NP-MRD: Showing NP-Card for 2-[5,10-dihydroxy-2-(2-hydroxypropan-2-yl)-11-methyl-6-oxo-1h,2h-furo[2,3-c]acridin-1-yl]-1-hydroxy-3,5,6-trimethoxy-10h-acridin-9-one (NP0328060)

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Record Information

Version

2.0

Created at

2022-09-12 11:11:19 UTC

Updated at

2022-09-12 11:11:19 UTC

NP-MRD ID

NP0328060

Secondary Accession Numbers

None

Natural Product Identification

Common Name

2-[5,10-dihydroxy-2-(2-hydroxypropan-2-yl)-11-methyl-6-oxo-1h,2h-furo[2,3-c]acridin-1-yl]-1-hydroxy-3,5,6-trimethoxy-10h-acridin-9-one

Description

Citbismine A 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. Citbismine A is an extremely weak basic (essentially neutral) compound (based on its pKa). Outside of the human body, Citbismine A has been detected, but not quantified in, citrus. 2-[5,10-dihydroxy-2-(2-hydroxypropan-2-yl)-11-methyl-6-oxo-1h,2h-furo[2,3-c]acridin-1-yl]-1-hydroxy-3,5,6-trimethoxy-10h-acridin-9-one is found in Citrus paradisi. This could make citbismine a a potential biomarker for the consumption of these foods.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv0541 05061312222D          

 47 53  0  0  0  0            999 V2000
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M  END

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M  END


  Mrv0541 05061312222D          

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    3.9077   -0.0008    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7439    7.3874    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.1628    3.1211    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8524    0.9626    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2021    4.4626    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.4639    0.6085    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4086    1.5719    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3417    3.0405    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0010    2.2891    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8835    5.9653    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.5764    1.8271    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2144    1.3948    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7218    5.1334    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.2697    0.4314    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8614    3.7112    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2242    6.7167    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1929    2.1231    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3726    2.4610    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3639    5.2946    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    4.7706    2.0041    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    5.9929    3.2315    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.9848   -0.8583    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.8836    5.3722    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.5761   -0.3722    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.8378    3.8720    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.6108    2.9061    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.9052    8.2576    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.7330    2.7265    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.0885    6.9271    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.1010    1.3033    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  8  7  2  0  0  0  0
  9  7  1  0  0  0  0
 11 10  2  0  0  0  0
 14 10  1  0  0  0  0
 15  8  1  0  0  0  0
 16 12  2  0  0  0  0
 17  9  2  0  0  0  0
 18 13  2  0  0  0  0
 19 11  1  0  0  0  0
 20 12  1  0  0  0  0
 21 13  1  0  0  0  0
 22 16  1  0  0  0  0
 23 18  1  0  0  0  0
 24 21  2  0  0  0  0
 25 20  2  0  0  0  0
 26 24  1  0  0  0  0
 26 25  1  0  0  0  0
 27 14  2  0  0  0  0
 28 15  2  0  0  0  0
 28 17  1  0  0  0  0
 29 23  2  0  0  0  0
 29 24  1  0  0  0  0
 30 14  1  0  0  0  0
 30 22  1  0  0  0  0
 31 15  1  0  0  0  0
 31 23  1  0  0  0  0
 32 22  2  0  0  0  0
 32 25  1  0  0  0  0
 33 19  2  0  0  0  0
 33 27  1  0  0  0  0
 34 26  1  0  0  0  0
 35  1  1  0  0  0  0
 35  2  1  0  0  0  0
 35 34  1  0  0  0  0
 36 16  1  0  0  0  0
 36 27  1  0  0  0  0
 37  3  1  0  0  0  0
 37 28  1  0  0  0  0
 37 29  1  0  0  0  0
 38 17  1  0  0  0  0
 39 18  1  0  0  0  0
 40 30  2  0  0  0  0
 41 31  2  0  0  0  0
 42 32  1  0  0  0  0
 43 35  1  0  0  0  0
 44  4  1  0  0  0  0
 44 19  1  0  0  0  0
 45  5  1  0  0  0  0
 45 20  1  0  0  0  0
 46  6  1  0  0  0  0
 46 33  1  0  0  0  0
 47 21  1  0  0  0  0
 47 34  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0328060

> <DATABASE_NAME>
NP-MRD

> <SMILES>
COC1=C(OC)C2=C(C=C1)C(=O)C1=C(O)C(C3C(OC4=C3C3=C(C(O)=C4)C(=O)C4=C(N3C)C(O)=CC=C4)C(C)(C)O)=C(OC)C=C1N2

> <INCHI_IDENTIFIER>
InChI=1S/C35H32N2O10/c1-35(2,43)34-26(24-21(47-34)13-18(39)23-29(24)37(3)28-15(31(23)41)8-7-9-17(28)38)25-20(45-5)12-16-22(32(25)42)30(40)14-10-11-19(44-4)33(46-6)27(14)36-16/h7-13,26,34,38-39,42-43H,1-6H3,(H,36,40)

> <INCHI_KEY>
FTTSBKFANOKIKQ-UHFFFAOYSA-N

> <FORMULA>
C35H32N2O10

> <MOLECULAR_WEIGHT>
640.636

> <EXACT_MASS>
640.205695254

> <JCHEM_ACCEPTOR_COUNT>
12

> <JCHEM_AVERAGE_POLARIZABILITY>
65.7462145483767

> <JCHEM_BIOAVAILABILITY>
0

> <JCHEM_DONOR_COUNT>
5

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
2-[5,10-dihydroxy-2-(2-hydroxypropan-2-yl)-11-methyl-6-oxo-1H,2H,6H,11H-furo[2,3-c]acridin-1-yl]-1-hydroxy-3,5,6-trimethoxy-9,10-dihydroacridin-9-one

> <ALOGPS_LOGP>
5.03

> <JCHEM_LOGP>
6.713088903666665

> <ALOGPS_LOGS>
-4.23

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
7

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
9.562643479007935

> <JCHEM_PKA_STRONGEST_ACIDIC>
8.975012127847528

> <JCHEM_PKA_STRONGEST_BASIC>
-3.1155125231255774

> <JCHEM_POLAR_SURFACE_AREA>
167.24999999999997

> <JCHEM_REFRACTIVITY>
171.6533

> <JCHEM_ROTATABLE_BOND_COUNT>
5

> <JCHEM_RULE_OF_FIVE>
0

> <ALOGPS_SOLUBILITY>
3.77e-02 g/l

> <JCHEM_TRADITIONAL_IUPAC>
2-[5,10-dihydroxy-2-(2-hydroxypropan-2-yl)-11-methyl-6-oxo-1H,2H-furo[2,3-c]acridin-1-yl]-1-hydroxy-3,5,6-trimethoxy-10H-acridin-9-one

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 06-MAY-13   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   06-MAY-13         0                                  
HETATM    1  C   UNK     0       1.360   3.496   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       3.528   5.854   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       7.661   4.467   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       6.570  16.844   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0      10.005   5.404   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0      10.557  14.127   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0      13.417   2.749   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0      12.379   1.612   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0      12.952   4.217   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       4.820  12.237   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       5.456  13.639   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       8.407   7.229   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       5.790   0.329   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       5.717  10.985   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0      10.875   1.943   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       7.510   8.481   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0      11.448   4.548   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       7.294  -0.001   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0       6.989  13.790   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0       7.771   5.826   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0       5.324   1.797   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0       5.977   8.330   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0       8.333   1.136   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0       6.363   2.934   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0       6.238   5.676   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0       5.602   4.273   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0       7.249  11.135   0.000  0.00  0.00           C+0
HETATM   28  C   UNK     0      10.409   3.411   0.000  0.00  0.00           C+0
HETATM   29  C   UNK     0       7.867   2.604   0.000  0.00  0.00           C+0
HETATM   30  C   UNK     0       5.081   9.582   0.000  0.00  0.00           C+0
HETATM   31  C   UNK     0       9.837   0.805   0.000  0.00  0.00           C+0
HETATM   32  C   UNK     0       5.341   6.928   0.000  0.00  0.00           C+0
HETATM   33  C   UNK     0       7.885  12.538   0.000  0.00  0.00           C+0
HETATM   34  C   UNK     0       4.093   3.963   0.000  0.00  0.00           C+0
HETATM   35  C   UNK     0       2.562   4.594   0.000  0.00  0.00           C+0
HETATM   36  N   UNK     0       8.146   9.883   0.000  0.00  0.00           N+0
HETATM   37  N   UNK     0       8.905   3.741   0.000  0.00  0.00           N+0
HETATM   38  O   UNK     0      11.187   6.032   0.000  0.00  0.00           O+0
HETATM   39  O   UNK     0       7.438  -1.602   0.000  0.00  0.00           O+0
HETATM   40  O   UNK     0       3.516  10.028   0.000  0.00  0.00           O+0
HETATM   41  O   UNK     0      10.409  -0.695   0.000  0.00  0.00           O+0
HETATM   42  O   UNK     0       3.431   7.228   0.000  0.00  0.00           O+0
HETATM   43  O   UNK     0       1.140   5.425   0.000  0.00  0.00           O+0
HETATM   44  O   UNK     0       7.290  15.414   0.000  0.00  0.00           O+0
HETATM   45  O   UNK     0       8.835   5.089   0.000  0.00  0.00           O+0
HETATM   46  O   UNK     0       9.499  12.931   0.000  0.00  0.00           O+0
HETATM   47  O   UNK     0       3.922   2.433   0.000  0.00  0.00           O+0
CONECT    1   35                                                            
CONECT    2   35                                                            
CONECT    3   37                                                            
CONECT    4   44                                                            
CONECT    5   45                                                            
CONECT    6   46                                                            
CONECT    7    8    9                                                       
CONECT    8    7   15                                                       
CONECT    9    7   17                                                       
CONECT   10   11   14                                                       
CONECT   11   10   19                                                       
CONECT   12   16   20                                                       
CONECT   13   18   21                                                       
CONECT   14   10   27   30                                                  
CONECT   15    8   28   31                                                  
CONECT   16   12   22   36                                                  
CONECT   17    9   28   38                                                  
CONECT   18   13   23   39                                                  
CONECT   19   11   33   44                                                  
CONECT   20   12   25   45                                                  
CONECT   21   13   24   47                                                  
CONECT   22   16   30   32                                                  
CONECT   23   18   29   31                                                  
CONECT   24   21   26   29                                                  
CONECT   25   20   26   32                                                  
CONECT   26   24   25   34                                                  
CONECT   27   14   33   36                                                  
CONECT   28   15   17   37                                                  
CONECT   29   23   24   37                                                  
CONECT   30   14   22   40                                                  
CONECT   31   15   23   41                                                  
CONECT   32   22   25   42                                                  
CONECT   33   19   27   46                                                  
CONECT   34   26   35   47                                                  
CONECT   35    1    2   34   43                                             
CONECT   36   16   27                                                       
CONECT   37    3   28   29                                                  
CONECT   38   17                                                            
CONECT   39   18                                                            
CONECT   40   30                                                            
CONECT   41   31                                                            
CONECT   42   32                                                            
CONECT   43   35                                                            
CONECT   44    4   19                                                       
CONECT   45    5   20                                                       
CONECT   46    6   33                                                       
CONECT   47   21   34                                                       
MASTER        0    0    0    0    0    0    0    0   47    0  106    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₃₅H₃₂N₂O₁₀

Average Mass

640.6360 Da

Monoisotopic Mass

640.20570 Da

IUPAC Name

2-[5,10-dihydroxy-2-(2-hydroxypropan-2-yl)-11-methyl-6-oxo-1H,2H,6H,11H-furo[2,3-c]acridin-1-yl]-1-hydroxy-3,5,6-trimethoxy-9,10-dihydroacridin-9-one

Traditional Name

2-[5,10-dihydroxy-2-(2-hydroxypropan-2-yl)-11-methyl-6-oxo-1H,2H-furo[2,3-c]acridin-1-yl]-1-hydroxy-3,5,6-trimethoxy-10H-acridin-9-one

CAS Registry Number

Not Available

SMILES

COC1=C(OC)C2=C(C=C1)C(=O)C1=C(O)C(C3C(OC4=C3C3=C(C(O)=C4)C(=O)C4=C(N3C)C(O)=CC=C4)C(C)(C)O)=C(OC)C=C1N2

InChI Identifier

InChI=1S/C35H32N2O10/c1-35(2,43)34-26(24-21(47-34)13-18(39)23-29(24)37(3)28-15(31(23)41)8-7-9-17(28)38)25-20(45-5)12-16-22(32(25)42)30(40)14-10-11-19(44-4)33(46-6)27(14)36-16/h7-13,26,34,38-39,42-43H,1-6H3,(H,36,40)

InChI Key

FTTSBKFANOKIKQ-UHFFFAOYSA-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
Citrus paradisi	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
Dihydroquinolone
8-hydroxyquinoline
Dihydroquinoline
Coumaran
Anisole
1-hydroxy-4-unsubstituted benzenoid
1-hydroxy-2-unsubstituted benzenoid
Alkyl aryl ether
Pyridine
Benzenoid
Heteroaromatic compound
Tertiary alcohol
Vinylogous acid
Vinylogous amide
Ether
Oxacycle
Azacycle
Alcohol
Organic nitrogen compound
Organooxygen compound
Organonitrogen compound
Hydrocarbon derivative
Organic oxide
Organic oxygen compound
Organopnictogen 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	5.03	ALOGPS
logP	6.71	ChemAxon
logS	-4.2	ALOGPS
pKa (Strongest Acidic)	8.98	ChemAxon
pKa (Strongest Basic)	-3.1	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	12	ChemAxon
Hydrogen Donor Count	5	ChemAxon
Polar Surface Area	167.25 Å²	ChemAxon
Rotatable Bond Count	5	ChemAxon
Refractivity	171.65 m³·mol⁻¹	ChemAxon
Polarizability	65.75 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

HMDB0041086

DrugBank ID

Not Available

Phenol Explorer Compound ID

Not Available

FoodDB ID

FDB020964

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

131753020

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for 2-[5,10-dihydroxy-2-(2-hydroxypropan-2-yl)-11-methyl-6-oxo-1h,2h-furo[2,3-c]acridin-1-yl]-1-hydroxy-3,5,6-trimethoxy-10h-acridin-9-one (NP0328060)

MOL for NP0328060 (2-[5,10-dihydroxy-2-(2-hydroxypropan-2-yl)-11-methyl-6-oxo-1h,2h-furo[2,3-c]acridin-1-yl]-1-hydroxy-3,5,6-trimethoxy-10h-acridin-9-one)

3D MOL for NP0328060 (2-[5,10-dihydroxy-2-(2-hydroxypropan-2-yl)-11-methyl-6-oxo-1h,2h-furo[2,3-c]acridin-1-yl]-1-hydroxy-3,5,6-trimethoxy-10h-acridin-9-one)

3D SDF for NP0328060 (2-[5,10-dihydroxy-2-(2-hydroxypropan-2-yl)-11-methyl-6-oxo-1h,2h-furo[2,3-c]acridin-1-yl]-1-hydroxy-3,5,6-trimethoxy-10h-acridin-9-one)

3D-SDF for NP0328060 (2-[5,10-dihydroxy-2-(2-hydroxypropan-2-yl)-11-methyl-6-oxo-1h,2h-furo[2,3-c]acridin-1-yl]-1-hydroxy-3,5,6-trimethoxy-10h-acridin-9-one)

PDB for NP0328060 (2-[5,10-dihydroxy-2-(2-hydroxypropan-2-yl)-11-methyl-6-oxo-1h,2h-furo[2,3-c]acridin-1-yl]-1-hydroxy-3,5,6-trimethoxy-10h-acridin-9-one)

3D PDB for NP0328060 (2-[5,10-dihydroxy-2-(2-hydroxypropan-2-yl)-11-methyl-6-oxo-1h,2h-furo[2,3-c]acridin-1-yl]-1-hydroxy-3,5,6-trimethoxy-10h-acridin-9-one)

SMILES for NP0328060 (2-[5,10-dihydroxy-2-(2-hydroxypropan-2-yl)-11-methyl-6-oxo-1h,2h-furo[2,3-c]acridin-1-yl]-1-hydroxy-3,5,6-trimethoxy-10h-acridin-9-one)

INCHI for NP0328060 (2-[5,10-dihydroxy-2-(2-hydroxypropan-2-yl)-11-methyl-6-oxo-1h,2h-furo[2,3-c]acridin-1-yl]-1-hydroxy-3,5,6-trimethoxy-10h-acridin-9-one)

Structure for NP0328060 (2-[5,10-dihydroxy-2-(2-hydroxypropan-2-yl)-11-methyl-6-oxo-1h,2h-furo[2,3-c]acridin-1-yl]-1-hydroxy-3,5,6-trimethoxy-10h-acridin-9-one)

3D Structure for NP0328060 (2-[5,10-dihydroxy-2-(2-hydroxypropan-2-yl)-11-methyl-6-oxo-1h,2h-furo[2,3-c]acridin-1-yl]-1-hydroxy-3,5,6-trimethoxy-10h-acridin-9-one)