NP-MRD: Showing NP-Card for Antibiotic DOB 41 (NP0061989)

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Record Information

Version

2.0

Created at

2022-04-28 06:40:53 UTC

Updated at

2022-04-28 06:40:53 UTC

NP-MRD ID

NP0061989

Secondary Accession Numbers

None

Natural Product Identification

Common Name

Antibiotic DOB 41

Description

6-[(S)-1-[(S)-3-Hydroxy-2-methoxy-1-oxopropoxy]ethyl]-1-phenazinecarboxylic acid belongs to the class of organic compounds known as phenazines and derivatives. These are polycyclic aromatic compounds containing a phenazine moiety, which is a linear tricyclic system that consists of a two benzene rings joined by a pyrazine ring. Antibiotic DOB 41 is found in Pseudomonas strain DOB-41. Based on a literature review very few articles have been published on 6-[(S)-1-[(S)-3-Hydroxy-2-methoxy-1-oxopropoxy]ethyl]-1-phenazinecarboxylic acid.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652304282208402D          

 27 29  0  0  1  0            999 V2000
    0.3020   -0.7441    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145   -1.4586    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5395   -1.4586    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    1.9520   -0.7441    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5395   -0.0296    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145   -0.0296    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    1.9520    0.6849    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7770    0.6849    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1895   -0.0296    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7770   -0.7441    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5395    1.3993    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9520    2.1138    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145    1.3993    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.3020   -2.1730    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5230   -2.1730    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9355   -1.4586    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5230   -0.7441    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145   -2.8875    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.3020   -3.6020    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5395   -2.8875    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.9520   -3.6020    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5395   -4.3164    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.7770   -3.6020    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.1895   -4.3164    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.0145   -4.3164    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1895   -2.8875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0145   -2.8875    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0  0  0  0
  2  3  1  0  0  0  0
  3  4  2  0  0  0  0
  4  5  1  0  0  0  0
  5  6  2  0  0  0  0
  1  6  1  0  0  0  0
  5  7  1  0  0  0  0
  7  8  2  0  0  0  0
  8  9  1  0  0  0  0
  9 10  2  0  0  0  0
  4 10  1  0  0  0  0
  7 11  1  0  0  0  0
 11 12  2  0  0  0  0
 11 13  1  0  0  0  0
  2 14  2  0  0  0  0
 14 15  1  0  0  0  0
 15 16  2  0  0  0  0
 16 17  1  0  0  0  0
  1 17  2  0  0  0  0
 14 18  1  0  0  0  0
 18 19  1  1  0  0  0
 18 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
 23 24  1  6  0  0  0
 24 25  1  0  0  0  0
 23 26  1  0  0  0  0
 26 27  1  0  0  0  0
M  END

     RDKit          3D

 45 47  0  0  0  0  0  0  0  0999 V2000
   -5.0959    0.4195   -1.8513 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7013    0.4012   -1.8255 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2048   -0.1588   -0.6650 C   0  0  1  0  0  0  0  0  0  0  0  0
   -2.3898   -1.4111   -0.9068 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3068   -1.1135   -1.7221 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3716    0.7892    0.1151 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1401    1.9622   -0.2386 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8287    0.3376    1.2945 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0108    1.0916    2.1663 C   0  0  1  0  0  0  0  0  0  0  0  0
   -1.6644    1.2762    3.5208 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2516    0.3374    2.3729 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6095   -0.1592    3.6135 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7930   -0.8577    3.7603 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5940   -1.0413    2.6472 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2386   -0.5468    1.4107 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0394   -0.7332    0.3212 N   0  0  0  0  0  0  0  0  0  0  0  0
    2.6592   -0.2338   -0.8672 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4849   -0.4352   -1.9506 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7290   -1.1725   -1.7771 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.5164   -1.3886   -2.7276 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.0569   -1.6524   -0.5230 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.1134    0.0715   -3.1898 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9429    0.7717   -3.3756 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1329    0.9599   -2.2740 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4712    0.4690   -1.0226 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6823    0.6519    0.0525 N   0  0  0  0  0  0  0  0  0  0  0  0
    1.0609    0.1511    1.2523 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.4993    0.8596   -2.7610 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.4083   -0.6595   -1.7366 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.4252    0.9334   -0.9227 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0724   -0.4566   -0.0392 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0691   -1.7705    0.1016 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0330   -2.1956   -1.3559 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5085   -0.4402   -2.3942 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8282    2.0974    1.7773 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9709    0.3490    4.0076 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9254    1.7826    4.1716 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5209    2.0128    3.4464 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0412   -0.0034    4.4883 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.0570   -1.2397    4.7400 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.5085   -1.5907    2.8004 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.4108   -1.0286    0.2062 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.7846   -0.1032   -4.0227 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.6670    1.1627   -4.3585 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.2127    1.5044   -2.3952 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
  3  6  1  0
  6  7  2  0
  6  8  1  0
  8  9  1  0
  9 10  1  0
  9 11  1  0
 11 27  2  0
 27 26  1  0
 26 25  2  0
 25 24  1  0
 24 23  2  0
 23 22  1  0
 22 18  2  0
 18 19  1  0
 19 21  1  0
 19 20  2  0
 18 17  1  0
 17 16  2  0
 16 15  1  0
 15 14  2  0
 14 13  1  0
 13 12  2  0
 12 11  1  0
 15 27  1  0
 17 25  1  0
  1 28  1  0
  1 29  1  0
  1 30  1  0
  3 31  1  1
  4 32  1  0
  4 33  1  0
  5 34  1  0
  9 35  1  6
 10 36  1  0
 10 37  1  0
 10 38  1  0
 24 45  1  0
 23 44  1  0
 22 43  1  0
 21 42  1  0
 14 41  1  0
 13 40  1  0
 12 39  1  0
M  END


  Mrv1652304282208402D          

 27 29  0  0  1  0            999 V2000
    0.3020   -0.7441    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145   -1.4586    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5395   -1.4586    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    1.9520   -0.7441    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5395   -0.0296    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145   -0.0296    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    1.9520    0.6849    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7770    0.6849    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1895   -0.0296    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7770   -0.7441    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5395    1.3993    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9520    2.1138    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145    1.3993    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.3020   -2.1730    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5230   -2.1730    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9355   -1.4586    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5230   -0.7441    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145   -2.8875    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.3020   -3.6020    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5395   -2.8875    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.9520   -3.6020    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5395   -4.3164    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.7770   -3.6020    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.1895   -4.3164    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.0145   -4.3164    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1895   -2.8875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0145   -2.8875    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0  0  0  0
  2  3  1  0  0  0  0
  3  4  2  0  0  0  0
  4  5  1  0  0  0  0
  5  6  2  0  0  0  0
  1  6  1  0  0  0  0
  5  7  1  0  0  0  0
  7  8  2  0  0  0  0
  8  9  1  0  0  0  0
  9 10  2  0  0  0  0
  4 10  1  0  0  0  0
  7 11  1  0  0  0  0
 11 12  2  0  0  0  0
 11 13  1  0  0  0  0
  2 14  2  0  0  0  0
 14 15  1  0  0  0  0
 15 16  2  0  0  0  0
 16 17  1  0  0  0  0
  1 17  2  0  0  0  0
 14 18  1  0  0  0  0
 18 19  1  1  0  0  0
 18 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
 23 24  1  6  0  0  0
 24 25  1  0  0  0  0
 23 26  1  0  0  0  0
 26 27  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0061989

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CO[C@@H](CO)C(=O)O[C@@H](C)C1=C2N=C3C=CC=C(C(O)=O)C3=NC2=CC=C1

> <INCHI_IDENTIFIER>
InChI=1S/C19H18N2O6/c1-10(27-19(25)15(9-22)26-2)11-5-3-7-13-16(11)20-14-8-4-6-12(18(23)24)17(14)21-13/h3-8,10,15,22H,9H2,1-2H3,(H,23,24)/t10-,15-/m0/s1

> <INCHI_KEY>
OSEDIRANPWGFRX-BONVTDFDSA-N

> <FORMULA>
C19H18N2O6

> <MOLECULAR_WEIGHT>
370.361

> <EXACT_MASS>
370.116486308

> <JCHEM_ACCEPTOR_COUNT>
7

> <JCHEM_ATOM_COUNT>
45

> <JCHEM_AVERAGE_POLARIZABILITY>
37.900083080705016

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
2

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
6-[(1S)-1-{[(2S)-3-hydroxy-2-methoxypropanoyl]oxy}ethyl]phenazine-1-carboxylic acid

> <ALOGPS_LOGP>
1.70

> <JCHEM_LOGP>
2.155922087

> <ALOGPS_LOGS>
-3.36

> <JCHEM_MDDR_LIKE_RULE>
1

> <JCHEM_NUMBER_OF_RINGS>
3

> <JCHEM_PHYSIOLOGICAL_CHARGE>
-1

> <JCHEM_PKA>
14.432875648681396

> <JCHEM_PKA_STRONGEST_ACIDIC>
3.6747337531672257

> <JCHEM_PKA_STRONGEST_BASIC>
-0.9948884563261894

> <JCHEM_POLAR_SURFACE_AREA>
118.84

> <JCHEM_REFRACTIVITY>
93.29

> <JCHEM_ROTATABLE_BOND_COUNT>
7

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
1.63e-01 g/l

> <JCHEM_TRADITIONAL_IUPAC>
6-[(1S)-1-{[(2S)-3-hydroxy-2-methoxypropanoyl]oxy}ethyl]phenazine-1-carboxylic acid

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 28-APR-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   28-APR-22         0                                  
HETATM    1  C   UNK     0       0.564  -1.389   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       1.334  -2.723   0.000  0.00  0.00           C+0
HETATM    3  N   UNK     0       2.874  -2.723   0.000  0.00  0.00           N+0
HETATM    4  C   UNK     0       3.644  -1.389   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       2.874  -0.055   0.000  0.00  0.00           C+0
HETATM    6  N   UNK     0       1.334  -0.055   0.000  0.00  0.00           N+0
HETATM    7  C   UNK     0       3.644   1.278   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       5.184   1.278   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       5.954  -0.055   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       5.184  -1.389   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       2.874   2.612   0.000  0.00  0.00           C+0
HETATM   12  O   UNK     0       3.644   3.946   0.000  0.00  0.00           O+0
HETATM   13  O   UNK     0       1.334   2.612   0.000  0.00  0.00           O+0
HETATM   14  C   UNK     0       0.564  -4.056   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0      -0.976  -4.056   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0      -1.746  -2.723   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0      -0.976  -1.389   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       1.334  -5.390   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0       0.564  -6.724   0.000  0.00  0.00           C+0
HETATM   20  O   UNK     0       2.874  -5.390   0.000  0.00  0.00           O+0
HETATM   21  C   UNK     0       3.644  -6.724   0.000  0.00  0.00           C+0
HETATM   22  O   UNK     0       2.874  -8.057   0.000  0.00  0.00           O+0
HETATM   23  C   UNK     0       5.184  -6.724   0.000  0.00  0.00           C+0
HETATM   24  O   UNK     0       5.954  -8.057   0.000  0.00  0.00           O+0
HETATM   25  C   UNK     0       7.494  -8.057   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0       5.954  -5.390   0.000  0.00  0.00           C+0
HETATM   27  O   UNK     0       7.494  -5.390   0.000  0.00  0.00           O+0
CONECT    1    2    6   17                                                  
CONECT    2    1    3   14                                                  
CONECT    3    2    4                                                       
CONECT    4    3    5   10                                                  
CONECT    5    4    6    7                                                  
CONECT    6    5    1                                                       
CONECT    7    5    8   11                                                  
CONECT    8    7    9                                                       
CONECT    9    8   10                                                       
CONECT   10    9    4                                                       
CONECT   11    7   12   13                                                  
CONECT   12   11                                                            
CONECT   13   11                                                            
CONECT   14    2   15   18                                                  
CONECT   15   14   16                                                       
CONECT   16   15   17                                                       
CONECT   17   16    1                                                       
CONECT   18   14   19   20                                                  
CONECT   19   18                                                            
CONECT   20   18   21                                                       
CONECT   21   20   22   23                                                  
CONECT   22   21                                                            
CONECT   23   21   24   26                                                  
CONECT   24   23   25                                                       
CONECT   25   24                                                            
CONECT   26   23   27                                                       
CONECT   27   26                                                            
MASTER        0    0    0    0    0    0    0    0   27    0   58    0
END

View in JSmol

Synonyms

Value	Source
6-[(S)-1-[(S)-3-Hydroxy-2-methoxy-1-oxopropoxy]ethyl]-1-phenazinecarboxylate	Generator

Chemical Formula

C₁₉H₁₈N₂O₆

Average Mass

370.3610 Da

Monoisotopic Mass

370.11649 Da

IUPAC Name

6-[(1S)-1-{[(2S)-3-hydroxy-2-methoxypropanoyl]oxy}ethyl]phenazine-1-carboxylic acid

Traditional Name

6-[(1S)-1-{[(2S)-3-hydroxy-2-methoxypropanoyl]oxy}ethyl]phenazine-1-carboxylic acid

CAS Registry Number

Not Available

SMILES

CO[C@@H](CO)C(=O)O[C@@H](C)C1=C2N=C3C=CC=C(C(O)=O)C3=NC2=CC=C1

InChI Identifier

InChI=1S/C19H18N2O6/c1-10(27-19(25)15(9-22)26-2)11-5-3-7-13-16(11)20-14-8-4-6-12(18(23)24)17(14)21-13/h3-8,10,15,22H,9H2,1-2H3,(H,23,24)/t10-,15-/m0/s1

InChI Key

OSEDIRANPWGFRX-BONVTDFDSA-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
Pseudomonas strain DOB-41	Bacteria	KNApSAcK

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as phenazines and derivatives. These are polycyclic aromatic compounds containing a phenazine moiety, which is a linear tricyclic system that consists of a two benzene rings joined by a pyrazine ring.

Kingdom

Organic compounds

Super Class

Organoheterocyclic compounds

Class

Diazanaphthalenes

Sub Class

Benzodiazines

Direct Parent

Phenazines and derivatives

Alternative Parents

Substituents

Phenazine
Beta-hydroxy acid
Glyceric_acid
Hydroxy acid
Monosaccharide
Benzenoid
Pyrazine
Heteroaromatic compound
Carboxylic acid ester
Carboxylic acid derivative
Carboxylic acid
Dialkyl ether
Ether
Monocarboxylic acid or derivatives
Azacycle
Organic oxide
Carbonyl group
Organic nitrogen compound
Alcohol
Hydrocarbon derivative
Organonitrogen compound
Organooxygen compound
Organic oxygen compound
Primary alcohol
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	1.7	ALOGPS
logP	2.16	ChemAxon
logS	-3.4	ALOGPS
pKa (Strongest Acidic)	3.67	ChemAxon
pKa (Strongest Basic)	-0.99	ChemAxon
Physiological Charge	-1	ChemAxon
Hydrogen Acceptor Count	7	ChemAxon
Hydrogen Donor Count	2	ChemAxon
Polar Surface Area	118.84 Å²	ChemAxon
Rotatable Bond Count	7	ChemAxon
Refractivity	93.29 m³·mol⁻¹	ChemAxon
Polarizability	37.9 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	Yes	ChemAxon

External Links

HMDB ID

Not Available

DrugBank ID

Not Available

Phenol Explorer Compound ID

Not Available

FoodDB ID

Not Available

KNApSAcK ID

Not Available

Chemspider ID

Not Available

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

101834249

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

Not Available

Showing NP-Card for Antibiotic DOB 41 (NP0061989)

MOL for NP0061989 (Antibiotic DOB 41)

3D MOL for NP0061989 (Antibiotic DOB 41)

3D SDF for NP0061989 (Antibiotic DOB 41)

3D-SDF for NP0061989 (Antibiotic DOB 41)

PDB for NP0061989 (Antibiotic DOB 41)

3D PDB for NP0061989 (Antibiotic DOB 41)

SMILES for NP0061989 (Antibiotic DOB 41)

INCHI for NP0061989 (Antibiotic DOB 41)

Structure for NP0061989 (Antibiotic DOB 41)

3D Structure for NP0061989 (Antibiotic DOB 41)