NP-MRD: Showing NP-Card for methyl 6-[1-hydroxy-3-methoxy-2-(6-methyloctyl)-3-oxopropyl]phenazine-1-carboxylate (NP0327397)

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Record Information

Version

1.0

Created at

2022-09-12 09:56:34 UTC

Updated at

2022-09-12 09:56:35 UTC

NP-MRD ID

NP0327397

Secondary Accession Numbers

None

Natural Product Identification

Common Name

methyl 6-[1-hydroxy-3-methoxy-2-(6-methyloctyl)-3-oxopropyl]phenazine-1-carboxylate

Description

Methyl 6-[1-hydroxy-3-methoxy-2-(6-methyloctyl)-3-oxopropyl]phenazine-1-carboxylate 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. Based on a literature review very few articles have been published on methyl 6-[1-hydroxy-3-methoxy-2-(6-methyloctyl)-3-oxopropyl]phenazine-1-carboxylate.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652309122211562D          

 34 36  0  0  0  0            999 V2000
    7.2234   -1.1823    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.7635   -1.8059    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.5737   -1.6500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.8437   -0.8704    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.1137   -2.2736    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.9239   -2.1177    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.4640   -2.7414    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   11.2741   -2.5855    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   11.8142   -3.2091    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   12.6243   -3.0532    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   12.8944   -2.2736    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   13.7045   -2.1177    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   12.3543   -1.6500    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   12.6243   -0.8704    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   13.1644   -3.6768    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   12.8944   -4.4564    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   13.9745   -3.5209    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   14.2446   -2.7414    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   15.0547   -2.5855    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   15.5948   -3.2091    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   15.3248   -3.9887    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   15.8649   -4.6123    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
   15.5948   -5.3918    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   16.1349   -6.0155    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   16.9450   -5.8596    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   17.2151   -5.0800    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   17.4851   -6.4832    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   18.2953   -6.3273    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   15.8649   -6.7950    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   15.0547   -6.9510    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   14.5146   -6.3273    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   14.7847   -5.5478    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   14.2446   -4.9241    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
   14.5146   -4.1446    0.0000 C   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  1  0  0  0  0
  3  5  1  0  0  0  0
  5  6  1  0  0  0  0
  6  7  1  0  0  0  0
  7  8  1  0  0  0  0
  8  9  1  0  0  0  0
  9 10  1  0  0  0  0
 10 11  1  0  0  0  0
 11 12  2  0  0  0  0
 11 13  1  0  0  0  0
 13 14  1  0  0  0  0
 10 15  1  0  0  0  0
 15 16  1  0  0  0  0
 15 17  1  0  0  0  0
 17 18  1  0  0  0  0
 18 19  2  0  0  0  0
 19 20  1  0  0  0  0
 20 21  2  0  0  0  0
 21 22  1  0  0  0  0
 22 23  2  0  0  0  0
 23 24  1  0  0  0  0
 24 25  1  0  0  0  0
 25 26  2  0  0  0  0
 25 27  1  0  0  0  0
 27 28  1  0  0  0  0
 24 29  2  0  0  0  0
 29 30  1  0  0  0  0
 30 31  2  0  0  0  0
 31 32  1  0  0  0  0
 23 32  1  0  0  0  0
 32 33  2  0  0  0  0
 33 34  1  0  0  0  0
 17 34  2  0  0  0  0
 21 34  1  0  0  0  0
M  END

     RDKit          3D

 68 70  0  0  0  0  0  0  0  0999 V2000
    7.1012    1.1902    2.7095 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.5102    0.7366    1.3245 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.9417    1.6810    0.2849 C   0  0  1  0  0  0  0  0  0  0  0  0
    7.3349    1.2508   -1.1024 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.4276    1.7783    0.4275 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7886    0.4187    0.2409 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2806    0.6286    0.4029 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5559   -0.7188    0.2255 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0893   -0.3942    0.4040 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1770   -1.5784    0.2812 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.5040   -2.5409   -0.7832 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3756   -2.8318   -1.6313 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.7267   -3.1738   -0.9366 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.9838   -4.0983   -1.9852 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2546   -1.2612    0.4442 C   0  0  1  0  0  0  0  0  0  0  0  0
   -1.4189   -0.7120    1.7268 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9517   -0.5157   -0.5851 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4694   -0.0306   -1.7628 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2491    0.6640   -2.6513 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5675    0.8830   -2.3497 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1185    0.4192   -1.1747 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.4311    0.6435   -0.8860 N   0  0  0  0  0  0  0  0  0  0  0  0
   -5.9473    0.1766    0.2758 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.2713    0.3929    0.5857 C   0  0  0  0  0  0  0  0  0  0  0  0
   -8.0825    1.1337   -0.3730 C   0  0  0  0  0  0  0  0  0  0  0  0
   -9.3073    1.3594   -0.1348 O   0  0  0  0  0  0  0  0  0  0  0  0
   -7.5737    1.6118   -1.5515 O   0  0  0  0  0  0  0  0  0  0  0  0
   -8.3615    2.3354   -2.4904 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.8025   -0.0800    1.7671 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.0326   -0.7841    2.6788 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.7104   -0.9873    2.3451 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.1684   -0.5129    1.1550 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8780   -0.7193    0.8445 N   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3144   -0.2709   -0.3081 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.1425    0.6752    3.0045 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.9019    0.9180    3.4072 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.9349    2.2918    2.6870 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.2394   -0.3220    1.1279 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.6159    0.7895    1.2729 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.3620    2.6846    0.4990 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.4925    1.4620   -1.8190 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.2563    1.7521   -1.4469 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.5620    0.1561   -1.0639 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.0426    2.4549   -0.3541 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.2310    2.1959    1.4310 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.1098   -0.2522    1.0468 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.9749    0.0541   -0.7674 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.9104    1.3698   -0.3043 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.1460    0.9973    1.4397 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.9048   -1.4059    1.0185 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.7949   -1.1368   -0.7749 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.0461   -0.0014    1.4783 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.7887    0.4926   -0.1793 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.4170   -2.1735    1.2492 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.8025   -3.7690   -2.6432 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.0515   -4.2306   -2.5747 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.2080   -5.1176   -1.5597 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7910   -2.2597    0.5197 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7072   -1.0170    2.3433 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4402   -0.1956   -2.0098 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8516    1.0522   -3.6001 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2438    1.4293   -3.0142 H   0  0  0  0  0  0  0  0  0  0  0  0
   -9.2492    1.7281   -2.7820 H   0  0  0  0  0  0  0  0  0  0  0  0
   -8.6453    3.2804   -1.9883 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.7287    2.5899   -3.3632 H   0  0  0  0  0  0  0  0  0  0  0  0
   -8.8546    0.0876    2.0215 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.4827   -1.1414    3.5978 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0767   -1.5325    3.0307 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
  3  5  1  0
  5  6  1  0
  6  7  1  0
  7  8  1  0
  8  9  1  0
  9 10  1  0
 10 15  1  0
 15 16  1  0
 15 17  1  0
 17 34  2  0
 34 33  1  0
 33 32  2  0
 32 31  1  0
 31 30  2  0
 30 29  1  0
 29 24  2  0
 24 25  1  0
 25 26  2  0
 25 27  1  0
 27 28  1  0
 24 23  1  0
 23 22  2  0
 22 21  1  0
 21 20  2  0
 20 19  1  0
 19 18  2  0
 10 11  1  0
 11 12  2  0
 11 13  1  0
 13 14  1  0
 18 17  1  0
 21 34  1  0
 23 32  1  0
  1 35  1  0
  1 36  1  0
  1 37  1  0
  2 38  1  0
  2 39  1  0
  3 40  1  1
  4 41  1  0
  4 42  1  0
  4 43  1  0
  5 44  1  0
  5 45  1  0
  6 46  1  0
  6 47  1  0
  7 48  1  0
  7 49  1  0
  8 50  1  0
  8 51  1  0
  9 52  1  0
  9 53  1  0
 10 54  1  1
 15 58  1  1
 16 59  1  0
 31 68  1  0
 30 67  1  0
 29 66  1  0
 28 63  1  0
 28 64  1  0
 28 65  1  0
 20 62  1  0
 19 61  1  0
 18 60  1  0
 14 55  1  0
 14 56  1  0
 14 57  1  0
M  END


  Mrv1652309122211562D          

 34 36  0  0  0  0            999 V2000
    7.2234   -1.1823    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.7635   -1.8059    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.5737   -1.6500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.8437   -0.8704    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.1137   -2.2736    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.9239   -2.1177    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.4640   -2.7414    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   11.2741   -2.5855    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   11.8142   -3.2091    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   12.6243   -3.0532    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   12.8944   -2.2736    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   13.7045   -2.1177    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   12.3543   -1.6500    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   12.6243   -0.8704    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   13.1644   -3.6768    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   12.8944   -4.4564    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   13.9745   -3.5209    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   14.2446   -2.7414    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   15.0547   -2.5855    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   15.5948   -3.2091    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   15.3248   -3.9887    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   15.8649   -4.6123    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
   15.5948   -5.3918    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   16.1349   -6.0155    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   16.9450   -5.8596    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   17.2151   -5.0800    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   17.4851   -6.4832    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   18.2953   -6.3273    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   15.8649   -6.7950    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   15.0547   -6.9510    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   14.5146   -6.3273    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   14.7847   -5.5478    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   14.2446   -4.9241    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
   14.5146   -4.1446    0.0000 C   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  1  0  0  0  0
  3  5  1  0  0  0  0
  5  6  1  0  0  0  0
  6  7  1  0  0  0  0
  7  8  1  0  0  0  0
  8  9  1  0  0  0  0
  9 10  1  0  0  0  0
 10 11  1  0  0  0  0
 11 12  2  0  0  0  0
 11 13  1  0  0  0  0
 13 14  1  0  0  0  0
 10 15  1  0  0  0  0
 15 16  1  0  0  0  0
 15 17  1  0  0  0  0
 17 18  1  0  0  0  0
 18 19  2  0  0  0  0
 19 20  1  0  0  0  0
 20 21  2  0  0  0  0
 21 22  1  0  0  0  0
 22 23  2  0  0  0  0
 23 24  1  0  0  0  0
 24 25  1  0  0  0  0
 25 26  2  0  0  0  0
 25 27  1  0  0  0  0
 27 28  1  0  0  0  0
 24 29  2  0  0  0  0
 29 30  1  0  0  0  0
 30 31  2  0  0  0  0
 31 32  1  0  0  0  0
 23 32  1  0  0  0  0
 32 33  2  0  0  0  0
 33 34  1  0  0  0  0
 17 34  2  0  0  0  0
 21 34  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0327397

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CCC(C)CCCCCC(C(O)C1=C2N=C3C=CC=C(C(=O)OC)C3=NC2=CC=C1)C(=O)OC

> <INCHI_IDENTIFIER>
InChI=1S/C27H34N2O5/c1-5-17(2)11-7-6-8-12-20(27(32)34-4)25(30)18-13-9-15-21-23(18)28-22-16-10-14-19(24(22)29-21)26(31)33-3/h9-10,13-17,20,25,30H,5-8,11-12H2,1-4H3

> <INCHI_KEY>
ZDFPHWFJRDWIPF-UHFFFAOYSA-N

> <FORMULA>
C27H34N2O5

> <MOLECULAR_WEIGHT>
466.578

> <EXACT_MASS>
466.246772203

> <JCHEM_ACCEPTOR_COUNT>
5

> <JCHEM_ATOM_COUNT>
68

> <JCHEM_AVERAGE_POLARIZABILITY>
52.33621374905199

> <JCHEM_BIOAVAILABILITY>
0

> <JCHEM_DONOR_COUNT>
1

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
methyl 6-[1-hydroxy-3-methoxy-2-(6-methyloctyl)-3-oxopropyl]phenazine-1-carboxylate

> <JCHEM_LOGP>
6.159026174999999

> <JCHEM_MDDR_LIKE_RULE>
1

> <JCHEM_NUMBER_OF_RINGS>
3

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA_STRONGEST_ACIDIC>
13.865940193602714

> <JCHEM_PKA_STRONGEST_BASIC>
-0.35235435133077553

> <JCHEM_POLAR_SURFACE_AREA>
98.61000000000001

> <JCHEM_REFRACTIVITY>
128.5512

> <JCHEM_ROTATABLE_BOND_COUNT>
13

> <JCHEM_RULE_OF_FIVE>
0

> <JCHEM_TRADITIONAL_IUPAC>
methyl 6-[1-hydroxy-3-methoxy-2-(6-methyloctyl)-3-oxopropyl]phenazine-1-carboxylate

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 12-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   12-SEP-22         0                                  
HETATM    1  C   UNK     0      13.484  -2.207   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0      14.492  -3.371   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0      16.004  -3.080   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0      16.508  -1.625   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0      17.012  -4.244   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0      18.525  -3.953   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0      19.533  -5.117   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0      21.045  -4.826   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0      22.053  -5.990   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0      23.565  -5.699   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0      24.069  -4.244   0.000  0.00  0.00           C+0
HETATM   12  O   UNK     0      25.582  -3.953   0.000  0.00  0.00           O+0
HETATM   13  O   UNK     0      23.061  -3.080   0.000  0.00  0.00           O+0
HETATM   14  C   UNK     0      23.565  -1.625   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0      24.574  -6.863   0.000  0.00  0.00           C+0
HETATM   16  O   UNK     0      24.069  -8.319   0.000  0.00  0.00           O+0
HETATM   17  C   UNK     0      26.086  -6.572   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0      26.590  -5.117   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0      28.102  -4.826   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0      29.110  -5.990   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0      28.606  -7.445   0.000  0.00  0.00           C+0
HETATM   22  N   UNK     0      29.614  -8.610   0.000  0.00  0.00           N+0
HETATM   23  C   UNK     0      29.110 -10.065   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0      30.118 -11.229   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0      31.631 -10.938   0.000  0.00  0.00           C+0
HETATM   26  O   UNK     0      32.135  -9.483   0.000  0.00  0.00           O+0
HETATM   27  O   UNK     0      32.639 -12.102   0.000  0.00  0.00           O+0
HETATM   28  C   UNK     0      34.151 -11.811   0.000  0.00  0.00           C+0
HETATM   29  C   UNK     0      29.614 -12.684   0.000  0.00  0.00           C+0
HETATM   30  C   UNK     0      28.102 -12.975   0.000  0.00  0.00           C+0
HETATM   31  C   UNK     0      27.094 -11.811   0.000  0.00  0.00           C+0
HETATM   32  C   UNK     0      27.598 -10.356   0.000  0.00  0.00           C+0
HETATM   33  N   UNK     0      26.590  -9.192   0.000  0.00  0.00           N+0
HETATM   34  C   UNK     0      27.094  -7.737   0.000  0.00  0.00           C+0
CONECT    1    2                                                            
CONECT    2    1    3                                                       
CONECT    3    2    4    5                                                  
CONECT    4    3                                                            
CONECT    5    3    6                                                       
CONECT    6    5    7                                                       
CONECT    7    6    8                                                       
CONECT    8    7    9                                                       
CONECT    9    8   10                                                       
CONECT   10    9   11   15                                                  
CONECT   11   10   12   13                                                  
CONECT   12   11                                                            
CONECT   13   11   14                                                       
CONECT   14   13                                                            
CONECT   15   10   16   17                                                  
CONECT   16   15                                                            
CONECT   17   15   18   34                                                  
CONECT   18   17   19                                                       
CONECT   19   18   20                                                       
CONECT   20   19   21                                                       
CONECT   21   20   22   34                                                  
CONECT   22   21   23                                                       
CONECT   23   22   24   32                                                  
CONECT   24   23   25   29                                                  
CONECT   25   24   26   27                                                  
CONECT   26   25                                                            
CONECT   27   25   28                                                       
CONECT   28   27                                                            
CONECT   29   24   30                                                       
CONECT   30   29   31                                                       
CONECT   31   30   32                                                       
CONECT   32   31   23   33                                                  
CONECT   33   32   34                                                       
CONECT   34   33   17   21                                                  
MASTER        0    0    0    0    0    0    0    0   34    0   72    0
END

View in JSmol

Synonyms

Value	Source
Methyl 6-[1-hydroxy-3-methoxy-2-(6-methyloctyl)-3-oxopropyl]phenazine-1-carboxylic acid	Generator

Chemical Formula

C₂₇H₃₄N₂O₅

Average Mass

466.5780 Da

Monoisotopic Mass

466.24677 Da

IUPAC Name

methyl 6-[1-hydroxy-3-methoxy-2-(6-methyloctyl)-3-oxopropyl]phenazine-1-carboxylate

Traditional Name

methyl 6-[1-hydroxy-3-methoxy-2-(6-methyloctyl)-3-oxopropyl]phenazine-1-carboxylate

CAS Registry Number

Not Available

SMILES

CCC(C)CCCCCC(C(O)C1=C2N=C3C=CC=C(C(=O)OC)C3=NC2=CC=C1)C(=O)OC

InChI Identifier

InChI=1S/C27H34N2O5/c1-5-17(2)11-7-6-8-12-20(27(32)34-4)25(30)18-13-9-15-21-23(18)28-22-16-10-14-19(24(22)29-21)26(31)33-3/h9-10,13-17,20,25,30H,5-8,11-12H2,1-4H3

InChI Key

ZDFPHWFJRDWIPF-UHFFFAOYSA-N

Experimental Spectra

Not Available

Predicted Spectra

Spectrum Type	Description	Depositor ID	Depositor Organization	Depositor	Deposition Date	View
1D NMR	¹³C NMR Spectrum (1D, 25 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 100 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 252 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 1000 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 50 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 200 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 75 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 300 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 101 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 400 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 126 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 500 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 151 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 600 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 176 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 700 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 201 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 800 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 226 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 900 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum

Chemical Shift Submissions

Not Available

Species

Species of Origin

Not Available

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as 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
Fatty acid ester
Beta-hydroxy acid
Fatty acyl
Benzenoid
Pyrazine
Hydroxy acid
Dicarboxylic acid or derivatives
Heteroaromatic compound
Methyl ester
Secondary alcohol
Carboxylic acid ester
Azacycle
Carboxylic acid derivative
Organic nitrogen compound
Organic oxygen compound
Organopnictogen compound
Organic oxide
Hydrocarbon derivative
Aromatic alcohol
Organooxygen compound
Organonitrogen compound
Carbonyl group
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	6.16	ChemAxon
pKa (Strongest Acidic)	13.87	ChemAxon
pKa (Strongest Basic)	-0.35	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	5	ChemAxon
Hydrogen Donor Count	1	ChemAxon
Polar Surface Area	98.61 Å²	ChemAxon
Rotatable Bond Count	13	ChemAxon
Refractivity	128.55 m³·mol⁻¹	ChemAxon
Polarizability	52.34 Å³	ChemAxon
Number of Rings	3	ChemAxon
Bioavailability	No	ChemAxon
Rule of Five	No	ChemAxon
Ghose Filter	No	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

163020160

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for methyl 6-[1-hydroxy-3-methoxy-2-(6-methyloctyl)-3-oxopropyl]phenazine-1-carboxylate (NP0327397)

MOL for NP0327397 (methyl 6-[1-hydroxy-3-methoxy-2-(6-methyloctyl)-3-oxopropyl]phenazine-1-carboxylate)

3D MOL for NP0327397 (methyl 6-[1-hydroxy-3-methoxy-2-(6-methyloctyl)-3-oxopropyl]phenazine-1-carboxylate)

3D SDF for NP0327397 (methyl 6-[1-hydroxy-3-methoxy-2-(6-methyloctyl)-3-oxopropyl]phenazine-1-carboxylate)

3D-SDF for NP0327397 (methyl 6-[1-hydroxy-3-methoxy-2-(6-methyloctyl)-3-oxopropyl]phenazine-1-carboxylate)

PDB for NP0327397 (methyl 6-[1-hydroxy-3-methoxy-2-(6-methyloctyl)-3-oxopropyl]phenazine-1-carboxylate)

3D PDB for NP0327397 (methyl 6-[1-hydroxy-3-methoxy-2-(6-methyloctyl)-3-oxopropyl]phenazine-1-carboxylate)

SMILES for NP0327397 (methyl 6-[1-hydroxy-3-methoxy-2-(6-methyloctyl)-3-oxopropyl]phenazine-1-carboxylate)

INCHI for NP0327397 (methyl 6-[1-hydroxy-3-methoxy-2-(6-methyloctyl)-3-oxopropyl]phenazine-1-carboxylate)

Structure for NP0327397 (methyl 6-[1-hydroxy-3-methoxy-2-(6-methyloctyl)-3-oxopropyl]phenazine-1-carboxylate)

3D Structure for NP0327397 (methyl 6-[1-hydroxy-3-methoxy-2-(6-methyloctyl)-3-oxopropyl]phenazine-1-carboxylate)