NP-MRD: Showing NP-Card for (2s,3r,4s,5r,6r)-4,5-dihydroxy-2-methyl-6-{[(2r,3s,4s,5r,6s)-3,4,5-trihydroxy-6-[(6-methoxy-2-oxochromen-7-yl)oxy]oxan-2-yl]methoxy}oxan-3-yl acetate (NP0308615)

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Record Information

Version

2.0

Created at

2022-09-11 02:31:01 UTC

Updated at

2022-09-11 02:31:02 UTC

NP-MRD ID

NP0308615

Secondary Accession Numbers

None

Natural Product Identification

Common Name

(2s,3r,4s,5r,6r)-4,5-dihydroxy-2-methyl-6-{[(2r,3s,4s,5r,6s)-3,4,5-trihydroxy-6-[(6-methoxy-2-oxochromen-7-yl)oxy]oxan-2-yl]methoxy}oxan-3-yl acetate

Description

(2S,3R,4S,5R,6R)-4,5-dihydroxy-2-methyl-6-{[(2R,3S,4S,5R,6S)-3,4,5-trihydroxy-6-[(6-methoxy-2-oxo-2H-chromen-7-yl)oxy]oxan-2-yl]methoxy}oxan-3-yl acetate belongs to the class of organic compounds known as coumarin glycosides. These are aromatic compounds containing a carbohydrate moiety glycosidically bound to a coumarin moiety. (2s,3r,4s,5r,6r)-4,5-dihydroxy-2-methyl-6-{[(2r,3s,4s,5r,6s)-3,4,5-trihydroxy-6-[(6-methoxy-2-oxochromen-7-yl)oxy]oxan-2-yl]methoxy}oxan-3-yl acetate is found in Haplophyllum acutifolium. Based on a literature review very few articles have been published on (2S,3R,4S,5R,6R)-4,5-dihydroxy-2-methyl-6-{[(2R,3S,4S,5R,6S)-3,4,5-trihydroxy-6-[(6-methoxy-2-oxo-2H-chromen-7-yl)oxy]oxan-2-yl]methoxy}oxan-3-yl acetate.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652309112204312D          

 38 41  0  0  1  0            999 V2000
    0.0000    0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000    0.0000    0.0000 O   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    0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
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    2.8579    0.0000    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
    3.5724   -1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2868   -1.6500    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
    2.1434   -1.2375    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
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    0.0000   -1.6500    0.0000 O   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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  8 10  1  0  0  0  0
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  5 11  1  0  0  0  0
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 20 19  1  6  0  0  0
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 21 22  1  0  0  0  0
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 35 37  1  0  0  0  0
 15 37  1  0  0  0  0
 37 38  1  6  0  0  0
M  END

     RDKit          3D

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M  END


  Mrv1652309112204312D          

 38 41  0  0  1  0            999 V2000
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  5  6  1  0  0  0  0
  6  7  2  0  0  0  0
  7  8  1  0  0  0  0
  8  9  2  0  0  0  0
  8 10  1  0  0  0  0
 10 11  1  0  0  0  0
  5 11  1  0  0  0  0
 11 12  2  0  0  0  0
 12 13  1  0  0  0  0
  3 13  2  0  0  0  0
 13 14  1  0  0  0  0
 15 14  1  1  0  0  0
 15 16  1  0  0  0  0
 16 17  1  0  0  0  0
 17 18  1  1  0  0  0
 18 19  1  0  0  0  0
 20 19  1  6  0  0  0
 20 21  1  0  0  0  0
 21 22  1  0  0  0  0
 22 23  1  1  0  0  0
 22 24  1  0  0  0  0
 24 25  1  6  0  0  0
 25 26  1  0  0  0  0
 26 27  1  0  0  0  0
 26 28  2  0  0  0  0
 24 29  1  0  0  0  0
 29 30  1  1  0  0  0
 29 31  1  0  0  0  0
 20 31  1  0  0  0  0
 31 32  1  1  0  0  0
 17 33  1  0  0  0  0
 33 34  1  6  0  0  0
 33 35  1  0  0  0  0
 35 36  1  1  0  0  0
 35 37  1  0  0  0  0
 15 37  1  0  0  0  0
 37 38  1  6  0  0  0
M  END
> <DATABASE_ID>
NP0308615

> <DATABASE_NAME>
NP-MRD

> <SMILES>
COC1=C(O[C@@H]2O[C@H](CO[C@@H]3O[C@@H](C)[C@H](OC(C)=O)[C@@H](O)[C@H]3O)[C@@H](O)[C@H](O)[C@H]2O)C=C2OC(=O)C=CC2=C1

> <INCHI_IDENTIFIER>
InChI=1S/C24H30O14/c1-9-22(35-10(2)25)19(29)21(31)23(34-9)33-8-15-17(27)18(28)20(30)24(38-15)37-14-7-12-11(6-13(14)32-3)4-5-16(26)36-12/h4-7,9,15,17-24,27-31H,8H2,1-3H3/t9-,15+,17+,18-,19-,20+,21+,22-,23+,24+/m0/s1

> <INCHI_KEY>
JHSMQTZUUFFCMO-IAAIIRFQSA-N

> <FORMULA>
C24H30O14

> <MOLECULAR_WEIGHT>
542.49

> <EXACT_MASS>
542.163555646

> <JCHEM_ACCEPTOR_COUNT>
12

> <JCHEM_ATOM_COUNT>
68

> <JCHEM_AVERAGE_POLARIZABILITY>
51.91107732521707

> <JCHEM_BIOAVAILABILITY>
0

> <JCHEM_DONOR_COUNT>
5

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
(2S,3R,4S,5R,6R)-4,5-dihydroxy-2-methyl-6-{[(2R,3S,4S,5R,6S)-3,4,5-trihydroxy-6-[(6-methoxy-2-oxo-2H-chromen-7-yl)oxy]oxan-2-yl]methoxy}oxan-3-yl acetate

> <JCHEM_LOGP>
-1.2287453339999996

> <JCHEM_MDDR_LIKE_RULE>
1

> <JCHEM_NUMBER_OF_RINGS>
4

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
12.484363091084173

> <JCHEM_PKA_STRONGEST_ACIDIC>
11.934787715573247

> <JCHEM_PKA_STRONGEST_BASIC>
-3.648686014482922

> <JCHEM_POLAR_SURFACE_AREA>
199.9

> <JCHEM_REFRACTIVITY>
122.15820000000004

> <JCHEM_ROTATABLE_BOND_COUNT>
8

> <JCHEM_RULE_OF_FIVE>
0

> <JCHEM_TRADITIONAL_IUPAC>
(2S,3R,4S,5R,6R)-4,5-dihydroxy-2-methyl-6-{[(2R,3S,4S,5R,6S)-3,4,5-trihydroxy-6-[(6-methoxy-2-oxochromen-7-yl)oxy]oxan-2-yl]methoxy}oxan-3-yl acetate

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 11-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   11-SEP-22         0                                  
HETATM    1  C   UNK     0       0.000   1.540   0.000  0.00  0.00           C+0
HETATM    2  O   UNK     0       0.000   0.000   0.000  0.00  0.00           O+0
HETATM    3  C   UNK     0       1.334  -0.770   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       2.667   0.000   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       4.001  -0.770   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       5.335   0.000   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       6.668  -0.770   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       6.668  -2.310   0.000  0.00  0.00           C+0
HETATM    9  O   UNK     0       8.002  -3.080   0.000  0.00  0.00           O+0
HETATM   10  O   UNK     0       5.335  -3.080   0.000  0.00  0.00           O+0
HETATM   11  C   UNK     0       4.001  -2.310   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       2.667  -3.080   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       1.334  -2.310   0.000  0.00  0.00           C+0
HETATM   14  O   UNK     0       0.000  -3.080   0.000  0.00  0.00           O+0
HETATM   15  C   UNK     0      -1.334  -2.310   0.000  0.00  0.00           C+0
HETATM   16  O   UNK     0      -1.334  -0.770   0.000  0.00  0.00           O+0
HETATM   17  C   UNK     0      -2.667  -0.000   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0      -2.667   1.540   0.000  0.00  0.00           C+0
HETATM   19  O   UNK     0      -1.334   2.310   0.000  0.00  0.00           O+0
HETATM   20  C   UNK     0      -1.334   3.850   0.000  0.00  0.00           C+0
HETATM   21  O   UNK     0      -2.667   4.620   0.000  0.00  0.00           O+0
HETATM   22  C   UNK     0      -2.667   6.160   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0      -4.001   6.930   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0      -1.334   6.930   0.000  0.00  0.00           C+0
HETATM   25  O   UNK     0      -1.334   8.470   0.000  0.00  0.00           O+0
HETATM   26  C   UNK     0      -0.000   9.240   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0      -0.000  10.780   0.000  0.00  0.00           C+0
HETATM   28  O   UNK     0       1.334   8.470   0.000  0.00  0.00           O+0
HETATM   29  C   UNK     0      -0.000   6.160   0.000  0.00  0.00           C+0
HETATM   30  O   UNK     0       1.334   6.930   0.000  0.00  0.00           O+0
HETATM   31  C   UNK     0      -0.000   4.620   0.000  0.00  0.00           C+0
HETATM   32  O   UNK     0       1.334   3.850   0.000  0.00  0.00           O+0
HETATM   33  C   UNK     0      -4.001  -0.770   0.000  0.00  0.00           C+0
HETATM   34  O   UNK     0      -5.335  -0.000   0.000  0.00  0.00           O+0
HETATM   35  C   UNK     0      -4.001  -2.310   0.000  0.00  0.00           C+0
HETATM   36  O   UNK     0      -5.335  -3.080   0.000  0.00  0.00           O+0
HETATM   37  C   UNK     0      -2.667  -3.080   0.000  0.00  0.00           C+0
HETATM   38  O   UNK     0      -2.667  -4.620   0.000  0.00  0.00           O+0
CONECT    1    2                                                            
CONECT    2    1    3                                                       
CONECT    3    2    4   13                                                  
CONECT    4    3    5                                                       
CONECT    5    4    6   11                                                  
CONECT    6    5    7                                                       
CONECT    7    6    8                                                       
CONECT    8    7    9   10                                                  
CONECT    9    8                                                            
CONECT   10    8   11                                                       
CONECT   11   10    5   12                                                  
CONECT   12   11   13                                                       
CONECT   13   12    3   14                                                  
CONECT   14   13   15                                                       
CONECT   15   14   16   37                                                  
CONECT   16   15   17                                                       
CONECT   17   16   18   33                                                  
CONECT   18   17   19                                                       
CONECT   19   18   20                                                       
CONECT   20   19   21   31                                                  
CONECT   21   20   22                                                       
CONECT   22   21   23   24                                                  
CONECT   23   22                                                            
CONECT   24   22   25   29                                                  
CONECT   25   24   26                                                       
CONECT   26   25   27   28                                                  
CONECT   27   26                                                            
CONECT   28   26                                                            
CONECT   29   24   30   31                                                  
CONECT   30   29                                                            
CONECT   31   29   20   32                                                  
CONECT   32   31                                                            
CONECT   33   17   34   35                                                  
CONECT   34   33                                                            
CONECT   35   33   36   37                                                  
CONECT   36   35                                                            
CONECT   37   35   15   38                                                  
CONECT   38   37                                                            
MASTER        0    0    0    0    0    0    0    0   38    0   82    0
END

View in JSmol

Synonyms

Value	Source
(2S,3R,4S,5R,6R)-4,5-Dihydroxy-2-methyl-6-{[(2R,3S,4S,5R,6S)-3,4,5-trihydroxy-6-[(6-methoxy-2-oxo-2H-chromen-7-yl)oxy]oxan-2-yl]methoxy}oxan-3-yl acetic acid	Generator

Chemical Formula

C₂₄H₃₀O₁₄

Average Mass

542.4900 Da

Monoisotopic Mass

542.16356 Da

IUPAC Name

(2S,3R,4S,5R,6R)-4,5-dihydroxy-2-methyl-6-{[(2R,3S,4S,5R,6S)-3,4,5-trihydroxy-6-[(6-methoxy-2-oxo-2H-chromen-7-yl)oxy]oxan-2-yl]methoxy}oxan-3-yl acetate

Traditional Name

(2S,3R,4S,5R,6R)-4,5-dihydroxy-2-methyl-6-{[(2R,3S,4S,5R,6S)-3,4,5-trihydroxy-6-[(6-methoxy-2-oxochromen-7-yl)oxy]oxan-2-yl]methoxy}oxan-3-yl acetate

CAS Registry Number

Not Available

SMILES

COC1=C(O[C@@H]2O[C@H](CO[C@@H]3O[C@@H](C)[C@H](OC(C)=O)[C@@H](O)[C@H]3O)[C@@H](O)[C@H](O)[C@H]2O)C=C2OC(=O)C=CC2=C1

InChI Identifier

InChI=1S/C24H30O14/c1-9-22(35-10(2)25)19(29)21(31)23(34-9)33-8-15-17(27)18(28)20(30)24(38-15)37-14-7-12-11(6-13(14)32-3)4-5-16(26)36-12/h4-7,9,15,17-24,27-31H,8H2,1-3H3/t9-,15+,17+,18-,19-,20+,21+,22-,23+,24+/m0/s1

InChI Key

JHSMQTZUUFFCMO-IAAIIRFQSA-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
Haplophyllum acutifolium	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as coumarin glycosides. These are aromatic compounds containing a carbohydrate moiety glycosidically bound to a coumarin moiety.

Kingdom

Organic compounds

Super Class

Phenylpropanoids and polyketides

Class

Coumarins and derivatives

Sub Class

Coumarin glycosides

Direct Parent

Coumarin glycosides

Alternative Parents

Substituents

Coumarin-7-o-glycoside
Coumarin o-glycoside
Phenolic glycoside
Disaccharide
Glycosyl compound
O-glycosyl compound
Benzopyran
1-benzopyran
Anisole
Alkyl aryl ether
Pyranone
Benzenoid
Oxane
Pyran
Heteroaromatic compound
Carboxylic acid ester
Secondary alcohol
Lactone
Polyol
Carboxylic acid derivative
Monocarboxylic acid or derivatives
Oxacycle
Organoheterocyclic compound
Ether
Acetal
Organic oxygen compound
Organooxygen compound
Alcohol
Organic oxide
Hydrocarbon derivative
Carbonyl group
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	-1.2	ChemAxon
pKa (Strongest Acidic)	11.93	ChemAxon
pKa (Strongest Basic)	-3.6	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	12	ChemAxon
Hydrogen Donor Count	5	ChemAxon
Polar Surface Area	199.9 Å²	ChemAxon
Rotatable Bond Count	8	ChemAxon
Refractivity	122.16 m³·mol⁻¹	ChemAxon
Polarizability	51.91 Å³	ChemAxon
Number of Rings	4	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

162903603

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for (2s,3r,4s,5r,6r)-4,5-dihydroxy-2-methyl-6-{[(2r,3s,4s,5r,6s)-3,4,5-trihydroxy-6-[(6-methoxy-2-oxochromen-7-yl)oxy]oxan-2-yl]methoxy}oxan-3-yl acetate (NP0308615)

MOL for NP0308615 ((2s,3r,4s,5r,6r)-4,5-dihydroxy-2-methyl-6-{[(2r,3s,4s,5r,6s)-3,4,5-trihydroxy-6-[(6-methoxy-2-oxochromen-7-yl)oxy]oxan-2-yl]methoxy}oxan-3-yl acetate)

3D MOL for NP0308615 ((2s,3r,4s,5r,6r)-4,5-dihydroxy-2-methyl-6-{[(2r,3s,4s,5r,6s)-3,4,5-trihydroxy-6-[(6-methoxy-2-oxochromen-7-yl)oxy]oxan-2-yl]methoxy}oxan-3-yl acetate)

3D SDF for NP0308615 ((2s,3r,4s,5r,6r)-4,5-dihydroxy-2-methyl-6-{[(2r,3s,4s,5r,6s)-3,4,5-trihydroxy-6-[(6-methoxy-2-oxochromen-7-yl)oxy]oxan-2-yl]methoxy}oxan-3-yl acetate)

3D-SDF for NP0308615 ((2s,3r,4s,5r,6r)-4,5-dihydroxy-2-methyl-6-{[(2r,3s,4s,5r,6s)-3,4,5-trihydroxy-6-[(6-methoxy-2-oxochromen-7-yl)oxy]oxan-2-yl]methoxy}oxan-3-yl acetate)

PDB for NP0308615 ((2s,3r,4s,5r,6r)-4,5-dihydroxy-2-methyl-6-{[(2r,3s,4s,5r,6s)-3,4,5-trihydroxy-6-[(6-methoxy-2-oxochromen-7-yl)oxy]oxan-2-yl]methoxy}oxan-3-yl acetate)

3D PDB for NP0308615 ((2s,3r,4s,5r,6r)-4,5-dihydroxy-2-methyl-6-{[(2r,3s,4s,5r,6s)-3,4,5-trihydroxy-6-[(6-methoxy-2-oxochromen-7-yl)oxy]oxan-2-yl]methoxy}oxan-3-yl acetate)

SMILES for NP0308615 ((2s,3r,4s,5r,6r)-4,5-dihydroxy-2-methyl-6-{[(2r,3s,4s,5r,6s)-3,4,5-trihydroxy-6-[(6-methoxy-2-oxochromen-7-yl)oxy]oxan-2-yl]methoxy}oxan-3-yl acetate)

INCHI for NP0308615 ((2s,3r,4s,5r,6r)-4,5-dihydroxy-2-methyl-6-{[(2r,3s,4s,5r,6s)-3,4,5-trihydroxy-6-[(6-methoxy-2-oxochromen-7-yl)oxy]oxan-2-yl]methoxy}oxan-3-yl acetate)

Structure for NP0308615 ((2s,3r,4s,5r,6r)-4,5-dihydroxy-2-methyl-6-{[(2r,3s,4s,5r,6s)-3,4,5-trihydroxy-6-[(6-methoxy-2-oxochromen-7-yl)oxy]oxan-2-yl]methoxy}oxan-3-yl acetate)

3D Structure for NP0308615 ((2s,3r,4s,5r,6r)-4,5-dihydroxy-2-methyl-6-{[(2r,3s,4s,5r,6s)-3,4,5-trihydroxy-6-[(6-methoxy-2-oxochromen-7-yl)oxy]oxan-2-yl]methoxy}oxan-3-yl acetate)