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Record Information

Version

5.0

Status

Detected but not Quantified

Creation Date

2020-11-01 18:41:31 UTC

Update Date

2022-03-07 03:18:21 UTC

HMDB ID

HMDB0240722

Secondary Accession Numbers

None

Metabolite Identification

Common Name

2-Acetylamino-7-methoxy-3H-phenoxazin-3-one

Description

2-Acetylamino-7-methoxy-3H-phenoxazin-3-one belongs to the class of organic compounds known as phenoxazines. These are polycyclic aromatic compounds containing a phenoxazine moiety, which is a linear tricyclic system that consists of a two benzene rings joined by a 1,4-oxazine ring. Based on a literature review very few articles have been published on 2-Acetylamino-7-methoxy-3H-phenoxazin-3-one.

Structure

MOL 3D MOL SDF 3D SDF PDB 3D PDB SMILES InChI

HMDB0240722
     RDKit          3D
2-Acetylamino-7-methoxy-3H-phenoxazin-3-one
 33 35  0  0  0  0  0  0  0  0999 V2000
   -6.6041    0.2261   -0.3490 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.5282    0.0847   -1.2549 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2262    0.0852   -0.7323 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0015    0.2190    0.6196 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7616    0.2273    1.1916 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6491    0.0922    0.3598 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4076    0.0986    0.9140 N   0  0  0  0  0  0  0  0  0  0  0  0
    0.6388   -0.0330    0.0889 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9480   -0.0381    0.5616 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0582   -0.1693   -0.2345 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3925   -0.1779    0.2156 N   0  0  0  0  0  0  0  0  0  0  0  0
    4.8198   -0.0550    1.5441 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.2948   -0.0833    1.8642 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0764    0.0819    2.5402 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.7913   -0.3030   -1.6021 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7673   -0.4274   -2.3871 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.5342   -0.3066   -2.1361 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4107   -0.1750   -1.3414 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8033   -0.1758   -1.8325 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8312   -0.0437   -0.9947 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1223   -0.0467   -1.5373 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.5165   -0.5847    0.4320 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.4357    1.1843    0.2198 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.5798    0.2148   -0.8316 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8868    0.3241    1.2594 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5942    0.3324    2.2497 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.0358    0.0712    1.6275 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.1444   -0.2869   -0.5133 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.8878    0.2655    0.9996 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.5031    0.5953    2.7114 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.5297   -1.1201    2.1634 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.3413   -0.4115   -3.2026 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2259   -0.1564   -2.6129 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  1  0
  3  4  2  0
  4  5  1  0
  5  6  2  0
  6  7  1  0
  7  8  2  0
  8  9  1  0
  9 10  2  0
 10 11  1  0
 11 12  1  0
 12 13  1  0
 12 14  2  0
 10 15  1  0
 15 16  2  0
 15 17  1  0
 17 18  2  0
 18 19  1  0
 19 20  1  0
 20 21  2  0
 21  3  1  0
 20  6  1  0
 18  8  1  0
  1 22  1  0
  1 23  1  0
  1 24  1  0
  4 25  1  0
  5 26  1  0
  9 27  1  0
 11 28  1  0
 13 29  1  0
 13 30  1  0
 13 31  1  0
 17 32  1  0
 21 33  1  0
M  END

  Mrv1652311012019412D          

 21 23  0  0  0  0            999 V2000
   -3.5724   -2.8875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8579   -2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8579   -1.6500    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1434   -2.8875    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4289   -2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7145   -2.8875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000   -2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145   -2.8875    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289   -2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289   -1.6500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434   -1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579   -1.6500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579   -2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434   -2.8875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5724   -1.2375    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.5724   -0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145   -1.2375    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000   -1.6500    0.0000 C   0  0  0  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
   -1.4289   -1.6500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1434   -1.2375    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0  0  0  0
  2  3  2  0  0  0  0
  2  4  1  0  0  0  0
  4  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  2  0  0  0  0
  9 14  1  0  0  0  0
 12 15  1  0  0  0  0
 15 16  1  0  0  0  0
 10 17  1  0  0  0  0
 17 18  1  0  0  0  0
  7 18  1  0  0  0  0
 18 19  2  0  0  0  0
 19 20  1  0  0  0  0
  5 20  1  0  0  0  0
 20 21  2  0  0  0  0
M  END
> <DATABASE_ID>
HMDB0240722

> <DATABASE_NAME>
hmdb

> <SMILES>
COC1=CC2=C(C=C1)N=C1C=C(NC(C)=O)C(=O)C=C1O2

> <INCHI_IDENTIFIER>
InChI=1S/C15H12N2O4/c1-8(18)16-11-6-12-15(7-13(11)19)21-14-5-9(20-2)3-4-10(14)17-12/h3-7H,1-2H3,(H,16,18)

> <INCHI_KEY>
DOTQQODPKREUTR-UHFFFAOYSA-N

> <FORMULA>
C15H12N2O4

> <MOLECULAR_WEIGHT>
284.271

> <EXACT_MASS>
284.079706874

> <JCHEM_ACCEPTOR_COUNT>
5

> <JCHEM_ATOM_COUNT>
33

> <JCHEM_AVERAGE_POLARIZABILITY>
29.105190621890394

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
1

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
N-(7-methoxy-3-oxo-3H-phenoxazin-2-yl)acetamide

> <ALOGPS_LOGP>
1.66

> <JCHEM_LOGP>
0.8549247983333332

> <ALOGPS_LOGS>
-3.32

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
3

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA_STRONGEST_ACIDIC>
12.884396536206783

> <JCHEM_PKA_STRONGEST_BASIC>
-1.1053999326085964

> <JCHEM_POLAR_SURFACE_AREA>
76.99000000000001

> <JCHEM_REFRACTIVITY>
79.47559999999999

> <JCHEM_ROTATABLE_BOND_COUNT>
2

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
1.37e-01 g/l

> <JCHEM_TRADITIONAL_IUPAC>
N-(7-methoxy-3-oxophenoxazin-2-yl)acetamide

> <JCHEM_VEBER_RULE>
0

$$$$

HMDB0240722
     RDKit          3D
2-Acetylamino-7-methoxy-3H-phenoxazin-3-one
 33 35  0  0  0  0  0  0  0  0999 V2000
   -6.6041    0.2261   -0.3490 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.5282    0.0847   -1.2549 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2262    0.0852   -0.7323 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0015    0.2190    0.6196 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7616    0.2273    1.1916 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6491    0.0922    0.3598 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4076    0.0986    0.9140 N   0  0  0  0  0  0  0  0  0  0  0  0
    0.6388   -0.0330    0.0889 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9480   -0.0381    0.5616 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0582   -0.1693   -0.2345 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3925   -0.1779    0.2156 N   0  0  0  0  0  0  0  0  0  0  0  0
    4.8198   -0.0550    1.5441 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.2948   -0.0833    1.8642 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0764    0.0819    2.5402 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.7913   -0.3030   -1.6021 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7673   -0.4274   -2.3871 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.5342   -0.3066   -2.1361 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4107   -0.1750   -1.3414 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8033   -0.1758   -1.8325 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8312   -0.0437   -0.9947 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1223   -0.0467   -1.5373 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.5165   -0.5847    0.4320 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.4357    1.1843    0.2198 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.5798    0.2148   -0.8316 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8868    0.3241    1.2594 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5942    0.3324    2.2497 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.0358    0.0712    1.6275 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.1444   -0.2869   -0.5133 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.8878    0.2655    0.9996 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.5031    0.5953    2.7114 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.5297   -1.1201    2.1634 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.3413   -0.4115   -3.2026 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2259   -0.1564   -2.6129 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  1  0
  3  4  2  0
  4  5  1  0
  5  6  2  0
  6  7  1  0
  7  8  2  0
  8  9  1  0
  9 10  2  0
 10 11  1  0
 11 12  1  0
 12 13  1  0
 12 14  2  0
 10 15  1  0
 15 16  2  0
 15 17  1  0
 17 18  2  0
 18 19  1  0
 19 20  1  0
 20 21  2  0
 21  3  1  0
 20  6  1  0
 18  8  1  0
  1 22  1  0
  1 23  1  0
  1 24  1  0
  4 25  1  0
  5 26  1  0
  9 27  1  0
 11 28  1  0
 13 29  1  0
 13 30  1  0
 13 31  1  0
 17 32  1  0
 21 33  1  0
M  END

HEADER    PROTEIN                                 01-NOV-20   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   01-NOV-20         0                                  
HETATM    1  C   UNK     0      -6.668  -5.390   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0      -5.335  -4.620   0.000  0.00  0.00           C+0
HETATM    3  O   UNK     0      -5.335  -3.080   0.000  0.00  0.00           O+0
HETATM    4  N   UNK     0      -4.001  -5.390   0.000  0.00  0.00           N+0
HETATM    5  C   UNK     0      -2.667  -4.620   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0      -1.334  -5.390   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       0.000  -4.620   0.000  0.00  0.00           C+0
HETATM    8  N   UNK     0       1.334  -5.390   0.000  0.00  0.00           N+0
HETATM    9  C   UNK     0       2.667  -4.620   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       2.667  -3.080   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       4.001  -2.310   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       5.335  -3.080   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       5.335  -4.620   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       4.001  -5.390   0.000  0.00  0.00           C+0
HETATM   15  O   UNK     0       6.668  -2.310   0.000  0.00  0.00           O+0
HETATM   16  C   UNK     0       6.668  -0.770   0.000  0.00  0.00           C+0
HETATM   17  O   UNK     0       1.334  -2.310   0.000  0.00  0.00           O+0
HETATM   18  C   UNK     0       0.000  -3.080   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0      -1.334  -2.310   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0      -2.667  -3.080   0.000  0.00  0.00           C+0
HETATM   21  O   UNK     0      -4.001  -2.310   0.000  0.00  0.00           O+0
CONECT    1    2                                                            
CONECT    2    1    3    4                                                  
CONECT    3    2                                                            
CONECT    4    2    5                                                       
CONECT    5    4    6   20                                                  
CONECT    6    5    7                                                       
CONECT    7    6    8   18                                                  
CONECT    8    7    9                                                       
CONECT    9    8   10   14                                                  
CONECT   10    9   11   17                                                  
CONECT   11   10   12                                                       
CONECT   12   11   13   15                                                  
CONECT   13   12   14                                                       
CONECT   14   13    9                                                       
CONECT   15   12   16                                                       
CONECT   16   15                                                            
CONECT   17   10   18                                                       
CONECT   18   17    7   19                                                  
CONECT   19   18   20                                                       
CONECT   20   19    5   21                                                  
CONECT   21   20                                                            
MASTER        0    0    0    0    0    0    0    0   21    0   46    0
END

COMPND    HMDB0240722
HETATM    1  C1  UNL     1      -6.604   0.226  -0.349  1.00  0.00           C  
HETATM    2  O1  UNL     1      -5.528   0.085  -1.255  1.00  0.00           O  
HETATM    3  C2  UNL     1      -4.226   0.085  -0.732  1.00  0.00           C  
HETATM    4  C3  UNL     1      -4.002   0.219   0.620  1.00  0.00           C  
HETATM    5  C4  UNL     1      -2.762   0.227   1.192  1.00  0.00           C  
HETATM    6  C5  UNL     1      -1.649   0.092   0.360  1.00  0.00           C  
HETATM    7  N1  UNL     1      -0.408   0.099   0.914  1.00  0.00           N  
HETATM    8  C6  UNL     1       0.639  -0.033   0.089  1.00  0.00           C  
HETATM    9  C7  UNL     1       1.948  -0.038   0.562  1.00  0.00           C  
HETATM   10  C8  UNL     1       3.058  -0.169  -0.235  1.00  0.00           C  
HETATM   11  N2  UNL     1       4.393  -0.178   0.216  1.00  0.00           N  
HETATM   12  C9  UNL     1       4.820  -0.055   1.544  1.00  0.00           C  
HETATM   13  C10 UNL     1       6.295  -0.083   1.864  1.00  0.00           C  
HETATM   14  O2  UNL     1       4.076   0.082   2.540  1.00  0.00           O  
HETATM   15  C11 UNL     1       2.791  -0.303  -1.602  1.00  0.00           C  
HETATM   16  O3  UNL     1       3.767  -0.427  -2.387  1.00  0.00           O  
HETATM   17  C12 UNL     1       1.534  -0.307  -2.136  1.00  0.00           C  
HETATM   18  C13 UNL     1       0.411  -0.175  -1.341  1.00  0.00           C  
HETATM   19  O4  UNL     1      -0.803  -0.176  -1.832  1.00  0.00           O  
HETATM   20  C14 UNL     1      -1.831  -0.044  -0.995  1.00  0.00           C  
HETATM   21  C15 UNL     1      -3.122  -0.047  -1.537  1.00  0.00           C  
HETATM   22  H1  UNL     1      -6.517  -0.585   0.432  1.00  0.00           H  
HETATM   23  H2  UNL     1      -6.436   1.184   0.220  1.00  0.00           H  
HETATM   24  H3  UNL     1      -7.580   0.215  -0.832  1.00  0.00           H  
HETATM   25  H4  UNL     1      -4.887   0.324   1.259  1.00  0.00           H  
HETATM   26  H5  UNL     1      -2.594   0.332   2.250  1.00  0.00           H  
HETATM   27  H6  UNL     1       2.036   0.071   1.627  1.00  0.00           H  
HETATM   28  H7  UNL     1       5.144  -0.287  -0.513  1.00  0.00           H  
HETATM   29  H8  UNL     1       6.888   0.265   1.000  1.00  0.00           H  
HETATM   30  H9  UNL     1       6.503   0.595   2.711  1.00  0.00           H  
HETATM   31  H10 UNL     1       6.530  -1.120   2.163  1.00  0.00           H  
HETATM   32  H11 UNL     1       1.341  -0.411  -3.203  1.00  0.00           H  
HETATM   33  H12 UNL     1      -3.226  -0.156  -2.613  1.00  0.00           H  
CONECT    1    2   22   23   24
CONECT    2    3
CONECT    3    4    4   21
CONECT    4    5   25
CONECT    5    6    6   26
CONECT    6    7   20
CONECT    7    8    8
CONECT    8    9   18
CONECT    9   10   10   27
CONECT   10   11   15
CONECT   11   12   28
CONECT   12   13   14   14
CONECT   13   29   30   31
CONECT   15   16   16   17
CONECT   17   18   18   32
CONECT   18   19
CONECT   19   20
CONECT   20   21   21
CONECT   21   33
END

HMDB0240722
     RDKit          3D
2-Acetylamino-7-methoxy-3H-phenoxazin-3-one
 33 35  0  0  0  0  0  0  0  0999 V2000
   -6.6041    0.2261   -0.3490 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.5282    0.0847   -1.2549 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2262    0.0852   -0.7323 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0015    0.2190    0.6196 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7616    0.2273    1.1916 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6491    0.0922    0.3598 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4076    0.0986    0.9140 N   0  0  0  0  0  0  0  0  0  0  0  0
    0.6388   -0.0330    0.0889 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9480   -0.0381    0.5616 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0582   -0.1693   -0.2345 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3925   -0.1779    0.2156 N   0  0  0  0  0  0  0  0  0  0  0  0
    4.8198   -0.0550    1.5441 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.2948   -0.0833    1.8642 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0764    0.0819    2.5402 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.7913   -0.3030   -1.6021 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7673   -0.4274   -2.3871 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.5342   -0.3066   -2.1361 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4107   -0.1750   -1.3414 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8033   -0.1758   -1.8325 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8312   -0.0437   -0.9947 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1223   -0.0467   -1.5373 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.5165   -0.5847    0.4320 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.4357    1.1843    0.2198 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.5798    0.2148   -0.8316 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8868    0.3241    1.2594 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5942    0.3324    2.2497 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.0358    0.0712    1.6275 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.1444   -0.2869   -0.5133 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.8878    0.2655    0.9996 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.5031    0.5953    2.7114 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.5297   -1.1201    2.1634 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.3413   -0.4115   -3.2026 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2259   -0.1564   -2.6129 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  1  0
  3  4  2  0
  4  5  1  0
  5  6  2  0
  6  7  1  0
  7  8  2  0
  8  9  1  0
  9 10  2  0
 10 11  1  0
 11 12  1  0
 12 13  1  0
 12 14  2  0
 10 15  1  0
 15 16  2  0
 15 17  1  0
 17 18  2  0
 18 19  1  0
 19 20  1  0
 20 21  2  0
 21  3  1  0
 20  6  1  0
 18  8  1  0
  1 22  1  0
  1 23  1  0
  1 24  1  0
  4 25  1  0
  5 26  1  0
  9 27  1  0
 11 28  1  0
 13 29  1  0
 13 30  1  0
 13 31  1  0
 17 32  1  0
 21 33  1  0
M  END

View in JSmol View Stereo Labels

Synonyms

Not Available

Chemical Formula

C₁₅H₁₂N₂O₄

Average Molecular Weight

284.271

Monoisotopic Molecular Weight

284.079706874

IUPAC Name

N-(7-methoxy-3-oxo-3H-phenoxazin-2-yl)acetamide

Traditional Name

N-(7-methoxy-3-oxophenoxazin-2-yl)acetamide

CAS Registry Number

Not Available

SMILES

COC1=CC2=C(C=C1)N=C1C=C(NC(C)=O)C(=O)C=C1O2

InChI Identifier

InChI=1S/C15H12N2O4/c1-8(18)16-11-6-12-15(7-13(11)19)21-14-5-9(20-2)3-4-10(14)17-12/h3-7H,1-2H3,(H,16,18)

InChI Key

DOTQQODPKREUTR-UHFFFAOYSA-N

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as phenoxazines. These are polycyclic aromatic compounds containing a phenoxazine moiety, which is a linear tricyclic system that consists of a two benzene rings joined by a 1,4-oxazine ring.

Kingdom

Organic compounds

Super Class

Organoheterocyclic compounds

Class

Benzoxazines

Sub Class

Phenoxazines

Direct Parent

Phenoxazines

Alternative Parents

Substituents

Phenoxazine
N-acetylarylamine
Anisole
N-arylamide
Alkyl aryl ether
Benzenoid
Heteroaromatic compound
Acetamide
Carboxamide group
Secondary carboxylic acid amide
Cyclic ketone
Carboxylic acid derivative
Ether
Oxacycle
Azacycle
Organooxygen compound
Organonitrogen compound
Organic oxygen compound
Organic nitrogen compound
Organopnictogen compound
Organic oxide
Hydrocarbon derivative
Carbonyl group
Aromatic heteropolycyclic compound

Molecular Framework

Aromatic heteropolycyclic compounds

External Descriptors

Not Available

Ontology

Physiological effect

Not Available

Disposition

Biological location

Non-excretory biofluid

Biofluid or Excreta

Blood (PMID: 32966057)

Excreta

Biofluid or Excreta

Urine (PMID: 32966057)

Source

Exogenous

Exogenous (HMDB: HMDB0240722)

Process

Not Available

Role

Not Available

Physical Properties

State

Not Available

Experimental Molecular 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

Experimental Chromatographic Properties

Not Available

Predicted Molecular Properties

Property	Value	Source
logP	1.66	ALOGPS
logP	0.85	ChemAxon
logS	-3.3	ALOGPS
pKa (Strongest Acidic)	12.88	ChemAxon
pKa (Strongest Basic)	-1.1	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	5	ChemAxon
Hydrogen Donor Count	1	ChemAxon
Polar Surface Area	76.99 Å²	ChemAxon
Rotatable Bond Count	2	ChemAxon
Refractivity	79.48 m³·mol⁻¹	ChemAxon
Polarizability	29.11 Å³	ChemAxon
Number of Rings	3	ChemAxon
Bioavailability	Yes	ChemAxon
Rule of Five	Yes	ChemAxon
Ghose Filter	Yes	ChemAxon
Veber's Rule	No	ChemAxon
MDDR-like Rule	No	ChemAxon

Predicted Chromatographic Properties

Predicted Collision Cross Sections

Predictor	Adduct Type	CCS Value (Å²)	Reference
DeepCCS	[M+H]+	169.3	30932474
DeepCCS	[M-H]-	166.942	30932474
DeepCCS	[M-2H]-	200.284	30932474
DeepCCS	[M+Na]+	175.511	30932474

Predicted Kovats Retention Indices

Underivatized

Metabolite	SMILES	Kovats RI Value	Column Type	Reference
2-Acetylamino-7-methoxy-3H-phenoxazin-3-one	COC1=CC2=C(C=C1)N=C1C=C(NC(C)=O)C(=O)C=C1O2	3864.4	Standard polar	33892256
2-Acetylamino-7-methoxy-3H-phenoxazin-3-one	COC1=CC2=C(C=C1)N=C1C=C(NC(C)=O)C(=O)C=C1O2	2820.8	Standard non polar	33892256
2-Acetylamino-7-methoxy-3H-phenoxazin-3-one	COC1=CC2=C(C=C1)N=C1C=C(NC(C)=O)C(=O)C=C1O2	2902.5	Semi standard non polar	33892256

Derivatized

Derivative Name / Structure	SMILES	Kovats RI Value	Column Type	Reference
2-Acetylamino-7-methoxy-3H-phenoxazin-3-one,1TMS,isomer #1	COC1=CC=C2N=C3C=C(N(C(C)=O)[Si](C)(C)C)C(=O)C=C3OC2=C1	2876.9	Semi standard non polar	33892256
2-Acetylamino-7-methoxy-3H-phenoxazin-3-one,1TMS,isomer #1	COC1=CC=C2N=C3C=C(N(C(C)=O)[Si](C)(C)C)C(=O)C=C3OC2=C1	2866.6	Standard non polar	33892256
2-Acetylamino-7-methoxy-3H-phenoxazin-3-one,1TMS,isomer #1	COC1=CC=C2N=C3C=C(N(C(C)=O)[Si](C)(C)C)C(=O)C=C3OC2=C1	3717.5	Standard polar	33892256
2-Acetylamino-7-methoxy-3H-phenoxazin-3-one,1TBDMS,isomer #1	COC1=CC=C2N=C3C=C(N(C(C)=O)[Si](C)(C)C(C)(C)C)C(=O)C=C3OC2=C1	3075.3	Semi standard non polar	33892256
2-Acetylamino-7-methoxy-3H-phenoxazin-3-one,1TBDMS,isomer #1	COC1=CC=C2N=C3C=C(N(C(C)=O)[Si](C)(C)C(C)(C)C)C(=O)C=C3OC2=C1	3076.4	Standard non polar	33892256
2-Acetylamino-7-methoxy-3H-phenoxazin-3-one,1TBDMS,isomer #1	COC1=CC=C2N=C3C=C(N(C(C)=O)[Si](C)(C)C(C)(C)C)C(=O)C=C3OC2=C1	3722.8	Standard polar	33892256

Spectra

GC-MS Spectra

Spectrum Type	Description	Splash Key	Deposition Date	Source	View
Predicted GC-MS	Predicted GC-MS Spectrum - 2-Acetylamino-7-methoxy-3H-phenoxazin-3-one GC-MS (Non-derivatized) - 70eV, Positive	Not Available	2021-10-12	Wishart Lab	View Spectrum

MS/MS Spectra

Spectrum Type	Description	Splash Key	Deposition Date	Source	View
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 2-Acetylamino-7-methoxy-3H-phenoxazin-3-one 10V, Positive-QTOF	splash10-000f-0090000000-71d2c60ec66d5c90daaf	2021-09-23	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 2-Acetylamino-7-methoxy-3H-phenoxazin-3-one 20V, Positive-QTOF	splash10-000f-0090000000-b32d1c809f8c711bceb8	2021-09-23	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 2-Acetylamino-7-methoxy-3H-phenoxazin-3-one 40V, Positive-QTOF	splash10-0076-0890000000-242476cd800d3ebfd812	2021-09-23	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 2-Acetylamino-7-methoxy-3H-phenoxazin-3-one 10V, Negative-QTOF	splash10-001i-0090000000-0cb9a28a142abe4c3533	2021-09-24	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 2-Acetylamino-7-methoxy-3H-phenoxazin-3-one 20V, Negative-QTOF	splash10-004i-0090000000-24990b029fa6408f169a	2021-09-24	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 2-Acetylamino-7-methoxy-3H-phenoxazin-3-one 40V, Negative-QTOF	splash10-004i-2190000000-514f55b396fe59c7fad4	2021-09-24	Wishart Lab	View Spectrum

Biological Properties

Cellular Locations

Not Available

Biospecimen Locations

Blood
Urine

Tissue Locations

Not Available

Pathways

Not Available

Name	SMPDB/PathBank	KEGG

Normal Concentrations

Biospecimen	Status	Value	Age	Sex	Condition	Reference	Details
Blood	Detected but not Quantified	Not Quantified	Adult (>18 years old)	Both	Normal	32966057	details
Urine	Detected but not Quantified	Not Quantified	Adult (>18 years old)	Both	Normal	32966057	details

Abnormal Concentrations

Not Available

Associated Disorders and Diseases

Disease References

None

Associated OMIM IDs

None

External Links

DrugBank ID

Not Available

Phenol Explorer Compound ID

Not Available

FooDB ID

Not Available

KNApSAcK ID

Not Available

Chemspider ID

28556321

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

68781031

PDB ID

Not Available

ChEBI ID

Not Available

Food Biomarker Ontology

Not Available

VMH ID

Not Available

MarkerDB ID

Not Available

Good Scents ID

Not Available

References

Synthesis Reference

Not Available

Material Safety Data Sheet (MSDS)

Not Available

General References

Not Available

Showing metabocard for 2-Acetylamino-7-methoxy-3H-phenoxazin-3-one (HMDB0240722)

MOL for HMDB0240722 (2-Acetylamino-7-methoxy-3H-phenoxazin-3-one)

3D MOL for HMDB0240722 (2-Acetylamino-7-methoxy-3H-phenoxazin-3-one)

3D SDF for HMDB0240722 (2-Acetylamino-7-methoxy-3H-phenoxazin-3-one)

3D-SDF for HMDB0240722 (2-Acetylamino-7-methoxy-3H-phenoxazin-3-one)

PDB for HMDB0240722 (2-Acetylamino-7-methoxy-3H-phenoxazin-3-one)

3D PDB for HMDB0240722 (2-Acetylamino-7-methoxy-3H-phenoxazin-3-one)

SMILES for HMDB0240722 (2-Acetylamino-7-methoxy-3H-phenoxazin-3-one)

INCHI for HMDB0240722 (2-Acetylamino-7-methoxy-3H-phenoxazin-3-one)

Structure for HMDB0240722 (2-Acetylamino-7-methoxy-3H-phenoxazin-3-one)

3D Structure for HMDB0240722 (2-Acetylamino-7-methoxy-3H-phenoxazin-3-one)

Predicted Collision Cross Sections

Predicted Kovats Retention Indices

Underivatized

Derivatized

GC-MS Spectra

MS/MS Spectra