NP-MRD: Showing NP-Card for [(2r,3r,4s,5r,6r)-3,4,5-tris(acetyloxy)-6-{[(2r,3r,4r,5s,6s)-3,4,5-tris(acetyloxy)-6-[5,7-bis(acetyloxy)-2-[3,4-bis(acetyloxy)phenyl]-4-oxochromen-6-yl]oxan-2-yl]methoxy}oxan-2-yl]methyl acetate (NP0324263)

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Record Information

Version

2.0

Created at

2022-09-12 04:13:55 UTC

Updated at

2022-09-12 04:13:55 UTC

NP-MRD ID

NP0324263

Secondary Accession Numbers

None

Natural Product Identification

Common Name

[(2r,3r,4s,5r,6r)-3,4,5-tris(acetyloxy)-6-{[(2r,3r,4r,5s,6s)-3,4,5-tris(acetyloxy)-6-[5,7-bis(acetyloxy)-2-[3,4-bis(acetyloxy)phenyl]-4-oxochromen-6-yl]oxan-2-yl]methoxy}oxan-2-yl]methyl acetate

Description

CHEMBL451429 belongs to the class of organic compounds known as flavonoid c-glycosides. Flavonoid C-glycosides are compounds containing a carbohydrate moiety which is C-glycosidically linked to the 2-phenylchromen-4-one flavonoid backbone. [(2r,3r,4s,5r,6r)-3,4,5-tris(acetyloxy)-6-{[(2r,3r,4r,5s,6s)-3,4,5-tris(acetyloxy)-6-[5,7-bis(acetyloxy)-2-[3,4-bis(acetyloxy)phenyl]-4-oxochromen-6-yl]oxan-2-yl]methoxy}oxan-2-yl]methyl acetate is found in Gentiana arisanensis. Based on a literature review very few articles have been published on CHEMBL451429.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652309122206132D          

 76 80  0  0  1  0            999 V2000
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M  END

     RDKit          3D

128132  0  0  0  0  0  0  0  0999 V2000
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M  END


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M  END
> <DATABASE_ID>
NP0324263

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CC(=O)OC[C@H]1O[C@@H](OC[C@H]2O[C@H]([C@H](OC(C)=O)[C@@H](OC(C)=O)[C@@H]2OC(C)=O)C2=C(OC(C)=O)C=C3OC(=CC(=O)C3=C2OC(C)=O)C2=CC=C(OC(C)=O)C(OC(C)=O)=C2)[C@H](OC(C)=O)[C@@H](OC(C)=O)[C@@H]1OC(C)=O

> <INCHI_IDENTIFIER>
InChI=1S/C49H52O27/c1-19(50)62-17-38-42(68-24(6)55)46(71-27(9)58)48(73-29(11)60)49(76-38)63-18-37-41(67-23(5)54)45(70-26(8)57)47(72-28(10)59)44(75-37)40-36(66-22(4)53)16-35-39(43(40)69-25(7)56)31(61)15-33(74-35)30-12-13-32(64-20(2)51)34(14-30)65-21(3)52/h12-16,37-38,41-42,44-49H,17-18H2,1-11H3/t37-,38-,41-,42-,44+,45+,46+,47+,48-,49-/m1/s1

> <INCHI_KEY>
NFJLYZJRENZWOI-FYKFRPLHSA-N

> <FORMULA>
C49H52O27

> <MOLECULAR_WEIGHT>
1072.928

> <EXACT_MASS>
1072.269596414

> <JCHEM_ACCEPTOR_COUNT>
16

> <JCHEM_ATOM_COUNT>
128

> <JCHEM_AVERAGE_POLARIZABILITY>
105.33400139063306

> <JCHEM_BIOAVAILABILITY>
0

> <JCHEM_DONOR_COUNT>
0

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
[(2R,3R,4S,5R,6R)-3,4,5-tris(acetyloxy)-6-{[(2R,3R,4R,5S,6S)-3,4,5-tris(acetyloxy)-6-[5,7-bis(acetyloxy)-2-[3,4-bis(acetyloxy)phenyl]-4-oxo-4H-chromen-6-yl]oxan-2-yl]methoxy}oxan-2-yl]methyl acetate

> <JCHEM_LOGP>
-0.04384968233333286

> <JCHEM_MDDR_LIKE_RULE>
1

> <JCHEM_NUMBER_OF_RINGS>
5

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA_STRONGEST_ACIDIC>
14.884049025962469

> <JCHEM_PKA_STRONGEST_BASIC>
-3.8394590812586205

> <JCHEM_POLAR_SURFACE_AREA>
343.29

> <JCHEM_REFRACTIVITY>
241.09290000000004

> <JCHEM_ROTATABLE_BOND_COUNT>
28

> <JCHEM_RULE_OF_FIVE>
0

> <JCHEM_TRADITIONAL_IUPAC>
[(2R,3R,4S,5R,6R)-3,4,5-tris(acetyloxy)-6-{[(2R,3R,4R,5S,6S)-3,4,5-tris(acetyloxy)-6-[5,7-bis(acetyloxy)-2-[3,4-bis(acetyloxy)phenyl]-4-oxochromen-6-yl]oxan-2-yl]methoxy}oxan-2-yl]methyl acetate

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 12-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   12-SEP-22         0                                  
HETATM    1  C   UNK     0       5.335  -9.240   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       4.001 -10.010   0.000  0.00  0.00           C+0
HETATM    3  O   UNK     0       2.667  -9.240   0.000  0.00  0.00           O+0
HETATM    4  O   UNK     0       4.001 -11.550   0.000  0.00  0.00           O+0
HETATM    5  C   UNK     0       2.667 -12.320   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       1.334 -11.550   0.000  0.00  0.00           C+0
HETATM    7  O   UNK     0       1.334 -10.010   0.000  0.00  0.00           O+0
HETATM    8  C   UNK     0       0.000  -9.240   0.000  0.00  0.00           C+0
HETATM    9  O   UNK     0       0.000  -7.700   0.000  0.00  0.00           O+0
HETATM   10  C   UNK     0      -1.334  -6.930   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0      -1.334  -5.390   0.000  0.00  0.00           C+0
HETATM   12  O   UNK     0       0.000  -4.620   0.000  0.00  0.00           O+0
HETATM   13  C   UNK     0       0.000  -3.080   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       1.334  -2.310   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       1.334  -0.770   0.000  0.00  0.00           C+0
HETATM   16  O   UNK     0       0.000   0.000   0.000  0.00  0.00           O+0
HETATM   17  C   UNK     0       0.000   1.540   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0      -1.334   2.310   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       2.667   0.000   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0       4.001  -0.770   0.000  0.00  0.00           C+0
HETATM   22  O   UNK     0       5.335   0.000   0.000  0.00  0.00           O+0
HETATM   23  C   UNK     0       6.668  -0.770   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0       8.002  -0.000   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0       9.336  -0.770   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0      10.669  -0.000   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0      10.669   1.540   0.000  0.00  0.00           C+0
HETATM   28  O   UNK     0      12.003   2.310   0.000  0.00  0.00           O+0
HETATM   29  C   UNK     0      13.337   1.540   0.000  0.00  0.00           C+0
HETATM   30  C   UNK     0      13.337  -0.000   0.000  0.00  0.00           C+0
HETATM   31  O   UNK     0      14.670   2.310   0.000  0.00  0.00           O+0
HETATM   32  C   UNK     0       9.336   2.310   0.000  0.00  0.00           C+0
HETATM   33  O   UNK     0       9.336   3.850   0.000  0.00  0.00           O+0
HETATM   34  C   UNK     0       8.002   4.620   0.000  0.00  0.00           C+0
HETATM   35  C   UNK     0       8.002   6.160   0.000  0.00  0.00           C+0
HETATM   36  O   UNK     0       6.668   3.850   0.000  0.00  0.00           O+0
HETATM   37  C   UNK     0       8.002   1.540   0.000  0.00  0.00           C+0
HETATM   38  C   UNK     0       6.668  -2.310   0.000  0.00  0.00           C+0
HETATM   39  C   UNK     0       5.335  -3.080   0.000  0.00  0.00           C+0
HETATM   40  O   UNK     0       5.335  -4.620   0.000  0.00  0.00           O+0
HETATM   41  C   UNK     0       4.001  -2.310   0.000  0.00  0.00           C+0
HETATM   42  C   UNK     0       2.667  -3.080   0.000  0.00  0.00           C+0
HETATM   43  O   UNK     0       2.667  -4.620   0.000  0.00  0.00           O+0
HETATM   44  C   UNK     0       4.001  -5.390   0.000  0.00  0.00           C+0
HETATM   45  C   UNK     0       4.001  -6.930   0.000  0.00  0.00           C+0
HETATM   46  O   UNK     0       5.533  -5.551   0.000  0.00  0.00           O+0
HETATM   47  C   UNK     0      -1.334  -2.310   0.000  0.00  0.00           C+0
HETATM   48  O   UNK     0      -1.334  -0.770   0.000  0.00  0.00           O+0
HETATM   49  C   UNK     0      -2.667  -0.000   0.000  0.00  0.00           C+0
HETATM   50  C   UNK     0      -2.667   1.540   0.000  0.00  0.00           C+0
HETATM   51  O   UNK     0      -4.001  -0.770   0.000  0.00  0.00           O+0
HETATM   52  C   UNK     0      -2.667  -3.080   0.000  0.00  0.00           C+0
HETATM   53  O   UNK     0      -4.001  -2.310   0.000  0.00  0.00           O+0
HETATM   54  C   UNK     0      -5.335  -3.080   0.000  0.00  0.00           C+0
HETATM   55  C   UNK     0      -6.668  -2.310   0.000  0.00  0.00           C+0
HETATM   56  O   UNK     0      -5.335  -4.620   0.000  0.00  0.00           O+0
HETATM   57  C   UNK     0      -2.667  -4.620   0.000  0.00  0.00           C+0
HETATM   58  O   UNK     0      -4.001  -5.390   0.000  0.00  0.00           O+0
HETATM   59  C   UNK     0      -4.001  -6.930   0.000  0.00  0.00           C+0
HETATM   60  C   UNK     0      -5.335  -7.700   0.000  0.00  0.00           C+0
HETATM   61  O   UNK     0      -2.667  -7.700   0.000  0.00  0.00           O+0
HETATM   62  C   UNK     0      -1.334 -10.010   0.000  0.00  0.00           C+0
HETATM   63  O   UNK     0      -2.667  -9.240   0.000  0.00  0.00           O+0
HETATM   64  C   UNK     0      -4.001 -10.010   0.000  0.00  0.00           C+0
HETATM   65  C   UNK     0      -5.335  -9.240   0.000  0.00  0.00           C+0
HETATM   66  O   UNK     0      -4.001 -11.550   0.000  0.00  0.00           O+0
HETATM   67  C   UNK     0      -1.334 -11.550   0.000  0.00  0.00           C+0
HETATM   68  O   UNK     0      -2.667 -12.320   0.000  0.00  0.00           O+0
HETATM   69  C   UNK     0      -2.667 -13.860   0.000  0.00  0.00           C+0
HETATM   70  C   UNK     0      -4.001 -14.630   0.000  0.00  0.00           C+0
HETATM   71  O   UNK     0      -1.334 -14.630   0.000  0.00  0.00           O+0
HETATM   72  C   UNK     0       0.000 -12.320   0.000  0.00  0.00           C+0
HETATM   73  O   UNK     0       0.000 -13.860   0.000  0.00  0.00           O+0
HETATM   74  C   UNK     0       1.334 -14.630   0.000  0.00  0.00           C+0
HETATM   75  C   UNK     0       2.667 -13.860   0.000  0.00  0.00           C+0
HETATM   76  O   UNK     0       1.334 -16.170   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                                                       
CONECT    6    5    7   72                                                  
CONECT    7    6    8                                                       
CONECT    8    7    9   62                                                  
CONECT    9    8   10                                                       
CONECT   10    9   11                                                       
CONECT   11   10   12   57                                                  
CONECT   12   11   13                                                       
CONECT   13   12   14   47                                                  
CONECT   14   13   15   42                                                  
CONECT   15   14   16   20                                                  
CONECT   16   15   17                                                       
CONECT   17   16   18   19                                                  
CONECT   18   17                                                            
CONECT   19   17                                                            
CONECT   20   15   21                                                       
CONECT   21   20   22   41                                                  
CONECT   22   21   23                                                       
CONECT   23   22   24   38                                                  
CONECT   24   23   25   37                                                  
CONECT   25   24   26                                                       
CONECT   26   25   27                                                       
CONECT   27   26   28   32                                                  
CONECT   28   27   29                                                       
CONECT   29   28   30   31                                                  
CONECT   30   29                                                            
CONECT   31   29                                                            
CONECT   32   27   33   37                                                  
CONECT   33   32   34                                                       
CONECT   34   33   35   36                                                  
CONECT   35   34                                                            
CONECT   36   34                                                            
CONECT   37   32   24                                                       
CONECT   38   23   39                                                       
CONECT   39   38   40   41                                                  
CONECT   40   39                                                            
CONECT   41   39   21   42                                                  
CONECT   42   41   14   43                                                  
CONECT   43   42   44                                                       
CONECT   44   43   45   46                                                  
CONECT   45   44                                                            
CONECT   46   44                                                            
CONECT   47   13   48   52                                                  
CONECT   48   47   49                                                       
CONECT   49   48   50   51                                                  
CONECT   50   49                                                            
CONECT   51   49                                                            
CONECT   52   47   53   57                                                  
CONECT   53   52   54                                                       
CONECT   54   53   55   56                                                  
CONECT   55   54                                                            
CONECT   56   54                                                            
CONECT   57   52   11   58                                                  
CONECT   58   57   59                                                       
CONECT   59   58   60   61                                                  
CONECT   60   59                                                            
CONECT   61   59                                                            
CONECT   62    8   63   67                                                  
CONECT   63   62   64                                                       
CONECT   64   63   65   66                                                  
CONECT   65   64                                                            
CONECT   66   64                                                            
CONECT   67   62   68   72                                                  
CONECT   68   67   69                                                       
CONECT   69   68   70   71                                                  
CONECT   70   69                                                            
CONECT   71   69                                                            
CONECT   72   67    6   73                                                  
CONECT   73   72   74                                                       
CONECT   74   73   75   76                                                  
CONECT   75   74                                                            
CONECT   76   74                                                            
MASTER        0    0    0    0    0    0    0    0   76    0  160    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₄₉H₅₂O₂₇

Average Mass

1072.9280 Da

Monoisotopic Mass

1072.26960 Da

IUPAC Name

[(2R,3R,4S,5R,6R)-3,4,5-tris(acetyloxy)-6-{[(2R,3R,4R,5S,6S)-3,4,5-tris(acetyloxy)-6-[5,7-bis(acetyloxy)-2-[3,4-bis(acetyloxy)phenyl]-4-oxo-4H-chromen-6-yl]oxan-2-yl]methoxy}oxan-2-yl]methyl acetate

Traditional Name

[(2R,3R,4S,5R,6R)-3,4,5-tris(acetyloxy)-6-{[(2R,3R,4R,5S,6S)-3,4,5-tris(acetyloxy)-6-[5,7-bis(acetyloxy)-2-[3,4-bis(acetyloxy)phenyl]-4-oxochromen-6-yl]oxan-2-yl]methoxy}oxan-2-yl]methyl acetate

CAS Registry Number

Not Available

SMILES

CC(=O)OC[C@H]1O[C@@H](OC[C@H]2O[C@H]([C@H](OC(C)=O)[C@@H](OC(C)=O)[C@@H]2OC(C)=O)C2=C(OC(C)=O)C=C3OC(=CC(=O)C3=C2OC(C)=O)C2=CC=C(OC(C)=O)C(OC(C)=O)=C2)[C@H](OC(C)=O)[C@@H](OC(C)=O)[C@@H]1OC(C)=O

InChI Identifier

InChI=1S/C49H52O27/c1-19(50)62-17-38-42(68-24(6)55)46(71-27(9)58)48(73-29(11)60)49(76-38)63-18-37-41(67-23(5)54)45(70-26(8)57)47(72-28(10)59)44(75-37)40-36(66-22(4)53)16-35-39(43(40)69-25(7)56)31(61)15-33(74-35)30-12-13-32(64-20(2)51)34(14-30)65-21(3)52/h12-16,37-38,41-42,44-49H,17-18H2,1-11H3/t37-,38-,41-,42-,44+,45+,46+,47+,48-,49-/m1/s1

InChI Key

NFJLYZJRENZWOI-FYKFRPLHSA-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
Gentiana arisanensis	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as flavonoid c-glycosides. Flavonoid C-glycosides are compounds containing a carbohydrate moiety which is C-glycosidically linked to the 2-phenylchromen-4-one flavonoid backbone.

Kingdom

Organic compounds

Super Class

Phenylpropanoids and polyketides

Class

Flavonoids

Sub Class

Flavonoid glycosides

Direct Parent

Flavonoid C-glycosides

Alternative Parents

Substituents

Flavonoid c-glycoside
Flavone
Phenolic glycoside
C-glycosyl compound
Chromone
Disaccharide
Glycosyl compound
O-glycosyl compound
Benzopyran
1-benzopyran
Phenol ester
Phenoxy compound
Pyranone
Monocyclic benzene moiety
Benzenoid
Pyran
Oxane
Heteroaromatic compound
Carboxylic acid ester
Organoheterocyclic compound
Oxacycle
Ether
Dialkyl ether
Carboxylic acid derivative
Acetal
Hydrocarbon derivative
Carbonyl group
Organic oxide
Organooxygen compound
Organic oxygen 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	-0.044	ChemAxon
pKa (Strongest Acidic)	14.88	ChemAxon
pKa (Strongest Basic)	-3.8	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	16	ChemAxon
Hydrogen Donor Count	0	ChemAxon
Polar Surface Area	343.29 Å²	ChemAxon
Rotatable Bond Count	28	ChemAxon
Refractivity	241.09 m³·mol⁻¹	ChemAxon
Polarizability	105.33 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

23339329

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

44566601

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,4s,5r,6r)-3,4,5-tris(acetyloxy)-6-{[(2r,3r,4r,5s,6s)-3,4,5-tris(acetyloxy)-6-[5,7-bis(acetyloxy)-2-[3,4-bis(acetyloxy)phenyl]-4-oxochromen-6-yl]oxan-2-yl]methoxy}oxan-2-yl]methyl acetate (NP0324263)

MOL for NP0324263 ([(2r,3r,4s,5r,6r)-3,4,5-tris(acetyloxy)-6-{[(2r,3r,4r,5s,6s)-3,4,5-tris(acetyloxy)-6-[5,7-bis(acetyloxy)-2-[3,4-bis(acetyloxy)phenyl]-4-oxochromen-6-yl]oxan-2-yl]methoxy}oxan-2-yl]methyl acetate)

3D MOL for NP0324263 ([(2r,3r,4s,5r,6r)-3,4,5-tris(acetyloxy)-6-{[(2r,3r,4r,5s,6s)-3,4,5-tris(acetyloxy)-6-[5,7-bis(acetyloxy)-2-[3,4-bis(acetyloxy)phenyl]-4-oxochromen-6-yl]oxan-2-yl]methoxy}oxan-2-yl]methyl acetate)

3D SDF for NP0324263 ([(2r,3r,4s,5r,6r)-3,4,5-tris(acetyloxy)-6-{[(2r,3r,4r,5s,6s)-3,4,5-tris(acetyloxy)-6-[5,7-bis(acetyloxy)-2-[3,4-bis(acetyloxy)phenyl]-4-oxochromen-6-yl]oxan-2-yl]methoxy}oxan-2-yl]methyl acetate)

3D-SDF for NP0324263 ([(2r,3r,4s,5r,6r)-3,4,5-tris(acetyloxy)-6-{[(2r,3r,4r,5s,6s)-3,4,5-tris(acetyloxy)-6-[5,7-bis(acetyloxy)-2-[3,4-bis(acetyloxy)phenyl]-4-oxochromen-6-yl]oxan-2-yl]methoxy}oxan-2-yl]methyl acetate)

PDB for NP0324263 ([(2r,3r,4s,5r,6r)-3,4,5-tris(acetyloxy)-6-{[(2r,3r,4r,5s,6s)-3,4,5-tris(acetyloxy)-6-[5,7-bis(acetyloxy)-2-[3,4-bis(acetyloxy)phenyl]-4-oxochromen-6-yl]oxan-2-yl]methoxy}oxan-2-yl]methyl acetate)

3D PDB for NP0324263 ([(2r,3r,4s,5r,6r)-3,4,5-tris(acetyloxy)-6-{[(2r,3r,4r,5s,6s)-3,4,5-tris(acetyloxy)-6-[5,7-bis(acetyloxy)-2-[3,4-bis(acetyloxy)phenyl]-4-oxochromen-6-yl]oxan-2-yl]methoxy}oxan-2-yl]methyl acetate)

SMILES for NP0324263 ([(2r,3r,4s,5r,6r)-3,4,5-tris(acetyloxy)-6-{[(2r,3r,4r,5s,6s)-3,4,5-tris(acetyloxy)-6-[5,7-bis(acetyloxy)-2-[3,4-bis(acetyloxy)phenyl]-4-oxochromen-6-yl]oxan-2-yl]methoxy}oxan-2-yl]methyl acetate)

INCHI for NP0324263 ([(2r,3r,4s,5r,6r)-3,4,5-tris(acetyloxy)-6-{[(2r,3r,4r,5s,6s)-3,4,5-tris(acetyloxy)-6-[5,7-bis(acetyloxy)-2-[3,4-bis(acetyloxy)phenyl]-4-oxochromen-6-yl]oxan-2-yl]methoxy}oxan-2-yl]methyl acetate)

Structure for NP0324263 ([(2r,3r,4s,5r,6r)-3,4,5-tris(acetyloxy)-6-{[(2r,3r,4r,5s,6s)-3,4,5-tris(acetyloxy)-6-[5,7-bis(acetyloxy)-2-[3,4-bis(acetyloxy)phenyl]-4-oxochromen-6-yl]oxan-2-yl]methoxy}oxan-2-yl]methyl acetate)

3D Structure for NP0324263 ([(2r,3r,4s,5r,6r)-3,4,5-tris(acetyloxy)-6-{[(2r,3r,4r,5s,6s)-3,4,5-tris(acetyloxy)-6-[5,7-bis(acetyloxy)-2-[3,4-bis(acetyloxy)phenyl]-4-oxochromen-6-yl]oxan-2-yl]methoxy}oxan-2-yl]methyl acetate)