NP-MRD: Showing NP-Card for 5,7,4'-Tri-O-methylcatechin (NP0138711)

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Record Information

Version

1.0

Created at

2022-06-29 18:32:42 UTC

Updated at

2022-06-29 18:32:42 UTC

NP-MRD ID

NP0138711

Secondary Accession Numbers

None

Natural Product Identification

Common Name

5,7,4'-Tri-O-methylcatechin

Description

3,3'-Dihydroxy-4',5,7-trimethoxyflavan, also known as 4',5,7-tri-O-methylcatechin or catechin 5,7,4'-trimethyl ether, belongs to the class of organic compounds known as catechins. Catechins are compounds containing a catechin moiety, which is a 3,4-dihydro-2-chromene-3,5.7-Tiol. 3,3'-Dihydroxy-4',5,7-trimethoxyflavan is an extremely weak basic (essentially neutral) compound (based on its pKa). Outside of the human body, 3,3'-Dihydroxy-4',5,7-trimethoxyflavan has been detected, but not quantified in, a few different foods, such as chinese cinnamons, green vegetables, and herbs and spices. 5,7,4'-Tri-O-methylcatechin is found in Byrsonima microphylla and Cinnamomum aromaticum. This could make 3,3'-dihydroxy-4',5,7-trimethoxyflavan a potential biomarker for the consumption of these foods.

Structure

MOL 3D MOL SDF PDB SMILES InChI

     RDKit          3D

 44 46  0  0  0  0  0  0  0  0999 V2000
   -4.2184    2.6073   -2.1466 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3880    1.7976   -1.0151 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4216    0.8626   -0.6137 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6537    0.1031    0.5045 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7419   -0.8328    0.9496 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0349   -1.5667    2.0836 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2357   -1.3592    2.7627 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5585   -1.0092    0.2456 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3218   -0.2579   -0.8660 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2492    0.6757   -1.2960 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1568   -0.4178   -1.5759 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.8572   -1.3412   -1.2302 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.9785   -0.5229   -0.6926 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6651   -0.7774    0.4518 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6831    0.0847    0.8184 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9883    1.1746    0.0361 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0091    2.0566    0.3847 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.7452    1.8051    1.5885 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2999    1.4443   -1.1267 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6235    2.5503   -1.9027 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.2929    0.5903   -1.4880 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3867   -2.4344   -0.3564 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.2746   -3.4414   -1.1009 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5861   -1.9941    0.7040 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2402    3.1687   -2.1340 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2752    2.0781   -3.0991 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0538    3.3655   -2.1188 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5791    0.2458    1.0491 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.1343   -1.5496    2.1096 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2493   -2.0589    3.6455 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3657   -0.2941    3.1092 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0523    1.2568   -2.1667 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.2223   -1.7767   -2.1863 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.4011   -1.6410    1.0481 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.2214   -0.1217    1.7227 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.0616    0.7379    1.5342 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.5947    2.4845    1.6849 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.0517    1.9727    2.4376 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.3756    3.1620   -1.6048 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.7538    0.8093   -2.4070 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.2271   -2.9490    0.1264 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4815   -4.2127   -0.5398 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1406   -2.8871    1.0824 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0255   -1.5877    1.5881 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
  4  5  1  0
  5  6  1  0
  6  7  1  0
  5  8  2  0
  8 24  1  0
 24 22  1  0
 22 23  1  0
 22 12  1  0
 12 11  1  0
 11  9  1  0
  9 10  2  0
 12 13  1  0
 13 21  2  0
 21 19  1  0
 19 20  1  0
 19 16  2  0
 16 17  1  0
 17 18  1  0
 16 15  1  0
 15 14  2  0
 10  3  1  0
 14 13  1  0
  9  8  1  0
  1 25  1  0
  1 26  1  0
  1 27  1  0
  4 28  1  0
  7 29  1  0
  7 30  1  0
  7 31  1  0
 24 43  1  0
 24 44  1  0
 22 41  1  1
 23 42  1  0
 12 33  1  6
 10 32  1  0
 21 40  1  0
 20 39  1  0
 18 36  1  0
 18 37  1  0
 18 38  1  0
 15 35  1  0
 14 34  1  0
M  END


  Mrv0541 05061305252D          

 24 26  0  0  0  0            999 V2000
   -0.7145   -1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.1447   -2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434    1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2868   -2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0013   -2.8875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0013   -1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145   -0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289   -1.6500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579    0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2868   -1.6500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145   -1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434   -0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7158   -1.6500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5724   -0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7158   -2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289    0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434   -1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5724   -1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.4302   -1.2375    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.2868    0.0000    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000   -1.6500    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.4302   -2.8875    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289    0.8250    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579   -1.6500    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  5  4  2  0  0  0  0
 10  4  1  0  0  0  0
 10  6  2  0  0  0  0
 11  7  2  0  0  0  0
 11  8  1  0  0  0  0
 12  9  1  0  0  0  0
 13  6  1  0  0  0  0
 14  9  1  0  0  0  0
 15  5  1  0  0  0  0
 15 13  2  0  0  0  0
 16  7  1  0  0  0  0
 16 12  2  0  0  0  0
 17  8  2  0  0  0  0
 17 12  1  0  0  0  0
 18 10  1  0  0  0  0
 18 14  1  0  0  0  0
 19 13  1  0  0  0  0
 20 14  1  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 15  1  0  0  0  0
 23  3  1  0  0  0  0
 23 16  1  0  0  0  0
 24 17  1  0  0  0  0
 24 18  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0138711

> <DATABASE_NAME>
NP-MRD

> <SMILES>
COC1=CC(OC)=C2CC(O)C(OC2=C1)C1=CC(O)=C(OC)C=C1

> <INCHI_IDENTIFIER>
InChI=1S/C18H20O6/c1-21-11-7-16(23-3)12-9-14(20)18(24-17(12)8-11)10-4-5-15(22-2)13(19)6-10/h4-8,14,18-20H,9H2,1-3H3

> <INCHI_KEY>
WCBCDLSKTYUDDL-UHFFFAOYSA-N

> <FORMULA>
C18H20O6

> <MOLECULAR_WEIGHT>
332.3478

> <EXACT_MASS>
332.125988372

> <JCHEM_ACCEPTOR_COUNT>
6

> <JCHEM_AVERAGE_POLARIZABILITY>
34.48734967623115

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
2

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
2-(3-hydroxy-4-methoxyphenyl)-5,7-dimethoxy-3,4-dihydro-2H-1-benzopyran-3-ol

> <ALOGPS_LOGP>
1.91

> <JCHEM_LOGP>
2.2327891833333338

> <ALOGPS_LOGS>
-3.30

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
3

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
13.898393310591281

> <JCHEM_PKA_STRONGEST_ACIDIC>
9.786657323400123

> <JCHEM_PKA_STRONGEST_BASIC>
-3.2919391902841353

> <JCHEM_POLAR_SURFACE_AREA>
77.38000000000001

> <JCHEM_REFRACTIVITY>
87.44659999999999

> <JCHEM_ROTATABLE_BOND_COUNT>
4

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
1.67e-01 g/l

> <JCHEM_TRADITIONAL_IUPAC>
2-(3-hydroxy-4-methoxyphenyl)-5,7-dimethoxy-3,4-dihydro-2H-1-benzopyran-3-ol

> <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      -1.334  -2.310   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0      13.337  -4.620   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       4.001   2.310   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       8.002  -4.620   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       9.336  -5.390   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       9.336  -2.310   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       1.334  -0.770   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       2.667  -3.080   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       5.335   0.000   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       8.002  -3.080   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       1.334  -2.310   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       4.001  -0.770   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0      10.669  -3.080   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       6.668  -0.770   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0      10.669  -4.620   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       2.667   0.000   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       4.001  -2.310   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       6.668  -2.310   0.000  0.00  0.00           C+0
HETATM   19  O   UNK     0      12.003  -2.310   0.000  0.00  0.00           O+0
HETATM   20  O   UNK     0       8.002   0.000   0.000  0.00  0.00           O+0
HETATM   21  O   UNK     0       0.000  -3.080   0.000  0.00  0.00           O+0
HETATM   22  O   UNK     0      12.003  -5.390   0.000  0.00  0.00           O+0
HETATM   23  O   UNK     0       2.667   1.540   0.000  0.00  0.00           O+0
HETATM   24  O   UNK     0       5.335  -3.080   0.000  0.00  0.00           O+0
CONECT    1   21                                                            
CONECT    2   22                                                            
CONECT    3   23                                                            
CONECT    4    5   10                                                       
CONECT    5    4   15                                                       
CONECT    6   10   13                                                       
CONECT    7   11   16                                                       
CONECT    8   11   17                                                       
CONECT    9   12   14                                                       
CONECT   10    4    6   18                                                  
CONECT   11    7    8   21                                                  
CONECT   12    9   16   17                                                  
CONECT   13    6   15   19                                                  
CONECT   14    9   18   20                                                  
CONECT   15    5   13   22                                                  
CONECT   16    7   12   23                                                  
CONECT   17    8   12   24                                                  
CONECT   18   10   14   24                                                  
CONECT   19   13                                                            
CONECT   20   14                                                            
CONECT   21    1   11                                                       
CONECT   22    2   15                                                       
CONECT   23    3   16                                                       
CONECT   24   17   18                                                       
MASTER        0    0    0    0    0    0    0    0   24    0   52    0
END

View in JSmol

Synonyms

Value	Source
4',5,7-Tri-O-methylcatechin	HMDB
Catechin 5,7,4'-trimethyl ether	HMDB

Chemical Formula

C₁₈H₂₀O₆

Average Mass

332.3478 Da

Monoisotopic Mass

332.12599 Da

IUPAC Name

2-(3-hydroxy-4-methoxyphenyl)-5,7-dimethoxy-3,4-dihydro-2H-1-benzopyran-3-ol

Traditional Name

2-(3-hydroxy-4-methoxyphenyl)-5,7-dimethoxy-3,4-dihydro-2H-1-benzopyran-3-ol

CAS Registry Number

105330-59-4

SMILES

COC1=CC(OC)=C2CC(O)C(OC2=C1)C1=CC(O)=C(OC)C=C1

InChI Identifier

InChI=1S/C18H20O6/c1-21-11-7-16(23-3)12-9-14(20)18(24-17(12)8-11)10-4-5-15(22-2)13(19)6-10/h4-8,14,18-20H,9H2,1-3H3

InChI Key

WCBCDLSKTYUDDL-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
Byrsonima microphylla	LOTUS Database	35616633
Cinnamomum aromaticum	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as catechins. Catechins are compounds containing a catechin moiety, which is a 3,4-dihydro-2-chromene-3,5.7-Tiol.

Kingdom

Organic compounds

Super Class

Phenylpropanoids and polyketides

Class

Flavonoids

Sub Class

Flavans

Direct Parent

Catechins

Alternative Parents

Substituents

Catechin
4p-methoxyflavonoid-skeleton
5-methoxyflavonoid-skeleton
7-methoxyflavonoid-skeleton
3'-hydroxyflavonoid
3-hydroxyflavonoid
Hydroxyflavonoid
Chromane
Benzopyran
1-benzopyran
Methoxyphenol
Phenoxy compound
Anisole
Methoxybenzene
Phenol ether
1-hydroxy-2-unsubstituted benzenoid
1-hydroxy-4-unsubstituted benzenoid
Alkyl aryl ether
Phenol
Benzenoid
Monocyclic benzene moiety
Secondary alcohol
Ether
Organoheterocyclic compound
Oxacycle
Alcohol
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	1.91	ALOGPS
logP	2.23	ChemAxon
logS	-3.3	ALOGPS
pKa (Strongest Acidic)	9.79	ChemAxon
pKa (Strongest Basic)	-3.3	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	6	ChemAxon
Hydrogen Donor Count	2	ChemAxon
Polar Surface Area	77.38 Å²	ChemAxon
Rotatable Bond Count	4	ChemAxon
Refractivity	87.45 m³·mol⁻¹	ChemAxon
Polarizability	34.49 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

HMDB0030664

DrugBank ID

Not Available

Phenol Explorer Compound ID

Not Available

FoodDB ID

FDB002575

KNApSAcK ID

C00008816

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

67233312

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

Not Available

Showing NP-Card for 5,7,4'-Tri-O-methylcatechin (NP0138711)

MOL for NP0138711 (5,7,4'-Tri-O-methylcatechin)

3D MOL for NP0138711 (5,7,4'-Tri-O-methylcatechin)

3D SDF for NP0138711 (5,7,4'-Tri-O-methylcatechin)

3D-SDF for NP0138711 (5,7,4'-Tri-O-methylcatechin)

PDB for NP0138711 (5,7,4'-Tri-O-methylcatechin)

3D PDB for NP0138711 (5,7,4'-Tri-O-methylcatechin)

SMILES for NP0138711 (5,7,4'-Tri-O-methylcatechin)

INCHI for NP0138711 (5,7,4'-Tri-O-methylcatechin)

Structure for NP0138711 (5,7,4'-Tri-O-methylcatechin)

3D Structure for NP0138711 (5,7,4'-Tri-O-methylcatechin)