NP-MRD: Showing NP-Card for (5s)-5-[(4-hydroxyphenyl)methyl]-4-(4-methoxy-2-{[(2s,3r,4s,5s,6r)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}phenyl)-5h-furan-2-one (NP0231625)

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Record Information

Version

2.0

Created at

2022-09-06 12:34:19 UTC

Updated at

2022-09-06 12:34:19 UTC

NP-MRD ID

NP0231625

Secondary Accession Numbers

None

Natural Product Identification

Common Name

(5s)-5-[(4-hydroxyphenyl)methyl]-4-(4-methoxy-2-{[(2s,3r,4s,5s,6r)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}phenyl)-5h-furan-2-one

Description

CHEMBL3426721 belongs to the class of organic compounds known as phenolic glycosides. These are organic compounds containing a phenolic structure attached to a glycosyl moiety. Some examples of phenolic structures include lignans, and flavonoids. Among the sugar units found in natural glycosides are D-glucose, L-Fructose, and L rhamnose. (5s)-5-[(4-hydroxyphenyl)methyl]-4-(4-methoxy-2-{[(2s,3r,4s,5s,6r)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}phenyl)-5h-furan-2-one is found in Pueraria montana. Based on a literature review very few articles have been published on CHEMBL3426721.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652309062214342D          

 34 37  0  0  1  0            999 V2000
   -0.6078    1.1759    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1067    0.7634    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.1067   -0.0616    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8212   -0.4741    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8212   -1.2991    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1067   -1.7116    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1067   -2.5366    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7741   -3.0215    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5192   -3.8062    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0041   -4.4736    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3058   -3.8062    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5607   -3.0215    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -1.3454   -2.7666    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9584   -3.3186    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7869   -4.1256    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4000   -4.6776    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1846   -4.4227    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7977   -4.9747    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3562   -3.6157    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7431   -3.0637    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6078   -1.2991    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3222   -1.7116    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0367   -1.2991    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -2.7512   -1.7116    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4656   -1.2991    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -4.1801   -1.7116    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1801   -2.5366    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4656   -0.4741    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -4.1801   -0.0616    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7512   -0.0616    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
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   -1.3222   -0.0616    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6078   -0.4741    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0  0  0  0
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M  END

     RDKit          3D

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    2.8013   -0.7371   -0.1297 C   0  0  1  0  0  0  0  0  0  0  0  0
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    4.8985    0.3063   -0.7396 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7665    0.5368    0.3087 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.1211    0.3031    0.1760 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.6698   -0.1691   -1.0032 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.0389   -0.3960   -1.1095 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.8047   -0.3999   -2.0513 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.4629   -0.1694   -1.9229 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7188    0.4623    0.9640 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5309   -0.0918    0.0102 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8747   -0.0124   -0.2226 C   0  0  2  0  0  0  0  0  0  0  0  0
   -3.4638   -1.2889   -0.1189 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8423   -1.1385    0.0535 C   0  0  2  0  0  0  0  0  0  0  0  0
   -5.4550   -2.4989    0.3036 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.1960   -3.3135   -0.7912 O   0  0  0  0  0  0  0  0  0  0  0  0
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    5.3778    0.9074    1.2517 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.8010    0.4801    0.9868 H   0  0  0  0  0  0  0  0  0  0  0  0
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   -3.4166    0.6196    0.4937 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0337   -0.5384    0.9787 H   0  0  0  0  0  0  0  0  0  0  0  0
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 31 57  1  0
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 33 59  1  0
 34 60  1  0
M  END


  Mrv1652309062214342D          

 34 37  0  0  1  0            999 V2000
   -0.6078    1.1759    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1067    0.7634    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.1067   -0.0616    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
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   -4.1801   -0.0616    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
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M  END
> <DATABASE_ID>
NP0231625

> <DATABASE_NAME>
NP-MRD

> <SMILES>
COC1=CC=C(C2=CC(=O)O[C@H]2CC2=CC=C(O)C=C2)C(O[C@@H]2O[C@H](CO)[C@@H](O)[C@H](O)[C@H]2O)=C1

> <INCHI_IDENTIFIER>
InChI=1S/C24H26O10/c1-31-14-6-7-15(16-10-20(27)32-17(16)8-12-2-4-13(26)5-3-12)18(9-14)33-24-23(30)22(29)21(28)19(11-25)34-24/h2-7,9-10,17,19,21-26,28-30H,8,11H2,1H3/t17-,19+,21+,22-,23+,24+/m0/s1

> <INCHI_KEY>
IOVBNDMOPKKFCH-SVBUQHLSSA-N

> <FORMULA>
C24H26O10

> <MOLECULAR_WEIGHT>
474.462

> <EXACT_MASS>
474.152597037

> <JCHEM_ACCEPTOR_COUNT>
9

> <JCHEM_ATOM_COUNT>
60

> <JCHEM_AVERAGE_POLARIZABILITY>
47.151730799661664

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
5

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
(5S)-5-[(4-hydroxyphenyl)methyl]-4-(4-methoxy-2-{[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}phenyl)-2,5-dihydrofuran-2-one

> <JCHEM_LOGP>
1.0925455563333335

> <JCHEM_MDDR_LIKE_RULE>
1

> <JCHEM_NUMBER_OF_RINGS>
4

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
9.525180164644832

> <JCHEM_PKA_STRONGEST_ACIDIC>
7.363555401754381

> <JCHEM_PKA_STRONGEST_BASIC>
-2.9810923462238517

> <JCHEM_POLAR_SURFACE_AREA>
155.14000000000001

> <JCHEM_REFRACTIVITY>
117.23160000000004

> <JCHEM_ROTATABLE_BOND_COUNT>
7

> <JCHEM_RULE_OF_FIVE>
1

> <JCHEM_TRADITIONAL_IUPAC>
(5S)-5-[(4-hydroxyphenyl)methyl]-4-(4-methoxy-2-{[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}phenyl)-5H-furan-2-one

> <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      -1.134   2.195   0.000  0.00  0.00           C+0
HETATM    2  O   UNK     0       0.199   1.425   0.000  0.00  0.00           O+0
HETATM    3  C   UNK     0       0.199  -0.115   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       1.533  -0.885   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       1.533  -2.425   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       0.199  -3.195   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       0.199  -4.735   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       1.445  -5.640   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       0.969  -7.105   0.000  0.00  0.00           C+0
HETATM   10  O   UNK     0       1.874  -8.351   0.000  0.00  0.00           O+0
HETATM   11  O   UNK     0      -0.571  -7.105   0.000  0.00  0.00           O+0
HETATM   12  C   UNK     0      -1.047  -5.640   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0      -2.511  -5.164   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0      -3.656  -6.195   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0      -3.336  -7.701   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0      -4.480  -8.732   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0      -5.945  -8.256   0.000  0.00  0.00           C+0
HETATM   18  O   UNK     0      -7.089  -9.286   0.000  0.00  0.00           O+0
HETATM   19  C   UNK     0      -6.265  -6.749   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0      -5.120  -5.719   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0      -1.134  -2.425   0.000  0.00  0.00           C+0
HETATM   22  O   UNK     0      -2.468  -3.195   0.000  0.00  0.00           O+0
HETATM   23  C   UNK     0      -3.802  -2.425   0.000  0.00  0.00           C+0
HETATM   24  O   UNK     0      -5.136  -3.195   0.000  0.00  0.00           O+0
HETATM   25  C   UNK     0      -6.469  -2.425   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0      -7.803  -3.195   0.000  0.00  0.00           C+0
HETATM   27  O   UNK     0      -7.803  -4.735   0.000  0.00  0.00           O+0
HETATM   28  C   UNK     0      -6.469  -0.885   0.000  0.00  0.00           C+0
HETATM   29  O   UNK     0      -7.803  -0.115   0.000  0.00  0.00           O+0
HETATM   30  C   UNK     0      -5.136  -0.115   0.000  0.00  0.00           C+0
HETATM   31  O   UNK     0      -5.136   1.425   0.000  0.00  0.00           O+0
HETATM   32  C   UNK     0      -3.802  -0.885   0.000  0.00  0.00           C+0
HETATM   33  O   UNK     0      -2.468  -0.115   0.000  0.00  0.00           O+0
HETATM   34  C   UNK     0      -1.134  -0.885   0.000  0.00  0.00           C+0
CONECT    1    2                                                            
CONECT    2    1    3                                                       
CONECT    3    2    4   34                                                  
CONECT    4    3    5                                                       
CONECT    5    4    6                                                       
CONECT    6    5    7   21                                                  
CONECT    7    6    8   12                                                  
CONECT    8    7    9                                                       
CONECT    9    8   10   11                                                  
CONECT   10    9                                                            
CONECT   11    9   12                                                       
CONECT   12   11    7   13                                                  
CONECT   13   12   14                                                       
CONECT   14   13   15   20                                                  
CONECT   15   14   16                                                       
CONECT   16   15   17                                                       
CONECT   17   16   18   19                                                  
CONECT   18   17                                                            
CONECT   19   17   20                                                       
CONECT   20   19   14                                                       
CONECT   21    6   22   34                                                  
CONECT   22   21   23                                                       
CONECT   23   22   24   32                                                  
CONECT   24   23   25                                                       
CONECT   25   24   26   28                                                  
CONECT   26   25   27                                                       
CONECT   27   26                                                            
CONECT   28   25   29   30                                                  
CONECT   29   28                                                            
CONECT   30   28   31   32                                                  
CONECT   31   30                                                            
CONECT   32   30   23   33                                                  
CONECT   33   32                                                            
CONECT   34   21    3                                                       
MASTER        0    0    0    0    0    0    0    0   34    0   74    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₂₄H₂₆O₁₀

Average Mass

474.4620 Da

Monoisotopic Mass

474.15260 Da

IUPAC Name

(5S)-5-[(4-hydroxyphenyl)methyl]-4-(4-methoxy-2-{[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}phenyl)-2,5-dihydrofuran-2-one

Traditional Name

(5S)-5-[(4-hydroxyphenyl)methyl]-4-(4-methoxy-2-{[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}phenyl)-5H-furan-2-one

CAS Registry Number

Not Available

SMILES

COC1=CC=C(C2=CC(=O)O[C@H]2CC2=CC=C(O)C=C2)C(O[C@@H]2O[C@H](CO)[C@@H](O)[C@H](O)[C@H]2O)=C1

InChI Identifier

InChI=1S/C24H26O10/c1-31-14-6-7-15(16-10-20(27)32-17(16)8-12-2-4-13(26)5-3-12)18(9-14)33-24-23(30)22(29)21(28)19(11-25)34-24/h2-7,9-10,17,19,21-26,28-30H,8,11H2,1H3/t17-,19+,21+,22-,23+,24+/m0/s1

InChI Key

IOVBNDMOPKKFCH-SVBUQHLSSA-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
Pueraria montana	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as phenolic glycosides. These are organic compounds containing a phenolic structure attached to a glycosyl moiety. Some examples of phenolic structures include lignans, and flavonoids. Among the sugar units found in natural glycosides are D-glucose, L-Fructose, and L rhamnose.

Kingdom

Organic compounds

Super Class

Organic oxygen compounds

Class

Organooxygen compounds

Sub Class

Carbohydrates and carbohydrate conjugates

Direct Parent

Phenolic glycosides

Alternative Parents

Substituents

Phenolic glycoside
Hexose monosaccharide
O-glycosyl compound
Phenoxy compound
Anisole
Methoxybenzene
Phenol ether
1-hydroxy-2-unsubstituted benzenoid
Alkyl aryl ether
Phenol
Monocyclic benzene moiety
2-furanone
Monosaccharide
Oxane
Benzenoid
Enoate ester
Alpha,beta-unsaturated carboxylic ester
Dihydrofuran
Secondary alcohol
Carboxylic acid ester
Lactone
Oxacycle
Ether
Organoheterocyclic compound
Carboxylic acid derivative
Acetal
Polyol
Monocarboxylic acid or derivatives
Carbonyl group
Alcohol
Hydrocarbon derivative
Primary alcohol
Organic oxide
Aromatic heteromonocyclic compound

Molecular Framework

Aromatic heteromonocyclic 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	1.09	ChemAxon
pKa (Strongest Acidic)	7.36	ChemAxon
pKa (Strongest Basic)	-3	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	9	ChemAxon
Hydrogen Donor Count	5	ChemAxon
Polar Surface Area	155.14 Å²	ChemAxon
Rotatable Bond Count	7	ChemAxon
Refractivity	117.23 m³·mol⁻¹	ChemAxon
Polarizability	47.15 Å³	ChemAxon
Number of Rings	4	ChemAxon
Bioavailability	Yes	ChemAxon
Rule of Five	Yes	ChemAxon
Ghose Filter	Yes	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

58990409

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

118737372

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for (5s)-5-[(4-hydroxyphenyl)methyl]-4-(4-methoxy-2-{[(2s,3r,4s,5s,6r)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}phenyl)-5h-furan-2-one (NP0231625)

MOL for NP0231625 ((5s)-5-[(4-hydroxyphenyl)methyl]-4-(4-methoxy-2-{[(2s,3r,4s,5s,6r)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}phenyl)-5h-furan-2-one)

3D MOL for NP0231625 ((5s)-5-[(4-hydroxyphenyl)methyl]-4-(4-methoxy-2-{[(2s,3r,4s,5s,6r)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}phenyl)-5h-furan-2-one)

3D SDF for NP0231625 ((5s)-5-[(4-hydroxyphenyl)methyl]-4-(4-methoxy-2-{[(2s,3r,4s,5s,6r)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}phenyl)-5h-furan-2-one)

3D-SDF for NP0231625 ((5s)-5-[(4-hydroxyphenyl)methyl]-4-(4-methoxy-2-{[(2s,3r,4s,5s,6r)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}phenyl)-5h-furan-2-one)

PDB for NP0231625 ((5s)-5-[(4-hydroxyphenyl)methyl]-4-(4-methoxy-2-{[(2s,3r,4s,5s,6r)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}phenyl)-5h-furan-2-one)

3D PDB for NP0231625 ((5s)-5-[(4-hydroxyphenyl)methyl]-4-(4-methoxy-2-{[(2s,3r,4s,5s,6r)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}phenyl)-5h-furan-2-one)

SMILES for NP0231625 ((5s)-5-[(4-hydroxyphenyl)methyl]-4-(4-methoxy-2-{[(2s,3r,4s,5s,6r)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}phenyl)-5h-furan-2-one)

INCHI for NP0231625 ((5s)-5-[(4-hydroxyphenyl)methyl]-4-(4-methoxy-2-{[(2s,3r,4s,5s,6r)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}phenyl)-5h-furan-2-one)

Structure for NP0231625 ((5s)-5-[(4-hydroxyphenyl)methyl]-4-(4-methoxy-2-{[(2s,3r,4s,5s,6r)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}phenyl)-5h-furan-2-one)

3D Structure for NP0231625 ((5s)-5-[(4-hydroxyphenyl)methyl]-4-(4-methoxy-2-{[(2s,3r,4s,5s,6r)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}phenyl)-5h-furan-2-one)