NP-MRD: Showing NP-Card for [(2r,3s,4s,5r,6r)-3,4,5-trihydroxy-6-{[4-hydroxy-2,2,6,6-tetramethyl-4-(2-methylpropyl)-3,5-dioxocyclohexyl]oxy}oxan-2-yl]methyl 3,4,5-trihydroxybenzoate (NP0310519)

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Record Information

Version

2.0

Created at

2022-09-11 05:53:11 UTC

Updated at

2022-09-11 05:53:11 UTC

NP-MRD ID

NP0310519

Secondary Accession Numbers

None

Natural Product Identification

Common Name

[(2r,3s,4s,5r,6r)-3,4,5-trihydroxy-6-{[4-hydroxy-2,2,6,6-tetramethyl-4-(2-methylpropyl)-3,5-dioxocyclohexyl]oxy}oxan-2-yl]methyl 3,4,5-trihydroxybenzoate

Description

Gallomyrtucommulone B belongs to the class of organic compounds known as terpene glycosides. These are prenol lipids containing a carbohydrate moiety glycosidically bound to a terpene backbone. [(2r,3s,4s,5r,6r)-3,4,5-trihydroxy-6-{[4-hydroxy-2,2,6,6-tetramethyl-4-(2-methylpropyl)-3,5-dioxocyclohexyl]oxy}oxan-2-yl]methyl 3,4,5-trihydroxybenzoate is found in Myrtus communis. [(2r,3s,4s,5r,6r)-3,4,5-trihydroxy-6-{[4-hydroxy-2,2,6,6-tetramethyl-4-(2-methylpropyl)-3,5-dioxocyclohexyl]oxy}oxan-2-yl]methyl 3,4,5-trihydroxybenzoate was first documented in 2006 (PMID: 16499325). Based on a literature review very few articles have been published on Gallomyrtucommulone B.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652309112207532D          

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  5 39  1  0  0  0  0
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M  END

     RDKit          3D

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M  END


  Mrv1652309112207532D          

 40 42  0  0  1  0            999 V2000
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   -0.7145  -12.7875    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000  -11.5500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7145  -11.1375    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145  -11.1375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434   -8.6625    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.4289   -9.0750    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434   -7.8375    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.4289   -7.4250    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579   -7.4250    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.8579   -6.6000    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.5724   -6.1875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2902   -6.9627    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7599   -6.0442    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5724   -5.3625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579   -4.9500    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0  0  0  0
  2  3  1  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
  5  7  1  0  0  0  0
  7  8  2  0  0  0  0
  7  9  1  0  0  0  0
  9 10  1  0  0  0  0
  9 11  1  0  0  0  0
  9 12  1  0  0  0  0
 12 13  1  0  0  0  0
 14 13  1  6  0  0  0
 14 15  1  0  0  0  0
 15 16  1  0  0  0  0
 16 17  1  6  0  0  0
 17 18  1  0  0  0  0
 18 19  1  0  0  0  0
 19 20  2  0  0  0  0
 19 21  1  0  0  0  0
 21 22  2  0  0  0  0
 22 23  1  0  0  0  0
 23 24  1  0  0  0  0
 23 25  2  0  0  0  0
 25 26  1  0  0  0  0
 25 27  1  0  0  0  0
 27 28  1  0  0  0  0
 27 29  2  0  0  0  0
 21 29  1  0  0  0  0
 16 30  1  0  0  0  0
 30 31  1  1  0  0  0
 30 32  1  0  0  0  0
 32 33  1  6  0  0  0
 32 34  1  0  0  0  0
 14 34  1  0  0  0  0
 34 35  1  1  0  0  0
 12 36  1  0  0  0  0
 36 37  1  0  0  0  0
 36 38  1  0  0  0  0
 36 39  1  0  0  0  0
  5 39  1  0  0  0  0
 39 40  2  0  0  0  0
M  END
> <DATABASE_ID>
NP0310519

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CC(C)CC1(O)C(=O)C(C)(C)C(O[C@@H]2O[C@H](COC(=O)C3=CC(O)=C(O)C(O)=C3)[C@@H](O)[C@H](O)[C@H]2O)C(C)(C)C1=O

> <INCHI_IDENTIFIER>
InChI=1S/C27H38O13/c1-11(2)9-27(37)22(35)25(3,4)24(26(5,6)23(27)36)40-21-19(33)18(32)17(31)15(39-21)10-38-20(34)12-7-13(28)16(30)14(29)8-12/h7-8,11,15,17-19,21,24,28-33,37H,9-10H2,1-6H3/t15-,17-,18+,19-,21+,24?,27?/m1/s1

> <INCHI_KEY>
VKHZSJBPCYWANI-XXZDZOCTSA-N

> <FORMULA>
C27H38O13

> <MOLECULAR_WEIGHT>
570.588

> <EXACT_MASS>
570.231241284

> <JCHEM_ACCEPTOR_COUNT>
12

> <JCHEM_ATOM_COUNT>
78

> <JCHEM_AVERAGE_POLARIZABILITY>
55.780402099192386

> <JCHEM_BIOAVAILABILITY>
0

> <JCHEM_DONOR_COUNT>
7

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
[(2R,3S,4S,5R,6R)-3,4,5-trihydroxy-6-{[4-hydroxy-2,2,6,6-tetramethyl-4-(2-methylpropyl)-3,5-dioxocyclohexyl]oxy}oxan-2-yl]methyl 3,4,5-trihydroxybenzoate

> <JCHEM_LOGP>
2.729494276666667

> <JCHEM_MDDR_LIKE_RULE>
1

> <JCHEM_NUMBER_OF_RINGS>
3

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
10.973842676356364

> <JCHEM_PKA_STRONGEST_ACIDIC>
8.107597441476724

> <JCHEM_PKA_STRONGEST_BASIC>
-3.6490926816260245

> <JCHEM_POLAR_SURFACE_AREA>
220.50999999999996

> <JCHEM_REFRACTIVITY>
136.3562

> <JCHEM_ROTATABLE_BOND_COUNT>
8

> <JCHEM_RULE_OF_FIVE>
0

> <JCHEM_TRADITIONAL_IUPAC>
[(2R,3S,4S,5R,6R)-3,4,5-trihydroxy-6-{[4-hydroxy-2,2,6,6-tetramethyl-4-(2-methylpropyl)-3,5-dioxocyclohexyl]oxy}oxan-2-yl]methyl 3,4,5-trihydroxybenzoate

> <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       6.949  -6.346   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       8.465  -6.613   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       9.455  -5.433   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       8.992  -8.060   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       8.002  -9.240   0.000  0.00  0.00           C+0
HETATM    6  O   UNK     0       7.012  -8.060   0.000  0.00  0.00           O+0
HETATM    7  C   UNK     0       9.336 -10.010   0.000  0.00  0.00           C+0
HETATM    8  O   UNK     0      10.669  -9.240   0.000  0.00  0.00           O+0
HETATM    9  C   UNK     0       9.336 -11.550   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0      10.852 -11.283   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       9.862 -12.997   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       8.002 -12.320   0.000  0.00  0.00           C+0
HETATM   13  O   UNK     0       8.002 -13.860   0.000  0.00  0.00           O+0
HETATM   14  C   UNK     0       6.668 -14.630   0.000  0.00  0.00           C+0
HETATM   15  O   UNK     0       6.668 -16.170   0.000  0.00  0.00           O+0
HETATM   16  C   UNK     0       5.335 -16.940   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       5.335 -18.480   0.000  0.00  0.00           C+0
HETATM   18  O   UNK     0       4.001 -19.250   0.000  0.00  0.00           O+0
HETATM   19  C   UNK     0       4.001 -20.790   0.000  0.00  0.00           C+0
HETATM   20  O   UNK     0       5.335 -21.560   0.000  0.00  0.00           O+0
HETATM   21  C   UNK     0       2.667 -21.560   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0       2.667 -23.100   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0       1.334 -23.870   0.000  0.00  0.00           C+0
HETATM   24  O   UNK     0       1.334 -25.410   0.000  0.00  0.00           O+0
HETATM   25  C   UNK     0      -0.000 -23.100   0.000  0.00  0.00           C+0
HETATM   26  O   UNK     0      -1.334 -23.870   0.000  0.00  0.00           O+0
HETATM   27  C   UNK     0       0.000 -21.560   0.000  0.00  0.00           C+0
HETATM   28  O   UNK     0      -1.334 -20.790   0.000  0.00  0.00           O+0
HETATM   29  C   UNK     0       1.334 -20.790   0.000  0.00  0.00           C+0
HETATM   30  C   UNK     0       4.001 -16.170   0.000  0.00  0.00           C+0
HETATM   31  O   UNK     0       2.667 -16.940   0.000  0.00  0.00           O+0
HETATM   32  C   UNK     0       4.001 -14.630   0.000  0.00  0.00           C+0
HETATM   33  O   UNK     0       2.667 -13.860   0.000  0.00  0.00           O+0
HETATM   34  C   UNK     0       5.335 -13.860   0.000  0.00  0.00           C+0
HETATM   35  O   UNK     0       5.335 -12.320   0.000  0.00  0.00           O+0
HETATM   36  C   UNK     0       6.668 -11.550   0.000  0.00  0.00           C+0
HETATM   37  C   UNK     0       6.142 -12.997   0.000  0.00  0.00           C+0
HETATM   38  C   UNK     0       5.152 -11.283   0.000  0.00  0.00           C+0
HETATM   39  C   UNK     0       6.668 -10.010   0.000  0.00  0.00           C+0
HETATM   40  O   UNK     0       5.335  -9.240   0.000  0.00  0.00           O+0
CONECT    1    2                                                            
CONECT    2    1    3    4                                                  
CONECT    3    2                                                            
CONECT    4    2    5                                                       
CONECT    5    4    6    7   39                                             
CONECT    6    5                                                            
CONECT    7    5    8    9                                                  
CONECT    8    7                                                            
CONECT    9    7   10   11   12                                             
CONECT   10    9                                                            
CONECT   11    9                                                            
CONECT   12    9   13   36                                                  
CONECT   13   12   14                                                       
CONECT   14   13   15   34                                                  
CONECT   15   14   16                                                       
CONECT   16   15   17   30                                                  
CONECT   17   16   18                                                       
CONECT   18   17   19                                                       
CONECT   19   18   20   21                                                  
CONECT   20   19                                                            
CONECT   21   19   22   29                                                  
CONECT   22   21   23                                                       
CONECT   23   22   24   25                                                  
CONECT   24   23                                                            
CONECT   25   23   26   27                                                  
CONECT   26   25                                                            
CONECT   27   25   28   29                                                  
CONECT   28   27                                                            
CONECT   29   27   21                                                       
CONECT   30   16   31   32                                                  
CONECT   31   30                                                            
CONECT   32   30   33   34                                                  
CONECT   33   32                                                            
CONECT   34   32   14   35                                                  
CONECT   35   34                                                            
CONECT   36   12   37   38   39                                             
CONECT   37   36                                                            
CONECT   38   36                                                            
CONECT   39   36    5   40                                                  
CONECT   40   39                                                            
MASTER        0    0    0    0    0    0    0    0   40    0   84    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₂₇H₃₈O₁₃

Average Mass

570.5880 Da

Monoisotopic Mass

570.23124 Da

IUPAC Name

[(2R,3S,4S,5R,6R)-3,4,5-trihydroxy-6-{[4-hydroxy-2,2,6,6-tetramethyl-4-(2-methylpropyl)-3,5-dioxocyclohexyl]oxy}oxan-2-yl]methyl 3,4,5-trihydroxybenzoate

Traditional Name

[(2R,3S,4S,5R,6R)-3,4,5-trihydroxy-6-{[4-hydroxy-2,2,6,6-tetramethyl-4-(2-methylpropyl)-3,5-dioxocyclohexyl]oxy}oxan-2-yl]methyl 3,4,5-trihydroxybenzoate

CAS Registry Number

Not Available

SMILES

CC(C)CC1(O)C(=O)C(C)(C)C(O[C@@H]2O[C@H](COC(=O)C3=CC(O)=C(O)C(O)=C3)[C@@H](O)[C@H](O)[C@H]2O)C(C)(C)C1=O

InChI Identifier

InChI=1S/C27H38O13/c1-11(2)9-27(37)22(35)25(3,4)24(26(5,6)23(27)36)40-21-19(33)18(32)17(31)15(39-21)10-38-20(34)12-7-13(28)16(30)14(29)8-12/h7-8,11,15,17-19,21,24,28-33,37H,9-10H2,1-6H3/t15-,17-,18+,19-,21+,24?,27?/m1/s1

InChI Key

VKHZSJBPCYWANI-XXZDZOCTSA-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
Myrtus communis	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as terpene glycosides. These are prenol lipids containing a carbohydrate moiety glycosidically bound to a terpene backbone.

Kingdom

Organic compounds

Super Class

Lipids and lipid-like molecules

Class

Prenol lipids

Sub Class

Terpene glycosides

Direct Parent

Terpene glycosides

Alternative Parents

Substituents

Terpene glycoside
Galloyl ester
Gallic acid or derivatives
P-hydroxybenzoic acid alkyl ester
Glycosyl compound
O-glycosyl compound
M-hydroxybenzoic acid ester
P-hydroxybenzoic acid ester
Monocyclic monoterpenoid
Monoterpenoid
Aromatic monoterpenoid
Benzoate ester
Benzoic acid or derivatives
Benzenetriol
Pyrogallol derivative
Benzoyl
1-hydroxy-4-unsubstituted benzenoid
1-hydroxy-2-unsubstituted benzenoid
Phenol
Oxane
Benzenoid
Monosaccharide
Acyloin
Monocyclic benzene moiety
Tertiary alcohol
Cyclic alcohol
Cyclic ketone
Carboxylic acid ester
Ketone
Secondary alcohol
Oxacycle
Organoheterocyclic compound
Polyol
Monocarboxylic acid or derivatives
Carboxylic acid derivative
Acetal
Organic oxygen compound
Organooxygen compound
Alcohol
Organic oxide
Carbonyl group
Hydrocarbon derivative
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	2.73	ChemAxon
pKa (Strongest Acidic)	8.11	ChemAxon
pKa (Strongest Basic)	-3.6	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	12	ChemAxon
Hydrogen Donor Count	7	ChemAxon
Polar Surface Area	220.51 Å²	ChemAxon
Rotatable Bond Count	8	ChemAxon
Refractivity	136.36 m³·mol⁻¹	ChemAxon
Polarizability	55.78 Å³	ChemAxon
Number of Rings	3	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

9838912

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

11664177

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

Appendino G, Maxia L, Bettoni P, Locatelli M, Valdivia C, Ballero M, Stavri M, Gibbons S, Sterner O: Antibacterial galloylated alkylphloroglucinol glucosides from myrtle (Myrtus communis). J Nat Prod. 2006 Feb;69(2):251-4. doi: 10.1021/np050462w. [PubMed:16499325 ]
LOTUS database [Link]

Showing NP-Card for [(2r,3s,4s,5r,6r)-3,4,5-trihydroxy-6-{[4-hydroxy-2,2,6,6-tetramethyl-4-(2-methylpropyl)-3,5-dioxocyclohexyl]oxy}oxan-2-yl]methyl 3,4,5-trihydroxybenzoate (NP0310519)

MOL for NP0310519 ([(2r,3s,4s,5r,6r)-3,4,5-trihydroxy-6-{[4-hydroxy-2,2,6,6-tetramethyl-4-(2-methylpropyl)-3,5-dioxocyclohexyl]oxy}oxan-2-yl]methyl 3,4,5-trihydroxybenzoate)

3D MOL for NP0310519 ([(2r,3s,4s,5r,6r)-3,4,5-trihydroxy-6-{[4-hydroxy-2,2,6,6-tetramethyl-4-(2-methylpropyl)-3,5-dioxocyclohexyl]oxy}oxan-2-yl]methyl 3,4,5-trihydroxybenzoate)

3D SDF for NP0310519 ([(2r,3s,4s,5r,6r)-3,4,5-trihydroxy-6-{[4-hydroxy-2,2,6,6-tetramethyl-4-(2-methylpropyl)-3,5-dioxocyclohexyl]oxy}oxan-2-yl]methyl 3,4,5-trihydroxybenzoate)

3D-SDF for NP0310519 ([(2r,3s,4s,5r,6r)-3,4,5-trihydroxy-6-{[4-hydroxy-2,2,6,6-tetramethyl-4-(2-methylpropyl)-3,5-dioxocyclohexyl]oxy}oxan-2-yl]methyl 3,4,5-trihydroxybenzoate)

PDB for NP0310519 ([(2r,3s,4s,5r,6r)-3,4,5-trihydroxy-6-{[4-hydroxy-2,2,6,6-tetramethyl-4-(2-methylpropyl)-3,5-dioxocyclohexyl]oxy}oxan-2-yl]methyl 3,4,5-trihydroxybenzoate)

3D PDB for NP0310519 ([(2r,3s,4s,5r,6r)-3,4,5-trihydroxy-6-{[4-hydroxy-2,2,6,6-tetramethyl-4-(2-methylpropyl)-3,5-dioxocyclohexyl]oxy}oxan-2-yl]methyl 3,4,5-trihydroxybenzoate)

SMILES for NP0310519 ([(2r,3s,4s,5r,6r)-3,4,5-trihydroxy-6-{[4-hydroxy-2,2,6,6-tetramethyl-4-(2-methylpropyl)-3,5-dioxocyclohexyl]oxy}oxan-2-yl]methyl 3,4,5-trihydroxybenzoate)

INCHI for NP0310519 ([(2r,3s,4s,5r,6r)-3,4,5-trihydroxy-6-{[4-hydroxy-2,2,6,6-tetramethyl-4-(2-methylpropyl)-3,5-dioxocyclohexyl]oxy}oxan-2-yl]methyl 3,4,5-trihydroxybenzoate)

Structure for NP0310519 ([(2r,3s,4s,5r,6r)-3,4,5-trihydroxy-6-{[4-hydroxy-2,2,6,6-tetramethyl-4-(2-methylpropyl)-3,5-dioxocyclohexyl]oxy}oxan-2-yl]methyl 3,4,5-trihydroxybenzoate)

3D Structure for NP0310519 ([(2r,3s,4s,5r,6r)-3,4,5-trihydroxy-6-{[4-hydroxy-2,2,6,6-tetramethyl-4-(2-methylpropyl)-3,5-dioxocyclohexyl]oxy}oxan-2-yl]methyl 3,4,5-trihydroxybenzoate)