NP-MRD: Showing NP-Card for 10a,10'a-dimethyl (5s,5's,10as,10'as)-1,1',5,5',8,8'-hexahydroxy-3,3'-dimethyl-9,9'-dioxo-5h,5'h,6h,6'h,7h,7'h-[2,2'-bixanthene]-10a,10'a-dicarboxylate (NP0198265)

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Record Information

Version

2.0

Created at

2022-09-04 16:41:04 UTC

Updated at

2022-09-04 16:41:04 UTC

NP-MRD ID

NP0198265

Secondary Accession Numbers

None

Natural Product Identification

Common Name

10a,10'a-dimethyl (5s,5's,10as,10'as)-1,1',5,5',8,8'-hexahydroxy-3,3'-dimethyl-9,9'-dioxo-5h,5'h,6h,6'h,7h,7'h-[2,2'-bixanthene]-10a,10'a-dicarboxylate

Description

10A,10'a-dimethyl (5S,5'S,10aS,10'aS)-1,1',5,5',8,8'-hexahydroxy-3,3'-dimethyl-9,9'-dioxo-5H,5'H,6H,6'H,7H,7'H,9H,9'H,10aH,10'aH-[2,2'-bixanthene]-10a,10'a-dicarboxylate belongs to the class of organic compounds known as xanthones. These are polycyclic aromatic compounds containing a xanthene moiety conjugated to a ketone group at carbon 9. Xanthene is a tricyclic compound made up of two benzene rings linearly fused to each other through a pyran ring. Based on a literature review very few articles have been published on 10a,10'a-dimethyl (5S,5'S,10aS,10'aS)-1,1',5,5',8,8'-hexahydroxy-3,3'-dimethyl-9,9'-dioxo-5H,5'H,6H,6'H,7H,7'H,9H,9'H,10aH,10'aH-[2,2'-bixanthene]-10a,10'a-dicarboxylate.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652309042218412D          

 46 51  0  0  1  0            999 V2000
    5.0013   -4.5375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
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    5.7158   -6.6000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
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  5 45  1  0  0  0  0
 45 46  1  6  0  0  0
M  END

     RDKit          3D

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M  END


  Mrv1652309042218412D          

 46 51  0  0  1  0            999 V2000
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    8.5737   -7.4250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.5737   -6.6000    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   10.0026   -7.4250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.0026   -6.6000    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   10.7171   -7.8375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   11.4315   -7.4250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   11.4315   -6.6000    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   12.1460   -7.8375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   12.1460   -8.6625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   11.4315   -9.0750    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   11.4315   -9.9000    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   10.7171   -8.6625    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   10.7171   -9.4875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   11.0526  -10.2412    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   10.0026   -9.9000    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   10.0026  -10.7250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.0026   -9.0750    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.4302   -7.8375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.4302   -8.6625    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.7158   -7.4250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0013   -7.8375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0013   -8.6625    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.2868   -7.4250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5724   -7.8375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5724   -8.6625    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579   -7.4250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579   -6.6000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5724   -6.1875    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    3.0874   -5.5201    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
  3  4  2  0  0  0  0
  5  3  1  6  0  0  0
  5  6  1  0  0  0  0
  6  7  1  0  0  0  0
  7  8  2  0  0  0  0
  8  9  1  0  0  0  0
  9 10  1  0  0  0  0
  9 11  2  0  0  0  0
 11 12  1  0  0  0  0
 12 13  2  0  0  0  0
 13 14  1  0  0  0  0
 13 15  1  0  0  0  0
 15 16  2  0  0  0  0
 16 17  1  0  0  0  0
 17 18  2  0  0  0  0
 12 18  1  0  0  0  0
 18 19  1  0  0  0  0
 17 20  1  0  0  0  0
 20 21  2  0  0  0  0
 20 22  1  0  0  0  0
 22 23  2  0  0  0  0
 23 24  1  0  0  0  0
 23 25  1  0  0  0  0
 25 26  1  0  0  0  0
 26 27  1  0  0  0  0
 27 28  1  6  0  0  0
 27 29  1  0  0  0  0
 22 29  1  0  0  0  0
 29 30  1  6  0  0  0
 30 31  2  0  0  0  0
 30 32  1  0  0  0  0
 32 33  1  0  0  0  0
 29 34  1  0  0  0  0
 16 34  1  0  0  0  0
 11 35  1  0  0  0  0
 35 36  1  0  0  0  0
 35 37  2  0  0  0  0
  7 37  1  0  0  0  0
 37 38  1  0  0  0  0
 38 39  2  0  0  0  0
 38 40  1  0  0  0  0
  5 40  1  0  0  0  0
 40 41  2  0  0  0  0
 41 42  1  0  0  0  0
 41 43  1  0  0  0  0
 43 44  1  0  0  0  0
 44 45  1  0  0  0  0
  5 45  1  0  0  0  0
 45 46  1  6  0  0  0
M  END
> <DATABASE_ID>
NP0198265

> <DATABASE_NAME>
NP-MRD

> <SMILES>
COC(=O)[C@]12OC3=CC(C)=C(C(O)=C3C(=O)C1=C(O)CC[C@@H]2O)C1=C(C)C=C2O[C@@]3([C@@H](O)CCC(O)=C3C(=O)C2=C1O)C(=O)OC

> <INCHI_IDENTIFIER>
InChI=1S/C32H30O14/c1-11-9-15-21(27(39)23-13(33)5-7-17(35)31(23,45-15)29(41)43-3)25(37)19(11)20-12(2)10-16-22(26(20)38)28(40)24-14(34)6-8-18(36)32(24,46-16)30(42)44-4/h9-10,17-18,33-38H,5-8H2,1-4H3/t17-,18-,31+,32+/m0/s1

> <INCHI_KEY>
NCPFIXCVFFDLAF-WOQPHPHSSA-N

> <FORMULA>
C32H30O14

> <MOLECULAR_WEIGHT>
638.578

> <EXACT_MASS>
638.163555646

> <JCHEM_ACCEPTOR_COUNT>
12

> <JCHEM_ATOM_COUNT>
76

> <JCHEM_AVERAGE_POLARIZABILITY>
63.34614297659952

> <JCHEM_BIOAVAILABILITY>
0

> <JCHEM_DONOR_COUNT>
6

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
10a,10'a-dimethyl (5S,5'S,10aS,10'aS)-1,1',5,5',8,8'-hexahydroxy-3,3'-dimethyl-9,9'-dioxo-5H,5'H,6H,6'H,7H,7'H,9H,9'H,10aH,10'aH-[2,2'-bixanthene]-10a,10'a-dicarboxylate

> <JCHEM_LOGP>
2.5441807540000005

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
6

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
8.15006177319631

> <JCHEM_PKA_STRONGEST_ACIDIC>
7.351400310178105

> <JCHEM_PKA_STRONGEST_BASIC>
-3.4037989278622174

> <JCHEM_POLAR_SURFACE_AREA>
226.57999999999996

> <JCHEM_REFRACTIVITY>
158.23759999999996

> <JCHEM_ROTATABLE_BOND_COUNT>
4

> <JCHEM_RULE_OF_FIVE>
0

> <JCHEM_TRADITIONAL_IUPAC>
10a,10'a-dimethyl (5S,5'S,10aS,10'aS)-1,1',5,5',8,8'-hexahydroxy-3,3'-dimethyl-9,9'-dioxo-5H,5'H,6H,6'H,7H,7'H-[2,2'-bixanthene]-10a,10'a-dicarboxylate

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 04-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   04-SEP-22         0                                  
HETATM    1  C   UNK     0       9.336  -8.470   0.000  0.00  0.00           C+0
HETATM    2  O   UNK     0       9.336 -10.010   0.000  0.00  0.00           O+0
HETATM    3  C   UNK     0       8.002 -10.780   0.000  0.00  0.00           C+0
HETATM    4  O   UNK     0       6.668 -10.010   0.000  0.00  0.00           O+0
HETATM    5  C   UNK     0       8.002 -12.320   0.000  0.00  0.00           C+0
HETATM    6  O   UNK     0       9.336 -11.550   0.000  0.00  0.00           O+0
HETATM    7  C   UNK     0      10.669 -12.320   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0      12.003 -11.550   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0      13.337 -12.320   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0      14.670 -11.550   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0      13.337 -13.860   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0      14.670 -14.630   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0      14.670 -16.170   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0      13.337 -16.940   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0      16.004 -16.940   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0      17.338 -16.170   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0      17.338 -14.630   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0      16.004 -13.860   0.000  0.00  0.00           C+0
HETATM   19  O   UNK     0      16.004 -12.320   0.000  0.00  0.00           O+0
HETATM   20  C   UNK     0      18.672 -13.860   0.000  0.00  0.00           C+0
HETATM   21  O   UNK     0      18.672 -12.320   0.000  0.00  0.00           O+0
HETATM   22  C   UNK     0      20.005 -14.630   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0      21.339 -13.860   0.000  0.00  0.00           C+0
HETATM   24  O   UNK     0      21.339 -12.320   0.000  0.00  0.00           O+0
HETATM   25  C   UNK     0      22.673 -14.630   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0      22.673 -16.170   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0      21.339 -16.940   0.000  0.00  0.00           C+0
HETATM   28  O   UNK     0      21.339 -18.480   0.000  0.00  0.00           O+0
HETATM   29  C   UNK     0      20.005 -16.170   0.000  0.00  0.00           C+0
HETATM   30  C   UNK     0      20.005 -17.710   0.000  0.00  0.00           C+0
HETATM   31  O   UNK     0      20.632 -19.117   0.000  0.00  0.00           O+0
HETATM   32  O   UNK     0      18.672 -18.480   0.000  0.00  0.00           O+0
HETATM   33  C   UNK     0      18.672 -20.020   0.000  0.00  0.00           C+0
HETATM   34  O   UNK     0      18.672 -16.940   0.000  0.00  0.00           O+0
HETATM   35  C   UNK     0      12.003 -14.630   0.000  0.00  0.00           C+0
HETATM   36  O   UNK     0      12.003 -16.170   0.000  0.00  0.00           O+0
HETATM   37  C   UNK     0      10.669 -13.860   0.000  0.00  0.00           C+0
HETATM   38  C   UNK     0       9.336 -14.630   0.000  0.00  0.00           C+0
HETATM   39  O   UNK     0       9.336 -16.170   0.000  0.00  0.00           O+0
HETATM   40  C   UNK     0       8.002 -13.860   0.000  0.00  0.00           C+0
HETATM   41  C   UNK     0       6.668 -14.630   0.000  0.00  0.00           C+0
HETATM   42  O   UNK     0       6.668 -16.170   0.000  0.00  0.00           O+0
HETATM   43  C   UNK     0       5.335 -13.860   0.000  0.00  0.00           C+0
HETATM   44  C   UNK     0       5.335 -12.320   0.000  0.00  0.00           C+0
HETATM   45  C   UNK     0       6.668 -11.550   0.000  0.00  0.00           C+0
HETATM   46  O   UNK     0       5.763 -10.304   0.000  0.00  0.00           O+0
CONECT    1    2                                                            
CONECT    2    1    3                                                       
CONECT    3    2    4    5                                                  
CONECT    4    3                                                            
CONECT    5    3    6   40   45                                             
CONECT    6    5    7                                                       
CONECT    7    6    8   37                                                  
CONECT    8    7    9                                                       
CONECT    9    8   10   11                                                  
CONECT   10    9                                                            
CONECT   11    9   12   35                                                  
CONECT   12   11   13   18                                                  
CONECT   13   12   14   15                                                  
CONECT   14   13                                                            
CONECT   15   13   16                                                       
CONECT   16   15   17   34                                                  
CONECT   17   16   18   20                                                  
CONECT   18   17   12   19                                                  
CONECT   19   18                                                            
CONECT   20   17   21   22                                                  
CONECT   21   20                                                            
CONECT   22   20   23   29                                                  
CONECT   23   22   24   25                                                  
CONECT   24   23                                                            
CONECT   25   23   26                                                       
CONECT   26   25   27                                                       
CONECT   27   26   28   29                                                  
CONECT   28   27                                                            
CONECT   29   27   22   30   34                                             
CONECT   30   29   31   32                                                  
CONECT   31   30                                                            
CONECT   32   30   33                                                       
CONECT   33   32                                                            
CONECT   34   29   16                                                       
CONECT   35   11   36   37                                                  
CONECT   36   35                                                            
CONECT   37   35    7   38                                                  
CONECT   38   37   39   40                                                  
CONECT   39   38                                                            
CONECT   40   38    5   41                                                  
CONECT   41   40   42   43                                                  
CONECT   42   41                                                            
CONECT   43   41   44                                                       
CONECT   44   43   45                                                       
CONECT   45   44    5   46                                                  
CONECT   46   45                                                            
MASTER        0    0    0    0    0    0    0    0   46    0  102    0
END

View in JSmol

Synonyms

Value	Source
10a,10'a-Dimethyl (5S,5's,10as,10'as)-1,1',5,5',8,8'-hexahydroxy-3,3'-dimethyl-9,9'-dioxo-5H,5'H,6H,6'H,7H,7'H,9H,9'H,10ah,10'ah-[2,2'-bixanthene]-10a,10'a-dicarboxylic acid	Generator

Chemical Formula

C₃₂H₃₀O₁₄

Average Mass

638.5780 Da

Monoisotopic Mass

638.16356 Da

IUPAC Name

10a,10'a-dimethyl (5S,5'S,10aS,10'aS)-1,1',5,5',8,8'-hexahydroxy-3,3'-dimethyl-9,9'-dioxo-5H,5'H,6H,6'H,7H,7'H,9H,9'H,10aH,10'aH-[2,2'-bixanthene]-10a,10'a-dicarboxylate

Traditional Name

10a,10'a-dimethyl (5S,5'S,10aS,10'aS)-1,1',5,5',8,8'-hexahydroxy-3,3'-dimethyl-9,9'-dioxo-5H,5'H,6H,6'H,7H,7'H-[2,2'-bixanthene]-10a,10'a-dicarboxylate

CAS Registry Number

Not Available

SMILES

COC(=O)[C@]12OC3=CC(C)=C(C(O)=C3C(=O)C1=C(O)CC[C@@H]2O)C1=C(C)C=C2O[C@@]3([C@@H](O)CCC(O)=C3C(=O)C2=C1O)C(=O)OC

InChI Identifier

InChI=1S/C32H30O14/c1-11-9-15-21(27(39)23-13(33)5-7-17(35)31(23,45-15)29(41)43-3)25(37)19(11)20-12(2)10-16-22(26(20)38)28(40)24-14(34)6-8-18(36)32(24,46-16)30(42)44-4/h9-10,17-18,33-38H,5-8H2,1-4H3/t17-,18-,31+,32+/m0/s1

InChI Key

NCPFIXCVFFDLAF-WOQPHPHSSA-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

Not Available

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as xanthones. These are polycyclic aromatic compounds containing a xanthene moiety conjugated to a ketone group at carbon 9. Xanthene is a tricyclic compound made up of two benzene rings linearly fused to each other through a pyran ring.

Kingdom

Organic compounds

Super Class

Organoheterocyclic compounds

Class

Benzopyrans

Sub Class

1-benzopyrans

Direct Parent

Xanthones

Alternative Parents

Substituents

Xanthone
Chromone
Aryl ketone
1-hydroxy-4-unsubstituted benzenoid
Alkyl aryl ether
Beta-hydroxy acid
Phenol
Dicarboxylic acid or derivatives
Benzenoid
Hydroxy acid
Vinylogous acid
Methyl ester
Carboxylic acid ester
Secondary alcohol
Ketone
Ether
Enol
Oxacycle
Carboxylic acid derivative
Polyol
Organic oxygen compound
Hydrocarbon derivative
Alcohol
Carbonyl group
Organic oxide
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	2.54	ChemAxon
pKa (Strongest Acidic)	7.35	ChemAxon
pKa (Strongest Basic)	-3.4	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	12	ChemAxon
Hydrogen Donor Count	6	ChemAxon
Polar Surface Area	226.58 Å²	ChemAxon
Rotatable Bond Count	4	ChemAxon
Refractivity	158.24 m³·mol⁻¹	ChemAxon
Polarizability	63.35 Å³	ChemAxon
Number of Rings	6	ChemAxon
Bioavailability	No	ChemAxon
Rule of Five	No	ChemAxon
Ghose Filter	No	ChemAxon
Veber's Rule	No	ChemAxon
MDDR-like Rule	No	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

10189061

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 10a,10'a-dimethyl (5s,5's,10as,10'as)-1,1',5,5',8,8'-hexahydroxy-3,3'-dimethyl-9,9'-dioxo-5h,5'h,6h,6'h,7h,7'h-[2,2'-bixanthene]-10a,10'a-dicarboxylate (NP0198265)

MOL for NP0198265 (10a,10'a-dimethyl (5s,5's,10as,10'as)-1,1',5,5',8,8'-hexahydroxy-3,3'-dimethyl-9,9'-dioxo-5h,5'h,6h,6'h,7h,7'h-[2,2'-bixanthene]-10a,10'a-dicarboxylate)

3D MOL for NP0198265 (10a,10'a-dimethyl (5s,5's,10as,10'as)-1,1',5,5',8,8'-hexahydroxy-3,3'-dimethyl-9,9'-dioxo-5h,5'h,6h,6'h,7h,7'h-[2,2'-bixanthene]-10a,10'a-dicarboxylate)

3D SDF for NP0198265 (10a,10'a-dimethyl (5s,5's,10as,10'as)-1,1',5,5',8,8'-hexahydroxy-3,3'-dimethyl-9,9'-dioxo-5h,5'h,6h,6'h,7h,7'h-[2,2'-bixanthene]-10a,10'a-dicarboxylate)

3D-SDF for NP0198265 (10a,10'a-dimethyl (5s,5's,10as,10'as)-1,1',5,5',8,8'-hexahydroxy-3,3'-dimethyl-9,9'-dioxo-5h,5'h,6h,6'h,7h,7'h-[2,2'-bixanthene]-10a,10'a-dicarboxylate)

PDB for NP0198265 (10a,10'a-dimethyl (5s,5's,10as,10'as)-1,1',5,5',8,8'-hexahydroxy-3,3'-dimethyl-9,9'-dioxo-5h,5'h,6h,6'h,7h,7'h-[2,2'-bixanthene]-10a,10'a-dicarboxylate)

3D PDB for NP0198265 (10a,10'a-dimethyl (5s,5's,10as,10'as)-1,1',5,5',8,8'-hexahydroxy-3,3'-dimethyl-9,9'-dioxo-5h,5'h,6h,6'h,7h,7'h-[2,2'-bixanthene]-10a,10'a-dicarboxylate)

SMILES for NP0198265 (10a,10'a-dimethyl (5s,5's,10as,10'as)-1,1',5,5',8,8'-hexahydroxy-3,3'-dimethyl-9,9'-dioxo-5h,5'h,6h,6'h,7h,7'h-[2,2'-bixanthene]-10a,10'a-dicarboxylate)

INCHI for NP0198265 (10a,10'a-dimethyl (5s,5's,10as,10'as)-1,1',5,5',8,8'-hexahydroxy-3,3'-dimethyl-9,9'-dioxo-5h,5'h,6h,6'h,7h,7'h-[2,2'-bixanthene]-10a,10'a-dicarboxylate)

Structure for NP0198265 (10a,10'a-dimethyl (5s,5's,10as,10'as)-1,1',5,5',8,8'-hexahydroxy-3,3'-dimethyl-9,9'-dioxo-5h,5'h,6h,6'h,7h,7'h-[2,2'-bixanthene]-10a,10'a-dicarboxylate)

3D Structure for NP0198265 (10a,10'a-dimethyl (5s,5's,10as,10'as)-1,1',5,5',8,8'-hexahydroxy-3,3'-dimethyl-9,9'-dioxo-5h,5'h,6h,6'h,7h,7'h-[2,2'-bixanthene]-10a,10'a-dicarboxylate)