NP-MRD: Showing NP-Card for 4a,7-dimethyl-2-oxo-8-(3-oxo-4-{5,6,6-trimethyl-1-[2-(methylsulfanyl)-2-oxoethyl]-2,7,8-trioxabicyclo[3.2.1]octan-3-yl}pentyl)-4b,5,6,7,8,8a,9,10-octahydrophenanthren-9-yl acetate (NP0179695)

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Record Information

Version

2.0

Created at

2022-09-03 17:55:20 UTC

Updated at

2022-09-03 17:55:20 UTC

NP-MRD ID

NP0179695

Secondary Accession Numbers

None

Natural Product Identification

Common Name

4a,7-dimethyl-2-oxo-8-(3-oxo-4-{5,6,6-trimethyl-1-[2-(methylsulfanyl)-2-oxoethyl]-2,7,8-trioxabicyclo[3.2.1]octan-3-yl}pentyl)-4b,5,6,7,8,8a,9,10-octahydrophenanthren-9-yl acetate

Description

4A,7-dimethyl-2-oxo-8-(3-oxo-4-{5,6,6-trimethyl-1-[2-(methylsulfanyl)-2-oxoethyl]-2,7,8-trioxabicyclo[3.2.1]Octan-3-yl}pentyl)-2,4a,4b,5,6,7,8,8a,9,10-decahydrophenanthren-9-yl acetate belongs to the class of organic compounds known as oxosteroids. These are steroid derivatives carrying a C=O group attached to steroid skeleton. 4a,7-dimethyl-2-oxo-8-(3-oxo-4-{5,6,6-trimethyl-1-[2-(methylsulfanyl)-2-oxoethyl]-2,7,8-trioxabicyclo[3.2.1]octan-3-yl}pentyl)-4b,5,6,7,8,8a,9,10-octahydrophenanthren-9-yl acetate is found in Petunia axillaris. 4A,7-dimethyl-2-oxo-8-(3-oxo-4-{5,6,6-trimethyl-1-[2-(methylsulfanyl)-2-oxoethyl]-2,7,8-trioxabicyclo[3.2.1]Octan-3-yl}pentyl)-2,4a,4b,5,6,7,8,8a,9,10-decahydrophenanthren-9-yl acetate is an extremely weak basic (essentially neutral) compound (based on its pKa).

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1533004241504582D          

 43 47  0  0  0  0            999 V2000
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M  END

     RDKit          3D

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M  END


  Mrv1533004241504582D          

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    9.6336   -1.6978    0.0000 S   0  0  0  0  0  0  0  0  0  0  0  0
    8.8452   -1.9410    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.2405   -1.3799    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    8.6617   -2.7453    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.8733   -2.9885    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.3122   -2.3837    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.4895   -2.4454    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.0247   -3.1270    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.2679   -3.9154    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.6631   -4.4765    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.9547   -3.2513    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.0359   -4.2168    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.5711   -4.8984    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.5970   -4.8216    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.7503   -3.8043    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.0770   -1.7309    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.4895   -1.0164    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.2520   -1.7309    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.8395   -2.4454    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.8395   -1.0164    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0145   -1.0164    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6020   -0.3020    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0145    0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.8395    0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6020    1.1270    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7770    1.1270    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3645    0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7770   -0.3020    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3645   -1.0164    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5395   -1.0164    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1270   -0.3020    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3020   -0.3020    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1105    0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9355    0.4125    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.3020    1.1270    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1270    1.1270    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5395    0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9520    1.1270    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7770   -1.7309    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.3645   -2.4454    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5395   -2.4454    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.7770   -3.1599    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
  3  4  2  0  0  0  0
  3  5  1  0  0  0  0
  5  6  1  0  0  0  0
  6  7  1  0  0  0  0
  7  8  1  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
 10 12  1  0  0  0  0
  6 12  1  0  0  0  0
 10 13  1  0  0  0  0
 13 14  1  0  0  0  0
 13 15  1  0  0  0  0
 13 16  1  0  0  0  0
  6 16  1  0  0  0  0
  8 17  1  0  0  0  0
 17 18  1  0  0  0  0
 17 19  1  0  0  0  0
 19 20  2  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
 23 24  1  0  0  0  0
 24 25  1  0  0  0  0
 24 26  1  0  0  0  0
 26 27  1  0  0  0  0
 27 28  1  0  0  0  0
 28 29  1  0  0  0  0
 23 29  1  0  0  0  0
 29 30  1  0  0  0  0
 30 31  1  0  0  0  0
 31 32  1  0  0  0  0
 32 33  2  0  0  0  0
 33 34  1  0  0  0  0
 34 35  2  0  0  0  0
 34 36  1  0  0  0  0
 36 37  2  0  0  0  0
 37 38  1  0  0  0  0
 28 38  1  0  0  0  0
 32 38  1  0  0  0  0
 38 39  1  0  0  0  0
 30 40  1  0  0  0  0
 40 41  1  0  0  0  0
 41 42  2  0  0  0  0
 41 43  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0179695

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CSC(=O)CC12OC(C)(C)C(C)(CC(O1)C(C)C(=O)CCC1C(C)CCC3C1C(CC1=CC(=O)C=CC31C)OC(C)=O)O2

> <INCHI_IDENTIFIER>
InChI=1S/C34H48O8S/c1-19-9-11-25-30(27(39-21(3)35)16-22-15-23(36)13-14-32(22,25)6)24(19)10-12-26(37)20(2)28-17-33(7)31(4,5)41-34(40-28,42-33)18-29(38)43-8/h13-15,19-20,24-25,27-28,30H,9-12,16-18H2,1-8H3

> <INCHI_KEY>
YIXGLWJISJIDND-UHFFFAOYSA-N

> <FORMULA>
C34H48O8S

> <MOLECULAR_WEIGHT>
616.81

> <EXACT_MASS>
616.30698968

> <JCHEM_ACCEPTOR_COUNT>
7

> <JCHEM_ATOM_COUNT>
91

> <JCHEM_AVERAGE_POLARIZABILITY>
66.3227681045372

> <JCHEM_BIOAVAILABILITY>
0

> <JCHEM_DONOR_COUNT>
0

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
4a,7-dimethyl-2-oxo-8-(3-oxo-4-{5,6,6-trimethyl-1-[2-(methylsulfanyl)-2-oxoethyl]-2,7,8-trioxabicyclo[3.2.1]octan-3-yl}pentyl)-2,4a,4b,5,6,7,8,8a,9,10-decahydrophenanthren-9-yl acetate

> <ALOGPS_LOGP>
4.45

> <JCHEM_LOGP>
5.919891707999998

> <ALOGPS_LOGS>
-6.07

> <JCHEM_MDDR_LIKE_RULE>
1

> <JCHEM_NUMBER_OF_RINGS>
5

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
19.000886487568014

> <JCHEM_PKA_STRONGEST_ACIDIC>
16.691529855573847

> <JCHEM_PKA_STRONGEST_BASIC>
-4.034758368050973

> <JCHEM_POLAR_SURFACE_AREA>
105.20000000000002

> <JCHEM_REFRACTIVITY>
166.3174

> <JCHEM_ROTATABLE_BOND_COUNT>
10

> <JCHEM_RULE_OF_FIVE>
0

> <ALOGPS_SOLUBILITY>
5.31e-04 g/l

> <JCHEM_TRADITIONAL_IUPAC>
4a,7-dimethyl-2-oxo-8-(3-oxo-4-{5,6,6-trimethyl-1-[2-(methylsulfanyl)-2-oxoethyl]-2,7,8-trioxabicyclo[3.2.1]octan-3-yl}pentyl)-4b,5,6,7,8,8a,9,10-octahydrophenanthren-9-yl acetate

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 24-APR-15   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   24-APR-15         0                                  
HETATM    1  C   UNK     0      18.325  -1.668   0.000  0.00  0.00           C+0
HETATM    2  S   UNK     0      17.983  -3.169   0.000  0.00  0.00           S+0
HETATM    3  C   UNK     0      16.511  -3.623   0.000  0.00  0.00           C+0
HETATM    4  O   UNK     0      15.382  -2.576   0.000  0.00  0.00           O+0
HETATM    5  C   UNK     0      16.168  -5.125   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0      14.697  -5.579   0.000  0.00  0.00           C+0
HETATM    7  O   UNK     0      13.649  -4.450   0.000  0.00  0.00           O+0
HETATM    8  C   UNK     0      12.114  -4.565   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0      11.246  -5.837   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0      11.700  -7.309   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0      10.571  -8.356   0.000  0.00  0.00           C+0
HETATM   12  O   UNK     0      12.982  -6.069   0.000  0.00  0.00           O+0
HETATM   13  C   UNK     0      13.134  -7.871   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0      12.266  -9.144   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0      14.181  -9.000   0.000  0.00  0.00           C+0
HETATM   16  O   UNK     0      14.467  -7.101   0.000  0.00  0.00           O+0
HETATM   17  C   UNK     0      11.344  -3.231   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0      12.114  -1.897   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0       9.804  -3.231   0.000  0.00  0.00           C+0
HETATM   20  O   UNK     0       9.034  -4.565   0.000  0.00  0.00           O+0
HETATM   21  C   UNK     0       9.034  -1.897   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0       7.494  -1.897   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0       6.724  -0.564   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0       7.494   0.770   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0       9.034   0.770   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0       6.724   2.104   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0       5.184   2.104   0.000  0.00  0.00           C+0
HETATM   28  C   UNK     0       4.414   0.770   0.000  0.00  0.00           C+0
HETATM   29  C   UNK     0       5.184  -0.564   0.000  0.00  0.00           C+0
HETATM   30  C   UNK     0       4.414  -1.897   0.000  0.00  0.00           C+0
HETATM   31  C   UNK     0       2.874  -1.897   0.000  0.00  0.00           C+0
HETATM   32  C   UNK     0       2.104  -0.564   0.000  0.00  0.00           C+0
HETATM   33  C   UNK     0       0.564  -0.564   0.000  0.00  0.00           C+0
HETATM   34  C   UNK     0      -0.206   0.770   0.000  0.00  0.00           C+0
HETATM   35  O   UNK     0      -1.746   0.770   0.000  0.00  0.00           O+0
HETATM   36  C   UNK     0       0.564   2.104   0.000  0.00  0.00           C+0
HETATM   37  C   UNK     0       2.104   2.104   0.000  0.00  0.00           C+0
HETATM   38  C   UNK     0       2.874   0.770   0.000  0.00  0.00           C+0
HETATM   39  C   UNK     0       3.644   2.104   0.000  0.00  0.00           C+0
HETATM   40  O   UNK     0       5.184  -3.231   0.000  0.00  0.00           O+0
HETATM   41  C   UNK     0       4.414  -4.565   0.000  0.00  0.00           C+0
HETATM   42  O   UNK     0       2.874  -4.565   0.000  0.00  0.00           O+0
HETATM   43  C   UNK     0       5.184  -5.898   0.000  0.00  0.00           C+0
CONECT    1    2                                                            
CONECT    2    1    3                                                       
CONECT    3    2    4    5                                                  
CONECT    4    3                                                            
CONECT    5    3    6                                                       
CONECT    6    5    7   12   16                                             
CONECT    7    6    8                                                       
CONECT    8    7    9   17                                                  
CONECT    9    8   10                                                       
CONECT   10    9   11   12   13                                             
CONECT   11   10                                                            
CONECT   12   10    6                                                       
CONECT   13   10   14   15   16                                             
CONECT   14   13                                                            
CONECT   15   13                                                            
CONECT   16   13    6                                                       
CONECT   17    8   18   19                                                  
CONECT   18   17                                                            
CONECT   19   17   20   21                                                  
CONECT   20   19                                                            
CONECT   21   19   22                                                       
CONECT   22   21   23                                                       
CONECT   23   22   24   29                                                  
CONECT   24   23   25   26                                                  
CONECT   25   24                                                            
CONECT   26   24   27                                                       
CONECT   27   26   28                                                       
CONECT   28   27   29   38                                                  
CONECT   29   28   23   30                                                  
CONECT   30   29   31   40                                                  
CONECT   31   30   32                                                       
CONECT   32   31   33   38                                                  
CONECT   33   32   34                                                       
CONECT   34   33   35   36                                                  
CONECT   35   34                                                            
CONECT   36   34   37                                                       
CONECT   37   36   38                                                       
CONECT   38   37   28   32   39                                             
CONECT   39   38                                                            
CONECT   40   30   41                                                       
CONECT   41   40   42   43                                                  
CONECT   42   41                                                            
CONECT   43   41                                                            
MASTER        0    0    0    0    0    0    0    0   43    0   94    0
END

View in JSmol

Synonyms

Value	Source
4a,7-Dimethyl-2-oxo-8-(3-oxo-4-{5,6,6-trimethyl-1-[2-(methylsulfanyl)-2-oxoethyl]-2,7,8-trioxabicyclo[3.2.1]octan-3-yl}pentyl)-2,4a,4b,5,6,7,8,8a,9,10-decahydrophenanthren-9-yl acetic acid	Generator
4a,7-Dimethyl-2-oxo-8-(3-oxo-4-{5,6,6-trimethyl-1-[2-(methylsulphanyl)-2-oxoethyl]-2,7,8-trioxabicyclo[3.2.1]octan-3-yl}pentyl)-2,4a,4b,5,6,7,8,8a,9,10-decahydrophenanthren-9-yl acetate	Generator
4a,7-Dimethyl-2-oxo-8-(3-oxo-4-{5,6,6-trimethyl-1-[2-(methylsulphanyl)-2-oxoethyl]-2,7,8-trioxabicyclo[3.2.1]octan-3-yl}pentyl)-2,4a,4b,5,6,7,8,8a,9,10-decahydrophenanthren-9-yl acetic acid	Generator

Chemical Formula

C₃₄H₄₈O₈S

Average Mass

616.8100 Da

Monoisotopic Mass

616.30699 Da

IUPAC Name

4a,7-dimethyl-2-oxo-8-(3-oxo-4-{5,6,6-trimethyl-1-[2-(methylsulfanyl)-2-oxoethyl]-2,7,8-trioxabicyclo[3.2.1]octan-3-yl}pentyl)-2,4a,4b,5,6,7,8,8a,9,10-decahydrophenanthren-9-yl acetate

Traditional Name

4a,7-dimethyl-2-oxo-8-(3-oxo-4-{5,6,6-trimethyl-1-[2-(methylsulfanyl)-2-oxoethyl]-2,7,8-trioxabicyclo[3.2.1]octan-3-yl}pentyl)-4b,5,6,7,8,8a,9,10-octahydrophenanthren-9-yl acetate

CAS Registry Number

Not Available

SMILES

CSC(=O)CC12OC(C)(C)C(C)(CC(O1)C(C)C(=O)CCC1C(C)CCC3C1C(CC1=CC(=O)C=CC31C)OC(C)=O)O2

InChI Identifier

InChI=1S/C34H48O8S/c1-19-9-11-25-30(27(39-21(3)35)16-22-15-23(36)13-14-32(22,25)6)24(19)10-12-26(37)20(2)28-17-33(7)31(4,5)41-34(40-28,42-33)18-29(38)43-8/h13-15,19-20,24-25,27-28,30H,9-12,16-18H2,1-8H3

InChI Key

YIXGLWJISJIDND-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
Petunia axillaris	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as oxosteroids. These are steroid derivatives carrying a C=O group attached to steroid skeleton.

Kingdom

Organic compounds

Super Class

Lipids and lipid-like molecules

Class

Steroids and steroid derivatives

Sub Class

Oxosteroids

Direct Parent

Oxosteroids

Alternative Parents

Substituents

3-oxosteroid
Oxosteroid
Phenanthrene
Hydrophenanthrene
1,3-dioxepane
Carboxylic acid orthoester
Dioxepane
Ortho ester
Meta-dioxane
Meta-dioxolane
Carboxylic acid ester
Carbothioic s-ester
Cyclic ketone
Thiocarboxylic acid ester
Orthocarboxylic acid derivative
Ketone
Oxacycle
Carboxylic acid derivative
Organoheterocyclic compound
Sulfenyl compound
Thiocarboxylic acid or derivatives
Monocarboxylic acid or derivatives
Organic oxide
Hydrocarbon derivative
Organic oxygen compound
Organosulfur compound
Organooxygen compound
Carbonyl group
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	4.45	ALOGPS
logP	5.92	ChemAxon
logS	-6.1	ALOGPS
pKa (Strongest Acidic)	16.69	ChemAxon
pKa (Strongest Basic)	-4	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	7	ChemAxon
Hydrogen Donor Count	0	ChemAxon
Polar Surface Area	105.2 Å²	ChemAxon
Rotatable Bond Count	10	ChemAxon
Refractivity	166.32 m³·mol⁻¹	ChemAxon
Polarizability	66.32 Å³	ChemAxon
Number of Rings	5	ChemAxon
Bioavailability	No	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

14777871

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for 4a,7-dimethyl-2-oxo-8-(3-oxo-4-{5,6,6-trimethyl-1-[2-(methylsulfanyl)-2-oxoethyl]-2,7,8-trioxabicyclo[3.2.1]octan-3-yl}pentyl)-4b,5,6,7,8,8a,9,10-octahydrophenanthren-9-yl acetate (NP0179695)

MOL for NP0179695 (4a,7-dimethyl-2-oxo-8-(3-oxo-4-{5,6,6-trimethyl-1-[2-(methylsulfanyl)-2-oxoethyl]-2,7,8-trioxabicyclo[3.2.1]octan-3-yl}pentyl)-4b,5,6,7,8,8a,9,10-octahydrophenanthren-9-yl acetate)

3D MOL for NP0179695 (4a,7-dimethyl-2-oxo-8-(3-oxo-4-{5,6,6-trimethyl-1-[2-(methylsulfanyl)-2-oxoethyl]-2,7,8-trioxabicyclo[3.2.1]octan-3-yl}pentyl)-4b,5,6,7,8,8a,9,10-octahydrophenanthren-9-yl acetate)

3D SDF for NP0179695 (4a,7-dimethyl-2-oxo-8-(3-oxo-4-{5,6,6-trimethyl-1-[2-(methylsulfanyl)-2-oxoethyl]-2,7,8-trioxabicyclo[3.2.1]octan-3-yl}pentyl)-4b,5,6,7,8,8a,9,10-octahydrophenanthren-9-yl acetate)

3D-SDF for NP0179695 (4a,7-dimethyl-2-oxo-8-(3-oxo-4-{5,6,6-trimethyl-1-[2-(methylsulfanyl)-2-oxoethyl]-2,7,8-trioxabicyclo[3.2.1]octan-3-yl}pentyl)-4b,5,6,7,8,8a,9,10-octahydrophenanthren-9-yl acetate)

PDB for NP0179695 (4a,7-dimethyl-2-oxo-8-(3-oxo-4-{5,6,6-trimethyl-1-[2-(methylsulfanyl)-2-oxoethyl]-2,7,8-trioxabicyclo[3.2.1]octan-3-yl}pentyl)-4b,5,6,7,8,8a,9,10-octahydrophenanthren-9-yl acetate)

3D PDB for NP0179695 (4a,7-dimethyl-2-oxo-8-(3-oxo-4-{5,6,6-trimethyl-1-[2-(methylsulfanyl)-2-oxoethyl]-2,7,8-trioxabicyclo[3.2.1]octan-3-yl}pentyl)-4b,5,6,7,8,8a,9,10-octahydrophenanthren-9-yl acetate)

SMILES for NP0179695 (4a,7-dimethyl-2-oxo-8-(3-oxo-4-{5,6,6-trimethyl-1-[2-(methylsulfanyl)-2-oxoethyl]-2,7,8-trioxabicyclo[3.2.1]octan-3-yl}pentyl)-4b,5,6,7,8,8a,9,10-octahydrophenanthren-9-yl acetate)

INCHI for NP0179695 (4a,7-dimethyl-2-oxo-8-(3-oxo-4-{5,6,6-trimethyl-1-[2-(methylsulfanyl)-2-oxoethyl]-2,7,8-trioxabicyclo[3.2.1]octan-3-yl}pentyl)-4b,5,6,7,8,8a,9,10-octahydrophenanthren-9-yl acetate)

Structure for NP0179695 (4a,7-dimethyl-2-oxo-8-(3-oxo-4-{5,6,6-trimethyl-1-[2-(methylsulfanyl)-2-oxoethyl]-2,7,8-trioxabicyclo[3.2.1]octan-3-yl}pentyl)-4b,5,6,7,8,8a,9,10-octahydrophenanthren-9-yl acetate)

3D Structure for NP0179695 (4a,7-dimethyl-2-oxo-8-(3-oxo-4-{5,6,6-trimethyl-1-[2-(methylsulfanyl)-2-oxoethyl]-2,7,8-trioxabicyclo[3.2.1]octan-3-yl}pentyl)-4b,5,6,7,8,8a,9,10-octahydrophenanthren-9-yl acetate)