NP-MRD: Showing NP-Card for (1s,3br,4s,5r,5ar,9ar,9br,11as)-5-methoxy-3b,6,6,9a,11a-pentamethyl-2,7-dioxo-1-[(2s)-1-oxobutan-2-yl]-1h,4h,5h,5ah,9bh,10h,11h-cyclopenta[a]phenanthren-4-yl acetate (NP0215157)

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Record Information

Version

2.0

Created at

2022-09-05 14:39:48 UTC

Updated at

2022-09-05 14:39:48 UTC

NP-MRD ID

NP0215157

Secondary Accession Numbers

None

Natural Product Identification

Common Name

(1s,3br,4s,5r,5ar,9ar,9br,11as)-5-methoxy-3b,6,6,9a,11a-pentamethyl-2,7-dioxo-1-[(2s)-1-oxobutan-2-yl]-1h,4h,5h,5ah,9bh,10h,11h-cyclopenta[a]phenanthren-4-yl acetate

Description

(1R,2R,7R,8R,9S,10R,14S,15S)-8-methoxy-2,6,6,10,15-pentamethyl-5,13-dioxo-14-[(2S)-1-oxobutan-2-yl]tetracyclo[8.7.0.0²,⁷.0¹¹,¹⁵]Heptadeca-3,11-dien-9-yl acetate belongs to the class of organic compounds known as bile acids, alcohols and derivatives. These are organic compounds containing an alcohol or acid derivative of cholic acid. (1s,3br,4s,5r,5ar,9ar,9br,11as)-5-methoxy-3b,6,6,9a,11a-pentamethyl-2,7-dioxo-1-[(2s)-1-oxobutan-2-yl]-1h,4h,5h,5ah,9bh,10h,11h-cyclopenta[a]phenanthren-4-yl acetate is found in Azadirachta indica. Based on a literature review very few articles have been published on (1R,2R,7R,8R,9S,10R,14S,15S)-8-methoxy-2,6,6,10,15-pentamethyl-5,13-dioxo-14-[(2S)-1-oxobutan-2-yl]tetracyclo[8.7.0.0²,⁷.0¹¹,¹⁵]Heptadeca-3,11-dien-9-yl acetate.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652309052216392D          

 35 38  0  0  1  0            999 V2000
    4.1657    2.4949    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.9830    2.3821    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
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    6.6175    2.1564    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.7875    0.9666    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    5.0168    0.1741    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7927   -0.1062    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
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M  END

     RDKit          3D

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M  END


  Mrv1652309052216392D          

 35 38  0  0  1  0            999 V2000
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    0.9948    1.1884    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5266    0.5577    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.8069    1.3336    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0  0  0  0
  3  2  1  6  0  0  0
  3  4  1  0  0  0  0
  4  5  2  0  0  0  0
  6  3  1  6  0  0  0
  6  7  1  0  0  0  0
  7  8  2  0  0  0  0
  7  9  1  0  0  0  0
  9 10  2  0  0  0  0
 10 11  1  0  0  0  0
  6 11  1  0  0  0  0
 11 12  1  6  0  0  0
 11 13  1  0  0  0  0
 13 14  1  0  0  0  0
 15 14  1  1  0  0  0
 15 16  1  0  0  0  0
 10 16  1  0  0  0  0
 16 17  1  1  0  0  0
 16 18  1  0  0  0  0
 18 19  1  6  0  0  0
 19 20  1  0  0  0  0
 20 21  1  0  0  0  0
 20 22  2  0  0  0  0
 18 23  1  0  0  0  0
 23 24  1  6  0  0  0
 24 25  1  0  0  0  0
 26 23  1  1  0  0  0
 26 27  1  0  0  0  0
 27 28  1  0  0  0  0
 27 29  1  0  0  0  0
 27 30  1  0  0  0  0
 30 31  2  0  0  0  0
 30 32  1  0  0  0  0
 32 33  2  0  0  0  0
 33 34  1  0  0  0  0
 26 34  1  0  0  0  0
 15 34  1  0  0  0  0
 34 35  1  1  0  0  0
M  END
> <DATABASE_ID>
NP0215157

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CC[C@H](C=O)[C@@H]1C(=O)C=C2[C@@]1(C)CC[C@@H]1[C@@]3(C)C=CC(=O)C(C)(C)[C@@H]3[C@@H](OC)[C@@H](OC(C)=O)[C@@]21C

> <INCHI_IDENTIFIER>
InChI=1S/C29H40O6/c1-9-17(15-30)22-18(32)14-20-27(22,5)12-10-19-28(6)13-11-21(33)26(3,4)24(28)23(34-8)25(29(19,20)7)35-16(2)31/h11,13-15,17,19,22-25H,9-10,12H2,1-8H3/t17-,19-,22-,23-,24+,25-,27-,28-,29-/m1/s1

> <INCHI_KEY>
YNXQXJIXLIRWJC-CPUFNKEJSA-N

> <FORMULA>
C29H40O6

> <MOLECULAR_WEIGHT>
484.633

> <EXACT_MASS>
484.282489008

> <JCHEM_ACCEPTOR_COUNT>
5

> <JCHEM_ATOM_COUNT>
75

> <JCHEM_AVERAGE_POLARIZABILITY>
53.697624251731874

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
0

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
(1R,2R,7R,8R,9S,10R,14S,15S)-8-methoxy-2,6,6,10,15-pentamethyl-5,13-dioxo-14-[(2S)-1-oxobutan-2-yl]tetracyclo[8.7.0.0^{2,7}.0^{11,15}]heptadeca-3,11-dien-9-yl acetate

> <JCHEM_LOGP>
4.166630668666669

> <JCHEM_MDDR_LIKE_RULE>
1

> <JCHEM_NUMBER_OF_RINGS>
4

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA_STRONGEST_ACIDIC>
15.94143508947089

> <JCHEM_PKA_STRONGEST_BASIC>
-4.07557991807168

> <JCHEM_POLAR_SURFACE_AREA>
86.74000000000001

> <JCHEM_REFRACTIVITY>
133.9933

> <JCHEM_ROTATABLE_BOND_COUNT>
6

> <JCHEM_RULE_OF_FIVE>
1

> <JCHEM_TRADITIONAL_IUPAC>
(1R,2R,7R,8R,9S,10R,14S,15S)-8-methoxy-2,6,6,10,15-pentamethyl-5,13-dioxo-14-[(2S)-1-oxobutan-2-yl]tetracyclo[8.7.0.0^{2,7}.0^{11,15}]heptadeca-3,11-dien-9-yl acetate

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 05-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   05-SEP-22         0                                  
HETATM    1  C   UNK     0       7.776   4.657   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       9.302   4.447   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       9.882   3.020   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0      11.407   2.809   0.000  0.00  0.00           C+0
HETATM    5  O   UNK     0      12.353   4.025   0.000  0.00  0.00           O+0
HETATM    6  C   UNK     0       8.937   1.804   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       9.365   0.325   0.000  0.00  0.00           C+0
HETATM    8  O   UNK     0      10.813  -0.198   0.000  0.00  0.00           O+0
HETATM    9  C   UNK     0       8.090  -0.539   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       6.874   0.406   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       7.398   1.854   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       8.069   3.240   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       6.405   3.032   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       4.889   2.761   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       4.366   1.312   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       5.358   0.135   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       6.351  -1.043   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       4.835  -1.314   0.000  0.00  0.00           C+0
HETATM   19  O   UNK     0       5.828  -2.491   0.000  0.00  0.00           O+0
HETATM   20  C   UNK     0       5.305  -3.939   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0       6.297  -5.117   0.000  0.00  0.00           C+0
HETATM   22  O   UNK     0       3.789  -4.210   0.000  0.00  0.00           O+0
HETATM   23  C   UNK     0       3.319  -1.585   0.000  0.00  0.00           C+0
HETATM   24  O   UNK     0       2.796  -3.033   0.000  0.00  0.00           O+0
HETATM   25  C   UNK     0       1.280  -3.304   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0       2.326  -0.407   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0       0.810  -0.678   0.000  0.00  0.00           C+0
HETATM   28  C   UNK     0      -0.521  -1.452   0.000  0.00  0.00           C+0
HETATM   29  C   UNK     0       1.341  -2.124   0.000  0.00  0.00           C+0
HETATM   30  C   UNK     0      -0.182   0.499   0.000  0.00  0.00           C+0
HETATM   31  O   UNK     0      -1.698   0.228   0.000  0.00  0.00           O+0
HETATM   32  C   UNK     0       0.341   1.947   0.000  0.00  0.00           C+0
HETATM   33  C   UNK     0       1.857   2.218   0.000  0.00  0.00           C+0
HETATM   34  C   UNK     0       2.850   1.041   0.000  0.00  0.00           C+0
HETATM   35  C   UNK     0       3.373   2.489   0.000  0.00  0.00           C+0
CONECT    1    2                                                            
CONECT    2    1    3                                                       
CONECT    3    2    4    6                                                  
CONECT    4    3    5                                                       
CONECT    5    4                                                            
CONECT    6    3    7   11                                                  
CONECT    7    6    8    9                                                  
CONECT    8    7                                                            
CONECT    9    7   10                                                       
CONECT   10    9   11   16                                                  
CONECT   11   10    6   12   13                                             
CONECT   12   11                                                            
CONECT   13   11   14                                                       
CONECT   14   13   15                                                       
CONECT   15   14   16   34                                                  
CONECT   16   15   10   17   18                                             
CONECT   17   16                                                            
CONECT   18   16   19   23                                                  
CONECT   19   18   20                                                       
CONECT   20   19   21   22                                                  
CONECT   21   20                                                            
CONECT   22   20                                                            
CONECT   23   18   24   26                                                  
CONECT   24   23   25                                                       
CONECT   25   24                                                            
CONECT   26   23   27   34                                                  
CONECT   27   26   28   29   30                                             
CONECT   28   27                                                            
CONECT   29   27                                                            
CONECT   30   27   31   32                                                  
CONECT   31   30                                                            
CONECT   32   30   33                                                       
CONECT   33   32   34                                                       
CONECT   34   33   26   15   35                                             
CONECT   35   34                                                            
MASTER        0    0    0    0    0    0    0    0   35    0   76    0
END

View in JSmol

Synonyms

Value	Source
(1R,2R,7R,8R,9S,10R,14S,15S)-8-Methoxy-2,6,6,10,15-pentamethyl-5,13-dioxo-14-[(2S)-1-oxobutan-2-yl]tetracyclo[8.7.0.0,.0,]heptadeca-3,11-dien-9-yl acetic acid	Generator

Chemical Formula

C₂₉H₄₀O₆

Average Mass

484.6330 Da

Monoisotopic Mass

484.28249 Da

IUPAC Name

(1R,2R,7R,8R,9S,10R,14S,15S)-8-methoxy-2,6,6,10,15-pentamethyl-5,13-dioxo-14-[(2S)-1-oxobutan-2-yl]tetracyclo[8.7.0.0^{2,7}.0^{11,15}]heptadeca-3,11-dien-9-yl acetate

Traditional Name

(1R,2R,7R,8R,9S,10R,14S,15S)-8-methoxy-2,6,6,10,15-pentamethyl-5,13-dioxo-14-[(2S)-1-oxobutan-2-yl]tetracyclo[8.7.0.0^{2,7}.0^{11,15}]heptadeca-3,11-dien-9-yl acetate

CAS Registry Number

Not Available

SMILES

CC[C@H](C=O)[C@@H]1C(=O)C=C2[C@@]1(C)CC[C@@H]1[C@@]3(C)C=CC(=O)C(C)(C)[C@@H]3[C@@H](OC)[C@@H](OC(C)=O)[C@@]21C

InChI Identifier

InChI=1S/C29H40O6/c1-9-17(15-30)22-18(32)14-20-27(22,5)12-10-19-28(6)13-11-21(33)26(3,4)24(28)23(34-8)25(29(19,20)7)35-16(2)31/h11,13-15,17,19,22-25H,9-10,12H2,1-8H3/t17-,19-,22-,23-,24+,25-,27-,28-,29-/m1/s1

InChI Key

YNXQXJIXLIRWJC-CPUFNKEJSA-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
Azadirachta indica	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as bile acids, alcohols and derivatives. These are organic compounds containing an alcohol or acid derivative of cholic acid.

Kingdom

Organic compounds

Super Class

Lipids and lipid-like molecules

Class

Steroids and steroid derivatives

Sub Class

Bile acids, alcohols and derivatives

Direct Parent

Bile acids, alcohols and derivatives

Alternative Parents

Substituents

Bile acid, alcohol, or derivatives
22-oxosteroid
21-oxosteroid
Steroid ester
3-oxo-delta-1-steroid
3-oxosteroid
3-oxo-5-alpha-steroid
Oxosteroid
16-oxosteroid
Delta-1-steroid
Cyclohexenone
Cyclic ketone
Carboxylic acid ester
Ketone
Carboxylic acid derivative
Monocarboxylic acid or derivatives
Dialkyl ether
Ether
Organic oxygen compound
Carbonyl group
Hydrocarbon derivative
Organooxygen compound
Organic oxide
Aldehyde
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	4.17	ChemAxon
pKa (Strongest Acidic)	15.94	ChemAxon
pKa (Strongest Basic)	-4.1	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	5	ChemAxon
Hydrogen Donor Count	0	ChemAxon
Polar Surface Area	86.74 Å²	ChemAxon
Rotatable Bond Count	6	ChemAxon
Refractivity	133.99 m³·mol⁻¹	ChemAxon
Polarizability	53.7 Å³	ChemAxon
Number of Rings	4	ChemAxon
Bioavailability	Yes	ChemAxon
Rule of Five	Yes	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

163082705

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for (1s,3br,4s,5r,5ar,9ar,9br,11as)-5-methoxy-3b,6,6,9a,11a-pentamethyl-2,7-dioxo-1-[(2s)-1-oxobutan-2-yl]-1h,4h,5h,5ah,9bh,10h,11h-cyclopenta[a]phenanthren-4-yl acetate (NP0215157)

MOL for NP0215157 ((1s,3br,4s,5r,5ar,9ar,9br,11as)-5-methoxy-3b,6,6,9a,11a-pentamethyl-2,7-dioxo-1-[(2s)-1-oxobutan-2-yl]-1h,4h,5h,5ah,9bh,10h,11h-cyclopenta[a]phenanthren-4-yl acetate)

3D MOL for NP0215157 ((1s,3br,4s,5r,5ar,9ar,9br,11as)-5-methoxy-3b,6,6,9a,11a-pentamethyl-2,7-dioxo-1-[(2s)-1-oxobutan-2-yl]-1h,4h,5h,5ah,9bh,10h,11h-cyclopenta[a]phenanthren-4-yl acetate)

3D SDF for NP0215157 ((1s,3br,4s,5r,5ar,9ar,9br,11as)-5-methoxy-3b,6,6,9a,11a-pentamethyl-2,7-dioxo-1-[(2s)-1-oxobutan-2-yl]-1h,4h,5h,5ah,9bh,10h,11h-cyclopenta[a]phenanthren-4-yl acetate)

3D-SDF for NP0215157 ((1s,3br,4s,5r,5ar,9ar,9br,11as)-5-methoxy-3b,6,6,9a,11a-pentamethyl-2,7-dioxo-1-[(2s)-1-oxobutan-2-yl]-1h,4h,5h,5ah,9bh,10h,11h-cyclopenta[a]phenanthren-4-yl acetate)

PDB for NP0215157 ((1s,3br,4s,5r,5ar,9ar,9br,11as)-5-methoxy-3b,6,6,9a,11a-pentamethyl-2,7-dioxo-1-[(2s)-1-oxobutan-2-yl]-1h,4h,5h,5ah,9bh,10h,11h-cyclopenta[a]phenanthren-4-yl acetate)

3D PDB for NP0215157 ((1s,3br,4s,5r,5ar,9ar,9br,11as)-5-methoxy-3b,6,6,9a,11a-pentamethyl-2,7-dioxo-1-[(2s)-1-oxobutan-2-yl]-1h,4h,5h,5ah,9bh,10h,11h-cyclopenta[a]phenanthren-4-yl acetate)

SMILES for NP0215157 ((1s,3br,4s,5r,5ar,9ar,9br,11as)-5-methoxy-3b,6,6,9a,11a-pentamethyl-2,7-dioxo-1-[(2s)-1-oxobutan-2-yl]-1h,4h,5h,5ah,9bh,10h,11h-cyclopenta[a]phenanthren-4-yl acetate)

INCHI for NP0215157 ((1s,3br,4s,5r,5ar,9ar,9br,11as)-5-methoxy-3b,6,6,9a,11a-pentamethyl-2,7-dioxo-1-[(2s)-1-oxobutan-2-yl]-1h,4h,5h,5ah,9bh,10h,11h-cyclopenta[a]phenanthren-4-yl acetate)

Structure for NP0215157 ((1s,3br,4s,5r,5ar,9ar,9br,11as)-5-methoxy-3b,6,6,9a,11a-pentamethyl-2,7-dioxo-1-[(2s)-1-oxobutan-2-yl]-1h,4h,5h,5ah,9bh,10h,11h-cyclopenta[a]phenanthren-4-yl acetate)

3D Structure for NP0215157 ((1s,3br,4s,5r,5ar,9ar,9br,11as)-5-methoxy-3b,6,6,9a,11a-pentamethyl-2,7-dioxo-1-[(2s)-1-oxobutan-2-yl]-1h,4h,5h,5ah,9bh,10h,11h-cyclopenta[a]phenanthren-4-yl acetate)