NP-MRD: Showing NP-Card for methyl (2s,3r,4r,5s,6r)-6-(3,4-dimethoxyphenyl)-2,3-dihydroxy-10,12-dimethoxy-5-phenyl-7-oxatricyclo[6.4.0.0²,⁶]dodeca-1(12),8,10-triene-4-carboxylate (NP0231190)

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Record Information

Version

2.0

Created at

2022-09-06 11:55:45 UTC

Updated at

2022-09-06 11:55:45 UTC

NP-MRD ID

NP0231190

Secondary Accession Numbers

None

Natural Product Identification

Common Name

methyl (2s,3r,4r,5s,6r)-6-(3,4-dimethoxyphenyl)-2,3-dihydroxy-10,12-dimethoxy-5-phenyl-7-oxatricyclo[6.4.0.0²,⁶]dodeca-1(12),8,10-triene-4-carboxylate

Description

(1R)-2,3-Dihydro-1,8bbeta-dihydroxy-3beta-phenyl-3abeta-(3,4-dimethoxyphenyl)-6,8-dimethoxy-1H-cyclopenta[b]benzofuran-2alpha-carboxylic acid methyl ester belongs to the class of organic compounds known as flavaglines. These are heterocyclic compounds with a structure characterized by a cyclopenta[b]benzofuran skeleton. methyl (2s,3r,4r,5s,6r)-6-(3,4-dimethoxyphenyl)-2,3-dihydroxy-10,12-dimethoxy-5-phenyl-7-oxatricyclo[6.4.0.0²,⁶]dodeca-1(12),8,10-triene-4-carboxylate is found in Aglaia spectabilis. Based on a literature review very few articles have been published on (1R)-2,3-Dihydro-1,8bbeta-dihydroxy-3beta-phenyl-3abeta-(3,4-dimethoxyphenyl)-6,8-dimethoxy-1H-cyclopenta[b]benzofuran-2alpha-carboxylic acid methyl ester.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652309062213552D          

 38 42  0  0  1  0            999 V2000
   -0.0633   -2.5357    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7162   -2.2653    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.8718   -1.4552    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2479   -0.9153    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.6512   -1.1848    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.8906   -0.3953    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.2138    0.0764    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4668   -0.2740    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2100    0.1977    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1400    1.0197    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6069    1.3701    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2838    0.8984    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7155   -0.3790    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.6992    0.4458    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4054    0.8723    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3891    1.6971    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
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  1  2  1  0  0  0  0
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  3  4  2  0  0  0  0
  5  3  1  6  0  0  0
  5  6  1  0  0  0  0
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  9 10  2  0  0  0  0
 10 11  1  0  0  0  0
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  7 12  1  0  0  0  0
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 14 23  1  0  0  0  0
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 35 36  1  1  0  0  0
 35 37  1  0  0  0  0
  5 37  1  0  0  0  0
 37 38  1  6  0  0  0
M  END

     RDKit          3D

 68 72  0  0  0  0  0  0  0  0999 V2000
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M  END


  Mrv1652309062213552D          

 38 42  0  0  1  0            999 V2000
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  9 10  2  0  0  0  0
 10 11  1  0  0  0  0
 11 12  2  0  0  0  0
  7 12  1  0  0  0  0
  6 13  1  0  0  0  0
 13 14  1  1  0  0  0
 14 15  2  0  0  0  0
 15 16  1  0  0  0  0
 16 17  2  0  0  0  0
 17 18  1  0  0  0  0
 18 19  1  0  0  0  0
 17 20  1  0  0  0  0
 20 21  1  0  0  0  0
 21 22  1  0  0  0  0
 20 23  2  0  0  0  0
 14 23  1  0  0  0  0
 13 24  1  0  0  0  0
 24 25  1  0  0  0  0
 25 26  2  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
 27 30  2  0  0  0  0
 30 31  1  0  0  0  0
 31 32  1  0  0  0  0
 32 33  1  0  0  0  0
 31 34  2  0  0  0  0
 25 34  1  0  0  0  0
 34 35  1  0  0  0  0
 13 35  1  0  0  0  0
 35 36  1  1  0  0  0
 35 37  1  0  0  0  0
  5 37  1  0  0  0  0
 37 38  1  6  0  0  0
M  END
> <DATABASE_ID>
NP0231190

> <DATABASE_NAME>
NP-MRD

> <SMILES>
COC(=O)[C@H]1[C@@H](O)[C@@]2(O)C3=C(OC)C=C(OC)C=C3O[C@]2([C@@H]1C1=CC=CC=C1)C1=CC=C(OC)C(OC)=C1

> <INCHI_IDENTIFIER>
InChI=1S/C29H30O9/c1-33-18-14-21(36-4)25-22(15-18)38-29(17-11-12-19(34-2)20(13-17)35-3)24(16-9-7-6-8-10-16)23(27(31)37-5)26(30)28(25,29)32/h6-15,23-24,26,30,32H,1-5H3/t23-,24-,26-,28+,29+/m1/s1

> <INCHI_KEY>
OWHOEKLNSDNYTQ-IDAMAFBJSA-N

> <FORMULA>
C29H30O9

> <MOLECULAR_WEIGHT>
522.55

> <EXACT_MASS>
522.188982546

> <JCHEM_ACCEPTOR_COUNT>
8

> <JCHEM_ATOM_COUNT>
68

> <JCHEM_AVERAGE_POLARIZABILITY>
53.53363718949443

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
2

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
methyl (2S,3R,4R,5S,6R)-6-(3,4-dimethoxyphenyl)-2,3-dihydroxy-10,12-dimethoxy-5-phenyl-7-oxatricyclo[6.4.0.0^{2,6}]dodeca-1(12),8,10-triene-4-carboxylate

> <JCHEM_LOGP>
2.736344814666666

> <JCHEM_MDDR_LIKE_RULE>
1

> <JCHEM_NUMBER_OF_RINGS>
5

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
14.033300949504998

> <JCHEM_PKA_STRONGEST_ACIDIC>
11.615148527373034

> <JCHEM_PKA_STRONGEST_BASIC>
-3.5729997133728704

> <JCHEM_POLAR_SURFACE_AREA>
112.91000000000003

> <JCHEM_REFRACTIVITY>
135.8782

> <JCHEM_ROTATABLE_BOND_COUNT>
8

> <JCHEM_RULE_OF_FIVE>
0

> <JCHEM_TRADITIONAL_IUPAC>
methyl (2S,3R,4R,5S,6R)-6-(3,4-dimethoxyphenyl)-2,3-dihydroxy-10,12-dimethoxy-5-phenyl-7-oxatricyclo[6.4.0.0^{2,6}]dodeca-1(12),8,10-triene-4-carboxylate

> <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      -0.118  -4.733   0.000  0.00  0.00           C+0
HETATM    2  O   UNK     0       1.337  -4.229   0.000  0.00  0.00           O+0
HETATM    3  C   UNK     0       1.627  -2.716   0.000  0.00  0.00           C+0
HETATM    4  O   UNK     0       0.463  -1.709   0.000  0.00  0.00           O+0
HETATM    5  C   UNK     0       3.082  -2.212   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       3.529  -0.738   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       2.266   0.143   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       0.871  -0.511   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0      -0.392   0.369   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0      -0.261   1.903   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       1.133   2.557   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       2.396   1.677   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       5.069  -0.708   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       5.039   0.832   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       6.357   1.628   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       6.326   3.168   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       4.978   3.912   0.000  0.00  0.00           C+0
HETATM   18  O   UNK     0       4.947   5.451   0.000  0.00  0.00           O+0
HETATM   19  C   UNK     0       6.266   6.247   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0       3.660   3.115   0.000  0.00  0.00           C+0
HETATM   21  O   UNK     0       2.311   3.859   0.000  0.00  0.00           O+0
HETATM   22  C   UNK     0       2.281   5.399   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0       3.690   1.576   0.000  0.00  0.00           C+0
HETATM   24  O   UNK     0       6.297   0.222   0.000  0.00  0.00           O+0
HETATM   25  C   UNK     0       7.560  -0.658   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0       9.060  -0.309   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0      10.113  -1.433   0.000  0.00  0.00           C+0
HETATM   28  O   UNK     0      11.612  -1.083   0.000  0.00  0.00           O+0
HETATM   29  C   UNK     0      12.665  -2.207   0.000  0.00  0.00           C+0
HETATM   30  C   UNK     0       9.666  -2.906   0.000  0.00  0.00           C+0
HETATM   31  C   UNK     0       8.166  -3.256   0.000  0.00  0.00           C+0
HETATM   32  O   UNK     0       7.719  -4.730   0.000  0.00  0.00           O+0
HETATM   33  C   UNK     0       8.772  -5.854   0.000  0.00  0.00           C+0
HETATM   34  C   UNK     0       7.113  -2.132   0.000  0.00  0.00           C+0
HETATM   35  C   UNK     0       5.574  -2.162   0.000  0.00  0.00           C+0
HETATM   36  O   UNK     0       6.078  -3.617   0.000  0.00  0.00           O+0
HETATM   37  C   UNK     0       4.346  -3.092   0.000  0.00  0.00           C+0
HETATM   38  O   UNK     0       4.376  -4.632   0.000  0.00  0.00           O+0
CONECT    1    2                                                            
CONECT    2    1    3                                                       
CONECT    3    2    4    5                                                  
CONECT    4    3                                                            
CONECT    5    3    6   37                                                  
CONECT    6    5    7   13                                                  
CONECT    7    6    8   12                                                  
CONECT    8    7    9                                                       
CONECT    9    8   10                                                       
CONECT   10    9   11                                                       
CONECT   11   10   12                                                       
CONECT   12   11    7                                                       
CONECT   13    6   14   24   35                                             
CONECT   14   13   15   23                                                  
CONECT   15   14   16                                                       
CONECT   16   15   17                                                       
CONECT   17   16   18   20                                                  
CONECT   18   17   19                                                       
CONECT   19   18                                                            
CONECT   20   17   21   23                                                  
CONECT   21   20   22                                                       
CONECT   22   21                                                            
CONECT   23   20   14                                                       
CONECT   24   13   25                                                       
CONECT   25   24   26   34                                                  
CONECT   26   25   27                                                       
CONECT   27   26   28   30                                                  
CONECT   28   27   29                                                       
CONECT   29   28                                                            
CONECT   30   27   31                                                       
CONECT   31   30   32   34                                                  
CONECT   32   31   33                                                       
CONECT   33   32                                                            
CONECT   34   31   25   35                                                  
CONECT   35   34   13   36   37                                             
CONECT   36   35                                                            
CONECT   37   35    5   38                                                  
CONECT   38   37                                                            
MASTER        0    0    0    0    0    0    0    0   38    0   84    0
END

View in JSmol

Synonyms

Value	Source
(1R)-2,3-Dihydro-1,8bbeta-dihydroxy-3b-phenyl-3abeta-(3,4-dimethoxyphenyl)-6,8-dimethoxy-1H-cyclopenta[b]benzofuran-2a-carboxylate methyl ester	Generator
(1R)-2,3-Dihydro-1,8bbeta-dihydroxy-3b-phenyl-3abeta-(3,4-dimethoxyphenyl)-6,8-dimethoxy-1H-cyclopenta[b]benzofuran-2a-carboxylic acid methyl ester	Generator
(1R)-2,3-Dihydro-1,8bbeta-dihydroxy-3beta-phenyl-3abeta-(3,4-dimethoxyphenyl)-6,8-dimethoxy-1H-cyclopenta[b]benzofuran-2alpha-carboxylate methyl ester	Generator
(1R)-2,3-Dihydro-1,8bbeta-dihydroxy-3β-phenyl-3abeta-(3,4-dimethoxyphenyl)-6,8-dimethoxy-1H-cyclopenta[b]benzofuran-2α-carboxylate methyl ester	Generator
(1R)-2,3-Dihydro-1,8bbeta-dihydroxy-3β-phenyl-3abeta-(3,4-dimethoxyphenyl)-6,8-dimethoxy-1H-cyclopenta[b]benzofuran-2α-carboxylic acid methyl ester	Generator

Chemical Formula

C₂₉H₃₀O₉

Average Mass

522.5500 Da

Monoisotopic Mass

522.18898 Da

IUPAC Name

methyl (2S,3R,4R,5S,6R)-6-(3,4-dimethoxyphenyl)-2,3-dihydroxy-10,12-dimethoxy-5-phenyl-7-oxatricyclo[6.4.0.0^{2,6}]dodeca-1(12),8,10-triene-4-carboxylate

Traditional Name

methyl (2S,3R,4R,5S,6R)-6-(3,4-dimethoxyphenyl)-2,3-dihydroxy-10,12-dimethoxy-5-phenyl-7-oxatricyclo[6.4.0.0^{2,6}]dodeca-1(12),8,10-triene-4-carboxylate

CAS Registry Number

Not Available

SMILES

COC(=O)[C@H]1[C@@H](O)[C@@]2(O)C3=C(OC)C=C(OC)C=C3O[C@]2([C@@H]1C1=CC=CC=C1)C1=CC=C(OC)C(OC)=C1

InChI Identifier

InChI=1S/C29H30O9/c1-33-18-14-21(36-4)25-22(15-18)38-29(17-11-12-19(34-2)20(13-17)35-3)24(16-9-7-6-8-10-16)23(27(31)37-5)26(30)28(25,29)32/h6-15,23-24,26,30,32H,1-5H3/t23-,24-,26-,28+,29+/m1/s1

InChI Key

OWHOEKLNSDNYTQ-IDAMAFBJSA-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 spectabilis	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as flavaglines. These are heterocyclic compounds with a structure characterized by a cyclopenta[b]benzofuran skeleton.

Kingdom

Organic compounds

Super Class

Organoheterocyclic compounds

Class

Benzofurans

Sub Class

Flavaglines

Direct Parent

Flavaglines

Alternative Parents

Substituents

Flavagline skeleton
Stilbene
O-dimethoxybenzene
Dimethoxybenzene
Coumaran
Phenoxy compound
Anisole
Methoxybenzene
Phenol ether
Beta-hydroxy acid
Alkyl aryl ether
Benzenoid
Hydroxy acid
Monocyclic benzene moiety
Cyclic alcohol
Methyl ester
Tertiary alcohol
1,2-diol
Carboxylic acid ester
Secondary alcohol
Carboxylic acid derivative
Oxacycle
Ether
Monocarboxylic acid or derivatives
Organic oxygen compound
Carbonyl group
Organooxygen compound
Hydrocarbon derivative
Organic oxide
Alcohol
Aromatic heteropolycyclic compound

Molecular Framework

Aromatic 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	2.74	ChemAxon
pKa (Strongest Acidic)	11.62	ChemAxon
pKa (Strongest Basic)	-3.6	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	8	ChemAxon
Hydrogen Donor Count	2	ChemAxon
Polar Surface Area	112.91 Å²	ChemAxon
Rotatable Bond Count	8	ChemAxon
Refractivity	135.88 m³·mol⁻¹	ChemAxon
Polarizability	53.53 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

8896142

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

10720804

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for methyl (2s,3r,4r,5s,6r)-6-(3,4-dimethoxyphenyl)-2,3-dihydroxy-10,12-dimethoxy-5-phenyl-7-oxatricyclo[6.4.0.0²,⁶]dodeca-1(12),8,10-triene-4-carboxylate (NP0231190)

MOL for NP0231190 (methyl (2s,3r,4r,5s,6r)-6-(3,4-dimethoxyphenyl)-2,3-dihydroxy-10,12-dimethoxy-5-phenyl-7-oxatricyclo[6.4.0.0²,⁶]dodeca-1(12),8,10-triene-4-carboxylate)

3D MOL for NP0231190 (methyl (2s,3r,4r,5s,6r)-6-(3,4-dimethoxyphenyl)-2,3-dihydroxy-10,12-dimethoxy-5-phenyl-7-oxatricyclo[6.4.0.0²,⁶]dodeca-1(12),8,10-triene-4-carboxylate)

3D SDF for NP0231190 (methyl (2s,3r,4r,5s,6r)-6-(3,4-dimethoxyphenyl)-2,3-dihydroxy-10,12-dimethoxy-5-phenyl-7-oxatricyclo[6.4.0.0²,⁶]dodeca-1(12),8,10-triene-4-carboxylate)

3D-SDF for NP0231190 (methyl (2s,3r,4r,5s,6r)-6-(3,4-dimethoxyphenyl)-2,3-dihydroxy-10,12-dimethoxy-5-phenyl-7-oxatricyclo[6.4.0.0²,⁶]dodeca-1(12),8,10-triene-4-carboxylate)

PDB for NP0231190 (methyl (2s,3r,4r,5s,6r)-6-(3,4-dimethoxyphenyl)-2,3-dihydroxy-10,12-dimethoxy-5-phenyl-7-oxatricyclo[6.4.0.0²,⁶]dodeca-1(12),8,10-triene-4-carboxylate)

3D PDB for NP0231190 (methyl (2s,3r,4r,5s,6r)-6-(3,4-dimethoxyphenyl)-2,3-dihydroxy-10,12-dimethoxy-5-phenyl-7-oxatricyclo[6.4.0.0²,⁶]dodeca-1(12),8,10-triene-4-carboxylate)

SMILES for NP0231190 (methyl (2s,3r,4r,5s,6r)-6-(3,4-dimethoxyphenyl)-2,3-dihydroxy-10,12-dimethoxy-5-phenyl-7-oxatricyclo[6.4.0.0²,⁶]dodeca-1(12),8,10-triene-4-carboxylate)

INCHI for NP0231190 (methyl (2s,3r,4r,5s,6r)-6-(3,4-dimethoxyphenyl)-2,3-dihydroxy-10,12-dimethoxy-5-phenyl-7-oxatricyclo[6.4.0.0²,⁶]dodeca-1(12),8,10-triene-4-carboxylate)

Structure for NP0231190 (methyl (2s,3r,4r,5s,6r)-6-(3,4-dimethoxyphenyl)-2,3-dihydroxy-10,12-dimethoxy-5-phenyl-7-oxatricyclo[6.4.0.0²,⁶]dodeca-1(12),8,10-triene-4-carboxylate)

3D Structure for NP0231190 (methyl (2s,3r,4r,5s,6r)-6-(3,4-dimethoxyphenyl)-2,3-dihydroxy-10,12-dimethoxy-5-phenyl-7-oxatricyclo[6.4.0.0²,⁶]dodeca-1(12),8,10-triene-4-carboxylate)