NP-MRD: Showing NP-Card for methyl 6-[(2r,3s)-3-hydroxy-1-methoxy-7-methyl-1-oxooctan-2-yl]phenazine-1-carboxylate (NP0144788)

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Record Information

Version

2.0

Created at

2022-09-01 23:51:03 UTC

Updated at

2022-09-01 23:51:03 UTC

NP-MRD ID

NP0144788

Secondary Accession Numbers

None

Natural Product Identification

Common Name

methyl 6-[(2r,3s)-3-hydroxy-1-methoxy-7-methyl-1-oxooctan-2-yl]phenazine-1-carboxylate

Description

Methyl 6-[(2R,3S)-3-hydroxy-1-methoxy-7-methyl-1-oxooctan-2-yl]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-[(2R,3S)-3-hydroxy-1-methoxy-7-methyl-1-oxooctan-2-yl]phenazine-1-carboxylate.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652309022201512D          

 31 33  0  0  1  0            999 V2000
   -6.1154   -3.1084    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.5753   -2.4848    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7651   -2.6407    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4951   -3.4202    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2251   -2.0171    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4951   -1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9550   -0.6139    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1449   -0.7698    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8748   -1.5493    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0647   -1.7052    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7946   -2.4848    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9845   -2.6407    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4444   -2.0171    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.7145   -1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1744   -0.6139    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5246   -1.0816    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7946   -0.3020    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3657   -2.1730    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.6358   -2.9525    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.9058   -1.5493    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7159   -1.7052    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2560   -1.0816    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0662   -1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6062   -0.6139    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3362   -2.0171    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7145   -3.4202    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2546   -4.0439    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0647   -3.8880    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3347   -3.1084    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1449   -2.9525    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4149   -2.1730    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  2  0  0  0  0
  3  5  1  0  0  0  0
  5  6  1  0  0  0  0
  6  7  2  0  0  0  0
  7  8  1  0  0  0  0
  8  9  2  0  0  0  0
  9 10  1  0  0  0  0
 10 11  2  0  0  0  0
 11 12  1  0  0  0  0
 12 13  1  0  0  0  0
 13 14  1  1  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  6  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
 12 26  2  0  0  0  0
 26 27  1  0  0  0  0
 27 28  2  0  0  0  0
 28 29  1  0  0  0  0
 11 29  1  0  0  0  0
 29 30  2  0  0  0  0
 30 31  1  0  0  0  0
  5 31  2  0  0  0  0
  9 31  1  0  0  0  0
M  END

     RDKit          3D

 59 61  0  0  0  0  0  0  0  0999 V2000
    7.7114    0.5770   -1.3600 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.4887    0.3570   -0.6647 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.5359    0.1066    0.6766 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.6284    0.0697    1.2907 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.3101   -0.1233    1.4221 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.3412   -0.3832    2.7924 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.1845   -0.5997    3.4867 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9860   -0.5562    2.8069 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9515   -0.2988    1.4483 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7908   -0.2597    0.7988 N   0  0  0  0  0  0  0  0  0  0  0  0
    1.6778   -0.0157   -0.5264 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4680    0.0081   -1.1713 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7762   -0.2001   -0.3810 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.9565    0.8263    0.6447 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7360    1.8130    0.4922 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2951    0.8198    1.8841 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5047    1.8349    2.8440 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9694   -0.5556   -1.2072 C   0  0  1  0  0  0  0  0  0  0  0  0
   -1.4720   -1.5489   -2.1353 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0601   -1.2679   -0.4860 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7945   -0.6427    0.6020 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6814    0.5120    0.3645 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.8670    0.2777   -0.5291 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.5579   -0.1482   -1.9287 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.8810   -0.6547    0.1293 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4425    0.2528   -2.5247 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6247    0.4730   -3.2294 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8336    0.4508   -2.5931 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8491    0.2062   -1.2452 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0211    0.1636   -0.5706 N   0  0  0  0  0  0  0  0  0  0  0  0
    4.1104   -0.0803    0.7450 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.5826    0.3190   -0.7397 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.7510    1.6342   -1.7209 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.6810   -0.0976   -2.2555 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.2792   -0.4162    3.3167 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.1738   -0.8053    4.5550 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.0608   -0.7233    3.3306 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5523   -1.1722    0.2037 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8814    2.7751    2.3634 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2383    1.5464    3.6227 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.4533    2.0675    3.3932 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2404    0.2936   -1.8196 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8929   -2.1633   -1.6245 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5123   -2.1677   -0.0016 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7268   -1.8382   -1.2123 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4038   -1.4521    1.1087 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0450   -0.3862    1.4220 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.1301    0.7698    1.3807 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2353    1.4499    0.0330 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.4172    1.2644   -0.5998 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5562    0.1023   -2.2942 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.7987   -1.2148   -2.1261 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.2478    0.3981   -2.6582 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.9557   -0.3221    1.1851 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.8627   -0.4690   -0.3407 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.5580   -1.7097    0.0983 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5071    0.2890   -3.0790 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.6071    0.6672   -4.3021 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.7692    0.6184   -3.1145 H   0  0  0  0  0  0  0  0  0  0  0  0
 17 16  1  0
 16 14  1  0
 14 15  2  0
 14 13  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
 13 12  1  0
 12 26  2  0
 26 27  1  0
 27 28  2  0
 28 29  1  0
 29 30  2  0
 30 31  1  0
 31  5  2  0
  5  6  1  0
  6  7  2  0
  7  8  1  0
  8  9  2  0
  9 10  1  0
 10 11  2  0
  5  3  1  0
  3  4  2  0
  3  2  1  0
  2  1  1  0
 11 12  1  0
 11 29  1  0
  9 31  1  0
 17 39  1  0
 17 40  1  0
 17 41  1  0
 13 38  1  1
 18 42  1  6
 19 43  1  0
 20 44  1  0
 20 45  1  0
 21 46  1  0
 21 47  1  0
 22 48  1  0
 22 49  1  0
 23 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
  6 35  1  0
  7 36  1  0
  8 37  1  0
  1 32  1  0
  1 33  1  0
  1 34  1  0
M  END


  Mrv1652309022201512D          

 31 33  0  0  1  0            999 V2000
   -6.1154   -3.1084    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.5753   -2.4848    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7651   -2.6407    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4951   -3.4202    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2251   -2.0171    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4951   -1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9550   -0.6139    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1449   -0.7698    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8748   -1.5493    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0647   -1.7052    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7946   -2.4848    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9845   -2.6407    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4444   -2.0171    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.7145   -1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1744   -0.6139    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5246   -1.0816    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7946   -0.3020    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3657   -2.1730    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.6358   -2.9525    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.9058   -1.5493    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7159   -1.7052    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2560   -1.0816    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0662   -1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6062   -0.6139    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3362   -2.0171    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7145   -3.4202    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2546   -4.0439    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0647   -3.8880    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3347   -3.1084    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1449   -2.9525    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4149   -2.1730    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  2  0  0  0  0
  3  5  1  0  0  0  0
  5  6  1  0  0  0  0
  6  7  2  0  0  0  0
  7  8  1  0  0  0  0
  8  9  2  0  0  0  0
  9 10  1  0  0  0  0
 10 11  2  0  0  0  0
 11 12  1  0  0  0  0
 12 13  1  0  0  0  0
 13 14  1  1  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  6  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
 12 26  2  0  0  0  0
 26 27  1  0  0  0  0
 27 28  2  0  0  0  0
 28 29  1  0  0  0  0
 11 29  1  0  0  0  0
 29 30  2  0  0  0  0
 30 31  1  0  0  0  0
  5 31  2  0  0  0  0
  9 31  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0144788

> <DATABASE_NAME>
NP-MRD

> <SMILES>
COC(=O)[C@@H]([C@@H](O)CCCC(C)C)C1=CC=CC2=NC3=C(C=CC=C3N=C12)C(=O)OC

> <INCHI_IDENTIFIER>
InChI=1S/C24H28N2O5/c1-14(2)8-5-13-19(27)20(24(29)31-4)15-9-6-11-17-21(15)25-18-12-7-10-16(22(18)26-17)23(28)30-3/h6-7,9-12,14,19-20,27H,5,8,13H2,1-4H3/t19-,20+/m0/s1

> <INCHI_KEY>
YNVFQWRFLIXGIL-VQTJNVASSA-N

> <FORMULA>
C24H28N2O5

> <MOLECULAR_WEIGHT>
424.497

> <EXACT_MASS>
424.19982201

> <JCHEM_ACCEPTOR_COUNT>
5

> <JCHEM_ATOM_COUNT>
59

> <JCHEM_AVERAGE_POLARIZABILITY>
46.265847080144866

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
1

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

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

> <ALOGPS_LOGP>
4.13

> <JCHEM_LOGP>
4.6694127199999995

> <ALOGPS_LOGS>
-4.73

> <JCHEM_MDDR_LIKE_RULE>
1

> <JCHEM_NUMBER_OF_RINGS>
3

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA_STRONGEST_ACIDIC>
14.507692811854909

> <JCHEM_PKA_STRONGEST_BASIC>
-0.2069983782602033

> <JCHEM_POLAR_SURFACE_AREA>
98.61

> <JCHEM_REFRACTIVITY>
114.90220000000001

> <JCHEM_ROTATABLE_BOND_COUNT>
10

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
7.89e-03 g/l

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

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 02-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   02-SEP-22         0                                  
HETATM    1  C   UNK     0     -11.415  -5.802   0.000  0.00  0.00           C+0
HETATM    2  O   UNK     0     -10.407  -4.638   0.000  0.00  0.00           O+0
HETATM    3  C   UNK     0      -8.895  -4.929   0.000  0.00  0.00           C+0
HETATM    4  O   UNK     0      -8.391  -6.384   0.000  0.00  0.00           O+0
HETATM    5  C   UNK     0      -7.887  -3.765   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0      -8.391  -2.310   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0      -7.383  -1.146   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0      -5.870  -1.437   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0      -5.366  -2.892   0.000  0.00  0.00           C+0
HETATM   10  N   UNK     0      -3.854  -3.183   0.000  0.00  0.00           N+0
HETATM   11  C   UNK     0      -3.350  -4.638   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0      -1.838  -4.929   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0      -0.830  -3.765   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0      -1.334  -2.310   0.000  0.00  0.00           C+0
HETATM   15  O   UNK     0      -0.326  -1.146   0.000  0.00  0.00           O+0
HETATM   16  O   UNK     0      -2.846  -2.019   0.000  0.00  0.00           O+0
HETATM   17  C   UNK     0      -3.350  -0.564   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       0.683  -4.056   0.000  0.00  0.00           C+0
HETATM   19  O   UNK     0       1.187  -5.511   0.000  0.00  0.00           O+0
HETATM   20  C   UNK     0       1.691  -2.892   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0       3.203  -3.183   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0       4.211  -2.019   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0       5.723  -2.310   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0       6.732  -1.146   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0       6.228  -3.765   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0      -1.334  -6.384   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0      -2.342  -7.549   0.000  0.00  0.00           C+0
HETATM   28  C   UNK     0      -3.854  -7.258   0.000  0.00  0.00           C+0
HETATM   29  C   UNK     0      -4.358  -5.802   0.000  0.00  0.00           C+0
HETATM   30  N   UNK     0      -5.870  -5.511   0.000  0.00  0.00           N+0
HETATM   31  C   UNK     0      -6.375  -4.056   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   31                                                  
CONECT    6    5    7                                                       
CONECT    7    6    8                                                       
CONECT    8    7    9                                                       
CONECT    9    8   10   31                                                  
CONECT   10    9   11                                                       
CONECT   11   10   12   29                                                  
CONECT   12   11   13   26                                                  
CONECT   13   12   14   18                                                  
CONECT   14   13   15   16                                                  
CONECT   15   14                                                            
CONECT   16   14   17                                                       
CONECT   17   16                                                            
CONECT   18   13   19   20                                                  
CONECT   19   18                                                            
CONECT   20   18   21                                                       
CONECT   21   20   22                                                       
CONECT   22   21   23                                                       
CONECT   23   22   24   25                                                  
CONECT   24   23                                                            
CONECT   25   23                                                            
CONECT   26   12   27                                                       
CONECT   27   26   28                                                       
CONECT   28   27   29                                                       
CONECT   29   28   11   30                                                  
CONECT   30   29   31                                                       
CONECT   31   30    5    9                                                  
MASTER        0    0    0    0    0    0    0    0   31    0   66    0
END

View in JSmol

Synonyms

Value	Source
Methyl 6-[(2R,3S)-3-hydroxy-1-methoxy-7-methyl-1-oxooctan-2-yl]phenazine-1-carboxylic acid	Generator

Chemical Formula

C₂₄H₂₈N₂O₅

Average Mass

424.4970 Da

Monoisotopic Mass

424.19982 Da

IUPAC Name

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

Traditional Name

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

CAS Registry Number

Not Available

SMILES

COC(=O)[C@@H]([C@@H](O)CCCC(C)C)C1=CC=CC2=NC3=C(C=CC=C3N=C12)C(=O)OC

InChI Identifier

InChI=1S/C24H28N2O5/c1-14(2)8-5-13-19(27)20(24(29)31-4)15-9-6-11-17-21(15)25-18-12-7-10-16(22(18)26-17)23(28)30-3/h6-7,9-12,14,19-20,27H,5,8,13H2,1-4H3/t19-,20+/m0/s1

InChI Key

YNVFQWRFLIXGIL-VQTJNVASSA-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
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	4.13	ALOGPS
logP	4.67	ChemAxon
logS	-4.7	ALOGPS
pKa (Strongest Acidic)	14.51	ChemAxon
pKa (Strongest Basic)	-0.21	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	10	ChemAxon
Refractivity	114.9 m³·mol⁻¹	ChemAxon
Polarizability	46.27 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

162863795

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-[(2r,3s)-3-hydroxy-1-methoxy-7-methyl-1-oxooctan-2-yl]phenazine-1-carboxylate (NP0144788)

MOL for NP0144788 (methyl 6-[(2r,3s)-3-hydroxy-1-methoxy-7-methyl-1-oxooctan-2-yl]phenazine-1-carboxylate)

3D MOL for NP0144788 (methyl 6-[(2r,3s)-3-hydroxy-1-methoxy-7-methyl-1-oxooctan-2-yl]phenazine-1-carboxylate)

3D SDF for NP0144788 (methyl 6-[(2r,3s)-3-hydroxy-1-methoxy-7-methyl-1-oxooctan-2-yl]phenazine-1-carboxylate)

3D-SDF for NP0144788 (methyl 6-[(2r,3s)-3-hydroxy-1-methoxy-7-methyl-1-oxooctan-2-yl]phenazine-1-carboxylate)

PDB for NP0144788 (methyl 6-[(2r,3s)-3-hydroxy-1-methoxy-7-methyl-1-oxooctan-2-yl]phenazine-1-carboxylate)

3D PDB for NP0144788 (methyl 6-[(2r,3s)-3-hydroxy-1-methoxy-7-methyl-1-oxooctan-2-yl]phenazine-1-carboxylate)

SMILES for NP0144788 (methyl 6-[(2r,3s)-3-hydroxy-1-methoxy-7-methyl-1-oxooctan-2-yl]phenazine-1-carboxylate)

INCHI for NP0144788 (methyl 6-[(2r,3s)-3-hydroxy-1-methoxy-7-methyl-1-oxooctan-2-yl]phenazine-1-carboxylate)

Structure for NP0144788 (methyl 6-[(2r,3s)-3-hydroxy-1-methoxy-7-methyl-1-oxooctan-2-yl]phenazine-1-carboxylate)

3D Structure for NP0144788 (methyl 6-[(2r,3s)-3-hydroxy-1-methoxy-7-methyl-1-oxooctan-2-yl]phenazine-1-carboxylate)