NP-MRD: Showing NP-Card for Diazaquinomycin A (NP0021283)

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Record Information

Version

1.0

Created at

2021-01-06 06:32:50 UTC

Updated at

2021-07-15 17:35:56 UTC

NP-MRD ID

NP0021283

Secondary Accession Numbers

None

Natural Product Identification

Common Name

Diazaquinomycin A

Provided By

NPAtlas

Description

Diazaquinomycin A is found in Streptomyces sp. It was first documented in 1985 (PMID: 3840154). Based on a literature review very few articles have been published on 2,8-dihydroxy-3,7-dimethyl-4,6-dipropyl-5H,10H-pyrido[3,2-g]quinoline-5,10-dione.

Structure

MOL 3D MOL SDF 3D SDF PDB SMILES InChI


  Mrv1652306242120423D          

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M  END

     RDKit          3D

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  Mrv1652306242120423D          

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  1 27  1  0  0  0  0
  1 28  1  0  0  0  0
  1 29  1  0  0  0  0
  2 30  1  0  0  0  0
  2 31  1  0  0  0  0
  3 32  1  0  0  0  0
  3 33  1  0  0  0  0
  7 34  1  0  0  0  0
 11 35  1  0  0  0  0
 11 36  1  0  0  0  0
 11 37  1  0  0  0  0
 15 38  1  0  0  0  0
 19 39  1  0  0  0  0
 19 40  1  0  0  0  0
 19 41  1  0  0  0  0
 21 42  1  0  0  0  0
 21 43  1  0  0  0  0
 22 44  1  0  0  0  0
 22 45  1  0  0  0  0
 23 46  1  0  0  0  0
 23 47  1  0  0  0  0
 23 48  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0021283

> <DATABASE_NAME>
NP-MRD

> <SMILES>
[H]N1C(=O)C(=C(C2=C1C(=O)C1=C(C2=O)C(=C(C(=O)N1[H])C([H])([H])[H])C([H])([H])C([H])([H])C([H])([H])[H])C([H])([H])C([H])([H])C([H])([H])[H])C([H])([H])[H]

> <INCHI_IDENTIFIER>
InChI=1S/C20H22N2O4/c1-5-7-11-9(3)19(25)21-15-13(11)17(23)14-12(8-6-2)10(4)20(26)22-16(14)18(15)24/h5-8H2,1-4H3,(H,21,25)(H,22,26)

> <INCHI_KEY>
WZZGVUSWZMBPPL-UHFFFAOYSA-N

> <FORMULA>
C20H22N2O4

> <MOLECULAR_WEIGHT>
354.406

> <EXACT_MASS>
354.157957196

> <JCHEM_ACCEPTOR_COUNT>
4

> <JCHEM_ATOM_COUNT>
48

> <JCHEM_AVERAGE_POLARIZABILITY>
37.9113576453973

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
2

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
3,7-dimethyl-4,6-dipropyl-1H,2H,5H,8H,9H,10H-pyrido[3,2-g]quinoline-2,5,8,10-tetrone

> <ALOGPS_LOGP>
2.74

> <JCHEM_LOGP>
2.3211251980000007

> <ALOGPS_LOGS>
-3.57

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
3

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
8.963662584502474

> <JCHEM_PKA_STRONGEST_ACIDIC>
8.037701710688264

> <JCHEM_PKA_STRONGEST_BASIC>
-3.4353192743471834

> <JCHEM_POLAR_SURFACE_AREA>
92.34

> <JCHEM_REFRACTIVITY>
100.19659999999999

> <JCHEM_ROTATABLE_BOND_COUNT>
4

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
9.64e-02 g/l

> <JCHEM_TRADITIONAL_IUPAC>
3,7-dimethyl-4,6-dipropyl-1H,9H-pyrido[3,2-g]quinoline-2,5,8,10-tetrone

> <JCHEM_VEBER_RULE>
0

$$$$

     RDKit          3D

 48 50  0  0  0  0  0  0  0  0999 V2000
    3.2790   -2.3314    1.1989 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1744   -1.4122    1.7670 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4311    0.0360    1.4615 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4525    0.3939    0.0402 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2443    0.5854   -0.6111 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2604    0.8477   -1.9937 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4105    0.9188   -2.6915 N   0  0  0  0  0  0  0  0  0  0  0  0
    3.5879    0.7434   -2.0923 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.6790    0.8017   -2.6964 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.6230    0.4807   -0.7239 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.9318    0.3328   -0.0644 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0083    1.0714   -2.6635 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0164    1.3028   -3.9052 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3035    1.0377   -1.9529 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4379    1.2502   -2.6386 N   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6232    1.2221   -2.0172 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7113    1.4200   -2.6434 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7483    0.9798   -0.6705 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0643    0.9581    0.0109 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5559    0.7569    0.0468 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6698    0.4890    1.4718 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0567   -0.8876    1.8957 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1649   -1.9975    1.4591 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3303    0.7837   -0.5853 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0414    0.5604    0.0675 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0284    0.3375    1.2861 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.9814   -3.3542    1.5353 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.2057   -2.0167    1.7231 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.3570   -2.2590    0.1159 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.2732   -1.7737    1.2359 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.1387   -1.6405    2.8333 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.9566    0.7571    2.1487 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.5282    0.1572    1.7936 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.3412    1.1144   -3.7079 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.0473    0.8956    0.8821 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.2065   -0.7219   -0.0284 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.7105    0.8143   -0.7585 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3781    1.4360   -3.6570 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.4752   -0.0403    0.1912 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.1623    1.6787    0.8438 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.7970    1.3891   -0.7541 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7856    0.7937    2.0155 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5587    1.1307    1.8544 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9641   -0.8813    3.0356 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1430   -1.1292    1.7836 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3954   -2.2864    2.2341 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6196   -1.8240    0.5317 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8132   -2.9212    1.3923 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  1  0
  3  4  1  0
  4  5  1  0
  5  6  2  0
  6  7  1  0
  7  8  1  0
  8  9  2  0
  8 10  1  0
 10 11  1  0
  6 12  1  0
 12 13  2  0
 12 14  1  0
 14 15  1  0
 15 16  1  0
 16 17  2  0
 16 18  1  0
 18 19  1  0
 18 20  2  0
 20 21  1  0
 21 22  1  0
 22 23  1  0
 20 24  1  0
 24 25  1  0
 25 26  2  0
 10  4  2  0
 24 14  2  0
 25  5  1  0
  1 27  1  0
  1 28  1  0
  1 29  1  0
  2 30  1  0
  2 31  1  0
  3 32  1  0
  3 33  1  0
  7 34  1  0
 11 35  1  0
 11 36  1  0
 11 37  1  0
 15 38  1  0
 19 39  1  0
 19 40  1  0
 19 41  1  0
 21 42  1  0
 21 43  1  0
 22 44  1  0
 22 45  1  0
 23 46  1  0
 23 47  1  0
 23 48  1  0
M  END

HEADER    PROTEIN                                 24-JUN-21   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   24-JUN-21         0                                  
HETATM    1  C   UNK     0       3.279  -2.331   1.199  0.00  0.00           C+0
HETATM    2  C   UNK     0       2.174  -1.412   1.767  0.00  0.00           C+0
HETATM    3  C   UNK     0       2.431   0.036   1.462  0.00  0.00           C+0
HETATM    4  C   UNK     0       2.453   0.394   0.040  0.00  0.00           C+0
HETATM    5  C   UNK     0       1.244   0.585  -0.611  0.00  0.00           C+0
HETATM    6  C   UNK     0       1.260   0.848  -1.994  0.00  0.00           C+0
HETATM    7  N   UNK     0       2.410   0.919  -2.692  0.00  0.00           N+0
HETATM    8  C   UNK     0       3.588   0.743  -2.092  0.00  0.00           C+0
HETATM    9  O   UNK     0       4.679   0.802  -2.696  0.00  0.00           O+0
HETATM   10  C   UNK     0       3.623   0.481  -0.724  0.00  0.00           C+0
HETATM   11  C   UNK     0       4.932   0.333  -0.064  0.00  0.00           C+0
HETATM   12  C   UNK     0      -0.008   1.071  -2.664  0.00  0.00           C+0
HETATM   13  O   UNK     0       0.016   1.303  -3.905  0.00  0.00           O+0
HETATM   14  C   UNK     0      -1.304   1.038  -1.953  0.00  0.00           C+0
HETATM   15  N   UNK     0      -2.438   1.250  -2.639  0.00  0.00           N+0
HETATM   16  C   UNK     0      -3.623   1.222  -2.017  0.00  0.00           C+0
HETATM   17  O   UNK     0      -4.711   1.420  -2.643  0.00  0.00           O+0
HETATM   18  C   UNK     0      -3.748   0.980  -0.671  0.00  0.00           C+0
HETATM   19  C   UNK     0      -5.064   0.958   0.011  0.00  0.00           C+0
HETATM   20  C   UNK     0      -2.556   0.757   0.047  0.00  0.00           C+0
HETATM   21  C   UNK     0      -2.670   0.489   1.472  0.00  0.00           C+0
HETATM   22  C   UNK     0      -3.057  -0.888   1.896  0.00  0.00           C+0
HETATM   23  C   UNK     0      -2.165  -1.998   1.459  0.00  0.00           C+0
HETATM   24  C   UNK     0      -1.330   0.784  -0.585  0.00  0.00           C+0
HETATM   25  C   UNK     0      -0.041   0.560   0.068  0.00  0.00           C+0
HETATM   26  O   UNK     0      -0.028   0.338   1.286  0.00  0.00           O+0
HETATM   27  H   UNK     0       2.981  -3.354   1.535  0.00  0.00           H+0
HETATM   28  H   UNK     0       4.206  -2.017   1.723  0.00  0.00           H+0
HETATM   29  H   UNK     0       3.357  -2.259   0.116  0.00  0.00           H+0
HETATM   30  H   UNK     0       1.273  -1.774   1.236  0.00  0.00           H+0
HETATM   31  H   UNK     0       2.139  -1.641   2.833  0.00  0.00           H+0
HETATM   32  H   UNK     0       1.957   0.757   2.149  0.00  0.00           H+0
HETATM   33  H   UNK     0       3.528   0.157   1.794  0.00  0.00           H+0
HETATM   34  H   UNK     0       2.341   1.114  -3.708  0.00  0.00           H+0
HETATM   35  H   UNK     0       5.047   0.896   0.882  0.00  0.00           H+0
HETATM   36  H   UNK     0       5.207  -0.722  -0.028  0.00  0.00           H+0
HETATM   37  H   UNK     0       5.710   0.814  -0.759  0.00  0.00           H+0
HETATM   38  H   UNK     0      -2.378   1.436  -3.657  0.00  0.00           H+0
HETATM   39  H   UNK     0      -5.475  -0.040   0.191  0.00  0.00           H+0
HETATM   40  H   UNK     0      -5.162   1.679   0.844  0.00  0.00           H+0
HETATM   41  H   UNK     0      -5.797   1.389  -0.754  0.00  0.00           H+0
HETATM   42  H   UNK     0      -1.786   0.794   2.015  0.00  0.00           H+0
HETATM   43  H   UNK     0      -3.559   1.131   1.854  0.00  0.00           H+0
HETATM   44  H   UNK     0      -2.964  -0.881   3.036  0.00  0.00           H+0
HETATM   45  H   UNK     0      -4.143  -1.129   1.784  0.00  0.00           H+0
HETATM   46  H   UNK     0      -1.395  -2.286   2.234  0.00  0.00           H+0
HETATM   47  H   UNK     0      -1.620  -1.824   0.532  0.00  0.00           H+0
HETATM   48  H   UNK     0      -2.813  -2.921   1.392  0.00  0.00           H+0
CONECT    1    2   27   28   29                                             
CONECT    2    1    3   30   31                                             
CONECT    3    2    4   32   33                                             
CONECT    4    3    5   10                                                  
CONECT    5    4    6   25                                                  
CONECT    6    5    7   12                                                  
CONECT    7    6    8   34                                                  
CONECT    8    7    9   10                                                  
CONECT    9    8                                                            
CONECT   10    8   11    4                                                  
CONECT   11   10   35   36   37                                             
CONECT   12    6   13   14                                                  
CONECT   13   12                                                            
CONECT   14   12   15   24                                                  
CONECT   15   14   16   38                                                  
CONECT   16   15   17   18                                                  
CONECT   17   16                                                            
CONECT   18   16   19   20                                                  
CONECT   19   18   39   40   41                                             
CONECT   20   18   21   24                                                  
CONECT   21   20   22   42   43                                             
CONECT   22   21   23   44   45                                             
CONECT   23   22   46   47   48                                             
CONECT   24   20   25   14                                                  
CONECT   25   24   26    5                                                  
CONECT   26   25                                                            
CONECT   27    1                                                            
CONECT   28    1                                                            
CONECT   29    1                                                            
CONECT   30    2                                                            
CONECT   31    2                                                            
CONECT   32    3                                                            
CONECT   33    3                                                            
CONECT   34    7                                                            
CONECT   35   11                                                            
CONECT   36   11                                                            
CONECT   37   11                                                            
CONECT   38   15                                                            
CONECT   39   19                                                            
CONECT   40   19                                                            
CONECT   41   19                                                            
CONECT   42   21                                                            
CONECT   43   21                                                            
CONECT   44   22                                                            
CONECT   45   22                                                            
CONECT   46   23                                                            
CONECT   47   23                                                            
CONECT   48   23                                                            
MASTER        0    0    0    0    0    0    0    0   48    0  100    0
END

RDKit          3D

48 50  0  0  0  0  0  0  0  0999 V2000
    3.2790   -2.3314    1.1989 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1744   -1.4122    1.7670 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4311    0.0360    1.4615 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4525    0.3939    0.0402 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2443    0.5854   -0.6111 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2604    0.8477   -1.9937 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4105    0.9188   -2.6915 N   0  0  0  0  0  0  0  0  0  0  0  0
    3.5879    0.7434   -2.0923 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.6790    0.8017   -2.6964 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.6230    0.4807   -0.7239 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.9318    0.3328   -0.0644 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0083    1.0714   -2.6635 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0164    1.3028   -3.9052 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3035    1.0377   -1.9529 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4379    1.2502   -2.6386 N   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6232    1.2221   -2.0172 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7113    1.4200   -2.6434 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7483    0.9798   -0.6705 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0643    0.9581    0.0109 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5559    0.7569    0.0468 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6698    0.4890    1.4718 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0567   -0.8876    1.8957 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1649   -1.9975    1.4591 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3303    0.7837   -0.5853 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0414    0.5604    0.0675 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0284    0.3375    1.2861 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.9814   -3.3542    1.5353 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.2057   -2.0167    1.7231 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.3570   -2.2590    0.1159 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.2732   -1.7737    1.2359 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.1387   -1.6405    2.8333 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.9566    0.7571    2.1487 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.5282    0.1572    1.7936 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.3412    1.1144   -3.7079 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.0473    0.8956    0.8821 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.2065   -0.7219   -0.0284 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.7105    0.8143   -0.7585 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3781    1.4360   -3.6570 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.4752   -0.0403    0.1912 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.1623    1.6787    0.8438 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.7970    1.3891   -0.7541 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7856    0.7937    2.0155 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5587    1.1307    1.8544 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9641   -0.8813    3.0356 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1430   -1.1292    1.7836 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3954   -2.2864    2.2341 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6196   -1.8240    0.5317 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8132   -2.9212    1.3923 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  1  0
  3  4  1  0
  4  5  1  0
  5  6  2  0
  6  7  1  0
  7  8  1  0
  8  9  2  0
  8 10  1  0
 10 11  1  0
  6 12  1  0
 12 13  2  0
 12 14  1  0
 14 15  1  0
 15 16  1  0
 16 17  2  0
 16 18  1  0
 18 19  1  0
 18 20  2  0
 20 21  1  0
 21 22  1  0
 22 23  1  0
 20 24  1  0
 24 25  1  0
 25 26  2  0
 10  4  2  0
 24 14  2  0
 25  5  1  0
  1 27  1  0
  1 28  1  0
  1 29  1  0
  2 30  1  0
  2 31  1  0
  3 32  1  0
  3 33  1  0
  7 34  1  0
 11 35  1  0
 11 36  1  0
 11 37  1  0
 15 38  1  0
 19 39  1  0
 19 40  1  0
 19 41  1  0
 21 42  1  0
 21 43  1  0
 22 44  1  0
 22 45  1  0
 23 46  1  0
 23 47  1  0
 23 48  1  0
M  END

View in JSmol View NMR Assignments

Synonyms

Value	Source
OM-704 a	MeSH
OM 704 a	MeSH
Antibiotic om 704a	MeSH
OM 704a	MeSH
Diazaquinomicin a	MeSH

Chemical Formula

C₂₀H₂₂N₂O₄

Average Mass

354.4060 Da

Monoisotopic Mass

354.15796 Da

IUPAC Name

3,7-dimethyl-4,6-dipropyl-1H,2H,5H,8H,9H,10H-pyrido[3,2-g]quinoline-2,5,8,10-tetrone

Traditional Name

3,7-dimethyl-4,6-dipropyl-1H,9H-pyrido[3,2-g]quinoline-2,5,8,10-tetrone

CAS Registry Number

Not Available

SMILES

CCCC1=C(C)C(=O)NC2=C1C(=O)C1=C(NC(=O)C(C)=C1CCC)C2=O

InChI Identifier

InChI=1S/C20H22N2O4/c1-5-7-11-9(3)19(25)21-15-13(11)17(23)14-12(8-6-2)10(4)20(26)22-16(14)18(15)24/h5-8H2,1-4H3,(H,21,25)(H,22,26)

InChI Key

WZZGVUSWZMBPPL-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, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 100 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 252 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 1000 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 50 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 200 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 75 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 300 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 101 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 400 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 126 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 500 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 151 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 600 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 176 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 700 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 201 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 800 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 226 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 900 MHz, D₂O, 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
Streptomyces sp.	NPAtlas	3840154

Chemical Taxonomy

Description

This compound belongs to the class of organic compounds known as quinoline quinones. These are quinoline derivative with a structure containing a 5,8-dihydroisoquinoline-5,8-dione skeleton.

Kingdom

Organic compounds

Super Class

Organoheterocyclic compounds

Class

Quinolines and derivatives

Sub Class

Quinoline quinones

Direct Parent

Quinoline quinones

Alternative Parents

Substituents

Quinoline quinone
Dihydroquinolone
Dihydroquinoline
Methylpyridine
Pyridinone
Pyridine
Benzenoid
Heteroaromatic compound
Vinylogous amide
Lactam
Azacycle
Organic nitrogen compound
Hydrocarbon derivative
Organic oxide
Organooxygen compound
Organonitrogen compound
Organopnictogen compound
Organic oxygen 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	2.74	ALOGPS
logP	2.32	ChemAxon
logS	-3.6	ALOGPS
pKa (Strongest Acidic)	8.04	ChemAxon
pKa (Strongest Basic)	-3.4	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	4	ChemAxon
Hydrogen Donor Count	2	ChemAxon
Polar Surface Area	92.34 Å²	ChemAxon
Rotatable Bond Count	4	ChemAxon
Refractivity	100.2 m³·mol⁻¹	ChemAxon
Polarizability	37.91 Å³	ChemAxon
Number of Rings	3	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

NPAtlas ID

NPA015760

HMDB ID

Not Available

DrugBank ID

Not Available

Phenol Explorer Compound ID

Not Available

FoodDB ID

Not Available

KNApSAcK ID

Not Available

Chemspider ID

108905

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

122105

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

Murata M, Miyasaka T, Tanaka H, Omura S: Diazaquinomycin A, a new antifolate antibiotic, inhibits thymidylate synthase. J Antibiot (Tokyo). 1985 Aug;38(8):1025-33. doi: 10.7164/antibiotics.38.1025. [PubMed:3840154 ]

Showing NP-Card for Diazaquinomycin A (NP0021283)

MOL for NP0021283 (Diazaquinomycin A)

3D MOL for NP0021283 (Diazaquinomycin A)

3D SDF for NP0021283 (Diazaquinomycin A)

3D-SDF for NP0021283 (Diazaquinomycin A)

PDB for NP0021283 (Diazaquinomycin A)

3D PDB for NP0021283 (Diazaquinomycin A)

SMILES for NP0021283 (Diazaquinomycin A)

INCHI for NP0021283 (Diazaquinomycin A)

Structure for NP0021283 (Diazaquinomycin A)

3D Structure for NP0021283 (Diazaquinomycin A)