NP-MRD: Showing NP-Card for methyl 2-(4-hydroxy-2-methoxyphenyl)-6-methoxy-1-benzofuran-3-carboxylate (NP0246734)

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Record Information

Version

2.0

Created at

2022-09-07 08:17:50 UTC

Updated at

2022-09-07 08:17:50 UTC

NP-MRD ID

NP0246734

Secondary Accession Numbers

None

Natural Product Identification

Common Name

methyl 2-(4-hydroxy-2-methoxyphenyl)-6-methoxy-1-benzofuran-3-carboxylate

Description

Methyl 2-(2-methoxy-4-hydroxyphenyl)-6-methoxy-3-benzofurancarboxylate belongs to the class of organic compounds known as 2-arylbenzofuran flavonoids. These are phenylpropanoids containing the 2-phenylbenzofuran moiety. Methyl 2-(2-methoxy-4-hydroxyphenyl)-6-methoxy-3-benzofurancarboxylate is an extremely weak basic (essentially neutral) compound (based on its pKa). Outside of the human body, Methyl 2-(2-methoxy-4-hydroxyphenyl)-6-methoxy-3-benzofurancarboxylate has been detected, but not quantified in, pulses. methyl 2-(4-hydroxy-2-methoxyphenyl)-6-methoxy-1-benzofuran-3-carboxylate is found in Medicago sativa. This could make methyl 2-(2-methoxy-4-hydroxyphenyl)-6-methoxy-3-benzofurancarboxylate a potential biomarker for the consumption of these foods.

Structure

MOL 3D MOL SDF PDB SMILES InChI

     RDKit          3D

 40 42  0  0  0  0  0  0  0  0999 V2000
   -0.3885    4.7343   -0.3091 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0956    3.3667   -0.5855 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.1988    2.5249    0.4817 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2134    2.9410    1.6904 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.4962    1.1210    0.1464 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3338    0.0542    0.0385 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7732    0.0288    0.2288 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5571    1.1024    0.5403 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9483    1.0183    0.7098 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5553   -0.1940    0.5571 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.9270   -0.2944    0.7208 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7992   -1.2905    0.2448 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4340   -1.1955    0.0809 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6626   -2.2999   -0.2350 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3023   -3.5497   -0.3906 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4245   -0.9822   -0.2787 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.6738   -0.6548   -0.3807 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8508   -1.3295   -0.6801 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0581   -0.6637   -0.7065 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.2365   -1.3630   -1.0112 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.2103   -2.7486   -1.2940 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.1503    0.6858   -0.4401 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9649    1.3663   -0.1383 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7896    0.6784   -0.1209 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3481    5.0994    0.4078 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2453    5.2861   -1.2642 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4256    4.7861    0.0513 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1172    2.0696    0.6662 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4788    1.9309    0.9565 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.4939   -0.1576   -0.1061 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2609   -2.2783    0.1160 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0610   -3.5300   -1.2096 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5768   -4.3453   -0.6618 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7858   -3.8819    0.5680 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.7751   -2.3908   -0.8892 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.1739   -3.3590   -0.3665 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.1642   -2.9589   -1.8586 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.3898   -2.9937   -1.9808 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.0819    1.2324   -0.4537 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.0221    2.4348    0.0747 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  1  0
  3  4  2  0
  3  5  1  0
  5  6  2  0
  6 16  1  0
 16 17  1  0
 17 24  2  0
 24 23  1  0
 23 22  2  0
 22 19  1  0
 19 20  1  0
 20 21  1  0
 19 18  2  0
  6  7  1  0
  7 13  2  0
 13 14  1  0
 14 15  1  0
 13 12  1  0
 12 10  2  0
 10 11  1  0
 10  9  1  0
  9  8  2  0
 24  5  1  0
  8  7  1  0
 18 17  1  0
  1 25  1  0
  1 26  1  0
  1 27  1  0
 23 40  1  0
 22 39  1  0
 21 36  1  0
 21 37  1  0
 21 38  1  0
 18 35  1  0
 15 32  1  0
 15 33  1  0
 15 34  1  0
 12 31  1  0
 11 30  1  0
  9 29  1  0
  8 28  1  0
M  END


  Mrv0541 05061312152D          

 24 26  0  0  0  0            999 V2000
    5.4223    0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2949   -1.0164    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8839    2.3061    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7676    1.1270    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9934    0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0574    1.1270    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2789    1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7676   -0.3020    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2789   -0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1801    0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9934    0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5645    0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4699    0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0574   -0.3020    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5645    0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7798    1.0799    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2949    0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5249    1.8646    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0051    0.4125    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.7179    2.0361    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.7079   -0.4125    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.4699   -1.0164    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.0769    2.4777    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.7798   -0.2549    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  6  4  2  0  0  0  0
  7  5  2  0  0  0  0
 10  4  1  0  0  0  0
 10  8  2  0  0  0  0
 11  5  1  0  0  0  0
 11  9  2  0  0  0  0
 12  7  1  0  0  0  0
 13  6  1  0  0  0  0
 14  8  1  0  0  0  0
 14 13  2  0  0  0  0
 15  9  1  0  0  0  0
 15 12  2  0  0  0  0
 16 12  1  0  0  0  0
 17 13  1  0  0  0  0
 17 16  2  0  0  0  0
 18 16  1  0  0  0  0
 19 10  1  0  0  0  0
 20 18  2  0  0  0  0
 21  1  1  0  0  0  0
 21 11  1  0  0  0  0
 22  2  1  0  0  0  0
 22 14  1  0  0  0  0
 23  3  1  0  0  0  0
 23 18  1  0  0  0  0
 24 15  1  0  0  0  0
 24 17  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0246734

> <DATABASE_NAME>
NP-MRD

> <SMILES>
COC(=O)C1=C(OC2=C1C=CC(OC)=C2)C1=C(OC)C=C(O)C=C1

> <INCHI_IDENTIFIER>
InChI=1S/C18H16O6/c1-21-11-5-7-12-15(9-11)24-17(16(12)18(20)23-3)13-6-4-10(19)8-14(13)22-2/h4-9,19H,1-3H3

> <INCHI_KEY>
FFAIKFRIUGUDRP-UHFFFAOYSA-N

> <FORMULA>
C18H16O6

> <MOLECULAR_WEIGHT>
328.316

> <EXACT_MASS>
328.094688244

> <JCHEM_ACCEPTOR_COUNT>
4

> <JCHEM_AVERAGE_POLARIZABILITY>
33.895548989652525

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
1

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
methyl 2-(4-hydroxy-2-methoxyphenyl)-6-methoxy-1-benzofuran-3-carboxylate

> <ALOGPS_LOGP>
3.03

> <JCHEM_LOGP>
3.0841648133333335

> <ALOGPS_LOGS>
-3.79

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
3

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA_STRONGEST_ACIDIC>
8.754361786170984

> <JCHEM_PKA_STRONGEST_BASIC>
-4.0759356344398

> <JCHEM_POLAR_SURFACE_AREA>
78.13000000000001

> <JCHEM_REFRACTIVITY>
86.8454

> <JCHEM_ROTATABLE_BOND_COUNT>
5

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
5.36e-02 g/l

> <JCHEM_TRADITIONAL_IUPAC>
methyl 2-(4-hydroxy-2-methoxyphenyl)-6-methoxy-1-benzofuran-3-carboxylate

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 06-MAY-13   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   06-MAY-13         0                                  
HETATM    1  C   UNK     0      10.122   0.000   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       2.417  -1.897   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       5.383   4.305   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0      -1.433   2.104   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       7.454   1.540   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       0.107   2.104   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       6.121   2.310   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0      -1.433  -0.564   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       6.121  -0.770   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0      -2.203   0.770   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       7.454   0.000   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       4.787   1.540   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       0.877   0.770   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       0.107  -0.564   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       4.787   0.000   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       3.322   2.016   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       2.417   0.770   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       2.846   3.481   0.000  0.00  0.00           C+0
HETATM   19  O   UNK     0      -3.743   0.770   0.000  0.00  0.00           O+0
HETATM   20  O   UNK     0       1.340   3.801   0.000  0.00  0.00           O+0
HETATM   21  O   UNK     0       8.788  -0.770   0.000  0.00  0.00           O+0
HETATM   22  O   UNK     0       0.877  -1.897   0.000  0.00  0.00           O+0
HETATM   23  O   UNK     0       3.877   4.625   0.000  0.00  0.00           O+0
HETATM   24  O   UNK     0       3.322  -0.476   0.000  0.00  0.00           O+0
CONECT    1   21                                                            
CONECT    2   22                                                            
CONECT    3   23                                                            
CONECT    4    6   10                                                       
CONECT    5    7   11                                                       
CONECT    6    4   13                                                       
CONECT    7    5   12                                                       
CONECT    8   10   14                                                       
CONECT    9   11   15                                                       
CONECT   10    4    8   19                                                  
CONECT   11    5    9   21                                                  
CONECT   12    7   15   16                                                  
CONECT   13    6   14   17                                                  
CONECT   14    8   13   22                                                  
CONECT   15    9   12   24                                                  
CONECT   16   12   17   18                                                  
CONECT   17   13   16   24                                                  
CONECT   18   16   20   23                                                  
CONECT   19   10                                                            
CONECT   20   18                                                            
CONECT   21    1   11                                                       
CONECT   22    2   14                                                       
CONECT   23    3   18                                                       
CONECT   24   15   17                                                       
MASTER        0    0    0    0    0    0    0    0   24    0   52    0
END

View in JSmol

Synonyms

Value	Source
Methyl 2-(2-methoxy-4-hydroxyphenyl)-6-methoxy-3-benzofurancarboxylic acid	Generator
Methyl 2-(4-hydroxy-2-methoxyphenyl)-6-methoxy-1-benzofuran-3-carboxylic acid	Generator

Chemical Formula

C₁₈H₁₆O₆

Average Mass

328.3160 Da

Monoisotopic Mass

328.09469 Da

IUPAC Name

methyl 2-(4-hydroxy-2-methoxyphenyl)-6-methoxy-1-benzofuran-3-carboxylate

Traditional Name

methyl 2-(4-hydroxy-2-methoxyphenyl)-6-methoxy-1-benzofuran-3-carboxylate

CAS Registry Number

Not Available

SMILES

COC(=O)C1=C(OC2=C1C=CC(OC)=C2)C1=C(OC)C=C(O)C=C1

InChI Identifier

InChI=1S/C18H16O6/c1-21-11-5-7-12-15(9-11)24-17(16(12)18(20)23-3)13-6-4-10(19)8-14(13)22-2/h4-9,19H,1-3H3

InChI Key

FFAIKFRIUGUDRP-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
Medicago sativa	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as 2-arylbenzofuran flavonoids. These are phenylpropanoids containing the 2-phenylbenzofuran moiety.

Kingdom

Organic compounds

Super Class

Phenylpropanoids and polyketides

Class

2-arylbenzofuran flavonoids

Sub Class

Not Available

Direct Parent

2-arylbenzofuran flavonoids

Alternative Parents

Substituents

2-arylbenzofuran flavonoid
2-phenylbenzofuran
Phenylbenzofuran
Methoxyphenol
Furoic acid ester
Benzofuran
Furoic acid or derivatives
Furan-3-carboxylic acid ester
Furan-3-carboxylic acid or derivatives
Phenoxy compound
Phenol ether
Anisole
Methoxybenzene
1-hydroxy-2-unsubstituted benzenoid
Alkyl aryl ether
Phenol
Monocyclic benzene moiety
Benzenoid
Heteroaromatic compound
Furan
Methyl ester
Carboxylic acid ester
Oxacycle
Organoheterocyclic compound
Carboxylic acid derivative
Ether
Monocarboxylic acid or derivatives
Organic oxide
Hydrocarbon derivative
Organooxygen compound
Organic oxygen compound
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	3.03	ALOGPS
logP	3.08	ChemAxon
logS	-3.8	ALOGPS
pKa (Strongest Acidic)	8.75	ChemAxon
pKa (Strongest Basic)	-4.1	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	4	ChemAxon
Hydrogen Donor Count	1	ChemAxon
Polar Surface Area	78.13 Å²	ChemAxon
Rotatable Bond Count	5	ChemAxon
Refractivity	86.85 m³·mol⁻¹	ChemAxon
Polarizability	33.9 Å³	ChemAxon
Number of Rings	3	ChemAxon
Bioavailability	Yes	ChemAxon
Rule of Five	Yes	ChemAxon
Ghose Filter	Yes	ChemAxon
Veber's Rule	No	ChemAxon
MDDR-like Rule	No	ChemAxon

External Links

HMDB ID

HMDB0040935

DrugBank ID

Not Available

Phenol Explorer Compound ID

Not Available

FoodDB ID

FDB020776

KNApSAcK ID

Not Available

Chemspider ID

9913646

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

11738939

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for methyl 2-(4-hydroxy-2-methoxyphenyl)-6-methoxy-1-benzofuran-3-carboxylate (NP0246734)

MOL for NP0246734 (methyl 2-(4-hydroxy-2-methoxyphenyl)-6-methoxy-1-benzofuran-3-carboxylate)

3D MOL for NP0246734 (methyl 2-(4-hydroxy-2-methoxyphenyl)-6-methoxy-1-benzofuran-3-carboxylate)

3D SDF for NP0246734 (methyl 2-(4-hydroxy-2-methoxyphenyl)-6-methoxy-1-benzofuran-3-carboxylate)

3D-SDF for NP0246734 (methyl 2-(4-hydroxy-2-methoxyphenyl)-6-methoxy-1-benzofuran-3-carboxylate)

PDB for NP0246734 (methyl 2-(4-hydroxy-2-methoxyphenyl)-6-methoxy-1-benzofuran-3-carboxylate)

3D PDB for NP0246734 (methyl 2-(4-hydroxy-2-methoxyphenyl)-6-methoxy-1-benzofuran-3-carboxylate)

SMILES for NP0246734 (methyl 2-(4-hydroxy-2-methoxyphenyl)-6-methoxy-1-benzofuran-3-carboxylate)

INCHI for NP0246734 (methyl 2-(4-hydroxy-2-methoxyphenyl)-6-methoxy-1-benzofuran-3-carboxylate)

Structure for NP0246734 (methyl 2-(4-hydroxy-2-methoxyphenyl)-6-methoxy-1-benzofuran-3-carboxylate)

3D Structure for NP0246734 (methyl 2-(4-hydroxy-2-methoxyphenyl)-6-methoxy-1-benzofuran-3-carboxylate)