2,7}.0^{11,15}]heptadec-3-ene-5,12-dione

CAS Registry Number

Not Available

SMILES

C[C@@]12CCC3[C@@]4(C)C=CC(=O)C(C)(C)C4C[C@@H](O)[C@@]3(C)C1C(=O)C[C@H]2CC(=O)CO

InChI Identifier

InChI=1S/C25H36O5/c1-22(2)18-12-20(30)25(5)17(24(18,4)9-7-19(22)29)6-8-23(3)14(10-15(27)13-26)11-16(28)21(23)25/h7,9,14,17-18,20-21,26,30H,6,8,10-13H2,1-5H3/t14-,17?,18?,20-,21?,23+,24-,25+/m1/s1

InChI Key

HGMJKTQTXZQERC-CVLJXKBESA-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

Not Available

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as androgens and derivatives. These are 3-hydroxylated C19 steroid hormones. They are known to favor the development of masculine characteristics. They also show profound effects on scalp and body hair in humans.

Kingdom

Organic compounds

Super Class

Lipids and lipid-like molecules

Class

Steroids and steroid derivatives

Sub Class

Androstane steroids

Direct Parent

Androgens and derivatives

Alternative Parents

Substituents

Androgen-skeleton
7-hydroxysteroid
Oxosteroid
15-oxosteroid
Hydroxysteroid
3-oxosteroid
3-oxo-delta-1-steroid
Delta-1-steroid
Cyclohexenone
Cyclic alcohol
Alpha-hydroxy ketone
Cyclic ketone
Secondary alcohol
Ketone
Organic oxygen compound
Organic oxide
Hydrocarbon derivative
Primary alcohol
Organooxygen compound
Carbonyl group
Alcohol
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
logP	2.96	ALOGPS
logP	2.81	ChemAxon
logS	-4.3	ALOGPS
pKa (Strongest Acidic)	13.81	ChemAxon
pKa (Strongest Basic)	-2.9	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	5	ChemAxon
Hydrogen Donor Count	2	ChemAxon
Polar Surface Area	91.67 Å²	ChemAxon
Rotatable Bond Count	3	ChemAxon
Refractivity	114.98 m³·mol⁻¹	ChemAxon
Polarizability	46.14 Å³	ChemAxon
Number of Rings	4	ChemAxon
Bioavailability	Yes	ChemAxon
Rule of Five	Yes	ChemAxon
Ghose Filter	Yes	ChemAxon
Veber's Rule	No	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

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

163048652

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for (1s,3br,4r,9ar,11as)-4-hydroxy-1-(3-hydroxy-2-oxopropyl)-3b,6,6,9a,11a-pentamethyl-1h,2h,3ah,4h,5h,5ah,9bh,10h,11h-cyclopenta[a]phenanthrene-3,7-dione (NP0161383)

MOL for NP0161383 ((1s,3br,4r,9ar,11as)-4-hydroxy-1-(3-hydroxy-2-oxopropyl)-3b,6,6,9a,11a-pentamethyl-1h,2h,3ah,4h,5h,5ah,9bh,10h,11h-cyclopenta[a]phenanthrene-3,7-dione)

3D MOL for NP0161383 ((1s,3br,4r,9ar,11as)-4-hydroxy-1-(3-hydroxy-2-oxopropyl)-3b,6,6,9a,11a-pentamethyl-1h,2h,3ah,4h,5h,5ah,9bh,10h,11h-cyclopenta[a]phenanthrene-3,7-dione)

3D SDF for NP0161383 ((1s,3br,4r,9ar,11as)-4-hydroxy-1-(3-hydroxy-2-oxopropyl)-3b,6,6,9a,11a-pentamethyl-1h,2h,3ah,4h,5h,5ah,9bh,10h,11h-cyclopenta[a]phenanthrene-3,7-dione)

3D-SDF for NP0161383 ((1s,3br,4r,9ar,11as)-4-hydroxy-1-(3-hydroxy-2-oxopropyl)-3b,6,6,9a,11a-pentamethyl-1h,2h,3ah,4h,5h,5ah,9bh,10h,11h-cyclopenta[a]phenanthrene-3,7-dione)

PDB for NP0161383 ((1s,3br,4r,9ar,11as)-4-hydroxy-1-(3-hydroxy-2-oxopropyl)-3b,6,6,9a,11a-pentamethyl-1h,2h,3ah,4h,5h,5ah,9bh,10h,11h-cyclopenta[a]phenanthrene-3,7-dione)

3D PDB for NP0161383 ((1s,3br,4r,9ar,11as)-4-hydroxy-1-(3-hydroxy-2-oxopropyl)-3b,6,6,9a,11a-pentamethyl-1h,2h,3ah,4h,5h,5ah,9bh,10h,11h-cyclopenta[a]phenanthrene-3,7-dione)

SMILES for NP0161383 ((1s,3br,4r,9ar,11as)-4-hydroxy-1-(3-hydroxy-2-oxopropyl)-3b,6,6,9a,11a-pentamethyl-1h,2h,3ah,4h,5h,5ah,9bh,10h,11h-cyclopenta[a]phenanthrene-3,7-dione)

INCHI for NP0161383 ((1s,3br,4r,9ar,11as)-4-hydroxy-1-(3-hydroxy-2-oxopropyl)-3b,6,6,9a,11a-pentamethyl-1h,2h,3ah,4h,5h,5ah,9bh,10h,11h-cyclopenta[a]phenanthrene-3,7-dione)

Structure for NP0161383 ((1s,3br,4r,9ar,11as)-4-hydroxy-1-(3-hydroxy-2-oxopropyl)-3b,6,6,9a,11a-pentamethyl-1h,2h,3ah,4h,5h,5ah,9bh,10h,11h-cyclopenta[a]phenanthrene-3,7-dione)

3D Structure for NP0161383 ((1s,3br,4r,9ar,11as)-4-hydroxy-1-(3-hydroxy-2-oxopropyl)-3b,6,6,9a,11a-pentamethyl-1h,2h,3ah,4h,5h,5ah,9bh,10h,11h-cyclopenta[a]phenanthrene-3,7-dione)