NP-MRD: Showing NP-Card for (9's,10r)-1,4',5',8,9'-pentahydroxy-2',6-dimethyl-10-[(2s,3r,4r,5s,6r)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]-10h-[2,9'-bianthracene]-9,10'-dione (NP0146594)

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Record Information

Version

2.0

Created at

2022-09-02 02:00:52 UTC

Updated at

2022-09-02 02:00:52 UTC

NP-MRD ID

NP0146594

Secondary Accession Numbers

None

Natural Product Identification

Common Name

(9's,10r)-1,4',5',8,9'-pentahydroxy-2',6-dimethyl-10-[(2s,3r,4r,5s,6r)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]-10h-[2,9'-bianthracene]-9,10'-dione

Description

(9'S,10R)-1,4',5',8,9'-pentahydroxy-2',6-dimethyl-10-[(2S,3R,4R,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]-9H,9'H,10H,10'H-[2,9'-bianthracene]-9,10'-dione belongs to the class of organic compounds known as anthracenes. These are organic compounds containing a system of three linearly fused benzene rings. (9's,10r)-1,4',5',8,9'-pentahydroxy-2',6-dimethyl-10-[(2s,3r,4r,5s,6r)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]-10h-[2,9'-bianthracene]-9,10'-dione is found in Asphodelus ramosus. Based on a literature review very few articles have been published on (9'S,10R)-1,4',5',8,9'-pentahydroxy-2',6-dimethyl-10-[(2S,3R,4R,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]-9H,9'H,10H,10'H-[2,9'-bianthracene]-9,10'-dione.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652309022204002D          

 48 54  0  0  1  0            999 V2000
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M  END

     RDKit          3D

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M  END


  Mrv1652309022204002D          

 48 54  0  0  1  0            999 V2000
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    5.1973   -2.3490    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    5.9118   -2.7615    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.9118   -3.5865    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    6.6262   -3.9990    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.6262   -4.8240    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.1973   -3.9990    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    5.1973   -4.8240    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.4828   -3.5865    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    3.7683   -3.9990    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.4828   -2.7615    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.7683   -2.3490    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.4828   -1.1115    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7683   -1.5240    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0539   -1.1115    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0539   -0.2865    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3394    0.1260    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.8697    0.7580    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.0572   -0.6493    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5875   -1.2813    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3054   -2.0565    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4929   -2.1998    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9626   -1.5678    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1501   -1.7110    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.2448   -0.7925    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145   -0.1605    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0980   -0.3038    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.9966    0.6147    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4663    1.2467    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3461    1.1034    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.7485    2.0219    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5610    2.1652    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8431    2.9404    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0913    1.5332    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8091    0.7580    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7683    0.1260    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7683    0.9510    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.4828   -0.2865    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.1973    0.1260    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.1973    0.9510    0.0000 O   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
  3  4  1  0  0  0  0
  4  5  1  0  0  0  0
  4  6  2  0  0  0  0
  6  7  1  0  0  0  0
  7  8  2  0  0  0  0
  2  8  1  0  0  0  0
  7  9  1  0  0  0  0
  9 10  1  6  0  0  0
 10 11  1  6  0  0  0
 11 12  1  0  0  0  0
 12 13  1  6  0  0  0
 13 14  1  0  0  0  0
 12 15  1  0  0  0  0
 15 16  1  1  0  0  0
 15 17  1  0  0  0  0
 17 18  1  6  0  0  0
 17 19  1  0  0  0  0
 10 19  1  0  0  0  0
 19 20  1  1  0  0  0
  9 21  1  0  0  0  0
 21 22  2  0  0  0  0
 22 23  1  0  0  0  0
 23 24  2  0  0  0  0
 25 24  1  6  0  0  0
 25 26  1  1  0  0  0
 25 27  1  0  0  0  0
 27 28  2  0  0  0  0
 28 29  1  0  0  0  0
 29 30  2  0  0  0  0
 30 31  1  0  0  0  0
 31 32  1  0  0  0  0
 31 33  2  0  0  0  0
 27 33  1  0  0  0  0
 33 34  1  0  0  0  0
 34 35  2  0  0  0  0
 34 36  1  0  0  0  0
 36 37  2  0  0  0  0
 37 38  1  0  0  0  0
 37 39  1  0  0  0  0
 39 40  2  0  0  0  0
 40 41  1  0  0  0  0
 40 42  1  0  0  0  0
 42 43  2  0  0  0  0
 36 43  1  0  0  0  0
 25 43  1  0  0  0  0
 24 44  1  0  0  0  0
 44 45  1  0  0  0  0
 44 46  2  0  0  0  0
 21 46  1  0  0  0  0
 46 47  1  0  0  0  0
  6 47  1  0  0  0  0
 47 48  2  0  0  0  0
M  END
> <DATABASE_ID>
NP0146594

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CC1=CC(O)=C2C(=O)C3=C(O)C(=CC=C3[C@@H]([C@@H]3O[C@H](CO)[C@@H](O)[C@H](O)[C@H]3O)C2=C1)[C@]1(O)C2=CC=CC(O)=C2C(=O)C2=C(O)C=C(C)C=C12

> <INCHI_IDENTIFIER>
InChI=1S/C36H32O12/c1-13-8-16-24(35-34(46)33(45)30(42)23(12-37)48-35)15-6-7-18(29(41)26(15)31(43)25(16)21(39)10-13)36(47)17-4-3-5-20(38)27(17)32(44)28-19(36)9-14(2)11-22(28)40/h3-11,23-24,30,33-35,37-42,45-47H,12H2,1-2H3/t23-,24-,30-,33+,34-,35+,36-/m1/s1

> <INCHI_KEY>
QBCODARMPHSBOD-QYTCQEDXSA-N

> <FORMULA>
C36H32O12

> <MOLECULAR_WEIGHT>
656.64

> <EXACT_MASS>
656.18937647

> <JCHEM_ACCEPTOR_COUNT>
12

> <JCHEM_ATOM_COUNT>
80

> <JCHEM_AVERAGE_POLARIZABILITY>
66.44823732603305

> <JCHEM_BIOAVAILABILITY>
0

> <JCHEM_DONOR_COUNT>
9

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
(9'S,10R)-1,4',5',8,9'-pentahydroxy-2',6-dimethyl-10-[(2S,3R,4R,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]-9H,9'H,10H,10'H-[2,9'-bianthracene]-9,10'-dione

> <ALOGPS_LOGP>
2.14

> <JCHEM_LOGP>
5.053291100666667

> <ALOGPS_LOGS>
-3.33

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
7

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
8.56913341617761

> <JCHEM_PKA_STRONGEST_ACIDIC>
8.110298631318077

> <JCHEM_PKA_STRONGEST_BASIC>
-3.625900281252382

> <JCHEM_POLAR_SURFACE_AREA>
225.43999999999997

> <JCHEM_REFRACTIVITY>
172.79240000000001

> <JCHEM_ROTATABLE_BOND_COUNT>
3

> <JCHEM_RULE_OF_FIVE>
0

> <ALOGPS_SOLUBILITY>
3.06e-01 g/l

> <JCHEM_TRADITIONAL_IUPAC>
(9'S,10R)-1,4',5',8,9'-pentahydroxy-2',6-dimethyl-10-[(2S,3R,4R,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]-10H-[2,9'-bianthracene]-9,10'-dione

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 02-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   02-SEP-22         0                                  
HETATM    1  C   UNK     0      15.036  -2.845   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0      13.703  -2.075   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0      13.703  -0.535   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0      12.369   0.235   0.000  0.00  0.00           C+0
HETATM    5  O   UNK     0      12.369   1.775   0.000  0.00  0.00           O+0
HETATM    6  C   UNK     0      11.035  -0.535   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0      11.035  -2.075   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0      12.369  -2.845   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       9.702  -2.845   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       9.702  -4.385   0.000  0.00  0.00           C+0
HETATM   11  O   UNK     0      11.035  -5.155   0.000  0.00  0.00           O+0
HETATM   12  C   UNK     0      11.035  -6.695   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0      12.369  -7.465   0.000  0.00  0.00           C+0
HETATM   14  O   UNK     0      12.369  -9.005   0.000  0.00  0.00           O+0
HETATM   15  C   UNK     0       9.702  -7.465   0.000  0.00  0.00           C+0
HETATM   16  O   UNK     0       9.702  -9.005   0.000  0.00  0.00           O+0
HETATM   17  C   UNK     0       8.368  -6.695   0.000  0.00  0.00           C+0
HETATM   18  O   UNK     0       7.034  -7.465   0.000  0.00  0.00           O+0
HETATM   19  C   UNK     0       8.368  -5.155   0.000  0.00  0.00           C+0
HETATM   20  O   UNK     0       7.034  -4.385   0.000  0.00  0.00           O+0
HETATM   21  C   UNK     0       8.368  -2.075   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0       7.034  -2.845   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0       5.701  -2.075   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0       5.701  -0.535   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0       4.367   0.235   0.000  0.00  0.00           C+0
HETATM   26  O   UNK     0       5.357   1.415   0.000  0.00  0.00           O+0
HETATM   27  C   UNK     0       3.840  -1.212   0.000  0.00  0.00           C+0
HETATM   28  C   UNK     0       4.830  -2.392   0.000  0.00  0.00           C+0
HETATM   29  C   UNK     0       4.303  -3.839   0.000  0.00  0.00           C+0
HETATM   30  C   UNK     0       2.787  -4.106   0.000  0.00  0.00           C+0
HETATM   31  C   UNK     0       1.797  -2.927   0.000  0.00  0.00           C+0
HETATM   32  O   UNK     0       0.280  -3.194   0.000  0.00  0.00           O+0
HETATM   33  C   UNK     0       2.324  -1.479   0.000  0.00  0.00           C+0
HETATM   34  C   UNK     0       1.334  -0.300   0.000  0.00  0.00           C+0
HETATM   35  O   UNK     0      -0.183  -0.567   0.000  0.00  0.00           O+0
HETATM   36  C   UNK     0       1.860   1.147   0.000  0.00  0.00           C+0
HETATM   37  C   UNK     0       0.870   2.327   0.000  0.00  0.00           C+0
HETATM   38  O   UNK     0      -0.646   2.060   0.000  0.00  0.00           O+0
HETATM   39  C   UNK     0       1.397   3.774   0.000  0.00  0.00           C+0
HETATM   40  C   UNK     0       2.914   4.042   0.000  0.00  0.00           C+0
HETATM   41  C   UNK     0       3.441   5.489   0.000  0.00  0.00           C+0
HETATM   42  C   UNK     0       3.904   2.862   0.000  0.00  0.00           C+0
HETATM   43  C   UNK     0       3.377   1.415   0.000  0.00  0.00           C+0
HETATM   44  C   UNK     0       7.034   0.235   0.000  0.00  0.00           C+0
HETATM   45  O   UNK     0       7.034   1.775   0.000  0.00  0.00           O+0
HETATM   46  C   UNK     0       8.368  -0.535   0.000  0.00  0.00           C+0
HETATM   47  C   UNK     0       9.702   0.235   0.000  0.00  0.00           C+0
HETATM   48  O   UNK     0       9.702   1.775   0.000  0.00  0.00           O+0
CONECT    1    2                                                            
CONECT    2    1    3    8                                                  
CONECT    3    2    4                                                       
CONECT    4    3    5    6                                                  
CONECT    5    4                                                            
CONECT    6    4    7   47                                                  
CONECT    7    6    8    9                                                  
CONECT    8    7    2                                                       
CONECT    9    7   10   21                                                  
CONECT   10    9   11   19                                                  
CONECT   11   10   12                                                       
CONECT   12   11   13   15                                                  
CONECT   13   12   14                                                       
CONECT   14   13                                                            
CONECT   15   12   16   17                                                  
CONECT   16   15                                                            
CONECT   17   15   18   19                                                  
CONECT   18   17                                                            
CONECT   19   17   10   20                                                  
CONECT   20   19                                                            
CONECT   21    9   22   46                                                  
CONECT   22   21   23                                                       
CONECT   23   22   24                                                       
CONECT   24   23   25   44                                                  
CONECT   25   24   26   27   43                                             
CONECT   26   25                                                            
CONECT   27   25   28   33                                                  
CONECT   28   27   29                                                       
CONECT   29   28   30                                                       
CONECT   30   29   31                                                       
CONECT   31   30   32   33                                                  
CONECT   32   31                                                            
CONECT   33   31   27   34                                                  
CONECT   34   33   35   36                                                  
CONECT   35   34                                                            
CONECT   36   34   37   43                                                  
CONECT   37   36   38   39                                                  
CONECT   38   37                                                            
CONECT   39   37   40                                                       
CONECT   40   39   41   42                                                  
CONECT   41   40                                                            
CONECT   42   40   43                                                       
CONECT   43   42   36   25                                                  
CONECT   44   24   45   46                                                  
CONECT   45   44                                                            
CONECT   46   44   21   47                                                  
CONECT   47   46    6   48                                                  
CONECT   48   47                                                            
MASTER        0    0    0    0    0    0    0    0   48    0  108    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₃₆H₃₂O₁₂

Average Mass

656.6400 Da

Monoisotopic Mass

656.18938 Da

IUPAC Name

(9'S,10R)-1,4',5',8,9'-pentahydroxy-2',6-dimethyl-10-[(2S,3R,4R,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]-9H,9'H,10H,10'H-[2,9'-bianthracene]-9,10'-dione

Traditional Name

(9'S,10R)-1,4',5',8,9'-pentahydroxy-2',6-dimethyl-10-[(2S,3R,4R,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]-10H-[2,9'-bianthracene]-9,10'-dione

CAS Registry Number

Not Available

SMILES

CC1=CC(O)=C2C(=O)C3=C(O)C(=CC=C3[C@@H]([C@@H]3O[C@H](CO)[C@@H](O)[C@H](O)[C@H]3O)C2=C1)[C@]1(O)C2=CC=CC(O)=C2C(=O)C2=C(O)C=C(C)C=C12

InChI Identifier

InChI=1S/C36H32O12/c1-13-8-16-24(35-34(46)33(45)30(42)23(12-37)48-35)15-6-7-18(29(41)26(15)31(43)25(16)21(39)10-13)36(47)17-4-3-5-20(38)27(17)32(44)28-19(36)9-14(2)11-22(28)40/h3-11,23-24,30,33-35,37-42,45-47H,12H2,1-2H3/t23-,24-,30-,33+,34-,35+,36-/m1/s1

InChI Key

QBCODARMPHSBOD-QYTCQEDXSA-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
Asphodelus ramosus	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as anthracenes. These are organic compounds containing a system of three linearly fused benzene rings.

Kingdom

Organic compounds

Super Class

Benzenoids

Class

Anthracenes

Sub Class

Not Available

Direct Parent

Anthracenes

Alternative Parents

Substituents

Anthracene
Hexose monosaccharide
C-glycosyl compound
Glycosyl compound
Aryl ketone
1-hydroxy-4-unsubstituted benzenoid
1-hydroxy-2-unsubstituted benzenoid
Monosaccharide
Oxane
Vinylogous acid
Tertiary alcohol
Ketone
Secondary alcohol
Dialkyl ether
Ether
Oxacycle
Organoheterocyclic compound
Polyol
Hydrocarbon derivative
Organic oxygen compound
Organic oxide
Primary alcohol
Organooxygen compound
Alcohol
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	2.14	ALOGPS
logP	5.05	ChemAxon
logS	-3.3	ALOGPS
pKa (Strongest Acidic)	8.11	ChemAxon
pKa (Strongest Basic)	-3.6	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	12	ChemAxon
Hydrogen Donor Count	9	ChemAxon
Polar Surface Area	225.44 Å²	ChemAxon
Rotatable Bond Count	3	ChemAxon
Refractivity	172.79 m³·mol⁻¹	ChemAxon
Polarizability	66.45 Å³	ChemAxon
Number of Rings	7	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

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

162932989

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for (9's,10r)-1,4',5',8,9'-pentahydroxy-2',6-dimethyl-10-[(2s,3r,4r,5s,6r)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]-10h-[2,9'-bianthracene]-9,10'-dione (NP0146594)

MOL for NP0146594 ((9's,10r)-1,4',5',8,9'-pentahydroxy-2',6-dimethyl-10-[(2s,3r,4r,5s,6r)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]-10h-[2,9'-bianthracene]-9,10'-dione)

3D MOL for NP0146594 ((9's,10r)-1,4',5',8,9'-pentahydroxy-2',6-dimethyl-10-[(2s,3r,4r,5s,6r)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]-10h-[2,9'-bianthracene]-9,10'-dione)

3D SDF for NP0146594 ((9's,10r)-1,4',5',8,9'-pentahydroxy-2',6-dimethyl-10-[(2s,3r,4r,5s,6r)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]-10h-[2,9'-bianthracene]-9,10'-dione)

3D-SDF for NP0146594 ((9's,10r)-1,4',5',8,9'-pentahydroxy-2',6-dimethyl-10-[(2s,3r,4r,5s,6r)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]-10h-[2,9'-bianthracene]-9,10'-dione)

PDB for NP0146594 ((9's,10r)-1,4',5',8,9'-pentahydroxy-2',6-dimethyl-10-[(2s,3r,4r,5s,6r)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]-10h-[2,9'-bianthracene]-9,10'-dione)

3D PDB for NP0146594 ((9's,10r)-1,4',5',8,9'-pentahydroxy-2',6-dimethyl-10-[(2s,3r,4r,5s,6r)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]-10h-[2,9'-bianthracene]-9,10'-dione)

SMILES for NP0146594 ((9's,10r)-1,4',5',8,9'-pentahydroxy-2',6-dimethyl-10-[(2s,3r,4r,5s,6r)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]-10h-[2,9'-bianthracene]-9,10'-dione)

INCHI for NP0146594 ((9's,10r)-1,4',5',8,9'-pentahydroxy-2',6-dimethyl-10-[(2s,3r,4r,5s,6r)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]-10h-[2,9'-bianthracene]-9,10'-dione)

Structure for NP0146594 ((9's,10r)-1,4',5',8,9'-pentahydroxy-2',6-dimethyl-10-[(2s,3r,4r,5s,6r)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]-10h-[2,9'-bianthracene]-9,10'-dione)

3D Structure for NP0146594 ((9's,10r)-1,4',5',8,9'-pentahydroxy-2',6-dimethyl-10-[(2s,3r,4r,5s,6r)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]-10h-[2,9'-bianthracene]-9,10'-dione)