NP-MRD: Showing NP-Card for Nocazine B (NP0010369)

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Record Information

Version

2.0

Created at

2021-01-05 19:54:50 UTC

Updated at

2021-07-15 17:05:54 UTC

NP-MRD ID

NP0010369

Secondary Accession Numbers

None

Natural Product Identification

Common Name

Nocazine B

Provided By

NPAtlas

Description

(3Z,6Z)-5-methoxy-6-[(4-methoxyphenyl)methylidene]-1-methyl-3-(phenylmethylidene)-1,2,3,6-tetrahydropyrazin-2-one belongs to the class of organic compounds known as methoxypyrazines. These are pyrazines containing a methoxyl group attached to the pyrazine ring. Nocazine B is found in Nocardiopsis and Nocardiopsis dassonvillei. Based on a literature review very few articles have been published on (3Z,6Z)-5-methoxy-6-[(4-methoxyphenyl)methylidene]-1-methyl-3-(phenylmethylidene)-1,2,3,6-tetrahydropyrazin-2-one.

Structure

MOL 3D MOL SDF 3D SDF PDB SMILES InChI


  Mrv1652306242107373D          

 46 48  0  0  0  0            999 V2000
    7.4939   -0.0750   -0.0129 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.6799   -0.2238    1.1274 O   0  0  0  0  0  0  0  0  0  0  0  0
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    4.7657    0.5360   -0.0479 C   0  0  0  0  0  0  0  0  0  0  0  0
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    2.6244    0.6944    1.0419 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2571    1.1242    0.9531 C   0  0  0  0  0  0  0  0  0  0  0  0
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M  END

     RDKit          3D

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M  END


  Mrv1652306242107373D          

 46 48  0  0  0  0            999 V2000
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 19 40  1  0  0  0  0
 20 41  1  0  0  0  0
 24 42  1  0  0  0  0
 24 43  1  0  0  0  0
 24 44  1  0  0  0  0
 25 45  1  0  0  0  0
 26 46  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0010369

> <DATABASE_NAME>
NP-MRD

> <SMILES>
[H]\C(C1=C([H])C([H])=C([H])C([H])=C1[H])=C1\N=C(OC([H])([H])[H])/C(=C(\[H])C2=C([H])C([H])=C(OC([H])([H])[H])C([H])=C2[H])/N(C1=O)C([H])([H])[H]

> <INCHI_IDENTIFIER>
InChI=1S/C21H20N2O3/c1-23-19(14-16-9-11-17(25-2)12-10-16)20(26-3)22-18(21(23)24)13-15-7-5-4-6-8-15/h4-14H,1-3H3/b18-13-,19-14-

> <INCHI_KEY>
NCBOROGHSUXZPE-SXQSXHJWSA-N

> <FORMULA>
C21H20N2O3

> <MOLECULAR_WEIGHT>
348.402

> <EXACT_MASS>
348.147392512

> <JCHEM_ACCEPTOR_COUNT>
3

> <JCHEM_ATOM_COUNT>
46

> <JCHEM_AVERAGE_POLARIZABILITY>
38.79056209645153

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
0

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
(3Z,6Z)-5-methoxy-6-[(4-methoxyphenyl)methylidene]-1-methyl-3-(phenylmethylidene)-1,2,3,6-tetrahydropyrazin-2-one

> <ALOGPS_LOGP>
3.65

> <JCHEM_LOGP>
3.5869829529999997

> <ALOGPS_LOGS>
-5.06

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
3

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA_STRONGEST_BASIC>
-1.6145985906065583

> <JCHEM_POLAR_SURFACE_AREA>
51.13

> <JCHEM_REFRACTIVITY>
103.60260000000002

> <JCHEM_ROTATABLE_BOND_COUNT>
4

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
3.06e-03 g/l

> <JCHEM_TRADITIONAL_IUPAC>
(3Z,6Z)-5-methoxy-6-[(4-methoxyphenyl)methylidene]-1-methyl-3-(phenylmethylidene)pyrazin-2-one

> <JCHEM_VEBER_RULE>
0

$$$$

     RDKit          3D

 46 48  0  0  0  0  0  0  0  0999 V2000
    7.4939   -0.0750   -0.0129 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.6799   -0.2238    1.1274 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.3286    0.0759    1.1207 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7657    0.5360   -0.0479 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4256    0.8349   -0.0606 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6244    0.6944    1.0419 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2571    1.1242    0.9531 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2799    0.4473    0.4247 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0182    1.0550    0.4340 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1543    2.3164    1.0089 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4377    2.9010    1.0103 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0646    0.4440   -0.0860 N   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9298   -0.7524   -0.6301 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9815   -1.3649   -1.1523 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3122   -0.7596   -1.1514 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6566    0.2073   -2.0806 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.8867    0.8077   -2.1264 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.8399    0.4390   -1.2054 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.5407   -0.5255   -0.2554 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.2790   -1.1178   -0.2353 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6885   -1.3467   -0.6451 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5417   -2.4853   -1.1595 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.4397   -0.7606   -0.1188 N   0  0  0  0  0  0  0  0  0  0  0  0
    1.6960   -1.4262   -0.1623 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2024    0.2340    2.2000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5294   -0.0707    2.2426 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.3250    0.9550   -0.4339 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.2506   -0.8260   -0.7974 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.5581   -0.1261    0.2340 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.3757    0.6629   -0.9567 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.0382    1.1959   -1.0189 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.0020    2.1249    1.3714 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5014    3.5145    1.9515 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1875    2.0776    1.0897 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6372    3.5110    0.1113 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8165   -2.3501   -1.5886 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9231    0.5068   -2.8073 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.1513    1.5559   -2.8464 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.8217    0.9052   -1.2273 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.3175   -0.7881    0.4517 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0639   -1.8713    0.5167 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.3672   -2.5394   -0.3697 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.2225   -1.6406    0.7536 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.2787   -1.3278   -1.1044 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.5882    0.1146    3.0854 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.0227   -0.4407    3.1514 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  1  0
  3  4  2  0
  4  5  1  0
  5  6  2  0
  6  7  1  0
  7  8  2  0
  8  9  1  0
  9 10  1  0
 10 11  1  0
  9 12  2  0
 12 13  1  0
 13 14  2  0
 14 15  1  0
 15 16  2  0
 16 17  1  0
 17 18  2  0
 18 19  1  0
 19 20  2  0
 13 21  1  0
 21 22  2  0
 21 23  1  0
 23 24  1  0
  6 25  1  0
 25 26  2  0
 26  3  1  0
 23  8  1  0
 20 15  1  0
  1 27  1  0
  1 28  1  0
  1 29  1  0
  4 30  1  0
  5 31  1  0
  7 32  1  0
 11 33  1  0
 11 34  1  0
 11 35  1  0
 14 36  1  0
 16 37  1  0
 17 38  1  0
 18 39  1  0
 19 40  1  0
 20 41  1  0
 24 42  1  0
 24 43  1  0
 24 44  1  0
 25 45  1  0
 26 46  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       7.494  -0.075  -0.013  0.00  0.00           C+0
HETATM    2  O   UNK     0       6.680  -0.224   1.127  0.00  0.00           O+0
HETATM    3  C   UNK     0       5.329   0.076   1.121  0.00  0.00           C+0
HETATM    4  C   UNK     0       4.766   0.536  -0.048  0.00  0.00           C+0
HETATM    5  C   UNK     0       3.426   0.835  -0.061  0.00  0.00           C+0
HETATM    6  C   UNK     0       2.624   0.694   1.042  0.00  0.00           C+0
HETATM    7  C   UNK     0       1.257   1.124   0.953  0.00  0.00           C+0
HETATM    8  C   UNK     0       0.280   0.447   0.425  0.00  0.00           C+0
HETATM    9  C   UNK     0      -1.018   1.055   0.434  0.00  0.00           C+0
HETATM   10  O   UNK     0      -1.154   2.316   1.009  0.00  0.00           O+0
HETATM   11  C   UNK     0      -2.438   2.901   1.010  0.00  0.00           C+0
HETATM   12  N   UNK     0      -2.065   0.444  -0.086  0.00  0.00           N+0
HETATM   13  C   UNK     0      -1.930  -0.752  -0.630  0.00  0.00           C+0
HETATM   14  C   UNK     0      -2.982  -1.365  -1.152  0.00  0.00           C+0
HETATM   15  C   UNK     0      -4.312  -0.760  -1.151  0.00  0.00           C+0
HETATM   16  C   UNK     0      -4.657   0.207  -2.081  0.00  0.00           C+0
HETATM   17  C   UNK     0      -5.887   0.808  -2.126  0.00  0.00           C+0
HETATM   18  C   UNK     0      -6.840   0.439  -1.205  0.00  0.00           C+0
HETATM   19  C   UNK     0      -6.541  -0.526  -0.255  0.00  0.00           C+0
HETATM   20  C   UNK     0      -5.279  -1.118  -0.235  0.00  0.00           C+0
HETATM   21  C   UNK     0      -0.689  -1.347  -0.645  0.00  0.00           C+0
HETATM   22  O   UNK     0      -0.542  -2.485  -1.159  0.00  0.00           O+0
HETATM   23  N   UNK     0       0.440  -0.761  -0.119  0.00  0.00           N+0
HETATM   24  C   UNK     0       1.696  -1.426  -0.162  0.00  0.00           C+0
HETATM   25  C   UNK     0       3.202   0.234   2.200  0.00  0.00           C+0
HETATM   26  C   UNK     0       4.529  -0.071   2.243  0.00  0.00           C+0
HETATM   27  H   UNK     0       7.325   0.955  -0.434  0.00  0.00           H+0
HETATM   28  H   UNK     0       7.251  -0.826  -0.797  0.00  0.00           H+0
HETATM   29  H   UNK     0       8.558  -0.126   0.234  0.00  0.00           H+0
HETATM   30  H   UNK     0       5.376   0.663  -0.957  0.00  0.00           H+0
HETATM   31  H   UNK     0       3.038   1.196  -1.019  0.00  0.00           H+0
HETATM   32  H   UNK     0       1.002   2.125   1.371  0.00  0.00           H+0
HETATM   33  H   UNK     0      -2.501   3.515   1.952  0.00  0.00           H+0
HETATM   34  H   UNK     0      -3.188   2.078   1.090  0.00  0.00           H+0
HETATM   35  H   UNK     0      -2.637   3.511   0.111  0.00  0.00           H+0
HETATM   36  H   UNK     0      -2.817  -2.350  -1.589  0.00  0.00           H+0
HETATM   37  H   UNK     0      -3.923   0.507  -2.807  0.00  0.00           H+0
HETATM   38  H   UNK     0      -6.151   1.556  -2.846  0.00  0.00           H+0
HETATM   39  H   UNK     0      -7.822   0.905  -1.227  0.00  0.00           H+0
HETATM   40  H   UNK     0      -7.317  -0.788   0.452  0.00  0.00           H+0
HETATM   41  H   UNK     0      -5.064  -1.871   0.517  0.00  0.00           H+0
HETATM   42  H   UNK     0       1.367  -2.539  -0.370  0.00  0.00           H+0
HETATM   43  H   UNK     0       2.223  -1.641   0.754  0.00  0.00           H+0
HETATM   44  H   UNK     0       2.279  -1.328  -1.104  0.00  0.00           H+0
HETATM   45  H   UNK     0       2.588   0.115   3.085  0.00  0.00           H+0
HETATM   46  H   UNK     0       5.023  -0.441   3.151  0.00  0.00           H+0
CONECT    1    2   27   28   29                                             
CONECT    2    1    3                                                       
CONECT    3    2    4   26                                                  
CONECT    4    3    5   30                                                  
CONECT    5    4    6   31                                                  
CONECT    6    5    7   25                                                  
CONECT    7    6    8   32                                                  
CONECT    8    7    9   23                                                  
CONECT    9    8   10   12                                                  
CONECT   10    9   11                                                       
CONECT   11   10   33   34   35                                             
CONECT   12    9   13                                                       
CONECT   13   12   14   21                                                  
CONECT   14   13   15   36                                                  
CONECT   15   14   16   20                                                  
CONECT   16   15   17   37                                                  
CONECT   17   16   18   38                                                  
CONECT   18   17   19   39                                                  
CONECT   19   18   20   40                                                  
CONECT   20   19   15   41                                                  
CONECT   21   13   22   23                                                  
CONECT   22   21                                                            
CONECT   23   21   24    8                                                  
CONECT   24   23   42   43   44                                             
CONECT   25    6   26   45                                                  
CONECT   26   25    3   46                                                  
CONECT   27    1                                                            
CONECT   28    1                                                            
CONECT   29    1                                                            
CONECT   30    4                                                            
CONECT   31    5                                                            
CONECT   32    7                                                            
CONECT   33   11                                                            
CONECT   34   11                                                            
CONECT   35   11                                                            
CONECT   36   14                                                            
CONECT   37   16                                                            
CONECT   38   17                                                            
CONECT   39   18                                                            
CONECT   40   19                                                            
CONECT   41   20                                                            
CONECT   42   24                                                            
CONECT   43   24                                                            
CONECT   44   24                                                            
CONECT   45   25                                                            
CONECT   46   26                                                            
MASTER        0    0    0    0    0    0    0    0   46    0   96    0
END

RDKit          3D

46 48  0  0  0  0  0  0  0  0999 V2000
    7.4939   -0.0750   -0.0129 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.6799   -0.2238    1.1274 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.3286    0.0759    1.1207 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7657    0.5360   -0.0479 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4256    0.8349   -0.0606 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6244    0.6944    1.0419 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2571    1.1242    0.9531 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2799    0.4473    0.4247 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0182    1.0550    0.4340 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1543    2.3164    1.0089 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4377    2.9010    1.0103 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0646    0.4440   -0.0860 N   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9298   -0.7524   -0.6301 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9815   -1.3649   -1.1523 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3122   -0.7596   -1.1514 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6566    0.2073   -2.0806 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.8867    0.8077   -2.1264 C   0  0  0  0  0  0  0  0  0  0  0  0
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    1.6960   -1.4262   -0.1623 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2024    0.2340    2.2000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5294   -0.0707    2.2426 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.3250    0.9550   -0.4339 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.2506   -0.8260   -0.7974 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.5581   -0.1261    0.2340 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.3757    0.6629   -0.9567 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.0382    1.1959   -1.0189 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.0020    2.1249    1.3714 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5014    3.5145    1.9515 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1875    2.0776    1.0897 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6372    3.5110    0.1113 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8165   -2.3501   -1.5886 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9231    0.5068   -2.8073 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.1513    1.5559   -2.8464 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.8217    0.9052   -1.2273 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.3175   -0.7881    0.4517 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0639   -1.8713    0.5167 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.3672   -2.5394   -0.3697 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.2225   -1.6406    0.7536 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.2787   -1.3278   -1.1044 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.5882    0.1146    3.0854 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.0227   -0.4407    3.1514 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  1  0
  3  4  2  0
  4  5  1  0
  5  6  2  0
  6  7  1  0
  7  8  2  0
  8  9  1  0
  9 10  1  0
 10 11  1  0
  9 12  2  0
 12 13  1  0
 13 14  2  0
 14 15  1  0
 15 16  2  0
 16 17  1  0
 17 18  2  0
 18 19  1  0
 19 20  2  0
 13 21  1  0
 21 22  2  0
 21 23  1  0
 23 24  1  0
  6 25  1  0
 25 26  2  0
 26  3  1  0
 23  8  1  0
 20 15  1  0
  1 27  1  0
  1 28  1  0
  1 29  1  0
  4 30  1  0
  5 31  1  0
  7 32  1  0
 11 33  1  0
 11 34  1  0
 11 35  1  0
 14 36  1  0
 16 37  1  0
 17 38  1  0
 18 39  1  0
 19 40  1  0
 20 41  1  0
 24 42  1  0
 24 43  1  0
 24 44  1  0
 25 45  1  0
 26 46  1  0
M  END

View in JSmol View NMR Assignments View DFT Assignments 3D Conformers

Synonyms

Not Available

Chemical Formula

C₂₁H₂₀N₂O₃

Average Mass

348.4020 Da

Monoisotopic Mass

348.14739 Da

IUPAC Name

(3Z,6Z)-5-methoxy-6-[(4-methoxyphenyl)methylidene]-1-methyl-3-(phenylmethylidene)-1,2,3,6-tetrahydropyrazin-2-one

Traditional Name

(3Z,6Z)-5-methoxy-6-[(4-methoxyphenyl)methylidene]-1-methyl-3-(phenylmethylidene)pyrazin-2-one

CAS Registry Number

Not Available

SMILES

COC1=CC=C(\C=C2/N(C)C(=O)\C(=C\C3=CC=CC=C3)N=C2OC)C=C1

InChI Identifier

InChI=1S/C21H20N2O3/c1-23-19(14-16-9-11-17(25-2)12-10-16)20(26-3)22-18(21(23)24)13-15-7-5-4-6-8-15/h4-14H,1-3H3/b18-13-,19-14-

InChI Key

NCBOROGHSUXZPE-SXQSXHJWSA-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
1D NMR	¹³C NMR Spectrum (1D, 100 MHz, chcl3, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 125 MHz, chcl3, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 150 MHz, chcl3, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 175 MHz, chcl3, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 200 MHz, chcl3, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 225 MHz, chcl3, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 25 MHz, chcl3, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 250 MHz, chcl3, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 50 MHz, chcl3, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 75 MHz, chcl3, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 100 MHz, chcl3, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 1000 MHz, chcl3, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 200 MHz, chcl3, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 300 MHz, chcl3, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 400 MHz, chcl3, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 500 MHz, chcl3, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 600 MHz, chcl3, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 700 MHz, chcl3, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 800 MHz, chcl3, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 900 MHz, chcl3, 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
Nocardiopsis	NPAtlas	21958359
Nocardiopsis dassonvillei	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as methoxypyrazines. These are pyrazines containing a methoxyl group attached to the pyrazine ring.

Kingdom

Organic compounds

Super Class

Organoheterocyclic compounds

Class

Diazines

Sub Class

Pyrazines

Direct Parent

Methoxypyrazines

Alternative Parents

Substituents

Phenoxy compound
Anisole
Methoxypyrazine
Phenol ether
Methoxybenzene
Alkyl aryl ether
Monocyclic benzene moiety
Benzenoid
Heteroaromatic compound
Lactam
Ether
Azacycle
Hydrocarbon derivative
Organooxygen compound
Organonitrogen compound
Organic oxide
Organic nitrogen compound
Organopnictogen compound
Organic oxygen compound
Aromatic heteromonocyclic compound

Molecular Framework

Aromatic heteromonocyclic compounds

External Descriptors

aromatic ether (CHEBI:69709 )
pyrazines (CHEBI:69709 )

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	3.65	ALOGPS
logP	3.59	ChemAxon
logS	-5.1	ALOGPS
pKa (Strongest Basic)	-1.6	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	3	ChemAxon
Hydrogen Donor Count	0	ChemAxon
Polar Surface Area	51.13 Å²	ChemAxon
Rotatable Bond Count	4	ChemAxon
Refractivity	103.6 m³·mol⁻¹	ChemAxon
Polarizability	38.79 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

NPA014715

HMDB ID

Not Available

DrugBank ID

Not Available

Phenol Explorer Compound ID

Not Available

FoodDB ID

Not Available

KNApSAcK ID

Not Available

Chemspider ID

26645373

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

Not Available

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

Showing NP-Card for Nocazine B (NP0010369)

MOL for NP0010369 (Nocazine B)

3D MOL for NP0010369 (Nocazine B)

3D SDF for NP0010369 (Nocazine B)

3D-SDF for NP0010369 (Nocazine B)

PDB for NP0010369 (Nocazine B)

3D PDB for NP0010369 (Nocazine B)

SMILES for NP0010369 (Nocazine B)

INCHI for NP0010369 (Nocazine B)

Structure for NP0010369 (Nocazine B)

3D Structure for NP0010369 (Nocazine B)