NP-MRD: Showing NP-Card for Streptophenazine H (NP0007686)

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Record Information

Version

1.0

Created at

2020-12-09 04:30:05 UTC

Updated at

2021-07-15 16:58:16 UTC

NP-MRD ID

NP0007686

Secondary Accession Numbers

None

Natural Product Identification

Common Name

Streptophenazine H

Provided By

NPAtlas

Description

Streptophenazine H is found in Streptomyces sp. It was first documented in 2008 (PMID: 18396903). Based on a literature review very few articles have been published on methyl 6-(3,7-dihydroxy-1-methoxy-7-methyl-1-oxooctan-2-yl)phenazine-1-carboxylate (PMID: 34383398) (PMID: 34383397) (PMID: 34383396) (PMID: 34384147).

Structure

MOL 3D MOL SDF 3D SDF PDB SMILES InChI


  Mrv1652306242119023D          

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M  END

     RDKit          3D

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M  END


  Mrv1652306242119023D          

 60 62  0  0  0  0            999 V2000
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   -0.0214   -0.9005   -2.7138 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2796   -1.1860   -2.4221 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9220   -0.4824   -1.3956 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2006   -0.8341   -1.0567 N   0  0  0  0  0  0  0  0  0  0  0  0
    3.8109   -0.2117   -0.0163 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.4592   -2.8542   -1.2027 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.9179   -3.7481   -1.3233 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.9392   -3.9603    0.1550 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.7494   -0.3216    1.7044 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.5606    1.4461    3.0070 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.2595    2.1382    2.3350 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6563    2.1100   -0.8784 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.5876    5.6625    0.2541 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.4307    5.3619    2.0140 H   0  0  0  0  0  0  0  0  0  0  0  0
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   -6.0847   -3.4905    0.0943 H   0  0  0  0  0  0  0  0  0  0  0  0
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   -7.1744   -1.5803   -0.1103 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.4096   -0.1189   -1.8342 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6492    0.3143   -2.2058 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5470   -1.4295   -3.5111 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.8092   -1.9425   -2.9673 H   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
  3  5  1  0  0  0  0
  5  6  2  0  0  0  0
  6  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
 10 11  1  0  0  0  0
 11 12  2  0  0  0  0
 12 13  1  0  0  0  0
 13 14  1  0  0  0  0
 14 15  2  0  0  0  0
 14 16  1  0  0  0  0
 16 17  1  0  0  0  0
 13 18  1  0  0  0  0
 18 19  1  0  0  0  0
 18 20  1  0  0  0  0
 20 21  1  0  0  0  0
 21 22  1  0  0  0  0
 22 23  1  0  0  0  0
 23 24  1  0  0  0  0
 23 25  1  0  0  0  0
 23 26  1  6  0  0  0
 12 27  1  0  0  0  0
 27 28  2  0  0  0  0
 28 29  1  0  0  0  0
 29 30  2  0  0  0  0
 30 31  1  0  0  0  0
 31 32  2  0  0  0  0
 32  5  1  0  0  0  0
 32  9  1  0  0  0  0
 30 11  1  0  0  0  0
  1 33  1  0  0  0  0
  1 34  1  0  0  0  0
  1 35  1  0  0  0  0
  6 36  1  0  0  0  0
  7 37  1  0  0  0  0
  8 38  1  0  0  0  0
 13 39  1  6  0  0  0
 17 40  1  0  0  0  0
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 19 44  1  0  0  0  0
 20 45  1  0  0  0  0
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 21 48  1  0  0  0  0
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 22 50  1  0  0  0  0
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 24 52  1  0  0  0  0
 24 53  1  0  0  0  0
 25 54  1  0  0  0  0
 25 55  1  0  0  0  0
 25 56  1  0  0  0  0
 26 57  1  0  0  0  0
 27 58  1  0  0  0  0
 28 59  1  0  0  0  0
 29 60  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0007686

> <DATABASE_NAME>
NP-MRD

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

> <INCHI_IDENTIFIER>
InChI=1S/C24H28N2O6/c1-24(2,30)13-7-12-18(27)19(23(29)32-4)14-8-5-10-16-20(14)25-17-11-6-9-15(21(17)26-16)22(28)31-3/h5-6,8-11,18-19,27,30H,7,12-13H2,1-4H3/t18-,19-/m0/s1

> <INCHI_KEY>
WLMRJQPFNIUWBX-UHFFFAOYSA-N

> <FORMULA>
C24H28N2O6

> <MOLECULAR_WEIGHT>
440.496

> <EXACT_MASS>
440.19473663

> <JCHEM_ACCEPTOR_COUNT>
6

> <JCHEM_ATOM_COUNT>
60

> <JCHEM_AVERAGE_POLARIZABILITY>
47.51184578719155

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
2

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
methyl 6-[(2S,3S)-3,7-dihydroxy-1-methoxy-7-methyl-1-oxooctan-2-yl]phenazine-1-carboxylate

> <ALOGPS_LOGP>
2.89

> <JCHEM_LOGP>
3.1982980349999988

> <ALOGPS_LOGS>
-4.12

> <JCHEM_MDDR_LIKE_RULE>
1

> <JCHEM_NUMBER_OF_RINGS>
3

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
18.53071836193327

> <JCHEM_PKA_STRONGEST_ACIDIC>
14.507561167125889

> <JCHEM_PKA_STRONGEST_BASIC>
-0.16971264742270098

> <JCHEM_POLAR_SURFACE_AREA>
118.84

> <JCHEM_REFRACTIVITY>
116.73830000000001

> <JCHEM_ROTATABLE_BOND_COUNT>
10

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
3.32e-02 g/l

> <JCHEM_TRADITIONAL_IUPAC>
methyl 6-[(2S,3S)-3,7-dihydroxy-1-methoxy-7-methyl-1-oxooctan-2-yl]phenazine-1-carboxylate

> <JCHEM_VEBER_RULE>
0

$$$$

     RDKit          3D

 60 62  0  0  0  0  0  0  0  0999 V2000
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    3.7934    1.3790    1.7955 C   0  0  0  0  0  0  0  0  0  0  0  0
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    1.9248    1.0966    0.3582 N   0  0  0  0  0  0  0  0  0  0  0  0
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   -0.0380    0.7880   -0.9507 C   0  0  0  0  0  0  0  0  0  0  0  0
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   -2.0545    2.2506    1.7468 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1140    0.0328    0.9184 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3765    0.0103    0.1261 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7991   -1.4517    0.0576 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.1037   -1.6429   -0.6248 C   0  0  1  0  0  0  0  0  0  0  0  0
   -5.3754   -3.1494   -0.6572 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.2524   -1.0917    0.2509 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.2113   -1.1101   -1.8801 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6312    0.0807   -1.9583 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0214   -0.9005   -2.7138 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2796   -1.1860   -2.4221 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9220   -0.4824   -1.3956 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2006   -0.8341   -1.0567 N   0  0  0  0  0  0  0  0  0  0  0  0
    3.8109   -0.2117   -0.0163 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.4592   -2.8542   -1.2027 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.9179   -3.7481   -1.3233 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.9392   -3.9603    0.1550 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.7494   -0.3216    1.7044 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.5606    1.4461    3.0070 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.2595    2.1382    2.3350 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6563    2.1100   -0.8784 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.5876    5.6625    0.2541 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.4307    5.3619    2.0140 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9217    6.1212    1.1763 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4230    1.0665    1.7155 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7889    2.6471    1.2356 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4580   -0.8549    0.6463 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4348   -0.2595    1.9872 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3717    0.5261   -0.8089 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2240    0.5070    0.7205 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8023   -1.8815    1.0598 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0291   -1.9674   -0.5772 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.0847   -3.4905    0.0943 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4376   -3.7184   -0.4762 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.7494   -3.4640   -1.6551 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.0818   -1.4138    1.3108 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.3536   -0.0012    0.1310 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.1744   -1.5803   -0.1103 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.4096   -0.1189   -1.8342 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6492    0.3143   -2.2058 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5470   -1.4295   -3.5111 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.8092   -1.9425   -2.9673 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
  3  5  1  0
  5  6  2  0
  6  7  1  0
  7  8  2  0
  8  9  1  0
  9 10  2  0
 10 11  1  0
 11 12  2  0
 12 13  1  0
 13 14  1  0
 14 15  2  0
 14 16  1  0
 16 17  1  0
 13 18  1  0
 18 19  1  0
 18 20  1  0
 20 21  1  0
 21 22  1  0
 22 23  1  0
 23 24  1  0
 23 25  1  0
 23 26  1  6
 12 27  1  0
 27 28  2  0
 28 29  1  0
 29 30  2  0
 30 31  1  0
 31 32  2  0
 32  5  1  0
 32  9  1  0
 30 11  1  0
  1 33  1  0
  1 34  1  0
  1 35  1  0
  6 36  1  0
  7 37  1  0
  8 38  1  0
 13 39  1  6
 17 40  1  0
 17 41  1  0
 17 42  1  0
 18 43  1  1
 19 44  1  0
 20 45  1  0
 20 46  1  0
 21 47  1  0
 21 48  1  0
 22 49  1  0
 22 50  1  0
 24 51  1  0
 24 52  1  0
 24 53  1  0
 25 54  1  0
 25 55  1  0
 25 56  1  0
 26 57  1  0
 27 58  1  0
 28 59  1  0
 29 60  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       7.600  -3.224  -0.608  0.00  0.00           C+0
HETATM    2  O   UNK     0       6.931  -2.167   0.058  0.00  0.00           O+0
HETATM    3  C   UNK     0       5.700  -1.653  -0.395  0.00  0.00           C+0
HETATM    4  O   UNK     0       5.185  -2.137  -1.425  0.00  0.00           O+0
HETATM    5  C   UNK     0       5.101  -0.588   0.374  0.00  0.00           C+0
HETATM    6  C   UNK     0       5.728  -0.003   1.441  0.00  0.00           C+0
HETATM    7  C   UNK     0       5.093   0.979   2.168  0.00  0.00           C+0
HETATM    8  C   UNK     0       3.793   1.379   1.796  0.00  0.00           C+0
HETATM    9  C   UNK     0       3.189   0.770   0.715  0.00  0.00           C+0
HETATM   10  N   UNK     0       1.925   1.097   0.358  0.00  0.00           N+0
HETATM   11  C   UNK     0       1.296   0.497  -0.661  0.00  0.00           C+0
HETATM   12  C   UNK     0      -0.038   0.788  -0.951  0.00  0.00           C+0
HETATM   13  C   UNK     0      -0.750   1.856  -0.206  0.00  0.00           C+0
HETATM   14  C   UNK     0      -0.058   3.097   0.027  0.00  0.00           C+0
HETATM   15  O   UNK     0       1.078   3.385  -0.392  0.00  0.00           O+0
HETATM   16  O   UNK     0      -0.694   4.094   0.783  0.00  0.00           O+0
HETATM   17  C   UNK     0      -0.113   5.344   1.058  0.00  0.00           C+0
HETATM   18  C   UNK     0      -1.357   1.277   1.052  0.00  0.00           C+0
HETATM   19  O   UNK     0      -2.054   2.251   1.747  0.00  0.00           O+0
HETATM   20  C   UNK     0      -2.114   0.033   0.918  0.00  0.00           C+0
HETATM   21  C   UNK     0      -3.377   0.010   0.126  0.00  0.00           C+0
HETATM   22  C   UNK     0      -3.799  -1.452   0.058  0.00  0.00           C+0
HETATM   23  C   UNK     0      -5.104  -1.643  -0.625  0.00  0.00           C+0
HETATM   24  C   UNK     0      -5.375  -3.149  -0.657  0.00  0.00           C+0
HETATM   25  C   UNK     0      -6.252  -1.092   0.251  0.00  0.00           C+0
HETATM   26  O   UNK     0      -5.211  -1.110  -1.880  0.00  0.00           O+0
HETATM   27  C   UNK     0      -0.631   0.081  -1.958  0.00  0.00           C+0
HETATM   28  C   UNK     0      -0.021  -0.901  -2.714  0.00  0.00           C+0
HETATM   29  C   UNK     0       1.280  -1.186  -2.422  0.00  0.00           C+0
HETATM   30  C   UNK     0       1.922  -0.482  -1.396  0.00  0.00           C+0
HETATM   31  N   UNK     0       3.201  -0.834  -1.057  0.00  0.00           N+0
HETATM   32  C   UNK     0       3.811  -0.212  -0.016  0.00  0.00           C+0
HETATM   33  H   UNK     0       8.459  -2.854  -1.203  0.00  0.00           H+0
HETATM   34  H   UNK     0       6.918  -3.748  -1.323  0.00  0.00           H+0
HETATM   35  H   UNK     0       7.939  -3.960   0.155  0.00  0.00           H+0
HETATM   36  H   UNK     0       6.749  -0.322   1.704  0.00  0.00           H+0
HETATM   37  H   UNK     0       5.561   1.446   3.007  0.00  0.00           H+0
HETATM   38  H   UNK     0       3.260   2.138   2.335  0.00  0.00           H+0
HETATM   39  H   UNK     0      -1.656   2.110  -0.878  0.00  0.00           H+0
HETATM   40  H   UNK     0       0.588   5.662   0.254  0.00  0.00           H+0
HETATM   41  H   UNK     0       0.431   5.362   2.014  0.00  0.00           H+0
HETATM   42  H   UNK     0      -0.922   6.121   1.176  0.00  0.00           H+0
HETATM   43  H   UNK     0      -0.423   1.067   1.716  0.00  0.00           H+0
HETATM   44  H   UNK     0      -2.789   2.647   1.236  0.00  0.00           H+0
HETATM   45  H   UNK     0      -1.458  -0.855   0.646  0.00  0.00           H+0
HETATM   46  H   UNK     0      -2.435  -0.260   1.987  0.00  0.00           H+0
HETATM   47  H   UNK     0      -3.372   0.526  -0.809  0.00  0.00           H+0
HETATM   48  H   UNK     0      -4.224   0.507   0.721  0.00  0.00           H+0
HETATM   49  H   UNK     0      -3.802  -1.882   1.060  0.00  0.00           H+0
HETATM   50  H   UNK     0      -3.029  -1.967  -0.577  0.00  0.00           H+0
HETATM   51  H   UNK     0      -6.085  -3.490   0.094  0.00  0.00           H+0
HETATM   52  H   UNK     0      -4.438  -3.718  -0.476  0.00  0.00           H+0
HETATM   53  H   UNK     0      -5.749  -3.464  -1.655  0.00  0.00           H+0
HETATM   54  H   UNK     0      -6.082  -1.414   1.311  0.00  0.00           H+0
HETATM   55  H   UNK     0      -6.354  -0.001   0.131  0.00  0.00           H+0
HETATM   56  H   UNK     0      -7.174  -1.580  -0.110  0.00  0.00           H+0
HETATM   57  H   UNK     0      -5.410  -0.119  -1.834  0.00  0.00           H+0
HETATM   58  H   UNK     0      -1.649   0.314  -2.206  0.00  0.00           H+0
HETATM   59  H   UNK     0      -0.547  -1.430  -3.511  0.00  0.00           H+0
HETATM   60  H   UNK     0       1.809  -1.942  -2.967  0.00  0.00           H+0
CONECT    1    2   33   34   35                                             
CONECT    2    1    3                                                       
CONECT    3    2    4    5                                                  
CONECT    4    3                                                            
CONECT    5    3    6   32                                                  
CONECT    6    5    7   36                                                  
CONECT    7    6    8   37                                                  
CONECT    8    7    9   38                                                  
CONECT    9    8   10   32                                                  
CONECT   10    9   11                                                       
CONECT   11   10   12   30                                                  
CONECT   12   11   13   27                                                  
CONECT   13   12   14   18   39                                             
CONECT   14   13   15   16                                                  
CONECT   15   14                                                            
CONECT   16   14   17                                                       
CONECT   17   16   40   41   42                                             
CONECT   18   13   19   20   43                                             
CONECT   19   18   44                                                       
CONECT   20   18   21   45   46                                             
CONECT   21   20   22   47   48                                             
CONECT   22   21   23   49   50                                             
CONECT   23   22   24   25   26                                             
CONECT   24   23   51   52   53                                             
CONECT   25   23   54   55   56                                             
CONECT   26   23   57                                                       
CONECT   27   12   28   58                                                  
CONECT   28   27   29   59                                                  
CONECT   29   28   30   60                                                  
CONECT   30   29   31   11                                                  
CONECT   31   30   32                                                       
CONECT   32   31    5    9                                                  
CONECT   33    1                                                            
CONECT   34    1                                                            
CONECT   35    1                                                            
CONECT   36    6                                                            
CONECT   37    7                                                            
CONECT   38    8                                                            
CONECT   39   13                                                            
CONECT   40   17                                                            
CONECT   41   17                                                            
CONECT   42   17                                                            
CONECT   43   18                                                            
CONECT   44   19                                                            
CONECT   45   20                                                            
CONECT   46   20                                                            
CONECT   47   21                                                            
CONECT   48   21                                                            
CONECT   49   22                                                            
CONECT   50   22                                                            
CONECT   51   24                                                            
CONECT   52   24                                                            
CONECT   53   24                                                            
CONECT   54   25                                                            
CONECT   55   25                                                            
CONECT   56   25                                                            
CONECT   57   26                                                            
CONECT   58   27                                                            
CONECT   59   28                                                            
CONECT   60   29                                                            
MASTER        0    0    0    0    0    0    0    0   60    0  124    0
END

RDKit          3D

60 62  0  0  0  0  0  0  0  0999 V2000
    7.6002   -3.2235   -0.6084 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.9315   -2.1675    0.0576 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.7000   -1.6531   -0.3952 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.1852   -2.1371   -1.4251 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.1006   -0.5875    0.3740 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7282   -0.0026    1.4414 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0926    0.9794    2.1681 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7934    1.3790    1.7955 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1890    0.7699    0.7145 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9248    1.0966    0.3582 N   0  0  0  0  0  0  0  0  0  0  0  0
    1.2963    0.4968   -0.6610 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0380    0.7880   -0.9507 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7502    1.8556   -0.2059 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.0577    3.0971    0.0273 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0783    3.3849   -0.3915 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6940    4.0941    0.7830 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1129    5.3440    1.0583 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3568    1.2774    1.0517 C   0  0  1  0  0  0  0  0  0  0  0  0
   -2.0545    2.2506    1.7468 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1140    0.0328    0.9184 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3765    0.0103    0.1261 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7991   -1.4517    0.0576 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.1037   -1.6429   -0.6248 C   0  0  1  0  0  0  0  0  0  0  0  0
   -5.3754   -3.1494   -0.6572 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.2524   -1.0917    0.2509 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.2113   -1.1101   -1.8801 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6312    0.0807   -1.9583 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0214   -0.9005   -2.7138 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2796   -1.1860   -2.4221 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9220   -0.4824   -1.3956 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2006   -0.8341   -1.0567 N   0  0  0  0  0  0  0  0  0  0  0  0
    3.8109   -0.2117   -0.0163 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.4592   -2.8542   -1.2027 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.9179   -3.7481   -1.3233 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.9392   -3.9603    0.1550 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.7494   -0.3216    1.7044 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.5606    1.4461    3.0070 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.2595    2.1382    2.3350 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6563    2.1100   -0.8784 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.5876    5.6625    0.2541 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.4307    5.3619    2.0140 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9217    6.1212    1.1763 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4230    1.0665    1.7155 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7889    2.6471    1.2356 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4580   -0.8549    0.6463 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4348   -0.2595    1.9872 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3717    0.5261   -0.8089 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2240    0.5070    0.7205 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8023   -1.8815    1.0598 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0291   -1.9674   -0.5772 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.0847   -3.4905    0.0943 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4376   -3.7184   -0.4762 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.7494   -3.4640   -1.6551 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.0818   -1.4138    1.3108 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.3536   -0.0012    0.1310 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.1744   -1.5803   -0.1103 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.4096   -0.1189   -1.8342 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6492    0.3143   -2.2058 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5470   -1.4295   -3.5111 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.8092   -1.9425   -2.9673 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
  3  5  1  0
  5  6  2  0
  6  7  1  0
  7  8  2  0
  8  9  1  0
  9 10  2  0
 10 11  1  0
 11 12  2  0
 12 13  1  0
 13 14  1  0
 14 15  2  0
 14 16  1  0
 16 17  1  0
 13 18  1  0
 18 19  1  0
 18 20  1  0
 20 21  1  0
 21 22  1  0
 22 23  1  0
 23 24  1  0
 23 25  1  0
 23 26  1  6
 12 27  1  0
 27 28  2  0
 28 29  1  0
 29 30  2  0
 30 31  1  0
 31 32  2  0
 32  5  1  0
 32  9  1  0
 30 11  1  0
  1 33  1  0
  1 34  1  0
  1 35  1  0
  6 36  1  0
  7 37  1  0
  8 38  1  0
 13 39  1  6
 17 40  1  0
 17 41  1  0
 17 42  1  0
 18 43  1  1
 19 44  1  0
 20 45  1  0
 20 46  1  0
 21 47  1  0
 21 48  1  0
 22 49  1  0
 22 50  1  0
 24 51  1  0
 24 52  1  0
 24 53  1  0
 25 54  1  0
 25 55  1  0
 25 56  1  0
 26 57  1  0
 27 58  1  0
 28 59  1  0
 29 60  1  0
M  END

View in JSmol View NMR Assignments

Synonyms

Value	Source
Methyl 6-(3,7-dihydroxy-1-methoxy-7-methyl-1-oxooctan-2-yl)phenazine-1-carboxylic acid	Generator

Chemical Formula

C₂₄H₂₈N₂O₆

Average Mass

440.4960 Da

Monoisotopic Mass

440.19474 Da

IUPAC Name

methyl 6-[(2S,3S)-3,7-dihydroxy-1-methoxy-7-methyl-1-oxooctan-2-yl]phenazine-1-carboxylate

Traditional Name

methyl 6-[(2S,3S)-3,7-dihydroxy-1-methoxy-7-methyl-1-oxooctan-2-yl]phenazine-1-carboxylate

CAS Registry Number

Not Available

SMILES

COC(=O)C(C(O)CCCC(C)(C)O)C1=CC=CC2=NC3=C(C=CC=C3N=C12)C(=O)OC

InChI Identifier

InChI=1S/C24H28N2O6/c1-24(2,30)13-7-12-18(27)19(23(29)32-4)14-8-5-10-16-20(14)25-17-11-6-9-15(21(17)26-16)22(28)31-3/h5-6,8-11,18-19,27,30H,7,12-13H2,1-4H3

InChI Key

WLMRJQPFNIUWBX-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	18396903

Chemical Taxonomy

Classification

Not classified

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	2.89	ALOGPS
logP	3.2	ChemAxon
logS	-4.1	ALOGPS
pKa (Strongest Acidic)	14.51	ChemAxon
pKa (Strongest Basic)	-0.17	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	6	ChemAxon
Hydrogen Donor Count	2	ChemAxon
Polar Surface Area	118.84 Å²	ChemAxon
Rotatable Bond Count	10	ChemAxon
Refractivity	116.74 m³·mol⁻¹	ChemAxon
Polarizability	47.51 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

NPAtlas ID

NPA001464

HMDB ID

Not Available

DrugBank ID

Not Available

Phenol Explorer Compound ID

Not Available

FoodDB ID

Not Available

KNApSAcK ID

Not Available

Chemspider ID

24695177

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

24879218

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

Mitova MI, Lang G, Wiese J, Imhoff JF: Subinhibitory concentrations of antibiotics induce phenazine production in a marine Streptomyces sp. J Nat Prod. 2008 May;71(5):824-7. doi: 10.1021/np800032a. Epub 2008 Apr 9. [PubMed:18396903 ]
Mitchell PM: The cost-effectiveness of what in health and care?. 2021 Feb. [PubMed:34383398 ]
Authors unspecified: Ozanimod. 2012. [PubMed:34383397 ]
Authors unspecified: Ponesimod. 2012. [PubMed:34383396 ]
Lee J, Cho Y, Choi KH, Hwang I, Oh YL: Metastatic leiomyosarcoma of the thyroid gland: cytologic findings and differential diagnosis. J Pathol Transl Med. 2021 Aug 13. pii: jptm.2021.06.23. doi: 10.4132/jptm.2021.06.23. [PubMed:34384147 ]

Showing NP-Card for Streptophenazine H (NP0007686)

MOL for NP0007686 (Streptophenazine H)

3D MOL for NP0007686 (Streptophenazine H)

3D SDF for NP0007686 (Streptophenazine H)

3D-SDF for NP0007686 (Streptophenazine H)

PDB for NP0007686 (Streptophenazine H)

3D PDB for NP0007686 (Streptophenazine H)

SMILES for NP0007686 (Streptophenazine H)

INCHI for NP0007686 (Streptophenazine H)

Structure for NP0007686 (Streptophenazine H)

3D Structure for NP0007686 (Streptophenazine H)