NP-MRD: Showing NP-Card for (2r,3r)-8-[(2r,3s,4s)-5,7-dihydroxy-2-(4-hydroxyphenyl)-3-{[(2s,3r,4r,5r,6s)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxy}-3,4-dihydro-2h-1-benzopyran-4-yl]-2-(3,4-dihydroxyphenyl)-5,7-dihydroxy-3,4-dihydro-2h-1-benzopyran-3-yl 4-hydroxy-3-methoxybenzoate (NP0207105)

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Record Information

Version

2.0

Created at

2022-09-05 03:35:18 UTC

Updated at

2022-09-05 03:35:18 UTC

NP-MRD ID

NP0207105

Secondary Accession Numbers

None

Natural Product Identification

Common Name

(2r,3r)-8-[(2r,3s,4s)-5,7-dihydroxy-2-(4-hydroxyphenyl)-3-{[(2s,3r,4r,5r,6s)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxy}-3,4-dihydro-2h-1-benzopyran-4-yl]-2-(3,4-dihydroxyphenyl)-5,7-dihydroxy-3,4-dihydro-2h-1-benzopyran-3-yl 4-hydroxy-3-methoxybenzoate

Description

(2R,3R)-8-[(2R,3S,4S)-5,7-dihydroxy-2-(4-hydroxyphenyl)-3-{[(2S,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxy}-3,4-dihydro-2H-1-benzopyran-4-yl]-2-(3,4-dihydroxyphenyl)-5,7-dihydroxy-3,4-dihydro-2H-1-benzopyran-3-yl 4-hydroxy-3-methoxybenzoate belongs to the class of organic compounds known as complex tannins. These are tannins made of a catechin bound to a gallotannin or elagitannin. (2r,3r)-8-[(2r,3s,4s)-5,7-dihydroxy-2-(4-hydroxyphenyl)-3-{[(2s,3r,4r,5r,6s)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxy}-3,4-dihydro-2h-1-benzopyran-4-yl]-2-(3,4-dihydroxyphenyl)-5,7-dihydroxy-3,4-dihydro-2h-1-benzopyran-3-yl 4-hydroxy-3-methoxybenzoate is found in Joannesia princeps. Based on a literature review very few articles have been published on (2R,3R)-8-[(2R,3S,4S)-5,7-dihydroxy-2-(4-hydroxyphenyl)-3-{[(2S,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxy}-3,4-dihydro-2H-1-benzopyran-4-yl]-2-(3,4-dihydroxyphenyl)-5,7-dihydroxy-3,4-dihydro-2H-1-benzopyran-3-yl 4-hydroxy-3-methoxybenzoate.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652309052205352D          

 62 69  0  0  1  0            999 V2000
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M  END

     RDKit          3D

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M  END


  Mrv1652309052205352D          

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M  END
> <DATABASE_ID>
NP0207105

> <DATABASE_NAME>
NP-MRD

> <SMILES>
COC1=CC(=CC=C1O)C(=O)O[C@@H]1CC2=C(O)C=C(O)C([C@H]3[C@H](O[C@@H]4O[C@@H](C)[C@H](O)[C@@H](O)[C@H]4O)[C@H](OC4=CC(O)=CC(O)=C34)C3=CC=C(O)C=C3)=C2O[C@@H]1C1=CC=C(O)C(O)=C1

> <INCHI_IDENTIFIER>
InChI=1S/C44H42O18/c1-17-36(53)37(54)38(55)44(58-17)62-42-35(33-28(51)13-22(46)14-31(33)59-40(42)18-3-7-21(45)8-4-18)34-29(52)16-26(49)23-15-32(60-43(56)20-6-10-25(48)30(12-20)57-2)39(61-41(23)34)19-5-9-24(47)27(50)11-19/h3-14,16-17,32,35-40,42,44-55H,15H2,1-2H3/t17-,32+,35-,36-,37+,38+,39+,40+,42-,44-/m0/s1

> <INCHI_KEY>
WOHNSGMEHDFINH-JMKADCDZSA-N

> <FORMULA>
C44H42O18

> <MOLECULAR_WEIGHT>
858.802

> <EXACT_MASS>
858.237114512

> <JCHEM_ACCEPTOR_COUNT>
17

> <JCHEM_ATOM_COUNT>
104

> <JCHEM_AVERAGE_POLARIZABILITY>
82.68136394206158

> <JCHEM_BIOAVAILABILITY>
0

> <JCHEM_DONOR_COUNT>
11

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
(2R,3R)-8-[(2R,3S,4S)-5,7-dihydroxy-2-(4-hydroxyphenyl)-3-{[(2S,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxy}-3,4-dihydro-2H-1-benzopyran-4-yl]-2-(3,4-dihydroxyphenyl)-5,7-dihydroxy-3,4-dihydro-2H-1-benzopyran-3-yl 4-hydroxy-3-methoxybenzoate

> <JCHEM_LOGP>
4.729447917666665

> <JCHEM_MDDR_LIKE_RULE>
1

> <JCHEM_NUMBER_OF_RINGS>
8

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
8.91715085380582

> <JCHEM_PKA_STRONGEST_ACIDIC>
8.505502949412037

> <JCHEM_PKA_STRONGEST_BASIC>
-5.204131809060045

> <JCHEM_POLAR_SURFACE_AREA>
294.97999999999996

> <JCHEM_REFRACTIVITY>
213.6628

> <JCHEM_ROTATABLE_BOND_COUNT>
9

> <JCHEM_RULE_OF_FIVE>
0

> <JCHEM_TRADITIONAL_IUPAC>
(2R,3R)-8-[(2R,3S,4S)-5,7-dihydroxy-2-(4-hydroxyphenyl)-3-{[(2S,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxy}-3,4-dihydro-2H-1-benzopyran-4-yl]-2-(3,4-dihydroxyphenyl)-5,7-dihydroxy-3,4-dihydro-2H-1-benzopyran-3-yl 4-hydroxy-3-methoxybenzoate

> <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      -7.875  -3.727   0.000  0.00  0.00           C+0
HETATM    2  O   UNK     0      -6.541  -4.497   0.000  0.00  0.00           O+0
HETATM    3  C   UNK     0      -5.207  -3.727   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0      -3.874  -4.497   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0      -2.540  -3.727   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0      -1.206  -4.497   0.000  0.00  0.00           C+0
HETATM    7  O   UNK     0       0.128  -3.727   0.000  0.00  0.00           O+0
HETATM    8  O   UNK     0      -1.206  -6.037   0.000  0.00  0.00           O+0
HETATM    9  C   UNK     0       0.128  -6.807   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       1.461  -6.037   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       2.795  -6.807   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       4.129  -6.037   0.000  0.00  0.00           C+0
HETATM   13  O   UNK     0       4.129  -4.497   0.000  0.00  0.00           O+0
HETATM   14  C   UNK     0       5.462  -6.807   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       5.462  -8.347   0.000  0.00  0.00           C+0
HETATM   16  O   UNK     0       6.165  -9.286   0.000  0.00  0.00           O+0
HETATM   17  C   UNK     0       4.129  -9.117   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       4.604 -10.582   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0       6.136 -10.421   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0       6.762  -9.014   0.000  0.00  0.00           C+0
HETATM   21  O   UNK     0       5.857  -7.768   0.000  0.00  0.00           O+0
HETATM   22  C   UNK     0       8.294  -8.853   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0       9.199 -10.099   0.000  0.00  0.00           C+0
HETATM   24  O   UNK     0      10.731  -9.938   0.000  0.00  0.00           O+0
HETATM   25  C   UNK     0       8.573 -11.506   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0       7.041 -11.667   0.000  0.00  0.00           C+0
HETATM   27  O   UNK     0       6.415 -13.073   0.000  0.00  0.00           O+0
HETATM   28  C   UNK     0       4.883 -13.234   0.000  0.00  0.00           C+0
HETATM   29  C   UNK     0       3.749 -14.230   0.000  0.00  0.00           C+0
HETATM   30  C   UNK     0       5.162 -15.887   0.000  0.00  0.00           C+0
HETATM   31  C   UNK     0       4.536 -17.294   0.000  0.00  0.00           C+0
HETATM   32  C   UNK     0       3.004 -17.455   0.000  0.00  0.00           C+0
HETATM   33  O   UNK     0       2.378 -18.862   0.000  0.00  0.00           O+0
HETATM   34  C   UNK     0       2.607 -16.620   0.000  0.00  0.00           C+0
HETATM   35  C   UNK     0       2.218 -14.391   0.000  0.00  0.00           C+0
HETATM   36  C   UNK     0       3.978 -11.989   0.000  0.00  0.00           C+0
HETATM   37  O   UNK     0       2.644 -11.219   0.000  0.00  0.00           O+0
HETATM   38  C   UNK     0       1.311 -11.989   0.000  0.00  0.00           C+0
HETATM   39  O   UNK     0      -0.192 -10.587   0.000  0.00  0.00           O+0
HETATM   40  C   UNK     0      -1.526 -11.357   0.000  0.00  0.00           C+0
HETATM   41  C   UNK     0      -2.880 -12.091   0.000  0.00  0.00           C+0
HETATM   42  C   UNK     0      -1.357 -13.529   0.000  0.00  0.00           C+0
HETATM   43  O   UNK     0      -2.387 -14.673   0.000  0.00  0.00           O+0
HETATM   44  C   UNK     0      -0.023 -14.299   0.000  0.00  0.00           C+0
HETATM   45  O   UNK     0      -0.928 -15.544   0.000  0.00  0.00           O+0
HETATM   46  C   UNK     0       1.311 -13.529   0.000  0.00  0.00           C+0
HETATM   47  O   UNK     0       1.937 -14.935   0.000  0.00  0.00           O+0
HETATM   48  C   UNK     0       2.795  -8.347   0.000  0.00  0.00           C+0
HETATM   49  O   UNK     0       1.461  -9.117   0.000  0.00  0.00           O+0
HETATM   50  C   UNK     0       0.128  -8.347   0.000  0.00  0.00           C+0
HETATM   51  C   UNK     0      -1.206  -9.117   0.000  0.00  0.00           C+0
HETATM   52  C   UNK     0      -1.206 -10.657   0.000  0.00  0.00           C+0
HETATM   53  C   UNK     0      -2.540 -11.427   0.000  0.00  0.00           C+0
HETATM   54  C   UNK     0      -3.874 -10.657   0.000  0.00  0.00           C+0
HETATM   55  O   UNK     0      -5.207 -11.427   0.000  0.00  0.00           O+0
HETATM   56  C   UNK     0      -3.874  -9.117   0.000  0.00  0.00           C+0
HETATM   57  O   UNK     0      -5.207  -8.347   0.000  0.00  0.00           O+0
HETATM   58  C   UNK     0      -2.540  -8.347   0.000  0.00  0.00           C+0
HETATM   59  C   UNK     0      -2.540  -2.187   0.000  0.00  0.00           C+0
HETATM   60  C   UNK     0      -3.874  -1.417   0.000  0.00  0.00           C+0
HETATM   61  C   UNK     0      -5.207  -2.187   0.000  0.00  0.00           C+0
HETATM   62  O   UNK     0      -6.541  -1.417   0.000  0.00  0.00           O+0
CONECT    1    2                                                            
CONECT    2    1    3                                                       
CONECT    3    2    4   61                                                  
CONECT    4    3    5                                                       
CONECT    5    4    6   59                                                  
CONECT    6    5    7    8                                                  
CONECT    7    6                                                            
CONECT    8    6    9                                                       
CONECT    9    8   10   50                                                  
CONECT   10    9   11                                                       
CONECT   11   10   12   48                                                  
CONECT   12   11   13   14                                                  
CONECT   13   12                                                            
CONECT   14   12   15                                                       
CONECT   15   14   16   17                                                  
CONECT   16   15                                                            
CONECT   17   15   18   48                                                  
CONECT   18   17   19   36                                                  
CONECT   19   18   20   26                                                  
CONECT   20   19   21   22                                                  
CONECT   21   20                                                            
CONECT   22   20   23                                                       
CONECT   23   22   24   25                                                  
CONECT   24   23                                                            
CONECT   25   23   26                                                       
CONECT   26   25   19   27                                                  
CONECT   27   26   28                                                       
CONECT   28   27   29   36                                                  
CONECT   29   28   30   35                                                  
CONECT   30   29   31                                                       
CONECT   31   30   32                                                       
CONECT   32   31   33   34                                                  
CONECT   33   32                                                            
CONECT   34   32   35                                                       
CONECT   35   34   29                                                       
CONECT   36   28   18   37                                                  
CONECT   37   36   38                                                       
CONECT   38   37   39   46                                                  
CONECT   39   38   40                                                       
CONECT   40   39   41   42                                                  
CONECT   41   40                                                            
CONECT   42   40   43   44                                                  
CONECT   43   42                                                            
CONECT   44   42   45   46                                                  
CONECT   45   44                                                            
CONECT   46   44   38   47                                                  
CONECT   47   46                                                            
CONECT   48   17   11   49                                                  
CONECT   49   48   50                                                       
CONECT   50   49    9   51                                                  
CONECT   51   50   52   58                                                  
CONECT   52   51   53                                                       
CONECT   53   52   54                                                       
CONECT   54   53   55   56                                                  
CONECT   55   54                                                            
CONECT   56   54   57   58                                                  
CONECT   57   56                                                            
CONECT   58   56   51                                                       
CONECT   59    5   60                                                       
CONECT   60   59   61                                                       
CONECT   61   60    3   62                                                  
CONECT   62   61                                                            
MASTER        0    0    0    0    0    0    0    0   62    0  138    0
END

View in JSmol

Synonyms

Value	Source
(2R,3R)-8-[(2R,3S,4S)-5,7-Dihydroxy-2-(4-hydroxyphenyl)-3-{[(2S,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxy}-3,4-dihydro-2H-1-benzopyran-4-yl]-2-(3,4-dihydroxyphenyl)-5,7-dihydroxy-3,4-dihydro-2H-1-benzopyran-3-yl 4-hydroxy-3-methoxybenzoic acid	Generator

Chemical Formula

C₄₄H₄₂O₁₈

Average Mass

858.8020 Da

Monoisotopic Mass

858.23711 Da

IUPAC Name

Traditional Name

CAS Registry Number

Not Available

SMILES

COC1=CC(=CC=C1O)C(=O)O[C@@H]1CC2=C(O)C=C(O)C([C@H]3[C@H](O[C@@H]4O[C@@H](C)[C@H](O)[C@@H](O)[C@H]4O)[C@H](OC4=CC(O)=CC(O)=C34)C3=CC=C(O)C=C3)=C2O[C@@H]1C1=CC=C(O)C(O)=C1

InChI Identifier

InChI=1S/C44H42O18/c1-17-36(53)37(54)38(55)44(58-17)62-42-35(33-28(51)13-22(46)14-31(33)59-40(42)18-3-7-21(45)8-4-18)34-29(52)16-26(49)23-15-32(60-43(56)20-6-10-25(48)30(12-20)57-2)39(61-41(23)34)19-5-9-24(47)27(50)11-19/h3-14,16-17,32,35-40,42,44-55H,15H2,1-2H3/t17-,32+,35-,36-,37+,38+,39+,40+,42-,44-/m0/s1

InChI Key

WOHNSGMEHDFINH-JMKADCDZSA-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
Joannesia princeps	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as complex tannins. These are tannins made of a catechin bound to a gallotannin or elagitannin.

Kingdom

Organic compounds

Super Class

Phenylpropanoids and polyketides

Class

Tannins

Sub Class

Complex tannins

Direct Parent

Complex tannins

Alternative Parents

Substituents

Complex tannin
B-type proanthocyanidin
Proanthocyanidin
Bi- and polyflavonoid skeleton
Flavonoid-3-o-glycoside
Flavonoid o-glycoside
Catechin
Hydroxyflavonoid
3'-hydroxyflavonoid
Flavan-3-ol
4'-hydroxyflavonoid
5-hydroxyflavonoid
7-hydroxyflavonoid
Flavan
Hexose monosaccharide
P-hydroxybenzoic acid alkyl ester
P-hydroxybenzoic acid ester
O-glycosyl compound
M-methoxybenzoic acid or derivatives
Glycosyl compound
Benzoate ester
Chromane
Benzopyran
1-benzopyran
Methoxyphenol
Benzoic acid or derivatives
Phenol ether
Anisole
Phenoxy compound
Benzoyl
Catechol
Methoxybenzene
Phenol
Alkyl aryl ether
1-hydroxy-4-unsubstituted benzenoid
1-hydroxy-2-unsubstituted benzenoid
Benzenoid
Monocyclic benzene moiety
Oxane
Monosaccharide
Secondary alcohol
Carboxylic acid ester
Polyol
Ether
Oxacycle
Organoheterocyclic compound
Monocarboxylic acid or derivatives
Acetal
Carboxylic acid derivative
Organooxygen compound
Hydrocarbon derivative
Organic oxygen compound
Alcohol
Organic oxide
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	4.73	ChemAxon
pKa (Strongest Acidic)	8.51	ChemAxon
pKa (Strongest Basic)	-5.2	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	17	ChemAxon
Hydrogen Donor Count	11	ChemAxon
Polar Surface Area	294.98 Å²	ChemAxon
Rotatable Bond Count	9	ChemAxon
Refractivity	213.66 m³·mol⁻¹	ChemAxon
Polarizability	82.68 Å³	ChemAxon
Number of Rings	8	ChemAxon
Bioavailability	No	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

162901994

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for (2r,3r)-8-[(2r,3s,4s)-5,7-dihydroxy-2-(4-hydroxyphenyl)-3-{[(2s,3r,4r,5r,6s)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxy}-3,4-dihydro-2h-1-benzopyran-4-yl]-2-(3,4-dihydroxyphenyl)-5,7-dihydroxy-3,4-dihydro-2h-1-benzopyran-3-yl 4-hydroxy-3-methoxybenzoate (NP0207105)

MOL for NP0207105 ((2r,3r)-8-[(2r,3s,4s)-5,7-dihydroxy-2-(4-hydroxyphenyl)-3-{[(2s,3r,4r,5r,6s)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxy}-3,4-dihydro-2h-1-benzopyran-4-yl]-2-(3,4-dihydroxyphenyl)-5,7-dihydroxy-3,4-dihydro-2h-1-benzopyran-3-yl 4-hydroxy-3-methoxybenzoate)

3D MOL for NP0207105 ((2r,3r)-8-[(2r,3s,4s)-5,7-dihydroxy-2-(4-hydroxyphenyl)-3-{[(2s,3r,4r,5r,6s)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxy}-3,4-dihydro-2h-1-benzopyran-4-yl]-2-(3,4-dihydroxyphenyl)-5,7-dihydroxy-3,4-dihydro-2h-1-benzopyran-3-yl 4-hydroxy-3-methoxybenzoate)

3D SDF for NP0207105 ((2r,3r)-8-[(2r,3s,4s)-5,7-dihydroxy-2-(4-hydroxyphenyl)-3-{[(2s,3r,4r,5r,6s)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxy}-3,4-dihydro-2h-1-benzopyran-4-yl]-2-(3,4-dihydroxyphenyl)-5,7-dihydroxy-3,4-dihydro-2h-1-benzopyran-3-yl 4-hydroxy-3-methoxybenzoate)

3D-SDF for NP0207105 ((2r,3r)-8-[(2r,3s,4s)-5,7-dihydroxy-2-(4-hydroxyphenyl)-3-{[(2s,3r,4r,5r,6s)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxy}-3,4-dihydro-2h-1-benzopyran-4-yl]-2-(3,4-dihydroxyphenyl)-5,7-dihydroxy-3,4-dihydro-2h-1-benzopyran-3-yl 4-hydroxy-3-methoxybenzoate)

PDB for NP0207105 ((2r,3r)-8-[(2r,3s,4s)-5,7-dihydroxy-2-(4-hydroxyphenyl)-3-{[(2s,3r,4r,5r,6s)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxy}-3,4-dihydro-2h-1-benzopyran-4-yl]-2-(3,4-dihydroxyphenyl)-5,7-dihydroxy-3,4-dihydro-2h-1-benzopyran-3-yl 4-hydroxy-3-methoxybenzoate)

3D PDB for NP0207105 ((2r,3r)-8-[(2r,3s,4s)-5,7-dihydroxy-2-(4-hydroxyphenyl)-3-{[(2s,3r,4r,5r,6s)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxy}-3,4-dihydro-2h-1-benzopyran-4-yl]-2-(3,4-dihydroxyphenyl)-5,7-dihydroxy-3,4-dihydro-2h-1-benzopyran-3-yl 4-hydroxy-3-methoxybenzoate)

SMILES for NP0207105 ((2r,3r)-8-[(2r,3s,4s)-5,7-dihydroxy-2-(4-hydroxyphenyl)-3-{[(2s,3r,4r,5r,6s)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxy}-3,4-dihydro-2h-1-benzopyran-4-yl]-2-(3,4-dihydroxyphenyl)-5,7-dihydroxy-3,4-dihydro-2h-1-benzopyran-3-yl 4-hydroxy-3-methoxybenzoate)

INCHI for NP0207105 ((2r,3r)-8-[(2r,3s,4s)-5,7-dihydroxy-2-(4-hydroxyphenyl)-3-{[(2s,3r,4r,5r,6s)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxy}-3,4-dihydro-2h-1-benzopyran-4-yl]-2-(3,4-dihydroxyphenyl)-5,7-dihydroxy-3,4-dihydro-2h-1-benzopyran-3-yl 4-hydroxy-3-methoxybenzoate)

Structure for NP0207105 ((2r,3r)-8-[(2r,3s,4s)-5,7-dihydroxy-2-(4-hydroxyphenyl)-3-{[(2s,3r,4r,5r,6s)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxy}-3,4-dihydro-2h-1-benzopyran-4-yl]-2-(3,4-dihydroxyphenyl)-5,7-dihydroxy-3,4-dihydro-2h-1-benzopyran-3-yl 4-hydroxy-3-methoxybenzoate)

3D Structure for NP0207105 ((2r,3r)-8-[(2r,3s,4s)-5,7-dihydroxy-2-(4-hydroxyphenyl)-3-{[(2s,3r,4r,5r,6s)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxy}-3,4-dihydro-2h-1-benzopyran-4-yl]-2-(3,4-dihydroxyphenyl)-5,7-dihydroxy-3,4-dihydro-2h-1-benzopyran-3-yl 4-hydroxy-3-methoxybenzoate)