NP-MRD: Showing NP-Card for 3,11-dihydroxy-2,2-dimethyl-3,5-dihydro-1-oxa-5-azatetraphene-4,10-dione (NP0323570)

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Record Information

Version

2.0

Created at

2022-09-12 03:04:48 UTC

Updated at

2022-09-12 03:04:48 UTC

NP-MRD ID

NP0323570

Secondary Accession Numbers

None

Natural Product Identification

Common Name

3,11-dihydroxy-2,2-dimethyl-3,5-dihydro-1-oxa-5-azatetraphene-4,10-dione

Description

3,11-Dihydroxy-2,2-dimethyl-3,4,5,10-tetrahydro-2H-1-oxa-5-azatetraphene-4,10-dione 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. 3,11-Dihydroxy-2,2-dimethyl-3,4,5,10-tetrahydro-2H-1-oxa-5-azatetraphene-4,10-dione is an extremely weak basic (essentially neutral) compound (based on its pKa).

Structure

MOL 3D MOL SDF PDB SMILES InChI

     RDKit          3D

 39 42  0  0  0  0  0  0  0  0999 V2000
   -4.6533    0.1820    1.3328 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4161    0.3612    0.4790 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8603    0.9400   -0.8453 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8669   -0.9248    0.2713 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5659   -1.1442   -0.1600 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1472   -2.0837   -1.0395 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1919   -2.1685   -1.3601 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5986   -3.1446   -2.2676 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.1058   -1.3048   -0.7935 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4213   -1.4056   -1.1277 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8025   -2.2791   -1.9418 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.3333   -0.5503   -0.5735 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.6669   -0.6452   -0.9052 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.5918    0.2132   -0.3507 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.1643    1.1789    0.5497 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8405    1.2526    0.8616 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9053    0.3972    0.3115 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6014    0.5192    0.6617 N   0  0  0  0  0  0  0  0  0  0  0  0
    0.7140   -0.3135    0.1241 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6253   -0.2729    0.4089 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1236    0.7200    1.3555 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4046    1.0036    2.3366 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4630    1.3445    1.1097 C   0  0  1  0  0  0  0  0  0  0  0  0
   -2.2462    2.4592    0.3016 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.3858    1.0116    1.1858 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.1813   -0.7621    1.1016 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3690    0.2213    2.4246 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0642    1.5930   -1.2576 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7327    1.5828   -0.6469 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0553    0.1600   -1.6049 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9050   -2.7442   -1.4627 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0637   -3.7776   -2.6843 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.9775   -1.4052   -1.6089 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.6581    0.1635   -0.5936 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.9209    1.8506    0.9774 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.5335    2.0141    1.5659 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.3577    1.2548    1.3099 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9097    1.6809    2.0639 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3462    2.8220    0.4902 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  1  0
  2  4  1  0
  4  5  1  0
  5  6  2  0
  6  7  1  0
  7  8  1  0
  7  9  2  0
  9 10  1  0
 10 11  2  0
 10 12  1  0
 12 13  2  0
 13 14  1  0
 14 15  2  0
 15 16  1  0
 16 17  2  0
 17 18  1  0
 18 19  1  0
 19 20  2  0
 20 21  1  0
 21 22  2  0
 21 23  1  0
 23 24  1  0
 23  2  1  0
 20  5  1  0
 19  9  1  0
 17 12  1  0
  1 25  1  0
  1 26  1  0
  1 27  1  0
  3 28  1  0
  3 29  1  0
  3 30  1  0
  6 31  1  0
  8 32  1  0
 13 33  1  0
 14 34  1  0
 15 35  1  0
 16 36  1  0
 18 37  1  0
 23 38  1  1
 24 39  1  0
M  END


  Mrv1533004241511092D          

 24 27  0  0  0  0            999 V2000
    2.0414   -1.8171    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7622   -2.2184    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2418   -2.8586    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0323   -1.4389    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.8424   -1.2829    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.1124   -0.5034    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.9226   -0.3475    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.1926    0.4321    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.4627   -0.9711    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.2728   -0.8152    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.5428   -0.0357    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.8129   -1.4389    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.6230   -1.2829    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.1631   -1.9066    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.8931   -2.6861    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.0829   -2.8421    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.5428   -2.2184    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7327   -2.3743    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    5.1926   -1.7507    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3825   -1.9066    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.1124   -2.6861    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.6525   -3.3098    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.3023   -2.8421    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0323   -3.6216    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
  2  4  1  0  0  0  0
  4  5  1  0  0  0  0
  5  6  2  0  0  0  0
  6  7  1  0  0  0  0
  7  8  1  0  0  0  0
  7  9  2  0  0  0  0
  9 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  2  0  0  0  0
 15 16  1  0  0  0  0
 16 17  2  0  0  0  0
 12 17  1  0  0  0  0
 17 18  1  0  0  0  0
 18 19  1  0  0  0  0
  9 19  1  0  0  0  0
 19 20  2  0  0  0  0
  5 20  1  0  0  0  0
 20 21  1  0  0  0  0
 21 22  2  0  0  0  0
 21 23  1  0  0  0  0
  2 23  1  0  0  0  0
 23 24  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0323570

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CC1(C)OC2=CC(O)=C3C(=O)C4=CC=CC=C4NC3=C2C(=O)C1O

> <INCHI_IDENTIFIER>
InChI=1S/C18H15NO5/c1-18(2)17(23)16(22)13-11(24-18)7-10(20)12-14(13)19-9-6-4-3-5-8(9)15(12)21/h3-7,17,20,23H,1-2H3,(H,19,21)

> <INCHI_KEY>
CREPQPLYKBVVSR-UHFFFAOYSA-N

> <FORMULA>
C18H15NO5

> <MOLECULAR_WEIGHT>
325.32

> <EXACT_MASS>
325.095022587

> <JCHEM_ACCEPTOR_COUNT>
6

> <JCHEM_ATOM_COUNT>
39

> <JCHEM_AVERAGE_POLARIZABILITY>
33.07406132018215

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
3

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
3,11-dihydroxy-2,2-dimethyl-3,4,5,10-tetrahydro-2H-1-oxa-5-azatetraphene-4,10-dione

> <ALOGPS_LOGP>
3.71

> <JCHEM_LOGP>
3.866024735333333

> <ALOGPS_LOGS>
-2.57

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
4

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
12.197522076011047

> <JCHEM_PKA_STRONGEST_ACIDIC>
7.114220884400343

> <JCHEM_PKA_STRONGEST_BASIC>
-4.042070624950619

> <JCHEM_POLAR_SURFACE_AREA>
95.86

> <JCHEM_REFRACTIVITY>
86.44409999999999

> <JCHEM_ROTATABLE_BOND_COUNT>
0

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
8.79e-01 g/l

> <JCHEM_TRADITIONAL_IUPAC>
3,11-dihydroxy-2,2-dimethyl-3,5-dihydro-1-oxa-5-azatetraphene-4,10-dione

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 24-APR-15   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   24-APR-15         0                                  
HETATM    1  C   UNK     0       3.811  -3.392   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       5.156  -4.141   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       4.185  -5.336   0.000  0.00  0.00           C+0
HETATM    4  O   UNK     0       5.660  -2.686   0.000  0.00  0.00           O+0
HETATM    5  C   UNK     0       7.172  -2.395   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       7.677  -0.940   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       9.189  -0.649   0.000  0.00  0.00           C+0
HETATM    8  O   UNK     0       9.693   0.807   0.000  0.00  0.00           O+0
HETATM    9  C   UNK     0      10.197  -1.813   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0      11.709  -1.522   0.000  0.00  0.00           C+0
HETATM   11  O   UNK     0      12.213  -0.067   0.000  0.00  0.00           O+0
HETATM   12  C   UNK     0      12.717  -2.686   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0      14.230  -2.395   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0      15.238  -3.559   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0      14.734  -5.014   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0      13.221  -5.305   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0      12.213  -4.141   0.000  0.00  0.00           C+0
HETATM   18  N   UNK     0      10.701  -4.432   0.000  0.00  0.00           N+0
HETATM   19  C   UNK     0       9.693  -3.268   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0       8.181  -3.559   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0       7.677  -5.014   0.000  0.00  0.00           C+0
HETATM   22  O   UNK     0       8.685  -6.178   0.000  0.00  0.00           O+0
HETATM   23  C   UNK     0       6.164  -5.305   0.000  0.00  0.00           C+0
HETATM   24  O   UNK     0       5.660  -6.760   0.000  0.00  0.00           O+0
CONECT    1    2                                                            
CONECT    2    1    3    4   23                                             
CONECT    3    2                                                            
CONECT    4    2    5                                                       
CONECT    5    4    6   20                                                  
CONECT    6    5    7                                                       
CONECT    7    6    8    9                                                  
CONECT    8    7                                                            
CONECT    9    7   10   19                                                  
CONECT   10    9   11   12                                                  
CONECT   11   10                                                            
CONECT   12   10   13   17                                                  
CONECT   13   12   14                                                       
CONECT   14   13   15                                                       
CONECT   15   14   16                                                       
CONECT   16   15   17                                                       
CONECT   17   16   12   18                                                  
CONECT   18   17   19                                                       
CONECT   19   18    9   20                                                  
CONECT   20   19    5   21                                                  
CONECT   21   20   22   23                                                  
CONECT   22   21                                                            
CONECT   23   21    2   24                                                  
CONECT   24   23                                                            
MASTER        0    0    0    0    0    0    0    0   24    0   54    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₁₈H₁₅NO₅

Average Mass

325.3200 Da

Monoisotopic Mass

325.09502 Da

IUPAC Name

3,11-dihydroxy-2,2-dimethyl-3,4,5,10-tetrahydro-2H-1-oxa-5-azatetraphene-4,10-dione

Traditional Name

3,11-dihydroxy-2,2-dimethyl-3,5-dihydro-1-oxa-5-azatetraphene-4,10-dione

CAS Registry Number

Not Available

SMILES

CC1(C)OC2=CC(O)=C3C(=O)C4=CC=CC=C4NC3=C2C(=O)C1O

InChI Identifier

InChI=1S/C18H15NO5/c1-18(2)17(23)16(22)13-11(24-18)7-10(20)12-14(13)19-9-6-4-3-5-8(9)15(12)21/h3-7,17,20,23H,1-2H3,(H,19,21)

InChI Key

CREPQPLYKBVVSR-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

Not Available

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
Chromenopyridine
2,2-dimethyl-1-benzopyran
Dihydroquinolone
Chromone
Chromane
Benzopyran
Dihydroquinoline
1-benzopyran
Aryl alkyl ketone
Aryl ketone
1-hydroxy-2-unsubstituted benzenoid
Alkyl aryl ether
Phenol
Benzenoid
Pyridine
Heteroaromatic compound
Vinylogous amide
Vinylogous acid
Ketone
Secondary alcohol
Oxacycle
Azacycle
Ether
Alcohol
Organic nitrogen compound
Hydrocarbon derivative
Organic oxide
Organic oxygen compound
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	3.71	ALOGPS
logP	3.87	ChemAxon
logS	-2.6	ALOGPS
pKa (Strongest Acidic)	7.11	ChemAxon
pKa (Strongest Basic)	-4	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	6	ChemAxon
Hydrogen Donor Count	3	ChemAxon
Polar Surface Area	95.86 Å²	ChemAxon
Rotatable Bond Count	0	ChemAxon
Refractivity	86.44 m³·mol⁻¹	ChemAxon
Polarizability	33.07 Å³	ChemAxon
Number of Rings	4	ChemAxon
Bioavailability	Yes	ChemAxon
Rule of Five	Yes	ChemAxon
Ghose Filter	Yes	ChemAxon
Veber's Rule	No	ChemAxon
MDDR-like Rule	No	ChemAxon

External Links

HMDB ID

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DrugBank ID

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Phenol Explorer Compound ID

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FoodDB ID

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KNApSAcK ID

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Chemspider ID

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KEGG Compound ID

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BioCyc ID

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BiGG ID

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Wikipedia Link

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METLIN ID

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PubChem Compound

101334257

PDB ID

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ChEBI ID

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Good Scents ID

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References

General References

LOTUS database [Link]

Showing NP-Card for 3,11-dihydroxy-2,2-dimethyl-3,5-dihydro-1-oxa-5-azatetraphene-4,10-dione (NP0323570)

MOL for NP0323570 (3,11-dihydroxy-2,2-dimethyl-3,5-dihydro-1-oxa-5-azatetraphene-4,10-dione)

3D MOL for NP0323570 (3,11-dihydroxy-2,2-dimethyl-3,5-dihydro-1-oxa-5-azatetraphene-4,10-dione)

3D SDF for NP0323570 (3,11-dihydroxy-2,2-dimethyl-3,5-dihydro-1-oxa-5-azatetraphene-4,10-dione)

3D-SDF for NP0323570 (3,11-dihydroxy-2,2-dimethyl-3,5-dihydro-1-oxa-5-azatetraphene-4,10-dione)

PDB for NP0323570 (3,11-dihydroxy-2,2-dimethyl-3,5-dihydro-1-oxa-5-azatetraphene-4,10-dione)

3D PDB for NP0323570 (3,11-dihydroxy-2,2-dimethyl-3,5-dihydro-1-oxa-5-azatetraphene-4,10-dione)

SMILES for NP0323570 (3,11-dihydroxy-2,2-dimethyl-3,5-dihydro-1-oxa-5-azatetraphene-4,10-dione)

INCHI for NP0323570 (3,11-dihydroxy-2,2-dimethyl-3,5-dihydro-1-oxa-5-azatetraphene-4,10-dione)

Structure for NP0323570 (3,11-dihydroxy-2,2-dimethyl-3,5-dihydro-1-oxa-5-azatetraphene-4,10-dione)

3D Structure for NP0323570 (3,11-dihydroxy-2,2-dimethyl-3,5-dihydro-1-oxa-5-azatetraphene-4,10-dione)