NP-MRD: Showing NP-Card for 2-(dimethylcarbamoyl)-3a-hydroxy-8a-(3-hydroxy-4-methoxyphenyl)-4,6-dimethoxy-1-phenyl-1h,2h,3h,8h-cyclopenta[a]inden-3-yl acetate (NP0325038)

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Record Information

Version

2.0

Created at

2022-09-12 05:29:35 UTC

Updated at

2022-09-12 05:29:35 UTC

NP-MRD ID

NP0325038

Secondary Accession Numbers

None

Natural Product Identification

Common Name

2-(dimethylcarbamoyl)-3a-hydroxy-8a-(3-hydroxy-4-methoxyphenyl)-4,6-dimethoxy-1-phenyl-1h,2h,3h,8h-cyclopenta[a]inden-3-yl acetate

Description

2-(Dimethylcarbamoyl)-3a-hydroxy-8a-(3-hydroxy-4-methoxyphenyl)-4,6-dimethoxy-1-phenyl-1H,2H,3H,3aH,8H,8aH-cyclopenta[a]inden-3-yl acetate belongs to the class of organic compounds known as stilbenes. These are organic compounds containing a 1,2-diphenylethylene moiety. Stilbenes (C6-C2-C6 ) are derived from the common phenylpropene (C6-C3) skeleton building block. The introduction of one or more hydroxyl groups to a phenyl ring lead to stilbenoids. 2-(dimethylcarbamoyl)-3a-hydroxy-8a-(3-hydroxy-4-methoxyphenyl)-4,6-dimethoxy-1-phenyl-1h,2h,3h,8h-cyclopenta[a]inden-3-yl acetate is found in Aglaia odorata. 2-(Dimethylcarbamoyl)-3a-hydroxy-8a-(3-hydroxy-4-methoxyphenyl)-4,6-dimethoxy-1-phenyl-1H,2H,3H,3aH,8H,8aH-cyclopenta[a]inden-3-yl acetate is an extremely weak basic (essentially neutral) compound (based on its pKa).

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1533004181502222D          

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M  END

     RDKit          3D

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M  END


  Mrv1533004181502222D          

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    4.1148    1.4437    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0448    2.2657    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7216    2.7374    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.4685    2.3870    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.5386    1.5650    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.8617    1.0933    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8835    1.7677    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6937    1.9233    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9640    2.7028    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4242    3.3266    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6945    4.1061    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.1547    4.7299    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6140    3.1710    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0741    3.7949    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.3436    2.3916    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
  4  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
 11 12  1  0  0  0  0
 12 13  2  0  0  0  0
 12 14  1  0  0  0  0
 10 15  1  0  0  0  0
  7 15  1  0  0  0  0
 15 16  1  0  0  0  0
 15 17  1  0  0  0  0
  5 17  2  0  0  0  0
 17 18  1  0  0  0  0
 18 19  1  0  0  0  0
 19 20  1  0  0  0  0
 18 21  2  0  0  0  0
  3 21  1  0  0  0  0
  9 22  1  0  0  0  0
 22 23  2  0  0  0  0
 22 24  1  0  0  0  0
 24 25  1  0  0  0  0
 24 26  1  0  0  0  0
  8 27  1  0  0  0  0
 27 28  2  0  0  0  0
 28 29  1  0  0  0  0
 29 30  2  0  0  0  0
 30 31  1  0  0  0  0
 31 32  2  0  0  0  0
 27 32  1  0  0  0  0
  7 33  1  0  0  0  0
 33 34  2  0  0  0  0
 34 35  1  0  0  0  0
 35 36  2  0  0  0  0
 36 37  1  0  0  0  0
 37 38  1  0  0  0  0
 36 39  1  0  0  0  0
 39 40  1  0  0  0  0
 39 41  2  0  0  0  0
 33 41  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0325038

> <DATABASE_NAME>
NP-MRD

> <SMILES>
COC1=CC2=C(C(OC)=C1)C1(O)C(OC(C)=O)C(C(C3=CC=CC=C3)C1(C2)C1=CC=C(OC)C(O)=C1)C(=O)N(C)C

> <INCHI_IDENTIFIER>
InChI=1S/C32H35NO8/c1-18(34)41-29-26(30(36)33(2)3)28(19-10-8-7-9-11-19)31(21-12-13-24(39-5)23(35)15-21)17-20-14-22(38-4)16-25(40-6)27(20)32(29,31)37/h7-16,26,28-29,35,37H,17H2,1-6H3

> <INCHI_KEY>
QLGZRYAIVAWYFO-UHFFFAOYSA-N

> <FORMULA>
C32H35NO8

> <MOLECULAR_WEIGHT>
561.631

> <EXACT_MASS>
561.236267091

> <JCHEM_ACCEPTOR_COUNT>
7

> <JCHEM_ATOM_COUNT>
76

> <JCHEM_AVERAGE_POLARIZABILITY>
59.26373382732511

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
2

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
2-(dimethylcarbamoyl)-3a-hydroxy-8a-(3-hydroxy-4-methoxyphenyl)-4,6-dimethoxy-1-phenyl-1H,2H,3H,3aH,8H,8aH-cyclopenta[a]inden-3-yl acetate

> <ALOGPS_LOGP>
4.06

> <JCHEM_LOGP>
2.995798344333333

> <ALOGPS_LOGS>
-4.80

> <JCHEM_MDDR_LIKE_RULE>
1

> <JCHEM_NUMBER_OF_RINGS>
5

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
12.502810563909811

> <JCHEM_PKA_STRONGEST_ACIDIC>
9.86667941578938

> <JCHEM_PKA_STRONGEST_BASIC>
-1.3182060762054508

> <JCHEM_POLAR_SURFACE_AREA>
114.76

> <JCHEM_REFRACTIVITY>
151.00799999999998

> <JCHEM_ROTATABLE_BOND_COUNT>
8

> <JCHEM_RULE_OF_FIVE>
0

> <ALOGPS_SOLUBILITY>
8.89e-03 g/l

> <JCHEM_TRADITIONAL_IUPAC>
2-(dimethylcarbamoyl)-3a-hydroxy-8a-(3-hydroxy-4-methoxyphenyl)-4,6-dimethoxy-1-phenyl-1H,2H,3H,8H-cyclopenta[a]inden-3-yl acetate

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 18-APR-15   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   18-APR-15         0                                  
HETATM    1  C   UNK     0      -2.719   0.346   0.000  0.00  0.00           C+0
HETATM    2  O   UNK     0      -1.666   1.470   0.000  0.00  0.00           O+0
HETATM    3  C   UNK     0      -0.166   1.120   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       0.887   2.244   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       2.387   1.894   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       3.650   2.774   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       4.878   1.845   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       6.417   1.814   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       6.864   0.341   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       5.601  -0.540   0.000  0.00  0.00           C+0
HETATM   11  O   UNK     0       5.571  -2.079   0.000  0.00  0.00           O+0
HETATM   12  C   UNK     0       6.889  -2.876   0.000  0.00  0.00           C+0
HETATM   13  O   UNK     0       6.858  -4.415   0.000  0.00  0.00           O+0
HETATM   14  C   UNK     0       8.237  -2.132   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       4.373   0.390   0.000  0.00  0.00           C+0
HETATM   16  O   UNK     0       3.868  -1.065   0.000  0.00  0.00           O+0
HETATM   17  C   UNK     0       2.833   0.420   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       1.781  -0.704   0.000  0.00  0.00           C+0
HETATM   19  O   UNK     0       2.228  -2.177   0.000  0.00  0.00           O+0
HETATM   20  C   UNK     0       1.175  -3.301   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0       0.281  -0.354   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0       8.319  -0.164   0.000  0.00  0.00           C+0
HETATM   23  O   UNK     0       9.484   0.844   0.000  0.00  0.00           O+0
HETATM   24  N   UNK     0       8.610  -1.676   0.000  0.00  0.00           N+0
HETATM   25  C   UNK     0      10.065  -2.181   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0       8.741  -3.211   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0       7.681   2.695   0.000  0.00  0.00           C+0
HETATM   28  C   UNK     0       7.550   4.229   0.000  0.00  0.00           C+0
HETATM   29  C   UNK     0       8.814   5.110   0.000  0.00  0.00           C+0
HETATM   30  C   UNK     0      10.208   4.456   0.000  0.00  0.00           C+0
HETATM   31  C   UNK     0      10.339   2.921   0.000  0.00  0.00           C+0
HETATM   32  C   UNK     0       9.075   2.041   0.000  0.00  0.00           C+0
HETATM   33  C   UNK     0       5.382   3.300   0.000  0.00  0.00           C+0
HETATM   34  C   UNK     0       6.895   3.590   0.000  0.00  0.00           C+0
HETATM   35  C   UNK     0       7.399   5.045   0.000  0.00  0.00           C+0
HETATM   36  C   UNK     0       6.392   6.210   0.000  0.00  0.00           C+0
HETATM   37  O   UNK     0       6.896   7.665   0.000  0.00  0.00           O+0
HETATM   38  C   UNK     0       5.889   8.829   0.000  0.00  0.00           C+0
HETATM   39  C   UNK     0       4.879   5.919   0.000  0.00  0.00           C+0
HETATM   40  O   UNK     0       3.872   7.084   0.000  0.00  0.00           O+0
HETATM   41  C   UNK     0       4.375   4.464   0.000  0.00  0.00           C+0
CONECT    1    2                                                            
CONECT    2    1    3                                                       
CONECT    3    2    4   21                                                  
CONECT    4    3    5                                                       
CONECT    5    4    6   17                                                  
CONECT    6    5    7                                                       
CONECT    7    6    8   15   33                                             
CONECT    8    7    9   27                                                  
CONECT    9    8   10   22                                                  
CONECT   10    9   11   15                                                  
CONECT   11   10   12                                                       
CONECT   12   11   13   14                                                  
CONECT   13   12                                                            
CONECT   14   12                                                            
CONECT   15   10    7   16   17                                             
CONECT   16   15                                                            
CONECT   17   15    5   18                                                  
CONECT   18   17   19   21                                                  
CONECT   19   18   20                                                       
CONECT   20   19                                                            
CONECT   21   18    3                                                       
CONECT   22    9   23   24                                                  
CONECT   23   22                                                            
CONECT   24   22   25   26                                                  
CONECT   25   24                                                            
CONECT   26   24                                                            
CONECT   27    8   28   32                                                  
CONECT   28   27   29                                                       
CONECT   29   28   30                                                       
CONECT   30   29   31                                                       
CONECT   31   30   32                                                       
CONECT   32   31   27                                                       
CONECT   33    7   34   41                                                  
CONECT   34   33   35                                                       
CONECT   35   34   36                                                       
CONECT   36   35   37   39                                                  
CONECT   37   36   38                                                       
CONECT   38   37                                                            
CONECT   39   36   40   41                                                  
CONECT   40   39                                                            
CONECT   41   39   33                                                       
MASTER        0    0    0    0    0    0    0    0   41    0   90    0
END

View in JSmol

Synonyms

Value	Source
2-(Dimethylcarbamoyl)-3a-hydroxy-8a-(3-hydroxy-4-methoxyphenyl)-4,6-dimethoxy-1-phenyl-1H,2H,3H,3ah,8H,8ah-cyclopenta[a]inden-3-yl acetic acid	Generator

Chemical Formula

C₃₂H₃₅NO₈

Average Mass

561.6310 Da

Monoisotopic Mass

561.23627 Da

IUPAC Name

2-(dimethylcarbamoyl)-3a-hydroxy-8a-(3-hydroxy-4-methoxyphenyl)-4,6-dimethoxy-1-phenyl-1H,2H,3H,3aH,8H,8aH-cyclopenta[a]inden-3-yl acetate

Traditional Name

2-(dimethylcarbamoyl)-3a-hydroxy-8a-(3-hydroxy-4-methoxyphenyl)-4,6-dimethoxy-1-phenyl-1H,2H,3H,8H-cyclopenta[a]inden-3-yl acetate

CAS Registry Number

Not Available

SMILES

COC1=CC2=C(C(OC)=C1)C1(O)C(OC(C)=O)C(C(C3=CC=CC=C3)C1(C2)C1=CC=C(OC)C(O)=C1)C(=O)N(C)C

InChI Identifier

InChI=1S/C32H35NO8/c1-18(34)41-29-26(30(36)33(2)3)28(19-10-8-7-9-11-19)31(21-12-13-24(39-5)23(35)15-21)17-20-14-22(38-4)16-25(40-6)27(20)32(29,31)37/h7-16,26,28-29,35,37H,17H2,1-6H3

InChI Key

QLGZRYAIVAWYFO-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
Aglaia odorata	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as stilbenes. These are organic compounds containing a 1,2-diphenylethylene moiety. Stilbenes (C6-C2-C6 ) are derived from the common phenylpropene (C6-C3) skeleton building block. The introduction of one or more hydroxyl groups to a phenyl ring lead to stilbenoids.

Kingdom

Organic compounds

Super Class

Phenylpropanoids and polyketides

Class

Stilbenes

Sub Class

Not Available

Direct Parent

Stilbenes

Alternative Parents

Substituents

Stilbene
Aromatic monoterpenoid
11-noriridane monoterpenoid
Methoxyphenol
Monoterpenoid
Indane
Phenoxy compound
Anisole
Methoxybenzene
Phenol ether
Alkyl aryl ether
1-hydroxy-4-unsubstituted benzenoid
1-hydroxy-2-unsubstituted benzenoid
Phenol
Monocyclic benzene moiety
Benzenoid
Tertiary carboxylic acid amide
Tertiary alcohol
Cyclic alcohol
Carboxylic acid ester
Carboxamide group
Carboxylic acid derivative
Ether
Monocarboxylic acid or derivatives
Organooxygen compound
Alcohol
Hydrocarbon derivative
Carbonyl group
Organic oxide
Organopnictogen compound
Organonitrogen compound
Organic nitrogen compound
Organic oxygen compound
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	4.06	ALOGPS
logP	3	ChemAxon
logS	-4.8	ALOGPS
pKa (Strongest Acidic)	9.87	ChemAxon
pKa (Strongest Basic)	-1.3	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	7	ChemAxon
Hydrogen Donor Count	2	ChemAxon
Polar Surface Area	114.76 Å²	ChemAxon
Rotatable Bond Count	8	ChemAxon
Refractivity	151.01 m³·mol⁻¹	ChemAxon
Polarizability	59.26 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

Not Available

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for 2-(dimethylcarbamoyl)-3a-hydroxy-8a-(3-hydroxy-4-methoxyphenyl)-4,6-dimethoxy-1-phenyl-1h,2h,3h,8h-cyclopenta[a]inden-3-yl acetate (NP0325038)

MOL for NP0325038 (2-(dimethylcarbamoyl)-3a-hydroxy-8a-(3-hydroxy-4-methoxyphenyl)-4,6-dimethoxy-1-phenyl-1h,2h,3h,8h-cyclopenta[a]inden-3-yl acetate)

3D MOL for NP0325038 (2-(dimethylcarbamoyl)-3a-hydroxy-8a-(3-hydroxy-4-methoxyphenyl)-4,6-dimethoxy-1-phenyl-1h,2h,3h,8h-cyclopenta[a]inden-3-yl acetate)

3D SDF for NP0325038 (2-(dimethylcarbamoyl)-3a-hydroxy-8a-(3-hydroxy-4-methoxyphenyl)-4,6-dimethoxy-1-phenyl-1h,2h,3h,8h-cyclopenta[a]inden-3-yl acetate)

3D-SDF for NP0325038 (2-(dimethylcarbamoyl)-3a-hydroxy-8a-(3-hydroxy-4-methoxyphenyl)-4,6-dimethoxy-1-phenyl-1h,2h,3h,8h-cyclopenta[a]inden-3-yl acetate)

PDB for NP0325038 (2-(dimethylcarbamoyl)-3a-hydroxy-8a-(3-hydroxy-4-methoxyphenyl)-4,6-dimethoxy-1-phenyl-1h,2h,3h,8h-cyclopenta[a]inden-3-yl acetate)

3D PDB for NP0325038 (2-(dimethylcarbamoyl)-3a-hydroxy-8a-(3-hydroxy-4-methoxyphenyl)-4,6-dimethoxy-1-phenyl-1h,2h,3h,8h-cyclopenta[a]inden-3-yl acetate)

SMILES for NP0325038 (2-(dimethylcarbamoyl)-3a-hydroxy-8a-(3-hydroxy-4-methoxyphenyl)-4,6-dimethoxy-1-phenyl-1h,2h,3h,8h-cyclopenta[a]inden-3-yl acetate)

INCHI for NP0325038 (2-(dimethylcarbamoyl)-3a-hydroxy-8a-(3-hydroxy-4-methoxyphenyl)-4,6-dimethoxy-1-phenyl-1h,2h,3h,8h-cyclopenta[a]inden-3-yl acetate)

Structure for NP0325038 (2-(dimethylcarbamoyl)-3a-hydroxy-8a-(3-hydroxy-4-methoxyphenyl)-4,6-dimethoxy-1-phenyl-1h,2h,3h,8h-cyclopenta[a]inden-3-yl acetate)

3D Structure for NP0325038 (2-(dimethylcarbamoyl)-3a-hydroxy-8a-(3-hydroxy-4-methoxyphenyl)-4,6-dimethoxy-1-phenyl-1h,2h,3h,8h-cyclopenta[a]inden-3-yl acetate)