NP-MRD: Showing NP-Card for 1-(2r,3s)-3-[(1r,3as,3bs,4r,9ar,9bs,11ar)-4-hydroxy-9a,11a-dimethyl-7-oxo-1h,2h,3h,3ah,3bh,4h,5h,9bh,10h,11h-cyclopenta[a]phenanthren-1-yl]-1-[(2s)-2,3,3-trimethyloxiran-2-yl]butan-2-yl 3-methyl propanedioate (NP0276980)

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Record Information

Version

2.0

Created at

2022-09-09 01:22:43 UTC

Updated at

2022-09-09 01:22:44 UTC

NP-MRD ID

NP0276980

Secondary Accession Numbers

None

Natural Product Identification

Common Name

1-(2r,3s)-3-[(1r,3as,3bs,4r,9ar,9bs,11ar)-4-hydroxy-9a,11a-dimethyl-7-oxo-1h,2h,3h,3ah,3bh,4h,5h,9bh,10h,11h-cyclopenta[a]phenanthren-1-yl]-1-[(2s)-2,3,3-trimethyloxiran-2-yl]butan-2-yl 3-methyl propanedioate

Description

1-(2R,3S)-3-[(1S,2R,9R,10S,11S,14R,15R)-9-hydroxy-2,15-dimethyl-5-oxotetracyclo[8.7.0.0²,⁷.0¹¹,¹⁵]Heptadeca-3,6-dien-14-yl]-1-[(2S)-2,3,3-trimethyloxiran-2-yl]butan-2-yl 3-methyl propanedioate belongs to the class of organic compounds known as monohydroxy bile acids, alcohols and derivatives. These are bile acids, alcohols or any of their derivatives bearing a hydroxyl group. Based on a literature review very few articles have been published on 1-(2R,3S)-3-[(1S,2R,9R,10S,11S,14R,15R)-9-hydroxy-2,15-dimethyl-5-oxotetracyclo[8.7.0.0²,⁷.0¹¹,¹⁵]Heptadeca-3,6-dien-14-yl]-1-[(2S)-2,3,3-trimethyloxiran-2-yl]butan-2-yl 3-methyl propanedioate.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652309092203222D          

 39 43  0  0  1  0            999 V2000
   -2.8518   -0.6141    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8518   -1.4391    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1373   -1.8516    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1373   -2.6766    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4228   -1.4391    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7084   -1.8516    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7084   -2.6766    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.0061   -1.4391    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.7206   -1.8516    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
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    1.4351   -3.0891    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.1529   -3.8644    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9654   -2.4571    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.2475   -3.2324    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0694   -3.3043    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
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  1  2  1  0  0  0  0
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 23 38  1  0  0  0  0
 38 39  1  1  0  0  0
M  END

     RDKit          3D

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M  END


  Mrv1652309092203222D          

 39 43  0  0  1  0            999 V2000
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    3.0694   -3.3043    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4611   -4.0293    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4351   -1.4391    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.1495   -1.8516    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4351   -0.6141    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.1025   -0.1292    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8476    0.6554    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0226    0.6554    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.4705    1.2685    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.3364    1.0970    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.5914    0.3124    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0394   -0.3007    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7676   -0.1292    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.5961   -0.9362    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8885    1.7101    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -1.1434    0.9255    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6955    1.5386    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2475    2.1517    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9925    2.9363    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5446    3.5494    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1856    3.1078    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6335    2.4947    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1734    2.6662    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7255    2.0531    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.5324    2.2247    0.0000 O   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
  3  4  2  0  0  0  0
  3  5  1  0  0  0  0
  5  6  1  0  0  0  0
  6  7  2  0  0  0  0
  6  8  1  0  0  0  0
  9  8  1  1  0  0  0
  9 10  1  0  0  0  0
 11 10  1  6  0  0  0
 11 12  1  1  0  0  0
 11 13  1  0  0  0  0
 13 14  1  0  0  0  0
 11 14  1  0  0  0  0
 14 15  1  0  0  0  0
 14 16  1  0  0  0  0
  9 17  1  0  0  0  0
 17 18  1  6  0  0  0
 19 17  1  6  0  0  0
 19 20  1  0  0  0  0
 20 21  1  0  0  0  0
 22 21  1  6  0  0  0
 23 22  1  1  0  0  0
 23 24  1  0  0  0  0
 24 25  1  6  0  0  0
 25 26  1  0  0  0  0
 26 27  1  0  0  0  0
 22 27  1  0  0  0  0
 19 27  1  0  0  0  0
 27 28  1  6  0  0  0
 24 29  1  0  0  0  0
 29 30  1  6  0  0  0
 29 31  1  0  0  0  0
 31 32  2  0  0  0  0
 32 33  1  0  0  0  0
 33 34  2  0  0  0  0
 33 35  1  0  0  0  0
 35 36  2  0  0  0  0
 29 36  1  0  0  0  0
 36 37  1  0  0  0  0
 37 38  1  0  0  0  0
 23 38  1  0  0  0  0
 38 39  1  1  0  0  0
M  END
> <DATABASE_ID>
NP0276980

> <DATABASE_NAME>
NP-MRD

> <SMILES>
COC(=O)CC(=O)O[C@H](C[C@]1(C)OC1(C)C)[C@@H](C)[C@H]1CC[C@H]2[C@@H]3[C@H](O)CC4=CC(=O)C=C[C@]4(C)[C@H]3CC[C@]12C

> <INCHI_IDENTIFIER>
InChI=1S/C32H46O7/c1-18(25(17-32(6)29(2,3)39-32)38-27(36)16-26(35)37-7)21-8-9-22-28-23(11-13-31(21,22)5)30(4)12-10-20(33)14-19(30)15-24(28)34/h10,12,14,18,21-25,28,34H,8-9,11,13,15-17H2,1-7H3/t18-,21+,22-,23-,24+,25+,28-,30-,31+,32-/m0/s1

> <INCHI_KEY>
HUNXSTIOGHPLRQ-GBQIVOSFSA-N

> <FORMULA>
C32H46O7

> <MOLECULAR_WEIGHT>
542.713

> <EXACT_MASS>
542.324353821

> <JCHEM_ACCEPTOR_COUNT>
5

> <JCHEM_ATOM_COUNT>
85

> <JCHEM_AVERAGE_POLARIZABILITY>
60.95775209043467

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
1

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
1-(2R,3S)-3-[(1S,2R,9R,10S,11S,14R,15R)-9-hydroxy-2,15-dimethyl-5-oxotetracyclo[8.7.0.0^{2,7}.0^{11,15}]heptadeca-3,6-dien-14-yl]-1-[(2S)-2,3,3-trimethyloxiran-2-yl]butan-2-yl 3-methyl propanedioate

> <JCHEM_LOGP>
4.363144729333332

> <JCHEM_MDDR_LIKE_RULE>
1

> <JCHEM_NUMBER_OF_RINGS>
5

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
16.874430422061707

> <JCHEM_PKA_STRONGEST_ACIDIC>
12.359403987967845

> <JCHEM_PKA_STRONGEST_BASIC>
-0.6106429756035282

> <JCHEM_POLAR_SURFACE_AREA>
102.43000000000002

> <JCHEM_REFRACTIVITY>
148.3902

> <JCHEM_ROTATABLE_BOND_COUNT>
9

> <JCHEM_RULE_OF_FIVE>
0

> <JCHEM_TRADITIONAL_IUPAC>
1-(2R,3S)-3-[(1S,2R,9R,10S,11S,14R,15R)-9-hydroxy-2,15-dimethyl-5-oxotetracyclo[8.7.0.0^{2,7}.0^{11,15}]heptadeca-3,6-dien-14-yl]-1-[(2S)-2,3,3-trimethyloxiran-2-yl]butan-2-yl 3-methyl propanedioate

> <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      -5.323  -1.146   0.000  0.00  0.00           C+0
HETATM    2  O   UNK     0      -5.323  -2.686   0.000  0.00  0.00           O+0
HETATM    3  C   UNK     0      -3.990  -3.456   0.000  0.00  0.00           C+0
HETATM    4  O   UNK     0      -3.990  -4.996   0.000  0.00  0.00           O+0
HETATM    5  C   UNK     0      -2.656  -2.686   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0      -1.322  -3.456   0.000  0.00  0.00           C+0
HETATM    7  O   UNK     0      -1.322  -4.996   0.000  0.00  0.00           O+0
HETATM    8  O   UNK     0       0.011  -2.686   0.000  0.00  0.00           O+0
HETATM    9  C   UNK     0       1.345  -3.456   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       1.345  -4.996   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       2.679  -5.766   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       2.152  -7.213   0.000  0.00  0.00           C+0
HETATM   13  O   UNK     0       3.669  -4.587   0.000  0.00  0.00           O+0
HETATM   14  C   UNK     0       4.195  -6.034   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       5.730  -6.168   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       4.594  -7.521   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       2.679  -2.686   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       4.012  -3.456   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0       2.679  -1.146   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0       3.925  -0.241   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0       3.449   1.223   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0       1.909   1.223   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0       0.878   2.368   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0      -0.628   2.048   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0      -1.104   0.583   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0      -0.073  -0.561   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0       1.433  -0.241   0.000  0.00  0.00           C+0
HETATM   28  C   UNK     0       1.113  -1.748   0.000  0.00  0.00           C+0
HETATM   29  C   UNK     0      -1.658   3.192   0.000  0.00  0.00           C+0
HETATM   30  C   UNK     0      -2.134   1.728   0.000  0.00  0.00           C+0
HETATM   31  C   UNK     0      -3.165   2.872   0.000  0.00  0.00           C+0
HETATM   32  C   UNK     0      -4.195   4.016   0.000  0.00  0.00           C+0
HETATM   33  C   UNK     0      -3.719   5.481   0.000  0.00  0.00           C+0
HETATM   34  O   UNK     0      -4.750   6.625   0.000  0.00  0.00           O+0
HETATM   35  C   UNK     0      -2.213   5.801   0.000  0.00  0.00           C+0
HETATM   36  C   UNK     0      -1.183   4.657   0.000  0.00  0.00           C+0
HETATM   37  C   UNK     0       0.324   4.977   0.000  0.00  0.00           C+0
HETATM   38  C   UNK     0       1.354   3.833   0.000  0.00  0.00           C+0
HETATM   39  O   UNK     0       2.861   4.153   0.000  0.00  0.00           O+0
CONECT    1    2                                                            
CONECT    2    1    3                                                       
CONECT    3    2    4    5                                                  
CONECT    4    3                                                            
CONECT    5    3    6                                                       
CONECT    6    5    7    8                                                  
CONECT    7    6                                                            
CONECT    8    6    9                                                       
CONECT    9    8   10   17                                                  
CONECT   10    9   11                                                       
CONECT   11   10   12   13   14                                             
CONECT   12   11                                                            
CONECT   13   11   14                                                       
CONECT   14   13   11   15   16                                             
CONECT   15   14                                                            
CONECT   16   14                                                            
CONECT   17    9   18   19                                                  
CONECT   18   17                                                            
CONECT   19   17   20   27                                                  
CONECT   20   19   21                                                       
CONECT   21   20   22                                                       
CONECT   22   21   23   27                                                  
CONECT   23   22   24   38                                                  
CONECT   24   23   25   29                                                  
CONECT   25   24   26                                                       
CONECT   26   25   27                                                       
CONECT   27   26   22   19   28                                             
CONECT   28   27                                                            
CONECT   29   24   30   31   36                                             
CONECT   30   29                                                            
CONECT   31   29   32                                                       
CONECT   32   31   33                                                       
CONECT   33   32   34   35                                                  
CONECT   34   33                                                            
CONECT   35   33   36                                                       
CONECT   36   35   29   37                                                  
CONECT   37   36   38                                                       
CONECT   38   37   23   39                                                  
CONECT   39   38                                                            
MASTER        0    0    0    0    0    0    0    0   39    0   86    0
END

View in JSmol

Synonyms

Value	Source
1-(2R,3S)-3-[(1S,2R,9R,10S,11S,14R,15R)-9-Hydroxy-2,15-dimethyl-5-oxotetracyclo[8.7.0.0,.0,]heptadeca-3,6-dien-14-yl]-1-[(2S)-2,3,3-trimethyloxiran-2-yl]butan-2-yl 3-methyl propanedioic acid	Generator

Chemical Formula

C₃₂H₄₆O₇

Average Mass

542.7130 Da

Monoisotopic Mass

542.32435 Da

IUPAC Name

1-(2R,3S)-3-[(1S,2R,9R,10S,11S,14R,15R)-9-hydroxy-2,15-dimethyl-5-oxotetracyclo[8.7.0.0^{2,7}.0^{11,15}]heptadeca-3,6-dien-14-yl]-1-[(2S)-2,3,3-trimethyloxiran-2-yl]butan-2-yl 3-methyl propanedioate

Traditional Name

1-(2R,3S)-3-[(1S,2R,9R,10S,11S,14R,15R)-9-hydroxy-2,15-dimethyl-5-oxotetracyclo[8.7.0.0^{2,7}.0^{11,15}]heptadeca-3,6-dien-14-yl]-1-[(2S)-2,3,3-trimethyloxiran-2-yl]butan-2-yl 3-methyl propanedioate

CAS Registry Number

Not Available

SMILES

COC(=O)CC(=O)O[C@H](C[C@]1(C)OC1(C)C)[C@@H](C)[C@H]1CC[C@H]2[C@@H]3[C@H](O)CC4=CC(=O)C=C[C@]4(C)[C@H]3CC[C@]12C

InChI Identifier

InChI=1S/C32H46O7/c1-18(25(17-32(6)29(2,3)39-32)38-27(36)16-26(35)37-7)21-8-9-22-28-23(11-13-31(21,22)5)30(4)12-10-20(33)14-19(30)15-24(28)34/h10,12,14,18,21-25,28,34H,8-9,11,13,15-17H2,1-7H3/t18-,21+,22-,23-,24+,25+,28-,30-,31+,32-/m0/s1

InChI Key

HUNXSTIOGHPLRQ-GBQIVOSFSA-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 monohydroxy bile acids, alcohols and derivatives. These are bile acids, alcohols or any of their derivatives bearing a hydroxyl group.

Kingdom

Organic compounds

Super Class

Lipids and lipid-like molecules

Class

Steroids and steroid derivatives

Sub Class

Bile acids, alcohols and derivatives

Direct Parent

Monohydroxy bile acids, alcohols and derivatives

Alternative Parents

Substituents

Cholesterol-skeleton
Cholestane-skeleton
Monohydroxy bile acid, alcohol, or derivatives
Steroid ester
3-oxo-delta-1,4-steroid
3-oxosteroid
Hydroxysteroid
Oxosteroid
7-hydroxysteroid
Delta-1,4-steroid
Dicarboxylic acid or derivatives
1,3-dicarbonyl compound
Methyl ester
Cyclic alcohol
Secondary alcohol
Cyclic ketone
Ketone
Carboxylic acid ester
Carboxylic acid derivative
Organoheterocyclic compound
Ether
Oxacycle
Dialkyl ether
Oxirane
Organooxygen compound
Hydrocarbon derivative
Alcohol
Carbonyl group
Organic oxygen compound
Organic oxide
Aliphatic heteropolycyclic compound

Molecular Framework

Aliphatic heteropolycyclic 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	4.36	ChemAxon
pKa (Strongest Acidic)	12.36	ChemAxon
pKa (Strongest Basic)	-0.61	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	5	ChemAxon
Hydrogen Donor Count	1	ChemAxon
Polar Surface Area	102.43 Å²	ChemAxon
Rotatable Bond Count	9	ChemAxon
Refractivity	148.39 m³·mol⁻¹	ChemAxon
Polarizability	60.96 Å³	ChemAxon
Number of Rings	5	ChemAxon
Bioavailability	Yes	ChemAxon
Rule of Five	No	ChemAxon
Ghose Filter	No	ChemAxon
Veber's Rule	No	ChemAxon
MDDR-like Rule	Yes	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

162927470

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for 1-(2r,3s)-3-[(1r,3as,3bs,4r,9ar,9bs,11ar)-4-hydroxy-9a,11a-dimethyl-7-oxo-1h,2h,3h,3ah,3bh,4h,5h,9bh,10h,11h-cyclopenta[a]phenanthren-1-yl]-1-[(2s)-2,3,3-trimethyloxiran-2-yl]butan-2-yl 3-methyl propanedioate (NP0276980)

MOL for NP0276980 (1-(2r,3s)-3-[(1r,3as,3bs,4r,9ar,9bs,11ar)-4-hydroxy-9a,11a-dimethyl-7-oxo-1h,2h,3h,3ah,3bh,4h,5h,9bh,10h,11h-cyclopenta[a]phenanthren-1-yl]-1-[(2s)-2,3,3-trimethyloxiran-2-yl]butan-2-yl 3-methyl propanedioate)

3D MOL for NP0276980 (1-(2r,3s)-3-[(1r,3as,3bs,4r,9ar,9bs,11ar)-4-hydroxy-9a,11a-dimethyl-7-oxo-1h,2h,3h,3ah,3bh,4h,5h,9bh,10h,11h-cyclopenta[a]phenanthren-1-yl]-1-[(2s)-2,3,3-trimethyloxiran-2-yl]butan-2-yl 3-methyl propanedioate)

3D SDF for NP0276980 (1-(2r,3s)-3-[(1r,3as,3bs,4r,9ar,9bs,11ar)-4-hydroxy-9a,11a-dimethyl-7-oxo-1h,2h,3h,3ah,3bh,4h,5h,9bh,10h,11h-cyclopenta[a]phenanthren-1-yl]-1-[(2s)-2,3,3-trimethyloxiran-2-yl]butan-2-yl 3-methyl propanedioate)

3D-SDF for NP0276980 (1-(2r,3s)-3-[(1r,3as,3bs,4r,9ar,9bs,11ar)-4-hydroxy-9a,11a-dimethyl-7-oxo-1h,2h,3h,3ah,3bh,4h,5h,9bh,10h,11h-cyclopenta[a]phenanthren-1-yl]-1-[(2s)-2,3,3-trimethyloxiran-2-yl]butan-2-yl 3-methyl propanedioate)

PDB for NP0276980 (1-(2r,3s)-3-[(1r,3as,3bs,4r,9ar,9bs,11ar)-4-hydroxy-9a,11a-dimethyl-7-oxo-1h,2h,3h,3ah,3bh,4h,5h,9bh,10h,11h-cyclopenta[a]phenanthren-1-yl]-1-[(2s)-2,3,3-trimethyloxiran-2-yl]butan-2-yl 3-methyl propanedioate)

3D PDB for NP0276980 (1-(2r,3s)-3-[(1r,3as,3bs,4r,9ar,9bs,11ar)-4-hydroxy-9a,11a-dimethyl-7-oxo-1h,2h,3h,3ah,3bh,4h,5h,9bh,10h,11h-cyclopenta[a]phenanthren-1-yl]-1-[(2s)-2,3,3-trimethyloxiran-2-yl]butan-2-yl 3-methyl propanedioate)

SMILES for NP0276980 (1-(2r,3s)-3-[(1r,3as,3bs,4r,9ar,9bs,11ar)-4-hydroxy-9a,11a-dimethyl-7-oxo-1h,2h,3h,3ah,3bh,4h,5h,9bh,10h,11h-cyclopenta[a]phenanthren-1-yl]-1-[(2s)-2,3,3-trimethyloxiran-2-yl]butan-2-yl 3-methyl propanedioate)

INCHI for NP0276980 (1-(2r,3s)-3-[(1r,3as,3bs,4r,9ar,9bs,11ar)-4-hydroxy-9a,11a-dimethyl-7-oxo-1h,2h,3h,3ah,3bh,4h,5h,9bh,10h,11h-cyclopenta[a]phenanthren-1-yl]-1-[(2s)-2,3,3-trimethyloxiran-2-yl]butan-2-yl 3-methyl propanedioate)

Structure for NP0276980 (1-(2r,3s)-3-[(1r,3as,3bs,4r,9ar,9bs,11ar)-4-hydroxy-9a,11a-dimethyl-7-oxo-1h,2h,3h,3ah,3bh,4h,5h,9bh,10h,11h-cyclopenta[a]phenanthren-1-yl]-1-[(2s)-2,3,3-trimethyloxiran-2-yl]butan-2-yl 3-methyl propanedioate)

3D Structure for NP0276980 (1-(2r,3s)-3-[(1r,3as,3bs,4r,9ar,9bs,11ar)-4-hydroxy-9a,11a-dimethyl-7-oxo-1h,2h,3h,3ah,3bh,4h,5h,9bh,10h,11h-cyclopenta[a]phenanthren-1-yl]-1-[(2s)-2,3,3-trimethyloxiran-2-yl]butan-2-yl 3-methyl propanedioate)