NP-MRD: Showing NP-Card for (5'r,6's,7'r,8's)-1',2,5',6',7',8,8'-heptahydroxy-3',6-dimethoxy-3,6'-dimethyl-7',8'-dihydro-5'h-[1,2'-bianthracene]-9,9',10,10'-tetrone (NP0175644)

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Record Information

Version

2.0

Created at

2022-09-03 13:09:38 UTC

Updated at

2022-09-03 13:09:39 UTC

NP-MRD ID

NP0175644

Secondary Accession Numbers

None

Natural Product Identification

Common Name

(5'r,6's,7'r,8's)-1',2,5',6',7',8,8'-heptahydroxy-3',6-dimethoxy-3,6'-dimethyl-7',8'-dihydro-5'h-[1,2'-bianthracene]-9,9',10,10'-tetrone

Description

Alterporriol C belongs to the class of organic compounds known as hydroxyanthraquinones. Hydroxyanthraquinones are compounds containing a hydroxyanthraquinone moiety, which consists of an anthracene bearing a quinone, and hydroxyl group. (5'r,6's,7'r,8's)-1',2,5',6',7',8,8'-heptahydroxy-3',6-dimethoxy-3,6'-dimethyl-7',8'-dihydro-5'h-[1,2'-bianthracene]-9,9',10,10'-tetrone is found in Alternaria porri and Alternaria solani. (5'r,6's,7'r,8's)-1',2,5',6',7',8,8'-heptahydroxy-3',6-dimethoxy-3,6'-dimethyl-7',8'-dihydro-5'h-[1,2'-bianthracene]-9,9',10,10'-tetrone was first documented in 2014 (PMID: 24840716). Based on a literature review very few articles have been published on Alterporriol C.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652309032215092D          

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M  END

     RDKit          3D

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M  END


  Mrv1652309032215092D          

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   -2.1434   -6.1875    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1434   -7.8375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8579   -7.4250    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1434   -8.6625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4289   -9.0750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7145   -8.6625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000   -9.0750    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4289   -9.9000    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.7145  -10.3125    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1434  -10.3125    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -1.6131  -10.9445    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6737  -10.9445    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8579   -9.9000    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -3.5724  -10.3125    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8579   -9.0750    0.0000 C   0  0  1  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
    0.0000   -4.9500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145   -5.3625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1994   -6.0299    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
  4  5  1  0  0  0  0
  5  6  1  0  0  0  0
  5  7  2  0  0  0  0
  7  8  1  0  0  0  0
  8  9  2  0  0  0  0
  3  9  1  0  0  0  0
  8 10  1  0  0  0  0
 10 11  2  0  0  0  0
 10 12  1  0  0  0  0
 12 13  2  0  0  0  0
 13 14  1  0  0  0  0
 14 15  1  0  0  0  0
 14 16  2  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
 19 20  2  0  0  0  0
 20 21  1  0  0  0  0
 21 22  1  0  0  0  0
 20 23  1  0  0  0  0
 23 24  2  0  0  0  0
 24 25  1  0  0  0  0
 25 26  2  0  0  0  0
 19 26  1  0  0  0  0
 26 27  1  0  0  0  0
 25 28  1  0  0  0  0
 28 29  2  0  0  0  0
 28 30  1  0  0  0  0
 30 31  2  0  0  0  0
 31 32  1  0  0  0  0
 24 32  1  0  0  0  0
 32 33  2  0  0  0  0
 31 34  1  0  0  0  0
 34 35  1  1  0  0  0
 34 36  1  0  0  0  0
 36 37  1  1  0  0  0
 36 38  1  6  0  0  0
 36 39  1  0  0  0  0
 39 40  1  6  0  0  0
 39 41  1  0  0  0  0
 30 41  1  0  0  0  0
 41 42  1  1  0  0  0
 18 43  2  0  0  0  0
 12 43  1  0  0  0  0
 43 44  1  0  0  0  0
  7 44  1  0  0  0  0
 44 45  2  0  0  0  0
M  END
> <DATABASE_ID>
NP0175644

> <DATABASE_NAME>
NP-MRD

> <SMILES>
COC1=CC(O)=C2C(=O)C3=C(C(O)=C(C)C=C3C(=O)C2=C1)C1=C(OC)C=C2C(=O)C3=C([C@H](O)[C@@H](O)[C@@](C)(O)[C@@H]3O)C(=O)C2=C1O

> <INCHI_IDENTIFIER>
InChI=1S/C32H26O13/c1-9-5-11-17(26(37)16-12(24(11)35)6-10(44-3)7-14(16)33)20(23(9)34)19-15(45-4)8-13-18(27(19)38)28(39)21-22(25(13)36)30(41)32(2,43)31(42)29(21)40/h5-8,29-31,33-34,38,40-43H,1-4H3/t29-,30+,31+,32-/m0/s1

> <INCHI_KEY>
PSGFKGASHCTNSI-BVEPWEIPSA-N

> <FORMULA>
C32H26O13

> <MOLECULAR_WEIGHT>
618.547

> <EXACT_MASS>
618.137340897

> <JCHEM_ACCEPTOR_COUNT>
13

> <JCHEM_ATOM_COUNT>
71

> <JCHEM_AVERAGE_POLARIZABILITY>
61.60780668717287

> <JCHEM_BIOAVAILABILITY>
0

> <JCHEM_DONOR_COUNT>
7

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
(5'R,6'S,7'R,8'S)-1',2,5',6',7',8,8'-heptahydroxy-3',6-dimethoxy-3,6'-dimethyl-5',6',7',8'-tetrahydro-9H,9'H,10H,10'H-[1,2'-bianthracene]-9,9',10,10'-tetrone

> <ALOGPS_LOGP>
2.69

> <JCHEM_LOGP>
1.871861110666667

> <ALOGPS_LOGS>
-3.12

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
6

> <JCHEM_PHYSIOLOGICAL_CHARGE>
-1

> <JCHEM_PKA>
7.420094518142655

> <JCHEM_PKA_STRONGEST_ACIDIC>
6.593902493751872

> <JCHEM_PKA_STRONGEST_BASIC>
-3.565771322632526

> <JCHEM_POLAR_SURFACE_AREA>
228.34999999999997

> <JCHEM_REFRACTIVITY>
156.52089999999998

> <JCHEM_ROTATABLE_BOND_COUNT>
2

> <JCHEM_RULE_OF_FIVE>
0

> <ALOGPS_SOLUBILITY>
4.66e-01 g/l

> <JCHEM_TRADITIONAL_IUPAC>
(5'R,6'S,7'R,8'S)-1',2,5',6',7',8,8'-heptahydroxy-3',6-dimethoxy-3,6'-dimethyl-7',8'-dihydro-5'H-[1,2'-bianthracene]-9,9',10,10'-tetrone

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 03-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   03-SEP-22         0                                  
HETATM    1  C   UNK     0       8.002  -7.700   0.000  0.00  0.00           C+0
HETATM    2  O   UNK     0       6.668  -6.930   0.000  0.00  0.00           O+0
HETATM    3  C   UNK     0       5.335  -7.700   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       5.335  -9.240   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       4.001 -10.010   0.000  0.00  0.00           C+0
HETATM    6  O   UNK     0       4.001 -11.550   0.000  0.00  0.00           O+0
HETATM    7  C   UNK     0       2.667  -9.240   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       2.667  -7.700   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       4.001  -6.930   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       1.334  -6.930   0.000  0.00  0.00           C+0
HETATM   11  O   UNK     0       1.334  -5.390   0.000  0.00  0.00           O+0
HETATM   12  C   UNK     0       0.000  -7.700   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0      -1.334  -6.930   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0      -2.667  -7.700   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0      -4.001  -6.930   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0      -2.667  -9.240   0.000  0.00  0.00           C+0
HETATM   17  O   UNK     0      -4.001 -10.010   0.000  0.00  0.00           O+0
HETATM   18  C   UNK     0      -1.334 -10.010   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0      -1.334 -11.550   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0       0.000 -12.320   0.000  0.00  0.00           C+0
HETATM   21  O   UNK     0       1.334 -11.550   0.000  0.00  0.00           O+0
HETATM   22  C   UNK     0       2.667 -12.320   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0       0.000 -13.860   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0      -1.334 -14.630   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0      -2.667 -13.860   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0      -2.667 -12.320   0.000  0.00  0.00           C+0
HETATM   27  O   UNK     0      -4.001 -11.550   0.000  0.00  0.00           O+0
HETATM   28  C   UNK     0      -4.001 -14.630   0.000  0.00  0.00           C+0
HETATM   29  O   UNK     0      -5.335 -13.860   0.000  0.00  0.00           O+0
HETATM   30  C   UNK     0      -4.001 -16.170   0.000  0.00  0.00           C+0
HETATM   31  C   UNK     0      -2.667 -16.940   0.000  0.00  0.00           C+0
HETATM   32  C   UNK     0      -1.334 -16.170   0.000  0.00  0.00           C+0
HETATM   33  O   UNK     0       0.000 -16.940   0.000  0.00  0.00           O+0
HETATM   34  C   UNK     0      -2.667 -18.480   0.000  0.00  0.00           C+0
HETATM   35  O   UNK     0      -1.334 -19.250   0.000  0.00  0.00           O+0
HETATM   36  C   UNK     0      -4.001 -19.250   0.000  0.00  0.00           C+0
HETATM   37  C   UNK     0      -3.011 -20.430   0.000  0.00  0.00           C+0
HETATM   38  O   UNK     0      -4.991 -20.430   0.000  0.00  0.00           O+0
HETATM   39  C   UNK     0      -5.335 -18.480   0.000  0.00  0.00           C+0
HETATM   40  O   UNK     0      -6.668 -19.250   0.000  0.00  0.00           O+0
HETATM   41  C   UNK     0      -5.335 -16.940   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       0.000  -9.240   0.000  0.00  0.00           C+0
HETATM   44  C   UNK     0       1.334 -10.010   0.000  0.00  0.00           C+0
HETATM   45  O   UNK     0       2.239 -11.256   0.000  0.00  0.00           O+0
CONECT    1    2                                                            
CONECT    2    1    3                                                       
CONECT    3    2    4    9                                                  
CONECT    4    3    5                                                       
CONECT    5    4    6    7                                                  
CONECT    6    5                                                            
CONECT    7    5    8   44                                                  
CONECT    8    7    9   10                                                  
CONECT    9    8    3                                                       
CONECT   10    8   11   12                                                  
CONECT   11   10                                                            
CONECT   12   10   13   43                                                  
CONECT   13   12   14                                                       
CONECT   14   13   15   16                                                  
CONECT   15   14                                                            
CONECT   16   14   17   18                                                  
CONECT   17   16                                                            
CONECT   18   16   19   43                                                  
CONECT   19   18   20   26                                                  
CONECT   20   19   21   23                                                  
CONECT   21   20   22                                                       
CONECT   22   21                                                            
CONECT   23   20   24                                                       
CONECT   24   23   25   32                                                  
CONECT   25   24   26   28                                                  
CONECT   26   25   19   27                                                  
CONECT   27   26                                                            
CONECT   28   25   29   30                                                  
CONECT   29   28                                                            
CONECT   30   28   31   41                                                  
CONECT   31   30   32   34                                                  
CONECT   32   31   24   33                                                  
CONECT   33   32                                                            
CONECT   34   31   35   36                                                  
CONECT   35   34                                                            
CONECT   36   34   37   38   39                                             
CONECT   37   36                                                            
CONECT   38   36                                                            
CONECT   39   36   40   41                                                  
CONECT   40   39                                                            
CONECT   41   39   30   42                                                  
CONECT   42   41                                                            
CONECT   43   18   12   44                                                  
CONECT   44   43    7   45                                                  
CONECT   45   44                                                            
MASTER        0    0    0    0    0    0    0    0   45    0  100    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₃₂H₂₆O₁₃

Average Mass

618.5470 Da

Monoisotopic Mass

618.13734 Da

IUPAC Name

(5'R,6'S,7'R,8'S)-1',2,5',6',7',8,8'-heptahydroxy-3',6-dimethoxy-3,6'-dimethyl-5',6',7',8'-tetrahydro-9H,9'H,10H,10'H-[1,2'-bianthracene]-9,9',10,10'-tetrone

Traditional Name

(5'R,6'S,7'R,8'S)-1',2,5',6',7',8,8'-heptahydroxy-3',6-dimethoxy-3,6'-dimethyl-7',8'-dihydro-5'H-[1,2'-bianthracene]-9,9',10,10'-tetrone

CAS Registry Number

Not Available

SMILES

COC1=CC(O)=C2C(=O)C3=C(C(O)=C(C)C=C3C(=O)C2=C1)C1=C(OC)C=C2C(=O)C3=C([C@H](O)[C@@H](O)[C@@](C)(O)[C@@H]3O)C(=O)C2=C1O

InChI Identifier

InChI=1S/C32H26O13/c1-9-5-11-17(26(37)16-12(24(11)35)6-10(44-3)7-14(16)33)20(23(9)34)19-15(45-4)8-13-18(27(19)38)28(39)21-22(25(13)36)30(41)32(2,43)31(42)29(21)40/h5-8,29-31,33-34,38,40-43H,1-4H3/t29-,30+,31+,32-/m0/s1

InChI Key

PSGFKGASHCTNSI-BVEPWEIPSA-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
Alternaria porri	LOTUS Database	35616633
Alternaria solani	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as hydroxyanthraquinones. Hydroxyanthraquinones are compounds containing a hydroxyanthraquinone moiety, which consists of an anthracene bearing a quinone, and hydroxyl group.

Kingdom

Super Class

Class

Sub Class

Direct Parent

Hydroxyanthraquinones

Alternative Parents

Substituents

Hydroxyanthraquinone
Anisole
Aryl ketone
Quinone
1-hydroxy-4-unsubstituted benzenoid
1-hydroxy-2-unsubstituted benzenoid
Alkyl aryl ether
Cyclitol or derivatives
Vinylogous acid
Tertiary alcohol
Secondary alcohol
Ketone
Ether
Polyol
Alcohol
Hydrocarbon derivative
Organic oxide
Organic oxygen compound
Organooxygen compound
Aromatic homopolycyclic compound

Molecular Framework

Aromatic homopolycyclic 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	2.69	ALOGPS
logP	1.87	ChemAxon
logS	-3.1	ALOGPS
pKa (Strongest Acidic)	6.59	ChemAxon
pKa (Strongest Basic)	-3.6	ChemAxon
Physiological Charge	-1	ChemAxon
Hydrogen Acceptor Count	13	ChemAxon
Hydrogen Donor Count	7	ChemAxon
Polar Surface Area	228.35 Å²	ChemAxon
Rotatable Bond Count	2	ChemAxon
Refractivity	156.52 m³·mol⁻¹	ChemAxon
Polarizability	61.61 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

28508740

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

14104232

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

Xia G, Li J, Li H, Long Y, Lin S, Lu Y, He L, Lin Y, Liu L, She Z: Alterporriol-type dimers from the mangrove endophytic fungus, Alternaria sp. (SK11), and their MptpB inhibitions. Mar Drugs. 2014 May 16;12(5):2953-69. doi: 10.3390/md12052953. [PubMed:24840716 ]
LOTUS database [Link]

Showing NP-Card for (5'r,6's,7'r,8's)-1',2,5',6',7',8,8'-heptahydroxy-3',6-dimethoxy-3,6'-dimethyl-7',8'-dihydro-5'h-[1,2'-bianthracene]-9,9',10,10'-tetrone (NP0175644)

MOL for NP0175644 ((5'r,6's,7'r,8's)-1',2,5',6',7',8,8'-heptahydroxy-3',6-dimethoxy-3,6'-dimethyl-7',8'-dihydro-5'h-[1,2'-bianthracene]-9,9',10,10'-tetrone)

3D MOL for NP0175644 ((5'r,6's,7'r,8's)-1',2,5',6',7',8,8'-heptahydroxy-3',6-dimethoxy-3,6'-dimethyl-7',8'-dihydro-5'h-[1,2'-bianthracene]-9,9',10,10'-tetrone)

3D SDF for NP0175644 ((5'r,6's,7'r,8's)-1',2,5',6',7',8,8'-heptahydroxy-3',6-dimethoxy-3,6'-dimethyl-7',8'-dihydro-5'h-[1,2'-bianthracene]-9,9',10,10'-tetrone)

3D-SDF for NP0175644 ((5'r,6's,7'r,8's)-1',2,5',6',7',8,8'-heptahydroxy-3',6-dimethoxy-3,6'-dimethyl-7',8'-dihydro-5'h-[1,2'-bianthracene]-9,9',10,10'-tetrone)

PDB for NP0175644 ((5'r,6's,7'r,8's)-1',2,5',6',7',8,8'-heptahydroxy-3',6-dimethoxy-3,6'-dimethyl-7',8'-dihydro-5'h-[1,2'-bianthracene]-9,9',10,10'-tetrone)

3D PDB for NP0175644 ((5'r,6's,7'r,8's)-1',2,5',6',7',8,8'-heptahydroxy-3',6-dimethoxy-3,6'-dimethyl-7',8'-dihydro-5'h-[1,2'-bianthracene]-9,9',10,10'-tetrone)

SMILES for NP0175644 ((5'r,6's,7'r,8's)-1',2,5',6',7',8,8'-heptahydroxy-3',6-dimethoxy-3,6'-dimethyl-7',8'-dihydro-5'h-[1,2'-bianthracene]-9,9',10,10'-tetrone)

INCHI for NP0175644 ((5'r,6's,7'r,8's)-1',2,5',6',7',8,8'-heptahydroxy-3',6-dimethoxy-3,6'-dimethyl-7',8'-dihydro-5'h-[1,2'-bianthracene]-9,9',10,10'-tetrone)

Structure for NP0175644 ((5'r,6's,7'r,8's)-1',2,5',6',7',8,8'-heptahydroxy-3',6-dimethoxy-3,6'-dimethyl-7',8'-dihydro-5'h-[1,2'-bianthracene]-9,9',10,10'-tetrone)

3D Structure for NP0175644 ((5'r,6's,7'r,8's)-1',2,5',6',7',8,8'-heptahydroxy-3',6-dimethoxy-3,6'-dimethyl-7',8'-dihydro-5'h-[1,2'-bianthracene]-9,9',10,10'-tetrone)