NP-MRD: Showing NP-Card for (3as,3bs,9ar,9bs,10r,11as)-10-hydroxy-9a,11a-dimethyl-2h,3h,3ah,3bh,4h,5h,9bh,10h,11h-cyclopenta[a]phenanthrene-1,7-dione (NP0286534)

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Record Information

Version

2.0

Created at

2022-09-09 15:09:17 UTC

Updated at

2022-09-09 15:09:17 UTC

NP-MRD ID

NP0286534

Secondary Accession Numbers

None

Natural Product Identification

Common Name

(3as,3bs,9ar,9bs,10r,11as)-10-hydroxy-9a,11a-dimethyl-2h,3h,3ah,3bh,4h,5h,9bh,10h,11h-cyclopenta[a]phenanthrene-1,7-dione

Description

11Alpha-Hydroxyandrosta-1,4-diene-3,17-dione, also known as 11-HADD, 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. (3as,3bs,9ar,9bs,10r,11as)-10-hydroxy-9a,11a-dimethyl-2h,3h,3ah,3bh,4h,5h,9bh,10h,11h-cyclopenta[a]phenanthrene-1,7-dione is found in Holarrhena pubescens. (3as,3bs,9ar,9bs,10r,11as)-10-hydroxy-9a,11a-dimethyl-2h,3h,3ah,3bh,4h,5h,9bh,10h,11h-cyclopenta[a]phenanthrene-1,7-dione was first documented in 2002 (PMID: 12462341). Based on a literature review very few articles have been published on 11alpha-Hydroxyandrosta-1,4-diene-3,17-dione.

Structure

MOL 3D MOL SDF PDB SMILES InChI

     RDKit          3D

 46 49  0  0  0  0  0  0  0  0999 V2000
   -2.5853    0.3643   -1.3175 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3243    0.6522    0.1325 C   0  0  2  0  0  0  0  0  0  0  0  0
   -1.5496    1.8743    0.3965 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1543    1.7619   -0.1362 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.5211    2.8969    0.3737 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.5444    0.5258    0.2642 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.3351   -0.7107   -0.0100 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.3021   -1.9818    0.4675 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5512   -2.2281   -0.3717 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4157   -1.0239   -0.0642 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5767   -1.2534    0.4670 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.4908   -0.1700    0.8082 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.6015   -0.4176    1.3168 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.0095    1.1674    0.5140 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8232    1.3789   -0.0261 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9091    0.3153   -0.3679 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.7830    0.3558   -1.9014 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5667   -0.4979    0.8026 C   0  0  2  0  0  0  0  0  0  0  0  0
   -2.5685   -1.6060    0.7377 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8985   -0.8995    0.9081 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6101    0.5517    0.8560 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2667    1.4515    1.2989 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9380    0.9157   -2.0122 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5188   -0.7020   -1.5745 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6342    0.6745   -1.5501 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0316    2.7429   -0.0970 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5420    2.0511    1.5017 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2041    1.9386   -1.2290 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.1878    3.7236   -0.0876 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.6899    0.5307    1.3600 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5345   -0.7536   -1.1033 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.6070   -1.8438    1.5364 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4315   -2.7834    0.3941 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.2475   -2.1813   -1.4349 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.1035   -3.1150   -0.0808 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.9149   -2.2857    0.6806 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.6612    2.0141    0.7529 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.5910    2.4512   -0.2155 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.7649    0.1156   -2.3584 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.0575   -0.3483   -2.2935 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.5234    1.3806   -2.2450 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3050   -0.1984    1.8143 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4267   -2.2428    1.6387 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5127   -2.2014   -0.1830 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5221   -1.1886    0.0204 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4164   -1.2012    1.8389 H   0  0  0  0  0  0  0  0  0  0  0  0
  2  1  1  6
  2  3  1  0
  3  4  1  0
  4  5  1  0
  4  6  1  0
  6  7  1  0
  7  8  1  0
  8  9  1  0
  9 10  1  0
 10 11  2  0
 11 12  1  0
 12 13  2  0
 12 14  1  0
 14 15  2  0
 15 16  1  0
 16 17  1  6
  7 18  1  0
 18 19  1  0
 19 20  1  0
 20 21  1  0
 21 22  2  0
 18  2  1  0
 21  2  1  0
 16  6  1  0
 16 10  1  0
  1 23  1  0
  1 24  1  0
  1 25  1  0
  3 26  1  0
  3 27  1  0
  4 28  1  6
  5 29  1  0
  6 30  1  1
  7 31  1  6
  8 32  1  0
  8 33  1  0
  9 34  1  0
  9 35  1  0
 11 36  1  0
 14 37  1  0
 15 38  1  0
 17 39  1  0
 17 40  1  0
 17 41  1  0
 18 42  1  1
 19 43  1  0
 19 44  1  0
 20 45  1  0
 20 46  1  0
M  END


  Mrv1652309092217092D          

 22 25  0  0  1  0            999 V2000
    3.5330   -3.2587    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
    4.4247   -3.1470    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.2368   -3.0018    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    5.7686   -3.6325    0.0000 O   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
    4.9853   -1.5952    0.0000 C   0  0  1  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
    8.7655   -1.6450    0.0000 O   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  2  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
    4.1731   -1.7404    0.0000 C   0  0  2  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
    2.8390   -1.6970    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0683   -2.4895    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5619   -3.1408    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  2  1  1  1  0  0  0
  2  3  1  0  0  0  0
  3  4  1  0  0  0  0
  4  5  1  6  0  0  0
  6  4  1  1  0  0  0
  6  7  1  0  0  0  0
  7  8  1  6  0  0  0
  8  9  1  0  0  0  0
  9 10  1  0  0  0  0
 10 11  2  0  0  0  0
 11 12  1  0  0  0  0
 12 13  2  0  0  0  0
 12 14  1  0  0  0  0
 14 15  2  0  0  0  0
 15 16  1  0  0  0  0
 10 16  1  0  0  0  0
  6 16  1  0  0  0  0
 16 17  1  1  0  0  0
  7 18  1  0  0  0  0
  2 18  1  0  0  0  0
 18 19  1  1  0  0  0
 19 20  1  0  0  0  0
 20 21  1  0  0  0  0
  2 21  1  0  0  0  0
 21 22  2  0  0  0  0
M  END
> <DATABASE_ID>
NP0286534

> <DATABASE_NAME>
NP-MRD

> <SMILES>
C[C@]12C[C@@H](O)[C@H]3[C@@H](CCC4=CC(=O)C=C[C@]34C)[C@@H]1CCC2=O

> <INCHI_IDENTIFIER>
InChI=1S/C19H24O3/c1-18-8-7-12(20)9-11(18)3-4-13-14-5-6-16(22)19(14,2)10-15(21)17(13)18/h7-9,13-15,17,21H,3-6,10H2,1-2H3/t13-,14-,15+,17+,18-,19-/m0/s1

> <INCHI_KEY>
ZHOLUHXKCIXGSR-GBHAUCNQSA-N

> <FORMULA>
C19H24O3

> <MOLECULAR_WEIGHT>
300.398

> <EXACT_MASS>
300.172544633

> <JCHEM_ACCEPTOR_COUNT>
3

> <JCHEM_ATOM_COUNT>
46

> <JCHEM_AVERAGE_POLARIZABILITY>
33.30106856457441

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
1

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
(1S,2R,10S,11S,15S,17R)-17-hydroxy-2,15-dimethyltetracyclo[8.7.0.0^{2,7}.0^{11,15}]heptadeca-3,6-diene-5,14-dione

> <JCHEM_LOGP>
2.6180096959999997

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
4

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
18.757563142612508

> <JCHEM_PKA_STRONGEST_ACIDIC>
14.868894545793875

> <JCHEM_PKA_STRONGEST_BASIC>
-2.8561165800519133

> <JCHEM_POLAR_SURFACE_AREA>
54.37

> <JCHEM_REFRACTIVITY>
86.29329999999999

> <JCHEM_ROTATABLE_BOND_COUNT>
0

> <JCHEM_RULE_OF_FIVE>
1

> <JCHEM_TRADITIONAL_IUPAC>
(1S,2R,10S,11S,15S,17R)-17-hydroxy-2,15-dimethyltetracyclo[8.7.0.0^{2,7}.0^{11,15}]heptadeca-3,6-diene-5,14-dione

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 09-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   09-SEP-22         0                                  
HETATM    1  C   UNK     0       6.595  -6.083   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       7.267  -4.697   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       8.259  -5.874   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       9.775  -5.603   0.000  0.00  0.00           C+0
HETATM    5  O   UNK     0      10.768  -6.781   0.000  0.00  0.00           O+0
HETATM    6  C   UNK     0      10.299  -4.155   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       9.306  -2.978   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       9.829  -1.529   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0      11.345  -1.258   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0      12.338  -2.436   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0      13.854  -2.164   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0      14.846  -3.342   0.000  0.00  0.00           C+0
HETATM   13  O   UNK     0      16.362  -3.071   0.000  0.00  0.00           O+0
HETATM   14  C   UNK     0      14.323  -4.790   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0      12.807  -5.061   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0      11.814  -3.884   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0      11.291  -5.332   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       7.790  -3.249   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0       6.574  -2.304   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0       5.299  -3.168   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0       5.727  -4.647   0.000  0.00  0.00           C+0
HETATM   22  O   UNK     0       4.782  -5.863   0.000  0.00  0.00           O+0
CONECT    1    2                                                            
CONECT    2    1    3   18   21                                             
CONECT    3    2    4                                                       
CONECT    4    3    5    6                                                  
CONECT    5    4                                                            
CONECT    6    4    7   16                                                  
CONECT    7    6    8   18                                                  
CONECT    8    7    9                                                       
CONECT    9    8   10                                                       
CONECT   10    9   11   16                                                  
CONECT   11   10   12                                                       
CONECT   12   11   13   14                                                  
CONECT   13   12                                                            
CONECT   14   12   15                                                       
CONECT   15   14   16                                                       
CONECT   16   15   10    6   17                                             
CONECT   17   16                                                            
CONECT   18    7    2   19                                                  
CONECT   19   18   20                                                       
CONECT   20   19   21                                                       
CONECT   21   20    2   22                                                  
CONECT   22   21                                                            
MASTER        0    0    0    0    0    0    0    0   22    0   50    0
END

View in JSmol

Synonyms

Value	Source
11a-Hydroxyandrosta-1,4-diene-3,17-dione	Generator
11Α-hydroxyandrosta-1,4-diene-3,17-dione	Generator
11-HADD	MeSH
11-Hydroxy-1,4-androstadiene-3,17-dione	MeSH
11-Hydroxy-1,4-androstadiene-3,17-dione, (11-beta)-isomer	MeSH

Chemical Formula

C₁₉H₂₄O₃

Average Mass

300.3980 Da

Monoisotopic Mass

300.17254 Da

IUPAC Name

(1S,2R,10S,11S,15S,17R)-17-hydroxy-2,15-dimethyltetracyclo[8.7.0.0^{2,7}.0^{11,15}]heptadeca-3,6-diene-5,14-dione

Traditional Name

(1S,2R,10S,11S,15S,17R)-17-hydroxy-2,15-dimethyltetracyclo[8.7.0.0^{2,7}.0^{11,15}]heptadeca-3,6-diene-5,14-dione

CAS Registry Number

Not Available

SMILES

C[C@]12C[C@@H](O)[C@H]3[C@@H](CCC4=CC(=O)C=C[C@]34C)[C@@H]1CCC2=O

InChI Identifier

InChI=1S/C19H24O3/c1-18-8-7-12(20)9-11(18)3-4-13-14-5-6-16(22)19(14,2)10-15(21)17(13)18/h7-9,13-15,17,21H,3-6,10H2,1-2H3/t13-,14-,15+,17+,18-,19-/m0/s1

InChI Key

ZHOLUHXKCIXGSR-GBHAUCNQSA-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
Holarrhena pubescens	LOTUS Database	35616633

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
3-oxo-delta-1,4-steroid
3-oxosteroid
11-hydroxysteroid
11-alpha-hydroxysteroid
Oxosteroid
17-oxosteroid
Hydroxysteroid
Delta-1,4-steroid
Cyclic alcohol
Cyclic ketone
Secondary alcohol
Ketone
Organic oxygen compound
Organooxygen compound
Carbonyl group
Hydrocarbon derivative
Alcohol
Organic oxide
Aliphatic homopolycyclic compound

Molecular Framework

Aliphatic homopolycyclic compounds

External Descriptors

3-hydroxy steroid (CHEBI:34139 )

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	2.62	ChemAxon
pKa (Strongest Acidic)	14.87	ChemAxon
pKa (Strongest Basic)	-2.9	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	3	ChemAxon
Hydrogen Donor Count	1	ChemAxon
Polar Surface Area	54.37 Å²	ChemAxon
Rotatable Bond Count	0	ChemAxon
Refractivity	86.29 m³·mol⁻¹	ChemAxon
Polarizability	33.3 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

99896

KEGG Compound ID

C14587

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

111337

PDB ID

Not Available

ChEBI ID

34139

Good Scents ID

Not Available

References

General References

Choudhary MI, Musharraf SG, Shaheen F, Atta-Ur-Rahman: Microbial transformation of (+)-androsta-1 ,4-diene-3,17-dione by Cephalosporium aphidicola. Nat Prod Lett. 2002 Dec;16(6):377-82. doi: 10.1080/10575630290033132. [PubMed:12462341 ]
LOTUS database [Link]

Showing NP-Card for (3as,3bs,9ar,9bs,10r,11as)-10-hydroxy-9a,11a-dimethyl-2h,3h,3ah,3bh,4h,5h,9bh,10h,11h-cyclopenta[a]phenanthrene-1,7-dione (NP0286534)

MOL for NP0286534 ((3as,3bs,9ar,9bs,10r,11as)-10-hydroxy-9a,11a-dimethyl-2h,3h,3ah,3bh,4h,5h,9bh,10h,11h-cyclopenta[a]phenanthrene-1,7-dione)

3D MOL for NP0286534 ((3as,3bs,9ar,9bs,10r,11as)-10-hydroxy-9a,11a-dimethyl-2h,3h,3ah,3bh,4h,5h,9bh,10h,11h-cyclopenta[a]phenanthrene-1,7-dione)

3D SDF for NP0286534 ((3as,3bs,9ar,9bs,10r,11as)-10-hydroxy-9a,11a-dimethyl-2h,3h,3ah,3bh,4h,5h,9bh,10h,11h-cyclopenta[a]phenanthrene-1,7-dione)

3D-SDF for NP0286534 ((3as,3bs,9ar,9bs,10r,11as)-10-hydroxy-9a,11a-dimethyl-2h,3h,3ah,3bh,4h,5h,9bh,10h,11h-cyclopenta[a]phenanthrene-1,7-dione)

PDB for NP0286534 ((3as,3bs,9ar,9bs,10r,11as)-10-hydroxy-9a,11a-dimethyl-2h,3h,3ah,3bh,4h,5h,9bh,10h,11h-cyclopenta[a]phenanthrene-1,7-dione)

3D PDB for NP0286534 ((3as,3bs,9ar,9bs,10r,11as)-10-hydroxy-9a,11a-dimethyl-2h,3h,3ah,3bh,4h,5h,9bh,10h,11h-cyclopenta[a]phenanthrene-1,7-dione)

SMILES for NP0286534 ((3as,3bs,9ar,9bs,10r,11as)-10-hydroxy-9a,11a-dimethyl-2h,3h,3ah,3bh,4h,5h,9bh,10h,11h-cyclopenta[a]phenanthrene-1,7-dione)

INCHI for NP0286534 ((3as,3bs,9ar,9bs,10r,11as)-10-hydroxy-9a,11a-dimethyl-2h,3h,3ah,3bh,4h,5h,9bh,10h,11h-cyclopenta[a]phenanthrene-1,7-dione)

Structure for NP0286534 ((3as,3bs,9ar,9bs,10r,11as)-10-hydroxy-9a,11a-dimethyl-2h,3h,3ah,3bh,4h,5h,9bh,10h,11h-cyclopenta[a]phenanthrene-1,7-dione)

3D Structure for NP0286534 ((3as,3bs,9ar,9bs,10r,11as)-10-hydroxy-9a,11a-dimethyl-2h,3h,3ah,3bh,4h,5h,9bh,10h,11h-cyclopenta[a]phenanthrene-1,7-dione)