NP-MRD: Showing NP-Card for (1s,5as,7s,8s,9ar,10s,11s,11as)-7-(acetyloxy)-8,10-dihydroxy-6,6,9a,11a-tetramethyl-1-[(2s)-6-methyl-5-methylideneheptan-2-yl]-1h,2h,4h,5h,5ah,7h,8h,9h,10h,11h-cyclopenta[a]phenanthren-11-yl acetate (NP0234867)

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Record Information

Version

2.0

Created at

2022-09-06 17:10:32 UTC

Updated at

2022-09-06 17:10:32 UTC

NP-MRD ID

NP0234867

Secondary Accession Numbers

None

Natural Product Identification

Common Name

(1s,5as,7s,8s,9ar,10s,11s,11as)-7-(acetyloxy)-8,10-dihydroxy-6,6,9a,11a-tetramethyl-1-[(2s)-6-methyl-5-methylideneheptan-2-yl]-1h,2h,4h,5h,5ah,7h,8h,9h,10h,11h-cyclopenta[a]phenanthren-11-yl acetate

Description

Integracide F belongs to the class of organic compounds known as ergostane steroids. These are steroids with a structure based on the ergostane skeleton, which arises from the methylation of cholestane at the 24-position. Based on a literature review very few articles have been published on Integracide F.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652309062219102D          

 40 43  0  0  1  0            999 V2000
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  1  2  2  0  0  0  0
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  5  6  1  6  0  0  0
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M  END

     RDKit          3D

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M  END


  Mrv1652309062219102D          

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   -2.4932   -3.7891    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7481   -4.5737    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1961   -5.1868    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -2.4510   -5.9714    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3891   -5.0152    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.8371   -5.6283    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0920   -6.4130    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5400   -7.0261    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8990   -6.5845    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1342   -4.2306    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.5211   -4.7827    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5551   -4.7452    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -3.0031   -5.3583    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8100   -5.5298    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6170   -5.7014    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -4.8719   -6.4860    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.1690   -5.0883    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -5.9760   -5.2598    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -6.5280   -4.6467    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.2731   -3.8621    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.3350   -4.8182    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9141   -4.3036    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.7311   -4.1888    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9429   -3.4791    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1071   -4.1321    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -3.8522   -3.3475    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0452   -3.1760    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1918   -4.3076    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9063   -3.8951    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1918   -5.1326    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  2  0  0  0  0
  2  3  1  0  0  0  0
  3  4  1  0  0  0  0
  4  5  1  0  0  0  0
  5  6  1  6  0  0  0
  7  5  1  1  0  0  0
  7  8  1  0  0  0  0
  8  9  1  0  0  0  0
  9 10  2  0  0  0  0
 10 11  1  0  0  0  0
 11 12  2  0  0  0  0
 12 13  1  0  0  0  0
 13 14  1  1  0  0  0
 13 15  1  0  0  0  0
 15 16  1  6  0  0  0
 16 17  1  0  0  0  0
 17 18  1  0  0  0  0
 17 19  2  0  0  0  0
 15 20  1  0  0  0  0
 10 20  1  0  0  0  0
  7 20  1  0  0  0  0
 20 21  1  1  0  0  0
 12 22  1  0  0  0  0
 22 23  1  1  0  0  0
 22 24  1  0  0  0  0
 24 25  1  0  0  0  0
 25 26  1  6  0  0  0
 25 27  1  0  0  0  0
 27 28  1  1  0  0  0
 28 29  1  0  0  0  0
 29 30  1  0  0  0  0
 29 31  2  0  0  0  0
 27 32  1  0  0  0  0
 32 33  1  0  0  0  0
 32 34  1  0  0  0  0
 32 35  1  0  0  0  0
 22 35  1  0  0  0  0
 35 36  1  1  0  0  0
 36 37  1  0  0  0  0
 11 37  1  0  0  0  0
  2 38  1  0  0  0  0
 38 39  1  0  0  0  0
 38 40  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0234867

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CC(C)C(=C)CC[C@H](C)[C@@H]1CC=C2C3=C([C@H](O)[C@@H](OC(C)=O)[C@@]12C)[C@]1(C)C[C@H](O)[C@@H](OC(C)=O)C(C)(C)[C@H]1CC3

> <INCHI_IDENTIFIER>
InChI=1S/C34H52O6/c1-18(2)19(3)11-12-20(4)24-14-15-25-23-13-16-27-32(7,8)30(39-21(5)35)26(37)17-33(27,9)28(23)29(38)31(34(24,25)10)40-22(6)36/h15,18,20,24,26-27,29-31,37-38H,3,11-14,16-17H2,1-2,4-10H3/t20-,24-,26-,27+,29-,30+,31+,33+,34-/m0/s1

> <INCHI_KEY>
GTJJCCFMWDWZHD-MHNSYPGMSA-N

> <FORMULA>
C34H52O6

> <MOLECULAR_WEIGHT>
556.784

> <EXACT_MASS>
556.376389394

> <JCHEM_ACCEPTOR_COUNT>
4

> <JCHEM_ATOM_COUNT>
92

> <JCHEM_AVERAGE_POLARIZABILITY>
65.34741488304695

> <JCHEM_BIOAVAILABILITY>
0

> <JCHEM_DONOR_COUNT>
2

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
(2R,4S,5S,7S,14S,15S,16S,17S)-5-(acetyloxy)-4,17-dihydroxy-2,6,6,15-tetramethyl-14-[(2S)-6-methyl-5-methylideneheptan-2-yl]tetracyclo[8.7.0.0^{2,7}.0^{11,15}]heptadeca-1(10),11-dien-16-yl acetate

> <JCHEM_LOGP>
5.003538685999998

> <JCHEM_MDDR_LIKE_RULE>
1

> <JCHEM_NUMBER_OF_RINGS>
4

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
14.22552622158804

> <JCHEM_PKA_STRONGEST_ACIDIC>
13.423649884946322

> <JCHEM_PKA_STRONGEST_BASIC>
-3.179192113058713

> <JCHEM_POLAR_SURFACE_AREA>
93.06000000000002

> <JCHEM_REFRACTIVITY>
156.78319999999997

> <JCHEM_ROTATABLE_BOND_COUNT>
9

> <JCHEM_RULE_OF_FIVE>
0

> <JCHEM_TRADITIONAL_IUPAC>
(2R,4S,5S,7S,14S,15S,16S,17S)-5-(acetyloxy)-4,17-dihydroxy-2,6,6,15-tetramethyl-14-[(2S)-6-methyl-5-methylideneheptan-2-yl]tetracyclo[8.7.0.0^{2,7}.0^{11,15}]heptadeca-1(10),11-dien-16-yl acetate

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 06-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   06-SEP-22         0                                  
HETATM    1  C   UNK     0       4.624  -5.731   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       4.624  -7.271   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       3.291  -8.041   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       1.957  -7.271   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       0.623  -8.041   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       0.623  -9.581   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0      -0.710  -7.271   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0      -0.871  -5.739   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0      -2.378  -5.419   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0      -3.148  -6.753   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0      -4.654  -7.073   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0      -5.130  -8.538   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0      -4.099  -9.682   0.000  0.00  0.00           C+0
HETATM   14  O   UNK     0      -4.575 -11.147   0.000  0.00  0.00           O+0
HETATM   15  C   UNK     0      -2.593  -9.362   0.000  0.00  0.00           C+0
HETATM   16  O   UNK     0      -1.563 -10.506   0.000  0.00  0.00           O+0
HETATM   17  C   UNK     0      -2.038 -11.971   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0      -1.008 -13.115   0.000  0.00  0.00           C+0
HETATM   19  O   UNK     0      -3.545 -12.291   0.000  0.00  0.00           O+0
HETATM   20  C   UNK     0      -2.117  -7.897   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0      -0.973  -8.928   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0      -6.636  -8.858   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0      -5.606 -10.002   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0      -7.112 -10.322   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0      -8.618 -10.643   0.000  0.00  0.00           C+0
HETATM   26  O   UNK     0      -9.094 -12.107   0.000  0.00  0.00           O+0
HETATM   27  C   UNK     0      -9.649  -9.498   0.000  0.00  0.00           C+0
HETATM   28  O   UNK     0     -11.155  -9.818   0.000  0.00  0.00           O+0
HETATM   29  C   UNK     0     -12.186  -8.674   0.000  0.00  0.00           C+0
HETATM   30  C   UNK     0     -11.710  -7.209   0.000  0.00  0.00           C+0
HETATM   31  O   UNK     0     -13.692  -8.994   0.000  0.00  0.00           O+0
HETATM   32  C   UNK     0      -9.173  -8.033   0.000  0.00  0.00           C+0
HETATM   33  C   UNK     0     -10.698  -7.819   0.000  0.00  0.00           C+0
HETATM   34  C   UNK     0      -9.227  -6.494   0.000  0.00  0.00           C+0
HETATM   35  C   UNK     0      -7.667  -7.713   0.000  0.00  0.00           C+0
HETATM   36  C   UNK     0      -7.191  -6.249   0.000  0.00  0.00           C+0
HETATM   37  C   UNK     0      -5.684  -5.928   0.000  0.00  0.00           C+0
HETATM   38  C   UNK     0       5.958  -8.041   0.000  0.00  0.00           C+0
HETATM   39  C   UNK     0       7.292  -7.271   0.000  0.00  0.00           C+0
HETATM   40  C   UNK     0       5.958  -9.581   0.000  0.00  0.00           C+0
CONECT    1    2                                                            
CONECT    2    1    3   38                                                  
CONECT    3    2    4                                                       
CONECT    4    3    5                                                       
CONECT    5    4    6    7                                                  
CONECT    6    5                                                            
CONECT    7    5    8   20                                                  
CONECT    8    7    9                                                       
CONECT    9    8   10                                                       
CONECT   10    9   11   20                                                  
CONECT   11   10   12   37                                                  
CONECT   12   11   13   22                                                  
CONECT   13   12   14   15                                                  
CONECT   14   13                                                            
CONECT   15   13   16   20                                                  
CONECT   16   15   17                                                       
CONECT   17   16   18   19                                                  
CONECT   18   17                                                            
CONECT   19   17                                                            
CONECT   20   15   10    7   21                                             
CONECT   21   20                                                            
CONECT   22   12   23   24   35                                             
CONECT   23   22                                                            
CONECT   24   22   25                                                       
CONECT   25   24   26   27                                                  
CONECT   26   25                                                            
CONECT   27   25   28   32                                                  
CONECT   28   27   29                                                       
CONECT   29   28   30   31                                                  
CONECT   30   29                                                            
CONECT   31   29                                                            
CONECT   32   27   33   34   35                                             
CONECT   33   32                                                            
CONECT   34   32                                                            
CONECT   35   32   22   36                                                  
CONECT   36   35   37                                                       
CONECT   37   36   11                                                       
CONECT   38    2   39   40                                                  
CONECT   39   38                                                            
CONECT   40   38                                                            
MASTER        0    0    0    0    0    0    0    0   40    0   86    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₃₄H₅₂O₆

Average Mass

556.7840 Da

Monoisotopic Mass

556.37639 Da

IUPAC Name

(2R,4S,5S,7S,14S,15S,16S,17S)-5-(acetyloxy)-4,17-dihydroxy-2,6,6,15-tetramethyl-14-[(2S)-6-methyl-5-methylideneheptan-2-yl]tetracyclo[8.7.0.0^{2,7}.0^{11,15}]heptadeca-1(10),11-dien-16-yl acetate

Traditional Name

(2R,4S,5S,7S,14S,15S,16S,17S)-5-(acetyloxy)-4,17-dihydroxy-2,6,6,15-tetramethyl-14-[(2S)-6-methyl-5-methylideneheptan-2-yl]tetracyclo[8.7.0.0^{2,7}.0^{11,15}]heptadeca-1(10),11-dien-16-yl acetate

CAS Registry Number

Not Available

SMILES

CC(C)C(=C)CC[C@H](C)[C@@H]1CC=C2C3=C([C@H](O)[C@@H](OC(C)=O)[C@@]12C)[C@]1(C)C[C@H](O)[C@@H](OC(C)=O)C(C)(C)[C@H]1CC3

InChI Identifier

InChI=1S/C34H52O6/c1-18(2)19(3)11-12-20(4)24-14-15-25-23-13-16-27-32(7,8)30(39-21(5)35)26(37)17-33(27,9)28(23)29(38)31(34(24,25)10)40-22(6)36/h15,18,20,24,26-27,29-31,37-38H,3,11-14,16-17H2,1-2,4-10H3/t20-,24-,26-,27+,29-,30+,31+,33+,34-/m0/s1

InChI Key

GTJJCCFMWDWZHD-MHNSYPGMSA-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 ergostane steroids. These are steroids with a structure based on the ergostane skeleton, which arises from the methylation of cholestane at the 24-position.

Kingdom

Organic compounds

Super Class

Lipids and lipid-like molecules

Class

Steroids and steroid derivatives

Sub Class

Ergostane steroids

Direct Parent

Ergostane steroids

Alternative Parents

Substituents

Ergostane-skeleton
Steroid ester
11-hydroxysteroid
11-alpha-hydroxysteroid
Hydroxysteroid
2-hydroxysteroid
Dicarboxylic acid or derivatives
Cyclic alcohol
Secondary alcohol
Carboxylic acid ester
Carboxylic acid derivative
Organic oxygen compound
Organic oxide
Hydrocarbon derivative
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	5	ChemAxon
pKa (Strongest Acidic)	13.42	ChemAxon
pKa (Strongest Basic)	-3.2	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	4	ChemAxon
Hydrogen Donor Count	2	ChemAxon
Polar Surface Area	93.06 Å²	ChemAxon
Rotatable Bond Count	9	ChemAxon
Refractivity	156.78 m³·mol⁻¹	ChemAxon
Polarizability	65.35 Å³	ChemAxon
Number of Rings	4	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

78442248

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

139587717

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for (1s,5as,7s,8s,9ar,10s,11s,11as)-7-(acetyloxy)-8,10-dihydroxy-6,6,9a,11a-tetramethyl-1-[(2s)-6-methyl-5-methylideneheptan-2-yl]-1h,2h,4h,5h,5ah,7h,8h,9h,10h,11h-cyclopenta[a]phenanthren-11-yl acetate (NP0234867)

MOL for NP0234867 ((1s,5as,7s,8s,9ar,10s,11s,11as)-7-(acetyloxy)-8,10-dihydroxy-6,6,9a,11a-tetramethyl-1-[(2s)-6-methyl-5-methylideneheptan-2-yl]-1h,2h,4h,5h,5ah,7h,8h,9h,10h,11h-cyclopenta[a]phenanthren-11-yl acetate)

3D MOL for NP0234867 ((1s,5as,7s,8s,9ar,10s,11s,11as)-7-(acetyloxy)-8,10-dihydroxy-6,6,9a,11a-tetramethyl-1-[(2s)-6-methyl-5-methylideneheptan-2-yl]-1h,2h,4h,5h,5ah,7h,8h,9h,10h,11h-cyclopenta[a]phenanthren-11-yl acetate)

3D SDF for NP0234867 ((1s,5as,7s,8s,9ar,10s,11s,11as)-7-(acetyloxy)-8,10-dihydroxy-6,6,9a,11a-tetramethyl-1-[(2s)-6-methyl-5-methylideneheptan-2-yl]-1h,2h,4h,5h,5ah,7h,8h,9h,10h,11h-cyclopenta[a]phenanthren-11-yl acetate)

3D-SDF for NP0234867 ((1s,5as,7s,8s,9ar,10s,11s,11as)-7-(acetyloxy)-8,10-dihydroxy-6,6,9a,11a-tetramethyl-1-[(2s)-6-methyl-5-methylideneheptan-2-yl]-1h,2h,4h,5h,5ah,7h,8h,9h,10h,11h-cyclopenta[a]phenanthren-11-yl acetate)

PDB for NP0234867 ((1s,5as,7s,8s,9ar,10s,11s,11as)-7-(acetyloxy)-8,10-dihydroxy-6,6,9a,11a-tetramethyl-1-[(2s)-6-methyl-5-methylideneheptan-2-yl]-1h,2h,4h,5h,5ah,7h,8h,9h,10h,11h-cyclopenta[a]phenanthren-11-yl acetate)

3D PDB for NP0234867 ((1s,5as,7s,8s,9ar,10s,11s,11as)-7-(acetyloxy)-8,10-dihydroxy-6,6,9a,11a-tetramethyl-1-[(2s)-6-methyl-5-methylideneheptan-2-yl]-1h,2h,4h,5h,5ah,7h,8h,9h,10h,11h-cyclopenta[a]phenanthren-11-yl acetate)

SMILES for NP0234867 ((1s,5as,7s,8s,9ar,10s,11s,11as)-7-(acetyloxy)-8,10-dihydroxy-6,6,9a,11a-tetramethyl-1-[(2s)-6-methyl-5-methylideneheptan-2-yl]-1h,2h,4h,5h,5ah,7h,8h,9h,10h,11h-cyclopenta[a]phenanthren-11-yl acetate)

INCHI for NP0234867 ((1s,5as,7s,8s,9ar,10s,11s,11as)-7-(acetyloxy)-8,10-dihydroxy-6,6,9a,11a-tetramethyl-1-[(2s)-6-methyl-5-methylideneheptan-2-yl]-1h,2h,4h,5h,5ah,7h,8h,9h,10h,11h-cyclopenta[a]phenanthren-11-yl acetate)

Structure for NP0234867 ((1s,5as,7s,8s,9ar,10s,11s,11as)-7-(acetyloxy)-8,10-dihydroxy-6,6,9a,11a-tetramethyl-1-[(2s)-6-methyl-5-methylideneheptan-2-yl]-1h,2h,4h,5h,5ah,7h,8h,9h,10h,11h-cyclopenta[a]phenanthren-11-yl acetate)

3D Structure for NP0234867 ((1s,5as,7s,8s,9ar,10s,11s,11as)-7-(acetyloxy)-8,10-dihydroxy-6,6,9a,11a-tetramethyl-1-[(2s)-6-methyl-5-methylideneheptan-2-yl]-1h,2h,4h,5h,5ah,7h,8h,9h,10h,11h-cyclopenta[a]phenanthren-11-yl acetate)