NP-MRD: Showing NP-Card for 3b,11a-dimethyl-1-oxo-2h,3h,3ah,4h,5h,9bh,10h,11h-cyclopenta[a]phenanthren-7-yl acetate (NP0152128)

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Record Information

Version

2.0

Created at

2022-09-02 08:33:02 UTC

Updated at

2022-09-02 08:33:02 UTC

NP-MRD ID

NP0152128

Secondary Accession Numbers

None

Natural Product Identification

Common Name

3b,11a-dimethyl-1-oxo-2h,3h,3ah,4h,5h,9bh,10h,11h-cyclopenta[a]phenanthren-7-yl acetate

Description

10,15-Dimethyl-14-oxotetracyclo[8.7.0.0²,⁷.0¹¹,¹⁵]Heptadeca-2,4,6-trien-5-yl acetate belongs to the class of organic compounds known as steroid esters. Steroid esters are compounds containing a steroid moiety which bears a carboxylic acid ester group. 3b,11a-dimethyl-1-oxo-2h,3h,3ah,4h,5h,9bh,10h,11h-cyclopenta[a]phenanthren-7-yl acetate is found in Holarrhena pubescens. 10,15-Dimethyl-14-oxotetracyclo[8.7.0.0²,⁷.0¹¹,¹⁵]Heptadeca-2,4,6-trien-5-yl acetate is an extremely weak basic (essentially neutral) compound (based on its pKa).

Structure

MOL 3D MOL SDF PDB SMILES InChI

     RDKit          3D

 50 53  0  0  0  0  0  0  0  0999 V2000
    6.9690    1.1721   -0.8336 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.5096    0.9814   -0.6402 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7103    1.5275   -1.4500 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.9855    0.2313    0.3886 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.6138    0.0550    0.5663 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8529    0.9059    1.3315 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5018    0.6981    1.4829 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8388   -0.3749    0.8752 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6058   -1.2130    0.1170 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9584   -1.0107   -0.0383 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9106   -2.3530   -0.5513 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2948   -1.6700   -1.2283 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2334   -1.1339   -0.1702 C   0  0  1  0  0  0  0  0  0  0  0  0
   -2.1388   -2.3403    0.1546 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5877   -0.6022    1.0481 C   0  0  2  0  0  0  0  0  0  0  0  0
   -1.2972    0.5812    1.6671 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7742    0.5234    1.4607 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1328    0.5065    0.0120 C   0  0  1  0  0  0  0  0  0  0  0  0
   -4.5241   -0.0703   -0.1352 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1774    1.9251   -0.5026 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9566    2.8041   -0.1212 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1557    2.1324   -1.5360 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2926    0.9161   -1.5207 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1239   -0.1350   -0.8694 C   0  0  1  0  0  0  0  0  0  0  0  0
    7.4794    0.5989   -0.0308 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.1648    2.2647   -0.6669 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.3129    0.9291   -1.8421 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.3272    1.7503    1.8202 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.9231    1.3601    2.0754 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.5695   -1.6750   -0.6394 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.5404   -2.7239   -1.3698 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.5872   -3.1170    0.1565 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.1680   -0.8480   -1.8362 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8335   -2.3478   -1.8841 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0962   -2.0545    0.5796 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5792   -3.1052    0.6987 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3861   -2.7803   -0.8568 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6780   -1.4209    1.8327 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9363    1.5467    1.2600 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0621    0.6011    2.7531 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1703    1.5092    1.8602 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2964   -0.2299    2.0836 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.2547    0.7224   -0.4268 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4993   -0.8279   -0.9282 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9046   -0.5019    0.8297 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5246    3.0327   -1.3452 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5934    2.2509   -2.5415 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0467    0.6127   -2.5758 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3144    1.0833   -1.0265 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6642   -0.6865   -1.6758 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  2  0
  2  4  1  0
  4  5  1  0
  5  6  2  0
  6  7  1  0
  7  8  2  0
  8 15  1  0
 15 16  1  0
 16 17  1  0
 17 18  1  0
 18 19  1  1
 18 24  1  0
 24 23  1  0
 23 22  1  0
 22 20  1  0
 20 21  2  0
 24 13  1  0
 13 14  1  1
 13 12  1  0
 12 11  1  0
 11  9  1  0
  9 10  2  0
 10  5  1  0
  9  8  1  0
 13 15  1  0
 20 18  1  0
  1 25  1  0
  1 26  1  0
  1 27  1  0
  6 28  1  0
  7 29  1  0
 15 38  1  1
 16 39  1  0
 16 40  1  0
 17 41  1  0
 17 42  1  0
 19 43  1  0
 19 44  1  0
 19 45  1  0
 24 50  1  6
 23 48  1  0
 23 49  1  0
 22 46  1  0
 22 47  1  0
 14 35  1  0
 14 36  1  0
 14 37  1  0
 12 33  1  0
 12 34  1  0
 11 31  1  0
 11 32  1  0
 10 30  1  0
M  END


  Mrv1533004251523432D          

 24 27  0  0  0  0            999 V2000
   -2.0022   -3.2741    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1901   -3.1289    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6582   -3.7596    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9098   -2.3529    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0976   -2.2077    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1827   -1.4318    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9948   -1.2866    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5266   -1.9173    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3387   -1.7721    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6190   -0.9961    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4311   -0.8509    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9629   -1.4816    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3228   -0.7393    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6826   -2.2576    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3340   -2.7639    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0168   -2.3009    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7875   -1.5084    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.2939   -0.8571    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.8705   -2.4028    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4023   -3.0335    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5902   -3.1787    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7781   -3.3239    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2463   -2.6932    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4342   -2.8384    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0  0  0  0
  2  3  2  0  0  0  0
  2  4  1  0  0  0  0
  4  5  1  0  0  0  0
  5  6  2  0  0  0  0
  6  7  1  0  0  0  0
  7  8  2  0  0  0  0
  8  9  1  0  0  0  0
  9 10  1  0  0  0  0
 10 11  1  0  0  0  0
 11 12  1  0  0  0  0
 12 13  1  0  0  0  0
 12 14  1  0  0  0  0
 14 15  1  0  0  0  0
 15 16  1  0  0  0  0
 16 17  1  0  0  0  0
 12 17  1  0  0  0  0
 17 18  2  0  0  0  0
 14 19  1  0  0  0  0
  9 19  1  0  0  0  0
 19 20  1  0  0  0  0
 19 21  1  0  0  0  0
 21 22  1  0  0  0  0
 22 23  1  0  0  0  0
  8 23  1  0  0  0  0
 23 24  2  0  0  0  0
  5 24  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0152128

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CC(=O)OC1=CC=C2C3CCC4(C)C(CCC4=O)C3(C)CCC2=C1

> <INCHI_IDENTIFIER>
InChI=1S/C21H26O3/c1-13(22)24-15-4-5-16-14(12-15)8-10-20(2)17(16)9-11-21(3)18(20)6-7-19(21)23/h4-5,12,17-18H,6-11H2,1-3H3

> <INCHI_KEY>
PYRGOWFQJKEJMV-UHFFFAOYSA-N

> <FORMULA>
C21H26O3

> <MOLECULAR_WEIGHT>
326.436

> <EXACT_MASS>
326.188194697

> <JCHEM_ACCEPTOR_COUNT>
2

> <JCHEM_ATOM_COUNT>
50

> <JCHEM_AVERAGE_POLARIZABILITY>
37.57388955840845

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
0

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
10,15-dimethyl-14-oxotetracyclo[8.7.0.0²,⁷.0¹¹,¹⁵]heptadeca-2,4,6-trien-5-yl acetate

> <ALOGPS_LOGP>
4.34

> <JCHEM_LOGP>
4.519902450000001

> <ALOGPS_LOGS>
-5.57

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
4

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA_STRONGEST_ACIDIC>
19.919580478723294

> <JCHEM_PKA_STRONGEST_BASIC>
-6.975979471070905

> <JCHEM_POLAR_SURFACE_AREA>
43.370000000000005

> <JCHEM_REFRACTIVITY>
92.70899999999999

> <JCHEM_ROTATABLE_BOND_COUNT>
2

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
8.69e-04 g/l

> <JCHEM_TRADITIONAL_IUPAC>
10,15-dimethyl-14-oxotetracyclo[8.7.0.0²,⁷.0¹¹,¹⁵]heptadeca-2,4,6-trien-5-yl acetate

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 25-APR-15   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   25-APR-15         0                                  
HETATM    1  C   UNK     0      -3.737  -6.112   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0      -2.221  -5.841   0.000  0.00  0.00           C+0
HETATM    3  O   UNK     0      -1.229  -7.018   0.000  0.00  0.00           O+0
HETATM    4  O   UNK     0      -1.698  -4.392   0.000  0.00  0.00           O+0
HETATM    5  C   UNK     0      -0.182  -4.121   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       0.341  -2.673   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       1.857  -2.402   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       2.850  -3.579   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       4.366  -3.308   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       4.889  -1.859   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       6.405  -1.588   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       7.398  -2.766   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       8.069  -1.380   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       6.874  -4.214   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       8.090  -5.159   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       9.365  -4.295   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       8.937  -2.816   0.000  0.00  0.00           C+0
HETATM   18  O   UNK     0       9.882  -1.600   0.000  0.00  0.00           O+0
HETATM   19  C   UNK     0       5.358  -4.485   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0       6.351  -5.663   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0       4.835  -5.934   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0       3.319  -6.205   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0       2.326  -5.027   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0       0.810  -5.298   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   24                                                  
CONECT    6    5    7                                                       
CONECT    7    6    8                                                       
CONECT    8    7    9   23                                                  
CONECT    9    8   10   19                                                  
CONECT   10    9   11                                                       
CONECT   11   10   12                                                       
CONECT   12   11   13   14   17                                             
CONECT   13   12                                                            
CONECT   14   12   15   19                                                  
CONECT   15   14   16                                                       
CONECT   16   15   17                                                       
CONECT   17   16   12   18                                                  
CONECT   18   17                                                            
CONECT   19   14    9   20   21                                             
CONECT   20   19                                                            
CONECT   21   19   22                                                       
CONECT   22   21   23                                                       
CONECT   23   22    8   24                                                  
CONECT   24   23    5                                                       
MASTER        0    0    0    0    0    0    0    0   24    0   54    0
END

View in JSmol

Synonyms

Value	Source
10,15-Dimethyl-14-oxotetracyclo[8.7.0.0,.0,]heptadeca-2,4,6-trien-5-yl acetic acid	Generator
10,15-Dimethyl-14-oxotetracyclo[8.7.0.0²,⁷.0¹¹,¹⁵]heptadeca-2,4,6-trien-5-yl acetic acid	Generator

Chemical Formula

C₂₁H₂₆O₃

Average Mass

326.4360 Da

Monoisotopic Mass

326.18819 Da

IUPAC Name

10,15-dimethyl-14-oxotetracyclo[8.7.0.0²,⁷.0¹¹,¹⁵]heptadeca-2,4,6-trien-5-yl acetate

Traditional Name

10,15-dimethyl-14-oxotetracyclo[8.7.0.0²,⁷.0¹¹,¹⁵]heptadeca-2,4,6-trien-5-yl acetate

CAS Registry Number

Not Available

SMILES

CC(=O)OC1=CC=C2C3CCC4(C)C(CCC4=O)C3(C)CCC2=C1

InChI Identifier

InChI=1S/C21H26O3/c1-13(22)24-15-4-5-16-14(12-15)8-10-20(2)17(16)9-11-21(3)18(20)6-7-19(21)23/h4-5,12,17-18H,6-11H2,1-3H3

InChI Key

PYRGOWFQJKEJMV-UHFFFAOYSA-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 steroid esters. Steroid esters are compounds containing a steroid moiety which bears a carboxylic acid ester group.

Kingdom

Organic compounds

Super Class

Lipids and lipid-like molecules

Class

Steroids and steroid derivatives

Sub Class

Steroid esters

Direct Parent

Steroid esters

Alternative Parents

Substituents

Steroid ester
17-oxosteroid
Oxosteroid
Phenanthrene
Tetralin
Benzenoid
Ketone
Carboxylic acid ester
Monocarboxylic acid or derivatives
Carboxylic acid derivative
Hydrocarbon derivative
Organic oxide
Organic oxygen compound
Organooxygen compound
Carbonyl group
Aromatic homopolycyclic compound

Molecular Framework

Aromatic 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	4.34	ALOGPS
logP	4.52	ChemAxon
logS	-5.6	ALOGPS
pKa (Strongest Acidic)	19.92	ChemAxon
pKa (Strongest Basic)	-7	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	2	ChemAxon
Hydrogen Donor Count	0	ChemAxon
Polar Surface Area	43.37 Å²	ChemAxon
Rotatable Bond Count	2	ChemAxon
Refractivity	92.71 m³·mol⁻¹	ChemAxon
Polarizability	37.57 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

124007420

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for 3b,11a-dimethyl-1-oxo-2h,3h,3ah,4h,5h,9bh,10h,11h-cyclopenta[a]phenanthren-7-yl acetate (NP0152128)

MOL for NP0152128 (3b,11a-dimethyl-1-oxo-2h,3h,3ah,4h,5h,9bh,10h,11h-cyclopenta[a]phenanthren-7-yl acetate)

3D MOL for NP0152128 (3b,11a-dimethyl-1-oxo-2h,3h,3ah,4h,5h,9bh,10h,11h-cyclopenta[a]phenanthren-7-yl acetate)

3D SDF for NP0152128 (3b,11a-dimethyl-1-oxo-2h,3h,3ah,4h,5h,9bh,10h,11h-cyclopenta[a]phenanthren-7-yl acetate)

3D-SDF for NP0152128 (3b,11a-dimethyl-1-oxo-2h,3h,3ah,4h,5h,9bh,10h,11h-cyclopenta[a]phenanthren-7-yl acetate)

PDB for NP0152128 (3b,11a-dimethyl-1-oxo-2h,3h,3ah,4h,5h,9bh,10h,11h-cyclopenta[a]phenanthren-7-yl acetate)

3D PDB for NP0152128 (3b,11a-dimethyl-1-oxo-2h,3h,3ah,4h,5h,9bh,10h,11h-cyclopenta[a]phenanthren-7-yl acetate)

SMILES for NP0152128 (3b,11a-dimethyl-1-oxo-2h,3h,3ah,4h,5h,9bh,10h,11h-cyclopenta[a]phenanthren-7-yl acetate)

INCHI for NP0152128 (3b,11a-dimethyl-1-oxo-2h,3h,3ah,4h,5h,9bh,10h,11h-cyclopenta[a]phenanthren-7-yl acetate)

Structure for NP0152128 (3b,11a-dimethyl-1-oxo-2h,3h,3ah,4h,5h,9bh,10h,11h-cyclopenta[a]phenanthren-7-yl acetate)

3D Structure for NP0152128 (3b,11a-dimethyl-1-oxo-2h,3h,3ah,4h,5h,9bh,10h,11h-cyclopenta[a]phenanthren-7-yl acetate)