NP-MRD: Showing NP-Card for 2-(furan-3-yl)-4a,9-dihydroxy-10b-methyl-4-oxo-7-{[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}-decahydronaphtho[2,1-c]pyran-10-yl acetate (NP0255601)

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Record Information

Version

1.0

Created at

2022-09-07 20:09:04 UTC

Updated at

2022-09-07 20:09:04 UTC

NP-MRD ID

NP0255601

Secondary Accession Numbers

None

Natural Product Identification

Common Name

2-(furan-3-yl)-4a,9-dihydroxy-10b-methyl-4-oxo-7-{[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}-decahydronaphtho[2,1-c]pyran-10-yl acetate

Description

2-(Furan-3-yl)-4a,9-dihydroxy-10b-methyl-4-oxo-7-{[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}-dodecahydro-1H-naphtho[2,1-c]pyran-10-yl acetate belongs to the class of organic compounds known as naphthopyrans. Naphthopyrans are compounds containing a pyran ring fused to a naphthalene moiety. Furan is a 6 membered-ring non-aromatic ring with five carbon and one oxygen atoms. Naphthalene is a polycyclic aromatic hydrocarbon made up of two fused benzene rings. 2-(furan-3-yl)-4a,9-dihydroxy-10b-methyl-4-oxo-7-{[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}-decahydronaphtho[2,1-c]pyran-10-yl acetate is found in Tinospora sinensis. 2-(Furan-3-yl)-4a,9-dihydroxy-10b-methyl-4-oxo-7-{[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}-dodecahydro-1H-naphtho[2,1-c]pyran-10-yl acetate is an extremely weak basic (essentially neutral) compound (based on its pKa).

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1533004251512382D          

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M  END

     RDKit          3D

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M  END


  Mrv1533004251512382D          

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    6.1579   -0.8250    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.7454   -1.5395    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.9204   -1.5395    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5079   -0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0954   -1.5395    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6829   -0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.1579   -2.2539    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.9784   -2.3402    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.1499   -3.1471    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.4354   -3.5596    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.8223   -3.0076    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0  0  0  0
  2  3  2  0  0  0  0
  2  4  1  0  0  0  0
  4  5  1  0  0  0  0
  5  6  1  0  0  0  0
  6  7  1  0  0  0  0
  6  8  1  0  0  0  0
  8  9  1  0  0  0  0
  9 10  1  0  0  0  0
 10 11  1  0  0  0  0
 11 12  1  0  0  0  0
 12 13  1  0  0  0  0
 13 14  1  0  0  0  0
 14 15  1  0  0  0  0
 13 16  1  0  0  0  0
 16 17  1  0  0  0  0
 16 18  1  0  0  0  0
 18 19  1  0  0  0  0
 18 20  1  0  0  0  0
 11 20  1  0  0  0  0
 20 21  1  0  0  0  0
  9 22  1  0  0  0  0
 22 23  1  0  0  0  0
 23 24  1  0  0  0  0
 24 25  1  0  0  0  0
 25 26  1  0  0  0  0
 25 27  1  0  0  0  0
 27 28  2  0  0  0  0
 27 29  1  0  0  0  0
 29 30  1  0  0  0  0
 30 31  1  0  0  0  0
 31 32  1  0  0  0  0
 25 32  1  0  0  0  0
 32 33  1  0  0  0  0
 32 34  1  0  0  0  0
  5 34  1  0  0  0  0
 22 34  1  0  0  0  0
 30 35  1  0  0  0  0
 35 36  2  0  0  0  0
 36 37  1  0  0  0  0
 37 38  1  0  0  0  0
 38 39  2  0  0  0  0
 35 39  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0255601

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CC(=O)OC1C(O)CC(OC2OC(CO)C(O)C(O)C2O)C2CCC3(O)C(=O)OC(CC3(C)C12)C1=COC=C1

> <INCHI_IDENTIFIER>
InChI=1S/C26H36O13/c1-11(28)36-22-14(29)7-15(37-23-21(32)20(31)19(30)17(9-27)38-23)13-3-5-26(34)24(33)39-16(12-4-6-35-10-12)8-25(26,2)18(13)22/h4,6,10,13-23,27,29-32,34H,3,5,7-9H2,1-2H3

> <INCHI_KEY>
GADVYUZLGRAFKB-UHFFFAOYSA-N

> <FORMULA>
C26H36O13

> <MOLECULAR_WEIGHT>
556.561

> <EXACT_MASS>
556.215591219

> <JCHEM_ACCEPTOR_COUNT>
10

> <JCHEM_ATOM_COUNT>
75

> <JCHEM_AVERAGE_POLARIZABILITY>
55.30394828802131

> <JCHEM_BIOAVAILABILITY>
0

> <JCHEM_DONOR_COUNT>
6

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
2-(furan-3-yl)-4a,9-dihydroxy-10b-methyl-4-oxo-7-{[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}-dodecahydro-1H-naphtho[2,1-c]pyran-10-yl acetate

> <ALOGPS_LOGP>
-1.21

> <JCHEM_LOGP>
-1.7688433450000005

> <ALOGPS_LOGS>
-1.63

> <JCHEM_MDDR_LIKE_RULE>
1

> <JCHEM_NUMBER_OF_RINGS>
5

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
12.389121747627016

> <JCHEM_PKA_STRONGEST_ACIDIC>
11.795728684604077

> <JCHEM_PKA_STRONGEST_BASIC>
-2.874229291356496

> <JCHEM_POLAR_SURFACE_AREA>
205.57999999999998

> <JCHEM_REFRACTIVITY>
126.66799999999999

> <JCHEM_ROTATABLE_BOND_COUNT>
6

> <JCHEM_RULE_OF_FIVE>
0

> <ALOGPS_SOLUBILITY>
1.31e+01 g/l

> <JCHEM_TRADITIONAL_IUPAC>
2-(furan-3-yl)-4a,9-dihydroxy-10b-methyl-4-oxo-7-{[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}-decahydronaphtho[2,1-c]pyran-10-yl acetate

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 25-APR-15   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   25-APR-15         0                                  
HETATM    1  C   UNK     0       4.565  -5.541   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       6.105  -5.541   0.000  0.00  0.00           C+0
HETATM    3  O   UNK     0       6.875  -6.875   0.000  0.00  0.00           O+0
HETATM    4  O   UNK     0       6.875  -4.207   0.000  0.00  0.00           O+0
HETATM    5  C   UNK     0       6.105  -2.874   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       4.565  -2.874   0.000  0.00  0.00           C+0
HETATM    7  O   UNK     0       3.795  -4.207   0.000  0.00  0.00           O+0
HETATM    8  C   UNK     0       3.795  -1.540   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       4.565  -0.206   0.000  0.00  0.00           C+0
HETATM   10  O   UNK     0       3.795   1.127   0.000  0.00  0.00           O+0
HETATM   11  C   UNK     0       2.255   1.127   0.000  0.00  0.00           C+0
HETATM   12  O   UNK     0       1.485   2.461   0.000  0.00  0.00           O+0
HETATM   13  C   UNK     0      -0.055   2.461   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0      -0.825   3.795   0.000  0.00  0.00           C+0
HETATM   15  O   UNK     0      -2.365   3.795   0.000  0.00  0.00           O+0
HETATM   16  C   UNK     0      -0.825   1.127   0.000  0.00  0.00           C+0
HETATM   17  O   UNK     0      -2.365   1.127   0.000  0.00  0.00           O+0
HETATM   18  C   UNK     0      -0.055  -0.206   0.000  0.00  0.00           C+0
HETATM   19  O   UNK     0      -0.825  -1.540   0.000  0.00  0.00           O+0
HETATM   20  C   UNK     0       1.485  -0.206   0.000  0.00  0.00           C+0
HETATM   21  O   UNK     0       2.255  -1.540   0.000  0.00  0.00           O+0
HETATM   22  C   UNK     0       6.105  -0.206   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0       6.875   1.127   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0       8.415   1.127   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0       9.185  -0.206   0.000  0.00  0.00           C+0
HETATM   26  O   UNK     0       9.955   1.127   0.000  0.00  0.00           O+0
HETATM   27  C   UNK     0      10.725  -0.206   0.000  0.00  0.00           C+0
HETATM   28  O   UNK     0      11.495   1.127   0.000  0.00  0.00           O+0
HETATM   29  O   UNK     0      11.495  -1.540   0.000  0.00  0.00           O+0
HETATM   30  C   UNK     0      10.725  -2.874   0.000  0.00  0.00           C+0
HETATM   31  C   UNK     0       9.185  -2.874   0.000  0.00  0.00           C+0
HETATM   32  C   UNK     0       8.415  -1.540   0.000  0.00  0.00           C+0
HETATM   33  C   UNK     0       7.645  -2.874   0.000  0.00  0.00           C+0
HETATM   34  C   UNK     0       6.875  -1.540   0.000  0.00  0.00           C+0
HETATM   35  C   UNK     0      11.495  -4.207   0.000  0.00  0.00           C+0
HETATM   36  C   UNK     0      13.026  -4.368   0.000  0.00  0.00           C+0
HETATM   37  O   UNK     0      13.346  -5.875   0.000  0.00  0.00           O+0
HETATM   38  C   UNK     0      12.013  -6.645   0.000  0.00  0.00           C+0
HETATM   39  C   UNK     0      10.868  -5.614   0.000  0.00  0.00           C+0
CONECT    1    2                                                            
CONECT    2    1    3    4                                                  
CONECT    3    2                                                            
CONECT    4    2    5                                                       
CONECT    5    4    6   34                                                  
CONECT    6    5    7    8                                                  
CONECT    7    6                                                            
CONECT    8    6    9                                                       
CONECT    9    8   10   22                                                  
CONECT   10    9   11                                                       
CONECT   11   10   12   20                                                  
CONECT   12   11   13                                                       
CONECT   13   12   14   16                                                  
CONECT   14   13   15                                                       
CONECT   15   14                                                            
CONECT   16   13   17   18                                                  
CONECT   17   16                                                            
CONECT   18   16   19   20                                                  
CONECT   19   18                                                            
CONECT   20   18   11   21                                                  
CONECT   21   20                                                            
CONECT   22    9   23   34                                                  
CONECT   23   22   24                                                       
CONECT   24   23   25                                                       
CONECT   25   24   26   27   32                                             
CONECT   26   25                                                            
CONECT   27   25   28   29                                                  
CONECT   28   27                                                            
CONECT   29   27   30                                                       
CONECT   30   29   31   35                                                  
CONECT   31   30   32                                                       
CONECT   32   31   25   33   34                                             
CONECT   33   32                                                            
CONECT   34   32    5   22                                                  
CONECT   35   30   36   39                                                  
CONECT   36   35   37                                                       
CONECT   37   36   38                                                       
CONECT   38   37   39                                                       
CONECT   39   38   35                                                       
MASTER        0    0    0    0    0    0    0    0   39    0   86    0
END

View in JSmol

Synonyms

Value	Source
2-(Furan-3-yl)-4a,9-dihydroxy-10b-methyl-4-oxo-7-{[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}-dodecahydro-1H-naphtho[2,1-c]pyran-10-yl acetic acid	Generator

Chemical Formula

C₂₆H₃₆O₁₃

Average Mass

556.5610 Da

Monoisotopic Mass

556.21559 Da

IUPAC Name

2-(furan-3-yl)-4a,9-dihydroxy-10b-methyl-4-oxo-7-{[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}-dodecahydro-1H-naphtho[2,1-c]pyran-10-yl acetate

Traditional Name

2-(furan-3-yl)-4a,9-dihydroxy-10b-methyl-4-oxo-7-{[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}-decahydronaphtho[2,1-c]pyran-10-yl acetate

CAS Registry Number

Not Available

SMILES

CC(=O)OC1C(O)CC(OC2OC(CO)C(O)C(O)C2O)C2CCC3(O)C(=O)OC(CC3(C)C12)C1=COC=C1

InChI Identifier

InChI=1S/C26H36O13/c1-11(28)36-22-14(29)7-15(37-23-21(32)20(31)19(30)17(9-27)38-23)13-3-5-26(34)24(33)39-16(12-4-6-35-10-12)8-25(26,2)18(13)22/h4,6,10,13-23,27,29-32,34H,3,5,7-9H2,1-2H3

InChI Key

GADVYUZLGRAFKB-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
Tinospora sinensis	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as naphthopyrans. Naphthopyrans are compounds containing a pyran ring fused to a naphthalene moiety. Furan is a 6 membered-ring non-aromatic ring with five carbon and one oxygen atoms. Naphthalene is a polycyclic aromatic hydrocarbon made up of two fused benzene rings.

Kingdom

Organic compounds

Super Class

Organoheterocyclic compounds

Class

Naphthopyrans

Sub Class

Not Available

Direct Parent

Naphthopyrans

Alternative Parents

Substituents

Naphthopyran
Hexose monosaccharide
Glycosyl compound
O-glycosyl compound
Naphthalene
Delta valerolactone
Delta_valerolactone
Cyclitol or derivatives
Dicarboxylic acid or derivatives
Monosaccharide
Pyran
Oxane
Cyclic alcohol
Furan
Heteroaromatic compound
Tertiary alcohol
Lactone
Carboxylic acid ester
Secondary alcohol
Oxacycle
Acetal
Carboxylic acid derivative
Polyol
Organic oxygen compound
Alcohol
Hydrocarbon derivative
Organic oxide
Carbonyl group
Primary alcohol
Organooxygen 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	-1.2	ALOGPS
logP	-1.8	ChemAxon
logS	-1.6	ALOGPS
pKa (Strongest Acidic)	11.8	ChemAxon
pKa (Strongest Basic)	-2.9	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	10	ChemAxon
Hydrogen Donor Count	6	ChemAxon
Polar Surface Area	205.58 Å²	ChemAxon
Rotatable Bond Count	6	ChemAxon
Refractivity	126.67 m³·mol⁻¹	ChemAxon
Polarizability	55.3 Å³	ChemAxon
Number of Rings	5	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

Not Available

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for 2-(furan-3-yl)-4a,9-dihydroxy-10b-methyl-4-oxo-7-{[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}-decahydronaphtho[2,1-c]pyran-10-yl acetate (NP0255601)

MOL for NP0255601 (2-(furan-3-yl)-4a,9-dihydroxy-10b-methyl-4-oxo-7-{[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}-decahydronaphtho[2,1-c]pyran-10-yl acetate)

3D MOL for NP0255601 (2-(furan-3-yl)-4a,9-dihydroxy-10b-methyl-4-oxo-7-{[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}-decahydronaphtho[2,1-c]pyran-10-yl acetate)

3D SDF for NP0255601 (2-(furan-3-yl)-4a,9-dihydroxy-10b-methyl-4-oxo-7-{[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}-decahydronaphtho[2,1-c]pyran-10-yl acetate)

3D-SDF for NP0255601 (2-(furan-3-yl)-4a,9-dihydroxy-10b-methyl-4-oxo-7-{[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}-decahydronaphtho[2,1-c]pyran-10-yl acetate)

PDB for NP0255601 (2-(furan-3-yl)-4a,9-dihydroxy-10b-methyl-4-oxo-7-{[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}-decahydronaphtho[2,1-c]pyran-10-yl acetate)

3D PDB for NP0255601 (2-(furan-3-yl)-4a,9-dihydroxy-10b-methyl-4-oxo-7-{[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}-decahydronaphtho[2,1-c]pyran-10-yl acetate)

SMILES for NP0255601 (2-(furan-3-yl)-4a,9-dihydroxy-10b-methyl-4-oxo-7-{[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}-decahydronaphtho[2,1-c]pyran-10-yl acetate)

INCHI for NP0255601 (2-(furan-3-yl)-4a,9-dihydroxy-10b-methyl-4-oxo-7-{[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}-decahydronaphtho[2,1-c]pyran-10-yl acetate)

Structure for NP0255601 (2-(furan-3-yl)-4a,9-dihydroxy-10b-methyl-4-oxo-7-{[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}-decahydronaphtho[2,1-c]pyran-10-yl acetate)

3D Structure for NP0255601 (2-(furan-3-yl)-4a,9-dihydroxy-10b-methyl-4-oxo-7-{[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}-decahydronaphtho[2,1-c]pyran-10-yl acetate)