NP-MRD: Showing NP-Card for 9-hydroxy-6,7-dimethoxy-2,5-dimethyl-2-[(1z)-2-(1,3,5-trihydroxy-10-methyl-9-oxoacridin-4-yl)ethenyl]-3h-1,4-dioxa-5-azatetraphen-10-one (NP0206297)

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Record Information

Version

2.0

Created at

2022-09-05 02:29:39 UTC

Updated at

2022-09-05 02:29:39 UTC

NP-MRD ID

NP0206297

Secondary Accession Numbers

None

Natural Product Identification

Common Name

9-hydroxy-6,7-dimethoxy-2,5-dimethyl-2-[(1z)-2-(1,3,5-trihydroxy-10-methyl-9-oxoacridin-4-yl)ethenyl]-3h-1,4-dioxa-5-azatetraphen-10-one

Description

Glycobismine D belongs to the class of organic compounds known as acridones. These are acridines containing a ketone group attached to the C9 carbon atom of the acridine moiety. 9-hydroxy-6,7-dimethoxy-2,5-dimethyl-2-[(1z)-2-(1,3,5-trihydroxy-10-methyl-9-oxoacridin-4-yl)ethenyl]-3h-1,4-dioxa-5-azatetraphen-10-one is found in Glycosmis citrifolia. Based on a literature review very few articles have been published on Glycobismine D.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652309052204292D          

 47 53  0  0  0  0            999 V2000
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M  END

     RDKit          3D

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M  END


  Mrv1652309052204292D          

 47 53  0  0  0  0            999 V2000
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   -3.2499    2.6804    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7802    3.3124    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5643    1.7029    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.2481    1.8462    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7784    1.2142    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3087    1.8462    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4929    0.8017    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2074    1.2142    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2074    2.0392    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4929    2.4517    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7784    2.0392    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.4929    3.2767    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2074    3.6892    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2074    4.5142    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.9218    3.2767    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6363    3.6892    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6363    4.5142    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.3508    3.2767    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0653    3.6892    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7797    3.2767    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7797    2.4517    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0653    2.0392    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0653    1.2142    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.3508    2.4517    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6363    2.0392    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    3.6363    1.2142    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9218    2.4517    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4963    0.4390    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
  8 10  1  0  0  0  0
 10 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
 14 15  2  0  0  0  0
 10 15  1  0  0  0  0
 15 16  1  0  0  0  0
 16 17  1  0  0  0  0
 16 18  1  0  0  0  0
  7 18  1  0  0  0  0
 18 19  2  0  0  0  0
  3 19  1  0  0  0  0
 19 20  1  0  0  0  0
 20 21  1  0  0  0  0
 14 22  1  0  0  0  0
 22 23  1  0  0  0  0
 23 24  1  0  0  0  0
 24 25  1  0  0  0  0
 24 26  1  0  0  0  0
 26 27  2  0  0  0  0
 27 28  1  0  0  0  0
 28 29  1  0  0  0  0
 29 30  1  0  0  0  0
 29 31  2  0  0  0  0
 31 32  1  0  0  0  0
 32 33  1  0  0  0  0
 32 34  2  0  0  0  0
 34 35  1  0  0  0  0
 35 36  2  0  0  0  0
 35 37  1  0  0  0  0
 37 38  2  0  0  0  0
 38 39  1  0  0  0  0
 39 40  2  0  0  0  0
 40 41  1  0  0  0  0
 41 42  1  0  0  0  0
 41 43  2  0  0  0  0
 37 43  1  0  0  0  0
 43 44  1  0  0  0  0
 44 45  1  0  0  0  0
 44 46  1  0  0  0  0
 28 46  2  0  0  0  0
 34 46  1  0  0  0  0
 24 47  1  0  0  0  0
 13 47  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0206297

> <DATABASE_NAME>
NP-MRD

> <SMILES>
COC1=CC(O)=C2C(=O)C3=CC=C4OC(C)(COC4=C3N(C)C2=C1OC)\C=C/C1=C2N(C)C3=C(O)C=CC=C3C(=O)C2=C(O)C=C1O

> <INCHI_IDENTIFIER>
InChI=1S/C35H30N2O10/c1-35(12-11-16-20(39)13-21(40)25-28(16)36(2)27-17(31(25)42)7-6-8-19(27)38)15-46-34-23(47-35)10-9-18-29(34)37(3)30-26(32(18)43)22(41)14-24(44-4)33(30)45-5/h6-14,38-41H,15H2,1-5H3/b12-11-

> <INCHI_KEY>
PQPGLMPQNHBXON-QXMHVHEDSA-N

> <FORMULA>
C35H30N2O10

> <MOLECULAR_WEIGHT>
638.629

> <EXACT_MASS>
638.190045174

> <JCHEM_ACCEPTOR_COUNT>
12

> <JCHEM_ATOM_COUNT>
77

> <JCHEM_AVERAGE_POLARIZABILITY>
64.61689291232337

> <JCHEM_BIOAVAILABILITY>
0

> <JCHEM_DONOR_COUNT>
4

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
9-hydroxy-6,7-dimethoxy-2,5-dimethyl-2-[(Z)-2-(1,3,5-trihydroxy-10-methyl-9-oxo-9,10-dihydroacridin-4-yl)ethenyl]-2,3,5,10-tetrahydro-1,4-dioxa-5-azatetraphen-10-one

> <JCHEM_LOGP>
6.230925176999998

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
7

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
8.882093647202478

> <JCHEM_PKA_STRONGEST_ACIDIC>
7.830065466330532

> <JCHEM_PKA_STRONGEST_BASIC>
-2.7649346279302254

> <JCHEM_POLAR_SURFACE_AREA>
158.46

> <JCHEM_REFRACTIVITY>
172.9058

> <JCHEM_ROTATABLE_BOND_COUNT>
4

> <JCHEM_RULE_OF_FIVE>
0

> <JCHEM_TRADITIONAL_IUPAC>
9-hydroxy-6,7-dimethoxy-2,5-dimethyl-2-[(Z)-2-(1,3,5-trihydroxy-10-methyl-9-oxoacridin-4-yl)ethenyl]-3H-1,4-dioxa-5-azatetraphen-10-one

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 05-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   05-SEP-22         0                                  
HETATM    1  C   UNK     0     -10.616   4.201   0.000  0.00  0.00           C+0
HETATM    2  O   UNK     0      -9.100   4.469   0.000  0.00  0.00           O+0
HETATM    3  C   UNK     0      -8.110   3.289   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0      -8.636   1.842   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0      -7.647   0.662   0.000  0.00  0.00           C+0
HETATM    6  O   UNK     0      -8.173  -0.785   0.000  0.00  0.00           O+0
HETATM    7  C   UNK     0      -6.130   0.929   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0      -5.140  -0.250   0.000  0.00  0.00           C+0
HETATM    9  O   UNK     0      -5.667  -1.697   0.000  0.00  0.00           O+0
HETATM   10  C   UNK     0      -3.623   0.017   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0      -2.634  -1.163   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0      -1.117  -0.895   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0      -0.590   0.552   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0      -1.580   1.732   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0      -3.097   1.464   0.000  0.00  0.00           C+0
HETATM   16  N   UNK     0      -4.087   2.644   0.000  0.00  0.00           N+0
HETATM   17  C   UNK     0      -3.560   4.091   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0      -5.603   2.377   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0      -6.593   3.556   0.000  0.00  0.00           C+0
HETATM   20  O   UNK     0      -6.066   5.003   0.000  0.00  0.00           O+0
HETATM   21  C   UNK     0      -7.056   6.183   0.000  0.00  0.00           C+0
HETATM   22  O   UNK     0      -1.053   3.179   0.000  0.00  0.00           O+0
HETATM   23  C   UNK     0       0.463   3.446   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0       1.453   2.267   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0       2.443   3.446   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0       2.787   1.497   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0       4.120   2.267   0.000  0.00  0.00           C+0
HETATM   28  C   UNK     0       4.120   3.807   0.000  0.00  0.00           C+0
HETATM   29  C   UNK     0       2.787   4.577   0.000  0.00  0.00           C+0
HETATM   30  O   UNK     0       1.453   3.807   0.000  0.00  0.00           O+0
HETATM   31  C   UNK     0       2.787   6.117   0.000  0.00  0.00           C+0
HETATM   32  C   UNK     0       4.120   6.887   0.000  0.00  0.00           C+0
HETATM   33  O   UNK     0       4.120   8.427   0.000  0.00  0.00           O+0
HETATM   34  C   UNK     0       5.454   6.117   0.000  0.00  0.00           C+0
HETATM   35  C   UNK     0       6.788   6.887   0.000  0.00  0.00           C+0
HETATM   36  O   UNK     0       6.788   8.427   0.000  0.00  0.00           O+0
HETATM   37  C   UNK     0       8.121   6.117   0.000  0.00  0.00           C+0
HETATM   38  C   UNK     0       9.455   6.887   0.000  0.00  0.00           C+0
HETATM   39  C   UNK     0      10.789   6.117   0.000  0.00  0.00           C+0
HETATM   40  C   UNK     0      10.789   4.577   0.000  0.00  0.00           C+0
HETATM   41  C   UNK     0       9.455   3.807   0.000  0.00  0.00           C+0
HETATM   42  O   UNK     0       9.455   2.267   0.000  0.00  0.00           O+0
HETATM   43  C   UNK     0       8.121   4.577   0.000  0.00  0.00           C+0
HETATM   44  N   UNK     0       6.788   3.807   0.000  0.00  0.00           N+0
HETATM   45  C   UNK     0       6.788   2.267   0.000  0.00  0.00           C+0
HETATM   46  C   UNK     0       5.454   4.577   0.000  0.00  0.00           C+0
HETATM   47  O   UNK     0       0.926   0.819   0.000  0.00  0.00           O+0
CONECT    1    2                                                            
CONECT    2    1    3                                                       
CONECT    3    2    4   19                                                  
CONECT    4    3    5                                                       
CONECT    5    4    6    7                                                  
CONECT    6    5                                                            
CONECT    7    5    8   18                                                  
CONECT    8    7    9   10                                                  
CONECT    9    8                                                            
CONECT   10    8   11   15                                                  
CONECT   11   10   12                                                       
CONECT   12   11   13                                                       
CONECT   13   12   14   47                                                  
CONECT   14   13   15   22                                                  
CONECT   15   14   10   16                                                  
CONECT   16   15   17   18                                                  
CONECT   17   16                                                            
CONECT   18   16    7   19                                                  
CONECT   19   18    3   20                                                  
CONECT   20   19   21                                                       
CONECT   21   20                                                            
CONECT   22   14   23                                                       
CONECT   23   22   24                                                       
CONECT   24   23   25   26   47                                             
CONECT   25   24                                                            
CONECT   26   24   27                                                       
CONECT   27   26   28                                                       
CONECT   28   27   29   46                                                  
CONECT   29   28   30   31                                                  
CONECT   30   29                                                            
CONECT   31   29   32                                                       
CONECT   32   31   33   34                                                  
CONECT   33   32                                                            
CONECT   34   32   35   46                                                  
CONECT   35   34   36   37                                                  
CONECT   36   35                                                            
CONECT   37   35   38   43                                                  
CONECT   38   37   39                                                       
CONECT   39   38   40                                                       
CONECT   40   39   41                                                       
CONECT   41   40   42   43                                                  
CONECT   42   41                                                            
CONECT   43   41   37   44                                                  
CONECT   44   43   45   46                                                  
CONECT   45   44                                                            
CONECT   46   44   28   34                                                  
CONECT   47   24   13                                                       
MASTER        0    0    0    0    0    0    0    0   47    0  106    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₃₅H₃₀N₂O₁₀

Average Mass

638.6290 Da

Monoisotopic Mass

638.19005 Da

IUPAC Name

9-hydroxy-6,7-dimethoxy-2,5-dimethyl-2-[(Z)-2-(1,3,5-trihydroxy-10-methyl-9-oxo-9,10-dihydroacridin-4-yl)ethenyl]-2,3,5,10-tetrahydro-1,4-dioxa-5-azatetraphen-10-one

Traditional Name

9-hydroxy-6,7-dimethoxy-2,5-dimethyl-2-[(Z)-2-(1,3,5-trihydroxy-10-methyl-9-oxoacridin-4-yl)ethenyl]-3H-1,4-dioxa-5-azatetraphen-10-one

CAS Registry Number

Not Available

SMILES

COC1=CC(O)=C2C(=O)C3=CC=C4OC(C)(COC4=C3N(C)C2=C1OC)\C=C/C1=C2N(C)C3=C(O)C=CC=C3C(=O)C2=C(O)C=C1O

InChI Identifier

InChI=1S/C35H30N2O10/c1-35(12-11-16-20(39)13-21(40)25-28(16)36(2)27-17(31(25)42)7-6-8-19(27)38)15-46-34-23(47-35)10-9-18-29(34)37(3)30-26(32(18)43)22(41)14-24(44-4)33(30)45-5/h6-14,38-41H,15H2,1-5H3/b12-11-

InChI Key

PQPGLMPQNHBXON-QXMHVHEDSA-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
Glycosmis citrifolia	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as acridones. These are acridines containing a ketone group attached to the C9 carbon atom of the acridine moiety.

Kingdom

Organic compounds

Super Class

Organoheterocyclic compounds

Class

Quinolines and derivatives

Sub Class

Benzoquinolines

Direct Parent

Acridones

Alternative Parents

Substituents

Acridone
8-hydroxyquinoline
Dihydroquinolone
Dihydroquinoline
Benzodioxane
Benzo-1,4-dioxane
Styrene
Anisole
1-hydroxy-4-unsubstituted benzenoid
1-hydroxy-2-unsubstituted benzenoid
Alkyl aryl ether
Benzenoid
Pyridine
Para-dioxin
Heteroaromatic compound
Vinylogous amide
Vinylogous acid
Oxacycle
Azacycle
Polyol
Ether
Organic nitrogen compound
Organic oxygen compound
Organopnictogen compound
Organic oxide
Hydrocarbon derivative
Organooxygen compound
Organonitrogen 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	6.23	ChemAxon
pKa (Strongest Acidic)	7.83	ChemAxon
pKa (Strongest Basic)	-2.8	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	12	ChemAxon
Hydrogen Donor Count	4	ChemAxon
Polar Surface Area	158.46 Å²	ChemAxon
Rotatable Bond Count	4	ChemAxon
Refractivity	172.91 m³·mol⁻¹	ChemAxon
Polarizability	64.62 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

134693664

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for 9-hydroxy-6,7-dimethoxy-2,5-dimethyl-2-[(1z)-2-(1,3,5-trihydroxy-10-methyl-9-oxoacridin-4-yl)ethenyl]-3h-1,4-dioxa-5-azatetraphen-10-one (NP0206297)

MOL for NP0206297 (9-hydroxy-6,7-dimethoxy-2,5-dimethyl-2-[(1z)-2-(1,3,5-trihydroxy-10-methyl-9-oxoacridin-4-yl)ethenyl]-3h-1,4-dioxa-5-azatetraphen-10-one)

3D MOL for NP0206297 (9-hydroxy-6,7-dimethoxy-2,5-dimethyl-2-[(1z)-2-(1,3,5-trihydroxy-10-methyl-9-oxoacridin-4-yl)ethenyl]-3h-1,4-dioxa-5-azatetraphen-10-one)

3D SDF for NP0206297 (9-hydroxy-6,7-dimethoxy-2,5-dimethyl-2-[(1z)-2-(1,3,5-trihydroxy-10-methyl-9-oxoacridin-4-yl)ethenyl]-3h-1,4-dioxa-5-azatetraphen-10-one)

3D-SDF for NP0206297 (9-hydroxy-6,7-dimethoxy-2,5-dimethyl-2-[(1z)-2-(1,3,5-trihydroxy-10-methyl-9-oxoacridin-4-yl)ethenyl]-3h-1,4-dioxa-5-azatetraphen-10-one)

PDB for NP0206297 (9-hydroxy-6,7-dimethoxy-2,5-dimethyl-2-[(1z)-2-(1,3,5-trihydroxy-10-methyl-9-oxoacridin-4-yl)ethenyl]-3h-1,4-dioxa-5-azatetraphen-10-one)

3D PDB for NP0206297 (9-hydroxy-6,7-dimethoxy-2,5-dimethyl-2-[(1z)-2-(1,3,5-trihydroxy-10-methyl-9-oxoacridin-4-yl)ethenyl]-3h-1,4-dioxa-5-azatetraphen-10-one)

SMILES for NP0206297 (9-hydroxy-6,7-dimethoxy-2,5-dimethyl-2-[(1z)-2-(1,3,5-trihydroxy-10-methyl-9-oxoacridin-4-yl)ethenyl]-3h-1,4-dioxa-5-azatetraphen-10-one)

INCHI for NP0206297 (9-hydroxy-6,7-dimethoxy-2,5-dimethyl-2-[(1z)-2-(1,3,5-trihydroxy-10-methyl-9-oxoacridin-4-yl)ethenyl]-3h-1,4-dioxa-5-azatetraphen-10-one)

Structure for NP0206297 (9-hydroxy-6,7-dimethoxy-2,5-dimethyl-2-[(1z)-2-(1,3,5-trihydroxy-10-methyl-9-oxoacridin-4-yl)ethenyl]-3h-1,4-dioxa-5-azatetraphen-10-one)

3D Structure for NP0206297 (9-hydroxy-6,7-dimethoxy-2,5-dimethyl-2-[(1z)-2-(1,3,5-trihydroxy-10-methyl-9-oxoacridin-4-yl)ethenyl]-3h-1,4-dioxa-5-azatetraphen-10-one)