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Record Information

Version

5.0

Status

Expected but not Quantified

Creation Date

2012-09-06 15:00:26 UTC

Update Date

2020-02-26 21:39:14 UTC

HMDB ID

HMDB0013913

Secondary Accession Numbers

HMDB13913

Metabolite Identification

Common Name

8-Hydroxynevirapine

Description

8-Hydroxynevirapine belongs to the class of organic compounds known as alkyldiarylamines. These are tertiary alkylarylamines having two aryl and one alkyl groups attached to the amino group. In humans, 8-hydroxynevirapine is involved in the nevirapine metabolism pathway. 8-Hydroxynevirapine is a primary metabolite. Primary metabolites are metabolically or physiologically essential metabolites. They are directly involved in an organism’s growth, development or reproduction. Based on a literature review a small amount of articles have been published on 8-Hydroxynevirapine.

Structure

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

HMDB0013913
     RDKit          3D
8-Hydroxynevirapine
 35 38  0  0  0  0  0  0  0  0999 V2000
    3.6995   -1.8825    0.1420 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9785   -0.6168   -0.1193 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5500    0.5161   -0.6292 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7922    1.6515   -0.8374 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4867    1.6471   -0.5385 N   0  0  0  0  0  0  0  0  0  0  0  0
    0.8810    0.5911   -0.0463 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6218   -0.5549    0.1689 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1480   -1.7825    0.6810 N   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1949   -2.2935    0.5637 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3108   -3.5307    0.7361 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3973   -1.5363    0.2728 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5203   -2.3334    0.1664 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7144   -1.7400   -0.1012 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8438   -2.5409   -0.2083 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8214   -0.3780   -0.2654 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7071    0.3672   -0.1550 N   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5030   -0.1631    0.1075 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4941    0.8813    0.1693 N   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9311    2.1952    0.4443 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1402    3.4095    0.6626 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0033    3.2817   -0.5497 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2136   -2.7559   -0.3530 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.7011   -1.7825   -0.3433 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.8695   -2.0572    1.2305 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.6225    0.4906   -0.8649 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.2906    2.5390   -1.2485 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.8487   -2.3644    1.1893 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4086   -3.4164    0.3015 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0640   -2.9029   -1.1456 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7968    0.0880   -0.4819 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8512    2.1624    1.1217 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.9417    3.5165    0.5950 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4948    4.1519    1.4633 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5573    3.1961   -1.5599 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8913    3.9466   -0.5687 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  2  0
  3  4  1  0
  4  5  2  0
  5  6  1  0
  6  7  2  0
  7  8  1  0
  8  9  1  0
  9 10  2  0
  9 11  1  0
 11 12  2  0
 12 13  1  0
 13 14  1  0
 13 15  2  0
 15 16  1  0
 16 17  2  0
 17 18  1  0
 18 19  1  0
 19 20  1  0
 20 21  1  0
  7  2  1  0
 17 11  1  0
 21 19  1  0
 18  6  1  0
  1 22  1  0
  1 23  1  0
  1 24  1  0
  3 25  1  0
  4 26  1  0
  8 27  1  0
 12 28  1  0
 14 29  1  0
 15 30  1  0
 19 31  1  0
 20 32  1  0
 20 33  1  0
 21 34  1  0
 21 35  1  0
M  END


  Mrv0541 06191310302D          

 21 24  0  0  0  0            999 V2000
    9.0940   -1.7777    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    8.3237   -4.3279    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    7.9112   -2.5208    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    6.9596   -4.5641    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    9.6876   -4.5641    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    8.3237   -5.1529    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.9112   -5.8671    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.7362   -5.8671    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.5805   -3.9700    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.0669   -3.9700    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.3969   -3.1659    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.2504   -3.1659    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.5799   -2.8999    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.7362   -2.5208    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.0675   -2.9000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.9455   -3.4794    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.1367   -4.3172    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.5106   -4.3172    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.4057   -2.0937    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.7019   -3.4794    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   11.4893   -3.2333    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  1 14  2  0  0  0  0
  2  6  1  0  0  0  0
  2  9  1  0  0  0  0
  2 10  1  0  0  0  0
  3 11  1  0  0  0  0
  3 14  1  0  0  0  0
  4  9  2  0  0  0  0
  4 17  1  0  0  0  0
  5 10  1  0  0  0  0
  5 18  2  0  0  0  0
  6  7  1  0  0  0  0
  6  8  1  0  0  0  0
  7  8  1  0  0  0  0
  9 11  1  0  0  0  0
 10 12  2  0  0  0  0
 11 13  2  0  0  0  0
 12 14  1  0  0  0  0
 12 15  1  0  0  0  0
 13 16  1  0  0  0  0
 13 19  1  0  0  0  0
 15 20  2  0  0  0  0
 16 17  2  0  0  0  0
 18 20  1  0  0  0  0
 20 21  1  0  0  0  0
M  END
> <DATABASE_ID>
HMDB0013913

> <DATABASE_NAME>
hmdb

> <SMILES>
CC1=C2NC(=O)C3=C(N=CC(O)=C3)N(C3CC3)C2=NC=C1

> <INCHI_IDENTIFIER>
InChI=1S/C15H14N4O2/c1-8-4-5-16-14-12(8)18-15(21)11-6-10(20)7-17-13(11)19(14)9-2-3-9/h4-7,9,20H,2-3H2,1H3,(H,18,21)

> <INCHI_KEY>
DZPVEPLRIKDBFC-UHFFFAOYSA-N

> <FORMULA>
C15H14N4O2

> <MOLECULAR_WEIGHT>
282.2973

> <EXACT_MASS>
282.111675712

> <JCHEM_ACCEPTOR_COUNT>
5

> <JCHEM_AVERAGE_POLARIZABILITY>
28.874732416289948

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
2

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
2-cyclopropyl-13-hydroxy-7-methyl-2,4,9,15-tetraazatricyclo[9.4.0.0³,⁸]pentadeca-1(11),3,5,7,12,14-hexaen-10-one

> <ALOGPS_LOGP>
1.20

> <JCHEM_LOGP>
2.184477457

> <ALOGPS_LOGS>
-2.85

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
4

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
10.517354836413626

> <JCHEM_PKA_STRONGEST_ACIDIC>
8.88068447850908

> <JCHEM_PKA_STRONGEST_BASIC>
5.060856736213049

> <JCHEM_POLAR_SURFACE_AREA>
78.35000000000001

> <JCHEM_REFRACTIVITY>
79.46289999999999

> <JCHEM_ROTATABLE_BOND_COUNT>
1

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
3.95e-01 g/l

> <JCHEM_TRADITIONAL_IUPAC>
2-cyclopropyl-13-hydroxy-7-methyl-2,4,9,15-tetraazatricyclo[9.4.0.0³,⁸]pentadeca-1(11),3,5,7,12,14-hexaen-10-one

> <JCHEM_VEBER_RULE>
0

$$$$

HMDB0013913
     RDKit          3D
8-Hydroxynevirapine
 35 38  0  0  0  0  0  0  0  0999 V2000
    3.6995   -1.8825    0.1420 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9785   -0.6168   -0.1193 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5500    0.5161   -0.6292 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7922    1.6515   -0.8374 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4867    1.6471   -0.5385 N   0  0  0  0  0  0  0  0  0  0  0  0
    0.8810    0.5911   -0.0463 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6218   -0.5549    0.1689 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1480   -1.7825    0.6810 N   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1949   -2.2935    0.5637 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3108   -3.5307    0.7361 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3973   -1.5363    0.2728 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5203   -2.3334    0.1664 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7144   -1.7400   -0.1012 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8438   -2.5409   -0.2083 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8214   -0.3780   -0.2654 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7071    0.3672   -0.1550 N   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5030   -0.1631    0.1075 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4941    0.8813    0.1693 N   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9311    2.1952    0.4443 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1402    3.4095    0.6626 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0033    3.2817   -0.5497 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2136   -2.7559   -0.3530 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.7011   -1.7825   -0.3433 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.8695   -2.0572    1.2305 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.6225    0.4906   -0.8649 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.2906    2.5390   -1.2485 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.8487   -2.3644    1.1893 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4086   -3.4164    0.3015 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0640   -2.9029   -1.1456 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7968    0.0880   -0.4819 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8512    2.1624    1.1217 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.9417    3.5165    0.5950 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4948    4.1519    1.4633 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5573    3.1961   -1.5599 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8913    3.9466   -0.5687 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  2  0
  3  4  1  0
  4  5  2  0
  5  6  1  0
  6  7  2  0
  7  8  1  0
  8  9  1  0
  9 10  2  0
  9 11  1  0
 11 12  2  0
 12 13  1  0
 13 14  1  0
 13 15  2  0
 15 16  1  0
 16 17  2  0
 17 18  1  0
 18 19  1  0
 19 20  1  0
 20 21  1  0
  7  2  1  0
 17 11  1  0
 21 19  1  0
 18  6  1  0
  1 22  1  0
  1 23  1  0
  1 24  1  0
  3 25  1  0
  4 26  1  0
  8 27  1  0
 12 28  1  0
 14 29  1  0
 15 30  1  0
 19 31  1  0
 20 32  1  0
 20 33  1  0
 21 34  1  0
 21 35  1  0
M  END

HEADER    PROTEIN                                 19-JUN-13   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   19-JUN-13         0                                  
HETATM    1  O   UNK     0      16.975  -3.318   0.000  0.00  0.00           O+0
HETATM    2  N   UNK     0      15.538  -8.079   0.000  0.00  0.00           N+0
HETATM    3  N   UNK     0      14.768  -4.706   0.000  0.00  0.00           N+0
HETATM    4  N   UNK     0      12.991  -8.520   0.000  0.00  0.00           N+0
HETATM    5  N   UNK     0      18.084  -8.520   0.000  0.00  0.00           N+0
HETATM    6  C   UNK     0      15.538  -9.619   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0      14.768 -10.952   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0      16.307 -10.952   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0      14.150  -7.411   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0      16.925  -7.411   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0      13.808  -5.910   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0      17.268  -5.910   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0      12.282  -5.413   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0      16.307  -4.706   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0      18.793  -5.413   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0      11.098  -6.495   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0      11.455  -8.059   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0      19.620  -8.059   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0      11.957  -3.908   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0      19.977  -6.495   0.000  0.00  0.00           C+0
HETATM   21  O   UNK     0      21.447  -6.035   0.000  0.00  0.00           O+0
CONECT    1   14                                                            
CONECT    2    6    9   10                                                  
CONECT    3   11   14                                                       
CONECT    4    9   17                                                       
CONECT    5   10   18                                                       
CONECT    6    2    7    8                                                  
CONECT    7    6    8                                                       
CONECT    8    6    7                                                       
CONECT    9    2    4   11                                                  
CONECT   10    2    5   12                                                  
CONECT   11    3    9   13                                                  
CONECT   12   10   14   15                                                  
CONECT   13   11   16   19                                                  
CONECT   14    1    3   12                                                  
CONECT   15   12   20                                                       
CONECT   16   13   17                                                       
CONECT   17    4   16                                                       
CONECT   18    5   20                                                       
CONECT   19   13                                                            
CONECT   20   15   18   21                                                  
CONECT   21   20                                                            
MASTER        0    0    0    0    0    0    0    0   21    0   48    0
END

COMPND    HMDB0013913
HETATM    1  C1  UNL     1       3.700  -1.883   0.142  1.00  0.00           C  
HETATM    2  C2  UNL     1       2.978  -0.617  -0.119  1.00  0.00           C  
HETATM    3  C3  UNL     1       3.550   0.516  -0.629  1.00  0.00           C  
HETATM    4  C4  UNL     1       2.792   1.651  -0.837  1.00  0.00           C  
HETATM    5  N1  UNL     1       1.487   1.647  -0.539  1.00  0.00           N  
HETATM    6  C5  UNL     1       0.881   0.591  -0.046  1.00  0.00           C  
HETATM    7  C6  UNL     1       1.622  -0.555   0.169  1.00  0.00           C  
HETATM    8  N2  UNL     1       1.148  -1.783   0.681  1.00  0.00           N  
HETATM    9  C7  UNL     1      -0.195  -2.294   0.564  1.00  0.00           C  
HETATM   10  O1  UNL     1      -0.311  -3.531   0.736  1.00  0.00           O  
HETATM   11  C8  UNL     1      -1.397  -1.536   0.273  1.00  0.00           C  
HETATM   12  C9  UNL     1      -2.520  -2.333   0.166  1.00  0.00           C  
HETATM   13  C10 UNL     1      -3.714  -1.740  -0.101  1.00  0.00           C  
HETATM   14  O2  UNL     1      -4.844  -2.541  -0.208  1.00  0.00           O  
HETATM   15  C11 UNL     1      -3.821  -0.378  -0.265  1.00  0.00           C  
HETATM   16  N3  UNL     1      -2.707   0.367  -0.155  1.00  0.00           N  
HETATM   17  C12 UNL     1      -1.503  -0.163   0.107  1.00  0.00           C  
HETATM   18  N4  UNL     1      -0.494   0.881   0.169  1.00  0.00           N  
HETATM   19  C13 UNL     1      -0.931   2.195   0.444  1.00  0.00           C  
HETATM   20  C14 UNL     1      -0.140   3.409   0.663  1.00  0.00           C  
HETATM   21  C15 UNL     1      -1.003   3.282  -0.550  1.00  0.00           C  
HETATM   22  H1  UNL     1       3.214  -2.756  -0.353  1.00  0.00           H  
HETATM   23  H2  UNL     1       4.701  -1.782  -0.343  1.00  0.00           H  
HETATM   24  H3  UNL     1       3.869  -2.057   1.230  1.00  0.00           H  
HETATM   25  H4  UNL     1       4.623   0.491  -0.865  1.00  0.00           H  
HETATM   26  H5  UNL     1       3.291   2.539  -1.249  1.00  0.00           H  
HETATM   27  H6  UNL     1       1.849  -2.364   1.189  1.00  0.00           H  
HETATM   28  H7  UNL     1      -2.409  -3.416   0.302  1.00  0.00           H  
HETATM   29  H8  UNL     1      -5.064  -2.903  -1.146  1.00  0.00           H  
HETATM   30  H9  UNL     1      -4.797   0.088  -0.482  1.00  0.00           H  
HETATM   31  H10 UNL     1      -1.851   2.162   1.122  1.00  0.00           H  
HETATM   32  H11 UNL     1       0.942   3.516   0.595  1.00  0.00           H  
HETATM   33  H12 UNL     1      -0.495   4.152   1.463  1.00  0.00           H  
HETATM   34  H13 UNL     1      -0.557   3.196  -1.560  1.00  0.00           H  
HETATM   35  H14 UNL     1      -1.891   3.947  -0.569  1.00  0.00           H  
CONECT    1    2   22   23   24
CONECT    2    3    3    7
CONECT    3    4   25
CONECT    4    5    5   26
CONECT    5    6
CONECT    6    7    7   18
CONECT    7    8
CONECT    8    9   27
CONECT    9   10   10   11
CONECT   11   12   12   17
CONECT   12   13   28
CONECT   13   14   15   15
CONECT   14   29
CONECT   15   16   30
CONECT   16   17   17
CONECT   17   18
CONECT   18   19
CONECT   19   20   21   31
CONECT   20   21   32   33
CONECT   21   34   35
END

HMDB0013913
     RDKit          3D
8-Hydroxynevirapine
 35 38  0  0  0  0  0  0  0  0999 V2000
    3.6995   -1.8825    0.1420 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9785   -0.6168   -0.1193 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5500    0.5161   -0.6292 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7922    1.6515   -0.8374 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4867    1.6471   -0.5385 N   0  0  0  0  0  0  0  0  0  0  0  0
    0.8810    0.5911   -0.0463 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6218   -0.5549    0.1689 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1480   -1.7825    0.6810 N   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1949   -2.2935    0.5637 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3108   -3.5307    0.7361 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3973   -1.5363    0.2728 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5203   -2.3334    0.1664 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7144   -1.7400   -0.1012 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8438   -2.5409   -0.2083 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8214   -0.3780   -0.2654 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7071    0.3672   -0.1550 N   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5030   -0.1631    0.1075 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4941    0.8813    0.1693 N   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9311    2.1952    0.4443 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1402    3.4095    0.6626 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0033    3.2817   -0.5497 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2136   -2.7559   -0.3530 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.7011   -1.7825   -0.3433 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.8695   -2.0572    1.2305 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.6225    0.4906   -0.8649 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.2906    2.5390   -1.2485 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.8487   -2.3644    1.1893 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4086   -3.4164    0.3015 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0640   -2.9029   -1.1456 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7968    0.0880   -0.4819 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8512    2.1624    1.1217 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.9417    3.5165    0.5950 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4948    4.1519    1.4633 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5573    3.1961   -1.5599 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8913    3.9466   -0.5687 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  2  0
  3  4  1  0
  4  5  2  0
  5  6  1  0
  6  7  2  0
  7  8  1  0
  8  9  1  0
  9 10  2  0
  9 11  1  0
 11 12  2  0
 12 13  1  0
 13 14  1  0
 13 15  2  0
 15 16  1  0
 16 17  2  0
 17 18  1  0
 18 19  1  0
 19 20  1  0
 20 21  1  0
  7  2  1  0
 17 11  1  0
 21 19  1  0
 18  6  1  0
  1 22  1  0
  1 23  1  0
  1 24  1  0
  3 25  1  0
  4 26  1  0
  8 27  1  0
 12 28  1  0
 14 29  1  0
 15 30  1  0
 19 31  1  0
 20 32  1  0
 20 33  1  0
 21 34  1  0
 21 35  1  0
M  END

View in JSmol View Stereo Labels

Synonyms

Not Available

Chemical Formula

C₁₅H₁₄N₄O₂

Average Molecular Weight

282.2973

Monoisotopic Molecular Weight

282.111675712

IUPAC Name

2-cyclopropyl-13-hydroxy-7-methyl-2,4,9,15-tetraazatricyclo[9.4.0.0³,⁸]pentadeca-1(11),3,5,7,12,14-hexaen-10-one

Traditional Name

2-cyclopropyl-13-hydroxy-7-methyl-2,4,9,15-tetraazatricyclo[9.4.0.0³,⁸]pentadeca-1(11),3,5,7,12,14-hexaen-10-one

CAS Registry Number

Not Available

SMILES

CC1=C2NC(=O)C3=C(N=CC(O)=C3)N(C3CC3)C2=NC=C1

InChI Identifier

InChI=1S/C15H14N4O2/c1-8-4-5-16-14-12(8)18-15(21)11-6-10(20)7-17-13(11)19(14)9-2-3-9/h4-7,9,20H,2-3H2,1H3,(H,18,21)

InChI Key

DZPVEPLRIKDBFC-UHFFFAOYSA-N

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as alkyldiarylamines. These are tertiary alkylarylamines having two aryl and one alkyl groups attached to the amino group.

Kingdom

Organic compounds

Super Class

Organic nitrogen compounds

Class

Organonitrogen compounds

Sub Class

Amines

Direct Parent

Alkyldiarylamines

Alternative Parents

Substituents

Alkyldiarylamine
Pyrido-para-diazepine
Para-diazepine
Methylpyridine
Hydroxypyridine
Imidolactam
Pyridine
Heteroaromatic compound
Vinylogous amide
Carboxamide group
Lactam
Secondary carboxylic acid amide
Carboxylic acid derivative
Azacycle
Organoheterocyclic compound
Organic oxygen compound
Organooxygen compound
Hydrocarbon derivative
Organic oxide
Organopnictogen compound
Aromatic heteropolycyclic compound

Molecular Framework

Aromatic heteropolycyclic compounds

External Descriptors

Not Available

Ontology

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
Water Solubility	0.4 g/L	ALOGPS
logP	1.2	ALOGPS
logP	2.18	ChemAxon
logS	-2.8	ALOGPS
pKa (Strongest Acidic)	8.88	ChemAxon
pKa (Strongest Basic)	5.06	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	5	ChemAxon
Hydrogen Donor Count	2	ChemAxon
Polar Surface Area	78.35 Å²	ChemAxon
Rotatable Bond Count	1	ChemAxon
Refractivity	79.46 m³·mol⁻¹	ChemAxon
Polarizability	28.87 Å³	ChemAxon
Number of Rings	4	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
DarkChem	[M+H]+	164.05	31661259
DarkChem	[M-H]-	162.448	31661259
DeepCCS	[M+H]+	171.486	30932474
DeepCCS	[M-H]-	169.128	30932474
DeepCCS	[M-2H]-	202.972	30932474
DeepCCS	[M+Na]+	178.199	30932474
AllCCS	[M+H]+	165.7	32859911
AllCCS	[M+H-H2O]+	162.2	32859911
AllCCS	[M+NH4]+	168.9	32859911
AllCCS	[M+Na]+	169.9	32859911
AllCCS	[M-H]-	167.4	32859911
AllCCS	[M+Na-2H]-	166.7	32859911
AllCCS	[M+HCOO]-	166.0	32859911

Predicted Retention Times

Underivatized

Chromatographic Method	Retention Time	Reference
Measured using a Waters Acquity ultraperformance liquid chromatography (UPLC) ethylene-bridged hybrid (BEH) C18 column (100 mm × 2.1 mm; 1.7 μmparticle diameter). Predicted by Afia on May 17, 2022. Predicted by Afia on May 17, 2022.	2.49 minutes	32390414
Predicted by Siyang on May 30, 2022	10.4344 minutes	33406817
Predicted by Siyang using ReTip algorithm on June 8, 2022	2.17 minutes	32390414
AjsUoB = Accucore 150 Amide HILIC with 10mM Ammonium Formate, 0.1% Formic Acid	28.0 seconds	40023050
Fem_Long = Waters ACQUITY UPLC HSS T3 C18 with Water:MeOH and 0.1% Formic Acid	907.9 seconds	40023050
Fem_Lipids = Ascentis Express C18 with (60:40 water:ACN):(90:10 IPA:ACN) and 10mM NH4COOH + 0.1% Formic Acid	219.8 seconds	40023050
Life_Old = Waters ACQUITY UPLC BEH C18 with Water:(20:80 acetone:ACN) and 0.1% Formic Acid	110.9 seconds	40023050
Life_New = RP Waters ACQUITY UPLC HSS T3 C18 with Water:(30:70 MeOH:ACN) and 0.1% Formic Acid	145.8 seconds	40023050
RIKEN = Waters ACQUITY UPLC BEH C18 with Water:ACN and 0.1% Formic Acid	62.9 seconds	40023050
Eawag_XBridgeC18 = XBridge C18 3.5u 2.1x50 mm with Water:MeOH and 0.1% Formic Acid	344.6 seconds	40023050
BfG_NTS_RP1 =Agilent Zorbax Eclipse Plus C18 (2.1 mm x 150 mm, 3.5 um) with Water:ACN and 0.1% Formic Acid	459.2 seconds	40023050
HILIC_BDD_2 = Merck SeQuant ZIC-HILIC with ACN(0.1% formic acid):water(16 mM ammonium formate)	115.7 seconds	40023050
UniToyama_Atlantis = RP Waters Atlantis T3 (2.1 x 150 mm, 5 um) with ACN:Water and 0.1% Formic Acid	718.9 seconds	40023050
BDD_C18 = Hypersil Gold 1.9µm C18 with Water:ACN and 0.1% Formic Acid	109.3 seconds	40023050
UFZ_Phenomenex = Kinetex Core-Shell C18 2.6 um, 3.0 x 100 mm, Phenomenex with Water:MeOH and 0.1% Formic Acid	1281.8 seconds	40023050
SNU_RIKEN_POS = Waters ACQUITY UPLC BEH C18 with Water:ACN and 0.1% Formic Acid	212.5 seconds	40023050
RPMMFDA = Waters ACQUITY UPLC BEH C18 with Water:ACN and 0.1% Formic Acid	288.5 seconds	40023050
MTBLS87 = Merck SeQuant ZIC-pHILIC column with ACN:Water and :ammonium carbonate	391.0 seconds	40023050
KI_GIAR_zic_HILIC_pH2_7 = Merck SeQuant ZIC-HILIC with ACN:Water and 0.1% FA	138.1 seconds	40023050
Meister zic-pHILIC pH9.3 = Merck SeQuant ZIC-pHILIC column with ACN:Water 5mM NH4Ac pH9.3 and 5mM ammonium acetate in water	153.7 seconds	40023050

Predicted Kovats Retention Indices

Underivatized

Metabolite	SMILES	Kovats RI Value	Column Type	Reference
8-Hydroxynevirapine	CC1=C2NC(=O)C3=C(N=CC(O)=C3)N(C3CC3)C2=NC=C1	3722.3	Standard polar	33892256
8-Hydroxynevirapine	CC1=C2NC(=O)C3=C(N=CC(O)=C3)N(C3CC3)C2=NC=C1	2640.4	Standard non polar	33892256
8-Hydroxynevirapine	CC1=C2NC(=O)C3=C(N=CC(O)=C3)N(C3CC3)C2=NC=C1	2577.2	Semi standard non polar	33892256

Derivatized

Derivative Name / Structure	SMILES	Kovats RI Value	Column Type	Reference
8-Hydroxynevirapine,1TMS,isomer #1	CC1=CC=NC2=C1NC(=O)C1=CC(O[Si](C)(C)C)=CN=C1N2C1CC1	2818.2	Semi standard non polar	33892256
8-Hydroxynevirapine,1TMS,isomer #2	CC1=CC=NC2=C1N([Si](C)(C)C)C(=O)C1=CC(O)=CN=C1N2C1CC1	2616.6	Semi standard non polar	33892256
8-Hydroxynevirapine,2TMS,isomer #1	CC1=CC=NC2=C1N([Si](C)(C)C)C(=O)C1=CC(O[Si](C)(C)C)=CN=C1N2C1CC1	2579.8	Semi standard non polar	33892256
8-Hydroxynevirapine,2TMS,isomer #1	CC1=CC=NC2=C1N([Si](C)(C)C)C(=O)C1=CC(O[Si](C)(C)C)=CN=C1N2C1CC1	2695.7	Standard non polar	33892256
8-Hydroxynevirapine,2TMS,isomer #1	CC1=CC=NC2=C1N([Si](C)(C)C)C(=O)C1=CC(O[Si](C)(C)C)=CN=C1N2C1CC1	3650.5	Standard polar	33892256
8-Hydroxynevirapine,1TBDMS,isomer #1	CC1=CC=NC2=C1NC(=O)C1=CC(O[Si](C)(C)C(C)(C)C)=CN=C1N2C1CC1	3016.8	Semi standard non polar	33892256
8-Hydroxynevirapine,1TBDMS,isomer #2	CC1=CC=NC2=C1N([Si](C)(C)C(C)(C)C)C(=O)C1=CC(O)=CN=C1N2C1CC1	2864.1	Semi standard non polar	33892256
8-Hydroxynevirapine,2TBDMS,isomer #1	CC1=CC=NC2=C1N([Si](C)(C)C(C)(C)C)C(=O)C1=CC(O[Si](C)(C)C(C)(C)C)=CN=C1N2C1CC1	2967.0	Semi standard non polar	33892256
8-Hydroxynevirapine,2TBDMS,isomer #1	CC1=CC=NC2=C1N([Si](C)(C)C(C)(C)C)C(=O)C1=CC(O[Si](C)(C)C(C)(C)C)=CN=C1N2C1CC1	3087.7	Standard non polar	33892256
8-Hydroxynevirapine,2TBDMS,isomer #1	CC1=CC=NC2=C1N([Si](C)(C)C(C)(C)C)C(=O)C1=CC(O[Si](C)(C)C(C)(C)C)=CN=C1N2C1CC1	3713.3	Standard polar	33892256

Spectra

GC-MS Spectra

Spectrum Type	Description	Splash Key	Deposition Date	Source	View
Predicted GC-MS	Predicted GC-MS Spectrum - 8-Hydroxynevirapine GC-MS (Non-derivatized) - 70eV, Positive	splash10-0gyd-1890000000-3cfd1974629bed42b767	2017-09-01	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - 8-Hydroxynevirapine GC-MS (1 TMS) - 70eV, Positive	splash10-002k-4869000000-743bd151da9f4be4e422	2017-10-06	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - 8-Hydroxynevirapine GC-MS (Non-derivatized) - 70eV, Positive	Not Available	2021-10-12	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - 8-Hydroxynevirapine 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 - 8-Hydroxynevirapine 10V, Positive-QTOF	splash10-001i-0090000000-4db90e3c8eec102dc152	2016-08-01	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 8-Hydroxynevirapine 20V, Positive-QTOF	splash10-001i-1090000000-6ea3809a97c81c186d3b	2016-08-01	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 8-Hydroxynevirapine 40V, Positive-QTOF	splash10-002f-9170000000-3221a4376c5aba7ebc60	2016-08-01	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 8-Hydroxynevirapine 10V, Negative-QTOF	splash10-001i-0090000000-083099581e2882f2398a	2016-08-03	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 8-Hydroxynevirapine 20V, Negative-QTOF	splash10-001l-0090000000-84dc076d6a97aa601ae1	2016-08-03	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 8-Hydroxynevirapine 40V, Negative-QTOF	splash10-05bg-1490000000-58b85aee49066a9e29e2	2016-08-03	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 8-Hydroxynevirapine 10V, Negative-QTOF	splash10-001i-0090000000-d72761c0346bc09759b0	2021-09-22	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 8-Hydroxynevirapine 20V, Negative-QTOF	splash10-001i-0090000000-4b8c21e2532f34918702	2021-09-22	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 8-Hydroxynevirapine 40V, Negative-QTOF	splash10-03di-1490000000-e98fafeba7360778c678	2021-09-22	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 8-Hydroxynevirapine 10V, Positive-QTOF	splash10-001i-0090000000-7c900f9f8b3f17914393	2021-09-22	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 8-Hydroxynevirapine 20V, Positive-QTOF	splash10-001l-0090000000-f426dd3b9af984da0078	2021-09-22	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 8-Hydroxynevirapine 40V, Positive-QTOF	splash10-004i-0190000000-ab9dbb520cbde3aefc95	2021-09-22	Wishart Lab	View Spectrum

Biological Properties

Cellular Locations

Extracellular

Biospecimen Locations

Blood
Urine

Tissue Locations

Kidney
Liver

Pathways

Name	SMPDB/PathBank	KEGG
Nevirapine Metabolism Pathway		Not Available

Normal Concentrations

Biospecimen	Status	Value	Age	Sex	Condition	Reference	Details
Blood	Expected but not Quantified	Not Quantified	Not Available	Not Available	Taking drug identified by DrugBank entry	21059682	details
Urine	Expected but not Quantified	Not Quantified	Not Available	Not Available	Taking drug identified by DrugBank entry	21059682	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

8930647

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

10755325

PDB ID

Not Available

ChEBI ID

174696

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 8-Hydroxynevirapine (HMDB0013913)

MOL for HMDB0013913 (8-Hydroxynevirapine)

3D MOL for HMDB0013913 (8-Hydroxynevirapine)

3D SDF for HMDB0013913 (8-Hydroxynevirapine)

3D-SDF for HMDB0013913 (8-Hydroxynevirapine)

PDB for HMDB0013913 (8-Hydroxynevirapine)

3D PDB for HMDB0013913 (8-Hydroxynevirapine)

SMILES for HMDB0013913 (8-Hydroxynevirapine)

INCHI for HMDB0013913 (8-Hydroxynevirapine)

Structure for HMDB0013913 (8-Hydroxynevirapine)

3D Structure for HMDB0013913 (8-Hydroxynevirapine)

Predicted Collision Cross Sections

Predicted Retention Times

Underivatized

Predicted Kovats Retention Indices

Underivatized

Derivatized

GC-MS Spectra

MS/MS Spectra