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Record Information

Version

5.0

Status

Expected but not Quantified

Creation Date

2013-07-04 18:56:32 UTC

Update Date

2019-07-23 07:14:59 UTC

HMDB ID

HMDB0060743

Secondary Accession Numbers

HMDB60743

Metabolite Identification

Common Name

3-Hydroxynevirapine glucuronide

Description

3-Hydroxynevirapine glucuronide is a metabolite of nevirapine. Nevirapine, also marketed under the trade name Viramune, is a non-nucleoside reverse transcriptase inhibitor (NNRTI) used to treat HIV-1 infection and AIDS. As with other antiretroviral drugs, HIV rapidly develops resistance if nevirapine is used alone, so recommended therapy consists of combinations of three or more antiretrovirals. (Wikipedia)

Structure

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

  Mrv0541 07041311562D          

 33 37  0  0  0  0            999 V2000
    1.9049   -0.5145    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.1237    0.8510    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.5189    0.2898    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2162    3.2347    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3912    3.2347    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.9401    1.6553    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6673    1.6553    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0884    0.2898    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8037    2.5203    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7305    0.5330    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4837    0.8510    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8768    0.5330    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.5775   -1.7219    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    7.0422   -1.0403    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    5.7548   -1.6603    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    6.6842   -0.2970    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    4.5470    1.3373    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0604    1.3373    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2162   -0.1120    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.1490    0.3847    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.3968   -0.9170    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.1517    1.8985    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    2.4556    1.8985    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    3.3912   -0.1120    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    3.8037    1.6953    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    0.6953    0.6078    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.9354   -2.4652    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.8649   -1.1019    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.2900   -2.3419    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.7910    1.1280    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.9717    0.3230    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.8616   -0.2353    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.5741   -0.8553    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  3  2  2  0  0  0  0
  5  4  1  0  0  0  0
  6  2  1  0  0  0  0
  8  1  1  0  0  0  0
  9  4  1  0  0  0  0
  9  5  1  0  0  0  0
 10  3  1  0  0  0  0
 11  7  2  0  0  0  0
 11  8  1  0  0  0  0
 12  8  2  0  0  0  0
 14 13  1  0  0  0  0
 15 13  1  0  0  0  0
 16 14  1  0  0  0  0
 17 10  2  0  0  0  0
 18 12  1  0  0  0  0
 19 10  1  0  0  0  0
 16 20  1  6  0  0  0
 21 15  1  0  0  0  0
 22  6  2  0  0  0  0
 22 17  1  0  0  0  0
 23  7  1  0  0  0  0
 23 18  2  0  0  0  0
 24 12  1  0  0  0  0
 24 19  2  0  0  0  0
 25  9  1  0  0  0  0
 25 17  1  0  0  0  0
 25 18  1  0  0  0  0
 26 11  1  0  0  0  0
 13 27  1  6  0  0  0
 14 28  1  1  0  0  0
 15 29  1  1  0  0  0
 30 20  2  0  0  0  0
 31 20  1  0  0  0  0
 32 16  1  0  0  0  0
 32 21  1  0  0  0  0
 33 19  1  0  0  0  0
 33 21  1  0  0  0  0
M  END

HMDB0060743
     RDKit          3D
3-Hydroxynevirapine glucuronide
 55 59  0  0  0  0  0  0  0  0999 V2000
   -0.2356    2.9039   -0.9939 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5061    2.1493   -0.8494 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6866    2.7057   -1.2854 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6788    3.9746   -1.8601 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8991    2.0200   -1.1625 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8553    0.8004   -0.6025 N   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7330    0.2194   -0.1648 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5095    0.8929   -0.2797 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2123    0.4630    0.1379 N   0  0  0  0  0  0  0  0  0  0  0  0
    0.0713   -0.5088    0.9513 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4184   -0.6623    1.1457 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.3870   -0.3602    0.1451 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2729    0.9834   -0.1920 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.2670    1.4078   -1.0228 C   0  0  2  0  0  0  0  0  0  0  0  0
    3.1789    0.8779   -2.4024 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0683    1.2311   -3.2194 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.1945    0.0268   -2.8565 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.6621    1.1904   -0.5122 C   0  0  1  0  0  0  0  0  0  0  0  0
    4.8613    2.0052    0.5884 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.8603   -0.2643   -0.1391 C   0  0  2  0  0  0  0  0  0  0  0  0
    4.8389   -1.0582   -1.2819 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.7269   -0.6145    0.8141 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.8119    0.3311    1.8616 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8392   -1.4186    1.6523 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2204   -2.0965    2.6751 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9274   -3.0064    3.4443 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2592   -3.2096    3.1555 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8748   -2.5376    2.1408 N   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1717   -1.6651    1.4130 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9919   -1.0627    0.3861 N   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1208   -1.7928   -0.0748 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9830   -1.5072   -1.2209 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.4991   -1.2774    0.1749 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4363    2.4823   -1.7578 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.3240    2.9138   -0.0161 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4426    3.9888   -1.1952 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5332    4.4025   -2.1871 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8082    2.4861   -1.5151 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.2744   -0.9739   -0.7476 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.1486    2.5278   -1.1257 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.4861   -0.9102   -3.1376 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.3636    1.3975   -1.3465 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.8004    2.1995    0.7757 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.8014   -0.3996    0.4418 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.5115   -1.9738   -1.1055 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.7961   -1.6241    1.2168 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.0216   -0.0753    2.7175 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.8219   -1.8949    2.8512 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4434   -3.5547    4.2650 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8107   -3.9217    3.7582 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0139   -2.9051    0.1492 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7824   -0.7013   -1.9243 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.4552   -2.3876   -1.7562 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.6644   -0.2335    0.5134 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.2481   -1.9833    0.5597 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
  3  5  1  0
  5  6  2  0
  6  7  1  0
  7  8  2  0
  8  9  1  0
  9 10  2  0
 10 11  1  0
 11 12  1  0
 12 13  1  0
 13 14  1  0
 14 15  1  0
 15 16  2  0
 15 17  1  0
 14 18  1  0
 18 19  1  0
 18 20  1  0
 20 21  1  0
 20 22  1  0
 22 23  1  0
 10 24  1  0
 24 25  2  0
 25 26  1  0
 26 27  2  0
 27 28  1  0
 28 29  2  0
 29 30  1  0
 30 31  1  0
 31 32  1  0
 32 33  1  0
  8  2  1  0
 22 12  1  0
 29 24  1  0
 33 31  1  0
 30  7  1  0
  1 34  1  0
  1 35  1  0
  1 36  1  0
  4 37  1  0
  5 38  1  0
 12 39  1  0
 14 40  1  6
 17 41  1  0
 18 42  1  6
 19 43  1  0
 20 44  1  1
 21 45  1  0
 22 46  1  1
 23 47  1  0
 25 48  1  0
 26 49  1  0
 27 50  1  0
 31 51  1  0
 32 52  1  0
 32 53  1  0
 33 54  1  0
 33 55  1  0
M  END

  Mrv0541 07041311562D          

 33 37  0  0  0  0            999 V2000
    1.9049   -0.5145    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.1237    0.8510    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.5189    0.2898    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2162    3.2347    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3912    3.2347    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.9401    1.6553    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6673    1.6553    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0884    0.2898    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8037    2.5203    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7305    0.5330    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4837    0.8510    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8768    0.5330    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.5775   -1.7219    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    7.0422   -1.0403    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    5.7548   -1.6603    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    6.6842   -0.2970    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    4.5470    1.3373    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0604    1.3373    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2162   -0.1120    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.1490    0.3847    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.3968   -0.9170    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.1517    1.8985    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    2.4556    1.8985    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    3.3912   -0.1120    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    3.8037    1.6953    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    0.6953    0.6078    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.9354   -2.4652    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.8649   -1.1019    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.2900   -2.3419    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.7910    1.1280    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.9717    0.3230    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.8616   -0.2353    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.5741   -0.8553    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  3  2  2  0  0  0  0
  5  4  1  0  0  0  0
  6  2  1  0  0  0  0
  8  1  1  0  0  0  0
  9  4  1  0  0  0  0
  9  5  1  0  0  0  0
 10  3  1  0  0  0  0
 11  7  2  0  0  0  0
 11  8  1  0  0  0  0
 12  8  2  0  0  0  0
 14 13  1  0  0  0  0
 15 13  1  0  0  0  0
 16 14  1  0  0  0  0
 17 10  2  0  0  0  0
 18 12  1  0  0  0  0
 19 10  1  0  0  0  0
 16 20  1  6  0  0  0
 21 15  1  0  0  0  0
 22  6  2  0  0  0  0
 22 17  1  0  0  0  0
 23  7  1  0  0  0  0
 23 18  2  0  0  0  0
 24 12  1  0  0  0  0
 24 19  2  0  0  0  0
 25  9  1  0  0  0  0
 25 17  1  0  0  0  0
 25 18  1  0  0  0  0
 26 11  1  0  0  0  0
 13 27  1  6  0  0  0
 14 28  1  1  0  0  0
 15 29  1  1  0  0  0
 30 20  2  0  0  0  0
 31 20  1  0  0  0  0
 32 16  1  0  0  0  0
 32 21  1  0  0  0  0
 33 19  1  0  0  0  0
 33 21  1  0  0  0  0
M  END
> <DATABASE_ID>
HMDB0060743

> <DATABASE_NAME>
hmdb

> <SMILES>
CC1=C2N=C(OC3O[C@@H]([C@@H](O)[C@H](O)[C@H]3O)C(O)=O)C3=C(N=CC=C3)N(C3CC3)C2=NC=C1O

> <INCHI_IDENTIFIER>
InChI=1S/C21H22N4O8/c1-8-11(26)7-23-18-12(8)24-19(10-3-2-6-22-17(10)25(18)9-4-5-9)33-21-15(29)13(27)14(28)16(32-21)20(30)31/h2-3,6-7,9,13-16,21,26-29H,4-5H2,1H3,(H,30,31)/t13-,14-,15+,16-,21?/m0/s1

> <INCHI_KEY>
GDAAYOYNGMRKSI-IQSUWLOCSA-N

> <FORMULA>
C21H22N4O8

> <MOLECULAR_WEIGHT>
458.4214

> <EXACT_MASS>
458.1437637

> <JCHEM_ACCEPTOR_COUNT>
11

> <JCHEM_AVERAGE_POLARIZABILITY>
44.31968020678327

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
5

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
(2S,3S,4S,5R)-6-({2-cyclopropyl-6-hydroxy-7-methyl-2,4,9,15-tetraazatricyclo[9.4.0.0³,⁸]pentadeca-1(11),3,5,7,9,12,14-heptaen-10-yl}oxy)-3,4,5-trihydroxyoxane-2-carboxylic acid

> <ALOGPS_LOGP>
0.48

> <JCHEM_LOGP>
-0.7376817121757181

> <ALOGPS_LOGS>
-2.51

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
5

> <JCHEM_PHYSIOLOGICAL_CHARGE>
-1

> <JCHEM_PKA>
9.542337218427836

> <JCHEM_PKA_STRONGEST_ACIDIC>
2.5412669074173544

> <JCHEM_PKA_STRONGEST_BASIC>
4.634766467036871

> <JCHEM_POLAR_SURFACE_AREA>
178.05999999999997

> <JCHEM_REFRACTIVITY>
112.49869999999999

> <JCHEM_ROTATABLE_BOND_COUNT>
4

> <JCHEM_RULE_OF_FIVE>
0

> <ALOGPS_SOLUBILITY>
1.43e+00 g/l

> <JCHEM_TRADITIONAL_IUPAC>
(2S,3S,4S,5R)-6-({2-cyclopropyl-6-hydroxy-7-methyl-2,4,9,15-tetraazatricyclo[9.4.0.0³,⁸]pentadeca-1(11),3,5,7,9,12,14-heptaen-10-yl}oxy)-3,4,5-trihydroxyoxane-2-carboxylic acid

> <JCHEM_VEBER_RULE>
0

$$$$

HMDB0060743
     RDKit          3D
3-Hydroxynevirapine glucuronide
 55 59  0  0  0  0  0  0  0  0999 V2000
   -0.2356    2.9039   -0.9939 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5061    2.1493   -0.8494 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6866    2.7057   -1.2854 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6788    3.9746   -1.8601 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8991    2.0200   -1.1625 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8553    0.8004   -0.6025 N   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7330    0.2194   -0.1648 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5095    0.8929   -0.2797 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2123    0.4630    0.1379 N   0  0  0  0  0  0  0  0  0  0  0  0
    0.0713   -0.5088    0.9513 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4184   -0.6623    1.1457 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.3870   -0.3602    0.1451 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2729    0.9834   -0.1920 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.2670    1.4078   -1.0228 C   0  0  2  0  0  0  0  0  0  0  0  0
    3.1789    0.8779   -2.4024 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0683    1.2311   -3.2194 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.1945    0.0268   -2.8565 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.6621    1.1904   -0.5122 C   0  0  1  0  0  0  0  0  0  0  0  0
    4.8613    2.0052    0.5884 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.8603   -0.2643   -0.1391 C   0  0  2  0  0  0  0  0  0  0  0  0
    4.8389   -1.0582   -1.2819 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.7269   -0.6145    0.8141 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.8119    0.3311    1.8616 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8392   -1.4186    1.6523 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2204   -2.0965    2.6751 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9274   -3.0064    3.4443 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2592   -3.2096    3.1555 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8748   -2.5376    2.1408 N   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1717   -1.6651    1.4130 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9919   -1.0627    0.3861 N   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1208   -1.7928   -0.0748 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9830   -1.5072   -1.2209 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.4991   -1.2774    0.1749 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4363    2.4823   -1.7578 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.3240    2.9138   -0.0161 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4426    3.9888   -1.1952 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5332    4.4025   -2.1871 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8082    2.4861   -1.5151 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.2744   -0.9739   -0.7476 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.1486    2.5278   -1.1257 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.4861   -0.9102   -3.1376 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.3636    1.3975   -1.3465 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.8004    2.1995    0.7757 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.8014   -0.3996    0.4418 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.5115   -1.9738   -1.1055 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.7961   -1.6241    1.2168 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.0216   -0.0753    2.7175 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.8219   -1.8949    2.8512 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4434   -3.5547    4.2650 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8107   -3.9217    3.7582 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0139   -2.9051    0.1492 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7824   -0.7013   -1.9243 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.4552   -2.3876   -1.7562 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.6644   -0.2335    0.5134 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.2481   -1.9833    0.5597 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
  3  5  1  0
  5  6  2  0
  6  7  1  0
  7  8  2  0
  8  9  1  0
  9 10  2  0
 10 11  1  0
 11 12  1  0
 12 13  1  0
 13 14  1  0
 14 15  1  0
 15 16  2  0
 15 17  1  0
 14 18  1  0
 18 19  1  0
 18 20  1  0
 20 21  1  0
 20 22  1  0
 22 23  1  0
 10 24  1  0
 24 25  2  0
 25 26  1  0
 26 27  2  0
 27 28  1  0
 28 29  2  0
 29 30  1  0
 30 31  1  0
 31 32  1  0
 32 33  1  0
  8  2  1  0
 22 12  1  0
 29 24  1  0
 33 31  1  0
 30  7  1  0
  1 34  1  0
  1 35  1  0
  1 36  1  0
  4 37  1  0
  5 38  1  0
 12 39  1  0
 14 40  1  6
 17 41  1  0
 18 42  1  6
 19 43  1  0
 20 44  1  1
 21 45  1  0
 22 46  1  1
 23 47  1  0
 25 48  1  0
 26 49  1  0
 27 50  1  0
 31 51  1  0
 32 52  1  0
 32 53  1  0
 33 54  1  0
 33 55  1  0
M  END

HEADER    PROTEIN                                 04-JUL-13   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   04-JUL-13         0                                  
HETATM    1  C   UNK     0       3.556  -0.960   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0      11.431   1.589   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0      10.302   0.541   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       7.870   6.038   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       6.330   6.038   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0      11.088   3.090   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       3.112   3.090   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       3.898   0.541   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       7.100   4.705   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       8.830   0.995   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       2.770   1.589   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       5.370   0.995   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0      12.278  -3.214   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0      13.145  -1.942   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0      10.742  -3.099   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0      12.477  -0.554   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       8.488   2.496   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       5.713   2.496   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0       7.870  -0.209   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0      13.345   0.718   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0      10.074  -1.712   0.000  0.00  0.00           C+0
HETATM   22  N   UNK     0       9.617   3.544   0.000  0.00  0.00           N+0
HETATM   23  N   UNK     0       4.584   3.544   0.000  0.00  0.00           N+0
HETATM   24  N   UNK     0       6.330  -0.209   0.000  0.00  0.00           N+0
HETATM   25  N   UNK     0       7.100   3.165   0.000  0.00  0.00           N+0
HETATM   26  O   UNK     0       1.298   1.135   0.000  0.00  0.00           O+0
HETATM   27  O   UNK     0      12.946  -4.602   0.000  0.00  0.00           O+0
HETATM   28  O   UNK     0      14.681  -2.057   0.000  0.00  0.00           O+0
HETATM   29  O   UNK     0       9.875  -4.372   0.000  0.00  0.00           O+0
HETATM   30  O   UNK     0      12.677   2.106   0.000  0.00  0.00           O+0
HETATM   31  O   UNK     0      14.881   0.603   0.000  0.00  0.00           O+0
HETATM   32  O   UNK     0      10.942  -0.439   0.000  0.00  0.00           O+0
HETATM   33  O   UNK     0       8.538  -1.597   0.000  0.00  0.00           O+0
CONECT    1    8                                                            
CONECT    2    3    6                                                       
CONECT    3    2   10                                                       
CONECT    4    5    9                                                       
CONECT    5    4    9                                                       
CONECT    6    2   22                                                       
CONECT    7   11   23                                                       
CONECT    8    1   11   12                                                  
CONECT    9    4    5   25                                                  
CONECT   10    3   17   19                                                  
CONECT   11    7    8   26                                                  
CONECT   12    8   18   24                                                  
CONECT   13   14   15   27                                                  
CONECT   14   13   16   28                                                  
CONECT   15   13   21   29                                                  
CONECT   16   14   20   32                                                  
CONECT   17   10   22   25                                                  
CONECT   18   12   23   25                                                  
CONECT   19   10   24   33                                                  
CONECT   20   16   30   31                                                  
CONECT   21   15   32   33                                                  
CONECT   22    6   17                                                       
CONECT   23    7   18                                                       
CONECT   24   12   19                                                       
CONECT   25    9   17   18                                                  
CONECT   26   11                                                            
CONECT   27   13                                                            
CONECT   28   14                                                            
CONECT   29   15                                                            
CONECT   30   20                                                            
CONECT   31   20                                                            
CONECT   32   16   21                                                       
CONECT   33   19   21                                                       
MASTER        0    0    0    0    0    0    0    0   33    0   74    0
END

COMPND    HMDB0060743
HETATM    1  C1  UNL     1      -0.236   2.904  -0.994  1.00  0.00           C  
HETATM    2  C2  UNL     1      -1.506   2.149  -0.849  1.00  0.00           C  
HETATM    3  C3  UNL     1      -2.687   2.706  -1.285  1.00  0.00           C  
HETATM    4  O1  UNL     1      -2.679   3.975  -1.860  1.00  0.00           O  
HETATM    5  C4  UNL     1      -3.899   2.020  -1.163  1.00  0.00           C  
HETATM    6  N1  UNL     1      -3.855   0.800  -0.603  1.00  0.00           N  
HETATM    7  C5  UNL     1      -2.733   0.219  -0.165  1.00  0.00           C  
HETATM    8  C6  UNL     1      -1.510   0.893  -0.280  1.00  0.00           C  
HETATM    9  N2  UNL     1      -0.212   0.463   0.138  1.00  0.00           N  
HETATM   10  C7  UNL     1       0.071  -0.509   0.951  1.00  0.00           C  
HETATM   11  O2  UNL     1       1.418  -0.662   1.146  1.00  0.00           O  
HETATM   12  C8  UNL     1       2.387  -0.360   0.145  1.00  0.00           C  
HETATM   13  O3  UNL     1       2.273   0.983  -0.192  1.00  0.00           O  
HETATM   14  C9  UNL     1       3.267   1.408  -1.023  1.00  0.00           C  
HETATM   15  C10 UNL     1       3.179   0.878  -2.402  1.00  0.00           C  
HETATM   16  O4  UNL     1       4.068   1.231  -3.219  1.00  0.00           O  
HETATM   17  O5  UNL     1       2.194   0.027  -2.857  1.00  0.00           O  
HETATM   18  C11 UNL     1       4.662   1.190  -0.512  1.00  0.00           C  
HETATM   19  O6  UNL     1       4.861   2.005   0.588  1.00  0.00           O  
HETATM   20  C12 UNL     1       4.860  -0.264  -0.139  1.00  0.00           C  
HETATM   21  O7  UNL     1       4.839  -1.058  -1.282  1.00  0.00           O  
HETATM   22  C13 UNL     1       3.727  -0.614   0.814  1.00  0.00           C  
HETATM   23  O8  UNL     1       3.812   0.331   1.862  1.00  0.00           O  
HETATM   24  C14 UNL     1      -0.839  -1.419   1.652  1.00  0.00           C  
HETATM   25  C15 UNL     1      -0.220  -2.096   2.675  1.00  0.00           C  
HETATM   26  C16 UNL     1      -0.927  -3.006   3.444  1.00  0.00           C  
HETATM   27  C17 UNL     1      -2.259  -3.210   3.155  1.00  0.00           C  
HETATM   28  N3  UNL     1      -2.875  -2.538   2.141  1.00  0.00           N  
HETATM   29  C18 UNL     1      -2.172  -1.665   1.413  1.00  0.00           C  
HETATM   30  N4  UNL     1      -2.992  -1.063   0.386  1.00  0.00           N  
HETATM   31  C19 UNL     1      -4.121  -1.793  -0.075  1.00  0.00           C  
HETATM   32  C20 UNL     1      -4.983  -1.507  -1.221  1.00  0.00           C  
HETATM   33  C21 UNL     1      -5.499  -1.277   0.175  1.00  0.00           C  
HETATM   34  H1  UNL     1       0.436   2.482  -1.758  1.00  0.00           H  
HETATM   35  H2  UNL     1       0.324   2.914  -0.016  1.00  0.00           H  
HETATM   36  H3  UNL     1      -0.443   3.989  -1.195  1.00  0.00           H  
HETATM   37  H4  UNL     1      -3.533   4.402  -2.187  1.00  0.00           H  
HETATM   38  H5  UNL     1      -4.808   2.486  -1.515  1.00  0.00           H  
HETATM   39  H6  UNL     1       2.274  -0.974  -0.748  1.00  0.00           H  
HETATM   40  H7  UNL     1       3.149   2.528  -1.126  1.00  0.00           H  
HETATM   41  H8  UNL     1       2.486  -0.910  -3.138  1.00  0.00           H  
HETATM   42  H9  UNL     1       5.364   1.397  -1.346  1.00  0.00           H  
HETATM   43  H10 UNL     1       5.800   2.199   0.776  1.00  0.00           H  
HETATM   44  H11 UNL     1       5.801  -0.400   0.442  1.00  0.00           H  
HETATM   45  H12 UNL     1       4.511  -1.974  -1.105  1.00  0.00           H  
HETATM   46  H13 UNL     1       3.796  -1.624   1.217  1.00  0.00           H  
HETATM   47  H14 UNL     1       4.022  -0.075   2.718  1.00  0.00           H  
HETATM   48  H15 UNL     1       0.822  -1.895   2.851  1.00  0.00           H  
HETATM   49  H16 UNL     1      -0.443  -3.555   4.265  1.00  0.00           H  
HETATM   50  H17 UNL     1      -2.811  -3.922   3.758  1.00  0.00           H  
HETATM   51  H18 UNL     1      -4.014  -2.905   0.149  1.00  0.00           H  
HETATM   52  H19 UNL     1      -4.782  -0.701  -1.924  1.00  0.00           H  
HETATM   53  H20 UNL     1      -5.455  -2.388  -1.756  1.00  0.00           H  
HETATM   54  H21 UNL     1      -5.664  -0.233   0.513  1.00  0.00           H  
HETATM   55  H22 UNL     1      -6.248  -1.983   0.560  1.00  0.00           H  
CONECT    1    2   34   35   36
CONECT    2    3    3    8
CONECT    3    4    5
CONECT    4   37
CONECT    5    6    6   38
CONECT    6    7
CONECT    7    8    8   30
CONECT    8    9
CONECT    9   10   10
CONECT   10   11   24
CONECT   11   12
CONECT   12   13   22   39
CONECT   13   14
CONECT   14   15   18   40
CONECT   15   16   16   17
CONECT   17   41
CONECT   18   19   20   42
CONECT   19   43
CONECT   20   21   22   44
CONECT   21   45
CONECT   22   23   46
CONECT   23   47
CONECT   24   25   25   29
CONECT   25   26   48
CONECT   26   27   27   49
CONECT   27   28   50
CONECT   28   29   29
CONECT   29   30
CONECT   30   31
CONECT   31   32   33   51
CONECT   32   33   52   53
CONECT   33   54   55
END

HMDB0060743
     RDKit          3D
3-Hydroxynevirapine glucuronide
 55 59  0  0  0  0  0  0  0  0999 V2000
   -0.2356    2.9039   -0.9939 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5061    2.1493   -0.8494 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6866    2.7057   -1.2854 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6788    3.9746   -1.8601 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8991    2.0200   -1.1625 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8553    0.8004   -0.6025 N   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7330    0.2194   -0.1648 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5095    0.8929   -0.2797 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2123    0.4630    0.1379 N   0  0  0  0  0  0  0  0  0  0  0  0
    0.0713   -0.5088    0.9513 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4184   -0.6623    1.1457 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.3870   -0.3602    0.1451 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2729    0.9834   -0.1920 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.2670    1.4078   -1.0228 C   0  0  2  0  0  0  0  0  0  0  0  0
    3.1789    0.8779   -2.4024 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0683    1.2311   -3.2194 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.1945    0.0268   -2.8565 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.6621    1.1904   -0.5122 C   0  0  1  0  0  0  0  0  0  0  0  0
    4.8613    2.0052    0.5884 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.8603   -0.2643   -0.1391 C   0  0  2  0  0  0  0  0  0  0  0  0
    4.8389   -1.0582   -1.2819 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.7269   -0.6145    0.8141 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.8119    0.3311    1.8616 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8392   -1.4186    1.6523 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2204   -2.0965    2.6751 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9274   -3.0064    3.4443 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2592   -3.2096    3.1555 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8748   -2.5376    2.1408 N   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1717   -1.6651    1.4130 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9919   -1.0627    0.3861 N   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1208   -1.7928   -0.0748 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9830   -1.5072   -1.2209 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.4991   -1.2774    0.1749 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4363    2.4823   -1.7578 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.3240    2.9138   -0.0161 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4426    3.9888   -1.1952 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5332    4.4025   -2.1871 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8082    2.4861   -1.5151 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.2744   -0.9739   -0.7476 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.1486    2.5278   -1.1257 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.4861   -0.9102   -3.1376 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.3636    1.3975   -1.3465 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.8004    2.1995    0.7757 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.8014   -0.3996    0.4418 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.5115   -1.9738   -1.1055 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.7961   -1.6241    1.2168 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.0216   -0.0753    2.7175 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.8219   -1.8949    2.8512 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4434   -3.5547    4.2650 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8107   -3.9217    3.7582 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0139   -2.9051    0.1492 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7824   -0.7013   -1.9243 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.4552   -2.3876   -1.7562 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.6644   -0.2335    0.5134 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.2481   -1.9833    0.5597 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
  3  5  1  0
  5  6  2  0
  6  7  1  0
  7  8  2  0
  8  9  1  0
  9 10  2  0
 10 11  1  0
 11 12  1  0
 12 13  1  0
 13 14  1  0
 14 15  1  0
 15 16  2  0
 15 17  1  0
 14 18  1  0
 18 19  1  0
 18 20  1  0
 20 21  1  0
 20 22  1  0
 22 23  1  0
 10 24  1  0
 24 25  2  0
 25 26  1  0
 26 27  2  0
 27 28  1  0
 28 29  2  0
 29 30  1  0
 30 31  1  0
 31 32  1  0
 32 33  1  0
  8  2  1  0
 22 12  1  0
 29 24  1  0
 33 31  1  0
 30  7  1  0
  1 34  1  0
  1 35  1  0
  1 36  1  0
  4 37  1  0
  5 38  1  0
 12 39  1  0
 14 40  1  6
 17 41  1  0
 18 42  1  6
 19 43  1  0
 20 44  1  1
 21 45  1  0
 22 46  1  1
 23 47  1  0
 25 48  1  0
 26 49  1  0
 27 50  1  0
 31 51  1  0
 32 52  1  0
 32 53  1  0
 33 54  1  0
 33 55  1  0
M  END

View in JSmol View NMR Assignments View Stereo Labels

Synonyms

Not Available

Chemical Formula

C₂₁H₂₂N₄O₈

Average Molecular Weight

458.4214

Monoisotopic Molecular Weight

458.1437637

IUPAC Name

(2S,3S,4S,5R)-6-({2-cyclopropyl-6-hydroxy-7-methyl-2,4,9,15-tetraazatricyclo[9.4.0.0³,⁸]pentadeca-1(11),3,5,7,9,12,14-heptaen-10-yl}oxy)-3,4,5-trihydroxyoxane-2-carboxylic acid

Traditional Name

(2S,3S,4S,5R)-6-({2-cyclopropyl-6-hydroxy-7-methyl-2,4,9,15-tetraazatricyclo[9.4.0.0³,⁸]pentadeca-1(11),3,5,7,9,12,14-heptaen-10-yl}oxy)-3,4,5-trihydroxyoxane-2-carboxylic acid

CAS Registry Number

Not Available

SMILES

CC1=C2N=C(OC3O[C@@H]([C@@H](O)[C@H](O)[C@H]3O)C(O)=O)C3=C(N=CC=C3)N(C3CC3)C2=NC=C1O

InChI Identifier

InChI=1S/C21H22N4O8/c1-8-11(26)7-23-18-12(8)24-19(10-3-2-6-22-17(10)25(18)9-4-5-9)33-21-15(29)13(27)14(28)16(32-21)20(30)31/h2-3,6-7,9,13-16,21,26-29H,4-5H2,1H3,(H,30,31)/t13-,14-,15+,16-,21?/m0/s1

InChI Key

GDAAYOYNGMRKSI-IQSUWLOCSA-N

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as o-glucuronides. These are glucuronides in which the aglycone is linked to the carbohydrate unit through an O-glycosidic bond.

Kingdom

Organic compounds

Super Class

Organic oxygen compounds

Class

Organooxygen compounds

Sub Class

Carbohydrates and carbohydrate conjugates

Direct Parent

O-glucuronides

Alternative Parents

Substituents

1-o-glucuronide
O-glucuronide
Hexose monosaccharide
Alkyldiarylamine
Glycosyl compound
O-glycosyl compound
Pyrido-para-diazepine
Beta-hydroxy acid
Methylpyridine
Hydroxypyridine
Hydroxy acid
Monosaccharide
Oxane
Pyran
Pyridine
Imidolactone
Imidolactam
Heteroaromatic compound
Secondary alcohol
Organoheterocyclic compound
Carboxylic acid
Carboxylic acid derivative
Organic 1,3-dipolar compound
Propargyl-type 1,3-dipolar organic compound
Azacycle
Acetal
Monocarboxylic acid or derivatives
Polyol
Oxacycle
Organopnictogen compound
Alcohol
Hydrocarbon derivative
Organic nitrogen compound
Organic oxide
Organonitrogen compound
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 (HMDB: HMDB0060743)

Organ

Kidney (HMDB: HMDB0060743)
Liver (HMDB: HMDB0060743)

Excreta

Biofluid or Excreta

Urine (HMDB: HMDB0060743)

Cellular substructure

Cytoplasm (HMDB: HMDB0060743)

Source

Endogenous

Endogenous (HMDB: HMDB0060743)

Process

Naturally occurring process

Biological process

Biochemical pathway

Metabolic pathway

Nevirapine Metabolism Pathway (PathBank: SMP0000642)

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
Water Solubility	1.43 g/L	ALOGPS
logP	0.48	ALOGPS
logP	-0.74	ChemAxon
logS	-2.5	ALOGPS
pKa (Strongest Acidic)	2.54	ChemAxon
pKa (Strongest Basic)	4.63	ChemAxon
Physiological Charge	-1	ChemAxon
Hydrogen Acceptor Count	11	ChemAxon
Hydrogen Donor Count	5	ChemAxon
Polar Surface Area	178.06 Å²	ChemAxon
Rotatable Bond Count	4	ChemAxon
Refractivity	112.5 m³·mol⁻¹	ChemAxon
Polarizability	44.32 Å³	ChemAxon
Number of Rings	5	ChemAxon
Bioavailability	Yes	ChemAxon
Rule of Five	No	ChemAxon
Ghose Filter	No	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]+	205.802	31661259
DarkChem	[M-H]-	198.652	31661259
DeepCCS	[M+H]+	205.601	30932474
DeepCCS	[M-H]-	203.65	30932474
DeepCCS	[M-2H]-	236.89	30932474
DeepCCS	[M+Na]+	211.342	30932474
AllCCS	[M+H]+	203.9	32859911
AllCCS	[M+H-H2O]+	201.8	32859911
AllCCS	[M+NH4]+	205.8	32859911
AllCCS	[M+Na]+	206.3	32859911
AllCCS	[M-H]-	197.9	32859911
AllCCS	[M+Na-2H]-	198.0	32859911
AllCCS	[M+HCOO]-	198.3	32859911

Predicted Kovats Retention Indices

Underivatized

Metabolite	SMILES	Kovats RI Value	Column Type	Reference
3-Hydroxynevirapine glucuronide	CC1=C2N=C(OC3O[C@@H]([C@@H](O)[C@H](O)[C@H]3O)C(O)=O)C3=C(N=CC=C3)N(C3CC3)C2=NC=C1O	4753.6	Standard polar	33892256
3-Hydroxynevirapine glucuronide	CC1=C2N=C(OC3O[C@@H]([C@@H](O)[C@H](O)[C@H]3O)C(O)=O)C3=C(N=CC=C3)N(C3CC3)C2=NC=C1O	3540.2	Standard non polar	33892256
3-Hydroxynevirapine glucuronide	CC1=C2N=C(OC3O[C@@H]([C@@H](O)[C@H](O)[C@H]3O)C(O)=O)C3=C(N=CC=C3)N(C3CC3)C2=NC=C1O	3922.1	Semi standard non polar	33892256

Derivatized

Derivative Name / Structure	SMILES	Kovats RI Value	Column Type	Reference
3-Hydroxynevirapine glucuronide,1TMS,isomer #1	CC1=C(O)C=NC2=C1N=C(OC1O[C@H](C(=O)O)[C@@H](O[Si](C)(C)C)[C@H](O)[C@H]1O)C1=CC=CN=C1N2C1CC1	3811.3	Semi standard non polar	33892256
3-Hydroxynevirapine glucuronide,1TMS,isomer #2	CC1=C(O)C=NC2=C1N=C(OC1O[C@H](C(=O)O)[C@@H](O)[C@H](O[Si](C)(C)C)[C@H]1O)C1=CC=CN=C1N2C1CC1	3818.7	Semi standard non polar	33892256
3-Hydroxynevirapine glucuronide,1TMS,isomer #3	CC1=C(O)C=NC2=C1N=C(OC1O[C@H](C(=O)O)[C@@H](O)[C@H](O)[C@H]1O[Si](C)(C)C)C1=CC=CN=C1N2C1CC1	3823.6	Semi standard non polar	33892256
3-Hydroxynevirapine glucuronide,1TMS,isomer #4	CC1=C(O)C=NC2=C1N=C(OC1O[C@H](C(=O)O[Si](C)(C)C)[C@@H](O)[C@H](O)[C@H]1O)C1=CC=CN=C1N2C1CC1	3779.3	Semi standard non polar	33892256
3-Hydroxynevirapine glucuronide,1TMS,isomer #5	CC1=C(O[Si](C)(C)C)C=NC2=C1N=C(OC1O[C@H](C(=O)O)[C@@H](O)[C@H](O)[C@H]1O)C1=CC=CN=C1N2C1CC1	3820.2	Semi standard non polar	33892256
3-Hydroxynevirapine glucuronide,2TMS,isomer #1	CC1=C(O[Si](C)(C)C)C=NC2=C1N=C(OC1O[C@H](C(=O)O)[C@@H](O[Si](C)(C)C)[C@H](O)[C@H]1O)C1=CC=CN=C1N2C1CC1	3707.3	Semi standard non polar	33892256
3-Hydroxynevirapine glucuronide,2TMS,isomer #10	CC1=C(O[Si](C)(C)C)C=NC2=C1N=C(OC1O[C@H](C(=O)O[Si](C)(C)C)[C@@H](O)[C@H](O)[C@H]1O)C1=CC=CN=C1N2C1CC1	3714.7	Semi standard non polar	33892256
3-Hydroxynevirapine glucuronide,2TMS,isomer #2	CC1=C(O)C=NC2=C1N=C(OC1O[C@H](C(=O)O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@H](O)[C@H]1O)C1=CC=CN=C1N2C1CC1	3720.9	Semi standard non polar	33892256
3-Hydroxynevirapine glucuronide,2TMS,isomer #3	CC1=C(O)C=NC2=C1N=C(OC1O[C@H](C(=O)O)[C@@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]1O)C1=CC=CN=C1N2C1CC1	3715.5	Semi standard non polar	33892256
3-Hydroxynevirapine glucuronide,2TMS,isomer #4	CC1=C(O)C=NC2=C1N=C(OC1O[C@H](C(=O)O)[C@@H](O[Si](C)(C)C)[C@H](O)[C@H]1O[Si](C)(C)C)C1=CC=CN=C1N2C1CC1	3724.5	Semi standard non polar	33892256
3-Hydroxynevirapine glucuronide,2TMS,isomer #5	CC1=C(O[Si](C)(C)C)C=NC2=C1N=C(OC1O[C@H](C(=O)O)[C@@H](O)[C@H](O[Si](C)(C)C)[C@H]1O)C1=CC=CN=C1N2C1CC1	3720.1	Semi standard non polar	33892256
3-Hydroxynevirapine glucuronide,2TMS,isomer #6	CC1=C(O)C=NC2=C1N=C(OC1O[C@H](C(=O)O[Si](C)(C)C)[C@@H](O)[C@H](O[Si](C)(C)C)[C@H]1O)C1=CC=CN=C1N2C1CC1	3707.4	Semi standard non polar	33892256
3-Hydroxynevirapine glucuronide,2TMS,isomer #7	CC1=C(O)C=NC2=C1N=C(OC1O[C@H](C(=O)O)[C@@H](O)[C@H](O[Si](C)(C)C)[C@H]1O[Si](C)(C)C)C1=CC=CN=C1N2C1CC1	3734.8	Semi standard non polar	33892256
3-Hydroxynevirapine glucuronide,2TMS,isomer #8	CC1=C(O[Si](C)(C)C)C=NC2=C1N=C(OC1O[C@H](C(=O)O)[C@@H](O)[C@H](O)[C@H]1O[Si](C)(C)C)C1=CC=CN=C1N2C1CC1	3715.7	Semi standard non polar	33892256
3-Hydroxynevirapine glucuronide,2TMS,isomer #9	CC1=C(O)C=NC2=C1N=C(OC1O[C@H](C(=O)O[Si](C)(C)C)[C@@H](O)[C@H](O)[C@H]1O[Si](C)(C)C)C1=CC=CN=C1N2C1CC1	3713.2	Semi standard non polar	33892256
3-Hydroxynevirapine glucuronide,3TMS,isomer #1	CC1=C(O[Si](C)(C)C)C=NC2=C1N=C(OC1O[C@H](C(=O)O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@H](O)[C@H]1O)C1=CC=CN=C1N2C1CC1	3700.3	Semi standard non polar	33892256
3-Hydroxynevirapine glucuronide,3TMS,isomer #10	CC1=C(O[Si](C)(C)C)C=NC2=C1N=C(OC1O[C@H](C(=O)O[Si](C)(C)C)[C@@H](O)[C@H](O)[C@H]1O[Si](C)(C)C)C1=CC=CN=C1N2C1CC1	3703.2	Semi standard non polar	33892256
3-Hydroxynevirapine glucuronide,3TMS,isomer #2	CC1=C(O[Si](C)(C)C)C=NC2=C1N=C(OC1O[C@H](C(=O)O)[C@@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]1O)C1=CC=CN=C1N2C1CC1	3680.7	Semi standard non polar	33892256
3-Hydroxynevirapine glucuronide,3TMS,isomer #3	CC1=C(O[Si](C)(C)C)C=NC2=C1N=C(OC1O[C@H](C(=O)O)[C@@H](O[Si](C)(C)C)[C@H](O)[C@H]1O[Si](C)(C)C)C1=CC=CN=C1N2C1CC1	3687.8	Semi standard non polar	33892256
3-Hydroxynevirapine glucuronide,3TMS,isomer #4	CC1=C(O)C=NC2=C1N=C(OC1O[C@H](C(=O)O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]1O)C1=CC=CN=C1N2C1CC1	3690.4	Semi standard non polar	33892256
3-Hydroxynevirapine glucuronide,3TMS,isomer #5	CC1=C(O)C=NC2=C1N=C(OC1O[C@H](C(=O)O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@H](O)[C@H]1O[Si](C)(C)C)C1=CC=CN=C1N2C1CC1	3694.9	Semi standard non polar	33892256
3-Hydroxynevirapine glucuronide,3TMS,isomer #6	CC1=C(O)C=NC2=C1N=C(OC1O[C@H](C(=O)O)[C@@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]1O[Si](C)(C)C)C1=CC=CN=C1N2C1CC1	3696.8	Semi standard non polar	33892256
3-Hydroxynevirapine glucuronide,3TMS,isomer #7	CC1=C(O[Si](C)(C)C)C=NC2=C1N=C(OC1O[C@H](C(=O)O[Si](C)(C)C)[C@@H](O)[C@H](O[Si](C)(C)C)[C@H]1O)C1=CC=CN=C1N2C1CC1	3688.9	Semi standard non polar	33892256
3-Hydroxynevirapine glucuronide,3TMS,isomer #8	CC1=C(O[Si](C)(C)C)C=NC2=C1N=C(OC1O[C@H](C(=O)O)[C@@H](O)[C@H](O[Si](C)(C)C)[C@H]1O[Si](C)(C)C)C1=CC=CN=C1N2C1CC1	3703.6	Semi standard non polar	33892256
3-Hydroxynevirapine glucuronide,3TMS,isomer #9	CC1=C(O)C=NC2=C1N=C(OC1O[C@H](C(=O)O[Si](C)(C)C)[C@@H](O)[C@H](O[Si](C)(C)C)[C@H]1O[Si](C)(C)C)C1=CC=CN=C1N2C1CC1	3692.7	Semi standard non polar	33892256
3-Hydroxynevirapine glucuronide,4TMS,isomer #1	CC1=C(O[Si](C)(C)C)C=NC2=C1N=C(OC1O[C@H](C(=O)O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]1O)C1=CC=CN=C1N2C1CC1	3694.6	Semi standard non polar	33892256
3-Hydroxynevirapine glucuronide,4TMS,isomer #2	CC1=C(O[Si](C)(C)C)C=NC2=C1N=C(OC1O[C@H](C(=O)O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@H](O)[C@H]1O[Si](C)(C)C)C1=CC=CN=C1N2C1CC1	3699.4	Semi standard non polar	33892256
3-Hydroxynevirapine glucuronide,4TMS,isomer #3	CC1=C(O[Si](C)(C)C)C=NC2=C1N=C(OC1O[C@H](C(=O)O)[C@@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]1O[Si](C)(C)C)C1=CC=CN=C1N2C1CC1	3698.9	Semi standard non polar	33892256
3-Hydroxynevirapine glucuronide,4TMS,isomer #4	CC1=C(O)C=NC2=C1N=C(OC1O[C@H](C(=O)O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]1O[Si](C)(C)C)C1=CC=CN=C1N2C1CC1	3705.3	Semi standard non polar	33892256
3-Hydroxynevirapine glucuronide,4TMS,isomer #5	CC1=C(O[Si](C)(C)C)C=NC2=C1N=C(OC1O[C@H](C(=O)O[Si](C)(C)C)[C@@H](O)[C@H](O[Si](C)(C)C)[C@H]1O[Si](C)(C)C)C1=CC=CN=C1N2C1CC1	3705.5	Semi standard non polar	33892256
3-Hydroxynevirapine glucuronide,5TMS,isomer #1	CC1=C(O[Si](C)(C)C)C=NC2=C1N=C(OC1O[C@H](C(=O)O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]1O[Si](C)(C)C)C1=CC=CN=C1N2C1CC1	3729.0	Semi standard non polar	33892256
3-Hydroxynevirapine glucuronide,1TBDMS,isomer #1	CC1=C(O)C=NC2=C1N=C(OC1O[C@H](C(=O)O)[C@@H](O[Si](C)(C)C(C)(C)C)[C@H](O)[C@H]1O)C1=CC=CN=C1N2C1CC1	3981.0	Semi standard non polar	33892256
3-Hydroxynevirapine glucuronide,1TBDMS,isomer #2	CC1=C(O)C=NC2=C1N=C(OC1O[C@H](C(=O)O)[C@@H](O)[C@H](O[Si](C)(C)C(C)(C)C)[C@H]1O)C1=CC=CN=C1N2C1CC1	3988.1	Semi standard non polar	33892256
3-Hydroxynevirapine glucuronide,1TBDMS,isomer #3	CC1=C(O)C=NC2=C1N=C(OC1O[C@H](C(=O)O)[C@@H](O)[C@H](O)[C@H]1O[Si](C)(C)C(C)(C)C)C1=CC=CN=C1N2C1CC1	3999.2	Semi standard non polar	33892256
3-Hydroxynevirapine glucuronide,1TBDMS,isomer #4	CC1=C(O)C=NC2=C1N=C(OC1O[C@H](C(=O)O[Si](C)(C)C(C)(C)C)[C@@H](O)[C@H](O)[C@H]1O)C1=CC=CN=C1N2C1CC1	3987.2	Semi standard non polar	33892256
3-Hydroxynevirapine glucuronide,1TBDMS,isomer #5	CC1=C(O[Si](C)(C)C(C)(C)C)C=NC2=C1N=C(OC1O[C@H](C(=O)O)[C@@H](O)[C@H](O)[C@H]1O)C1=CC=CN=C1N2C1CC1	4004.4	Semi standard non polar	33892256
3-Hydroxynevirapine glucuronide,2TBDMS,isomer #1	CC1=C(O[Si](C)(C)C(C)(C)C)C=NC2=C1N=C(OC1O[C@H](C(=O)O)[C@@H](O[Si](C)(C)C(C)(C)C)[C@H](O)[C@H]1O)C1=CC=CN=C1N2C1CC1	4027.7	Semi standard non polar	33892256
3-Hydroxynevirapine glucuronide,2TBDMS,isomer #10	CC1=C(O[Si](C)(C)C(C)(C)C)C=NC2=C1N=C(OC1O[C@H](C(=O)O[Si](C)(C)C(C)(C)C)[C@@H](O)[C@H](O)[C@H]1O)C1=CC=CN=C1N2C1CC1	4039.8	Semi standard non polar	33892256
3-Hydroxynevirapine glucuronide,2TBDMS,isomer #2	CC1=C(O)C=NC2=C1N=C(OC1O[C@H](C(=O)O[Si](C)(C)C(C)(C)C)[C@@H](O[Si](C)(C)C(C)(C)C)[C@H](O)[C@H]1O)C1=CC=CN=C1N2C1CC1	4043.7	Semi standard non polar	33892256
3-Hydroxynevirapine glucuronide,2TBDMS,isomer #3	CC1=C(O)C=NC2=C1N=C(OC1O[C@H](C(=O)O)[C@@H](O[Si](C)(C)C(C)(C)C)[C@H](O[Si](C)(C)C(C)(C)C)[C@H]1O)C1=CC=CN=C1N2C1CC1	4006.3	Semi standard non polar	33892256
3-Hydroxynevirapine glucuronide,2TBDMS,isomer #4	CC1=C(O)C=NC2=C1N=C(OC1O[C@H](C(=O)O)[C@@H](O[Si](C)(C)C(C)(C)C)[C@H](O)[C@H]1O[Si](C)(C)C(C)(C)C)C1=CC=CN=C1N2C1CC1	4025.8	Semi standard non polar	33892256
3-Hydroxynevirapine glucuronide,2TBDMS,isomer #5	CC1=C(O[Si](C)(C)C(C)(C)C)C=NC2=C1N=C(OC1O[C@H](C(=O)O)[C@@H](O)[C@H](O[Si](C)(C)C(C)(C)C)[C@H]1O)C1=CC=CN=C1N2C1CC1	4038.3	Semi standard non polar	33892256
3-Hydroxynevirapine glucuronide,2TBDMS,isomer #6	CC1=C(O)C=NC2=C1N=C(OC1O[C@H](C(=O)O[Si](C)(C)C(C)(C)C)[C@@H](O)[C@H](O[Si](C)(C)C(C)(C)C)[C@H]1O)C1=CC=CN=C1N2C1CC1	4026.0	Semi standard non polar	33892256
3-Hydroxynevirapine glucuronide,2TBDMS,isomer #7	CC1=C(O)C=NC2=C1N=C(OC1O[C@H](C(=O)O)[C@@H](O)[C@H](O[Si](C)(C)C(C)(C)C)[C@H]1O[Si](C)(C)C(C)(C)C)C1=CC=CN=C1N2C1CC1	4035.7	Semi standard non polar	33892256
3-Hydroxynevirapine glucuronide,2TBDMS,isomer #8	CC1=C(O[Si](C)(C)C(C)(C)C)C=NC2=C1N=C(OC1O[C@H](C(=O)O)[C@@H](O)[C@H](O)[C@H]1O[Si](C)(C)C(C)(C)C)C1=CC=CN=C1N2C1CC1	4044.4	Semi standard non polar	33892256
3-Hydroxynevirapine glucuronide,2TBDMS,isomer #9	CC1=C(O)C=NC2=C1N=C(OC1O[C@H](C(=O)O[Si](C)(C)C(C)(C)C)[C@@H](O)[C@H](O)[C@H]1O[Si](C)(C)C(C)(C)C)C1=CC=CN=C1N2C1CC1	4050.1	Semi standard non polar	33892256
3-Hydroxynevirapine glucuronide,3TBDMS,isomer #1	CC1=C(O[Si](C)(C)C(C)(C)C)C=NC2=C1N=C(OC1O[C@H](C(=O)O[Si](C)(C)C(C)(C)C)[C@@H](O[Si](C)(C)C(C)(C)C)[C@H](O)[C@H]1O)C1=CC=CN=C1N2C1CC1	4121.3	Semi standard non polar	33892256
3-Hydroxynevirapine glucuronide,3TBDMS,isomer #10	CC1=C(O[Si](C)(C)C(C)(C)C)C=NC2=C1N=C(OC1O[C@H](C(=O)O[Si](C)(C)C(C)(C)C)[C@@H](O)[C@H](O)[C@H]1O[Si](C)(C)C(C)(C)C)C1=CC=CN=C1N2C1CC1	4138.2	Semi standard non polar	33892256
3-Hydroxynevirapine glucuronide,3TBDMS,isomer #2	CC1=C(O[Si](C)(C)C(C)(C)C)C=NC2=C1N=C(OC1O[C@H](C(=O)O)[C@@H](O[Si](C)(C)C(C)(C)C)[C@H](O[Si](C)(C)C(C)(C)C)[C@H]1O)C1=CC=CN=C1N2C1CC1	4091.8	Semi standard non polar	33892256
3-Hydroxynevirapine glucuronide,3TBDMS,isomer #3	CC1=C(O[Si](C)(C)C(C)(C)C)C=NC2=C1N=C(OC1O[C@H](C(=O)O)[C@@H](O[Si](C)(C)C(C)(C)C)[C@H](O)[C@H]1O[Si](C)(C)C(C)(C)C)C1=CC=CN=C1N2C1CC1	4107.9	Semi standard non polar	33892256
3-Hydroxynevirapine glucuronide,3TBDMS,isomer #4	CC1=C(O)C=NC2=C1N=C(OC1O[C@H](C(=O)O[Si](C)(C)C(C)(C)C)[C@@H](O[Si](C)(C)C(C)(C)C)[C@H](O[Si](C)(C)C(C)(C)C)[C@H]1O)C1=CC=CN=C1N2C1CC1	4096.2	Semi standard non polar	33892256
3-Hydroxynevirapine glucuronide,3TBDMS,isomer #5	CC1=C(O)C=NC2=C1N=C(OC1O[C@H](C(=O)O[Si](C)(C)C(C)(C)C)[C@@H](O[Si](C)(C)C(C)(C)C)[C@H](O)[C@H]1O[Si](C)(C)C(C)(C)C)C1=CC=CN=C1N2C1CC1	4117.9	Semi standard non polar	33892256
3-Hydroxynevirapine glucuronide,3TBDMS,isomer #6	CC1=C(O)C=NC2=C1N=C(OC1O[C@H](C(=O)O)[C@@H](O[Si](C)(C)C(C)(C)C)[C@H](O[Si](C)(C)C(C)(C)C)[C@H]1O[Si](C)(C)C(C)(C)C)C1=CC=CN=C1N2C1CC1	4111.1	Semi standard non polar	33892256
3-Hydroxynevirapine glucuronide,3TBDMS,isomer #7	CC1=C(O[Si](C)(C)C(C)(C)C)C=NC2=C1N=C(OC1O[C@H](C(=O)O[Si](C)(C)C(C)(C)C)[C@@H](O)[C@H](O[Si](C)(C)C(C)(C)C)[C@H]1O)C1=CC=CN=C1N2C1CC1	4109.1	Semi standard non polar	33892256
3-Hydroxynevirapine glucuronide,3TBDMS,isomer #8	CC1=C(O[Si](C)(C)C(C)(C)C)C=NC2=C1N=C(OC1O[C@H](C(=O)O)[C@@H](O)[C@H](O[Si](C)(C)C(C)(C)C)[C@H]1O[Si](C)(C)C(C)(C)C)C1=CC=CN=C1N2C1CC1	4121.7	Semi standard non polar	33892256
3-Hydroxynevirapine glucuronide,3TBDMS,isomer #9	CC1=C(O)C=NC2=C1N=C(OC1O[C@H](C(=O)O[Si](C)(C)C(C)(C)C)[C@@H](O)[C@H](O[Si](C)(C)C(C)(C)C)[C@H]1O[Si](C)(C)C(C)(C)C)C1=CC=CN=C1N2C1CC1	4112.0	Semi standard non polar	33892256

Spectra

GC-MS Spectra

Spectrum Type	Description	Splash Key	Deposition Date	Source	View
Predicted GC-MS	Predicted GC-MS Spectrum - 3-Hydroxynevirapine glucuronide GC-MS (Non-derivatized) - 70eV, Positive	splash10-06r6-9317400000-2486a8005a174aa31d9c	2017-09-20	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - 3-Hydroxynevirapine glucuronide GC-MS (3 TMS) - 70eV, Positive	splash10-0a4r-6614149000-bdd1a5d57eb2510cbf83	2017-10-06	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - 3-Hydroxynevirapine glucuronide 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 - 3-Hydroxynevirapine glucuronide 10V, Positive-QTOF	splash10-052f-0040900000-eac92ad12a89af325070	2017-10-06	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 3-Hydroxynevirapine glucuronide 20V, Positive-QTOF	splash10-00lr-0190000000-b1c04c610709f115b3a6	2017-10-06	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 3-Hydroxynevirapine glucuronide 40V, Positive-QTOF	splash10-016u-4190000000-8f19cc71fca2b4d1d15e	2017-10-06	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 3-Hydroxynevirapine glucuronide 10V, Negative-QTOF	splash10-0bt9-1220900000-79e85e6a466fdfa81581	2017-10-06	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 3-Hydroxynevirapine glucuronide 20V, Negative-QTOF	splash10-0040-7724900000-5ba110269c9e13ba9a3c	2017-10-06	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 3-Hydroxynevirapine glucuronide 40V, Negative-QTOF	splash10-001l-7491000000-2b21884c17147ef12b8a	2017-10-06	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 3-Hydroxynevirapine glucuronide 10V, Positive-QTOF	splash10-06r6-0200900000-392527fcbc53c24997d5	2021-10-12	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 3-Hydroxynevirapine glucuronide 20V, Positive-QTOF	splash10-053u-0138900000-e1edc6b7ef0b0839f035	2021-10-12	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 3-Hydroxynevirapine glucuronide 40V, Positive-QTOF	splash10-000x-1391000000-969715dedf14da6e7cb7	2021-10-12	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 3-Hydroxynevirapine glucuronide 10V, Negative-QTOF	splash10-0a4i-0010900000-92d9d6816c3293890bc0	2021-10-12	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 3-Hydroxynevirapine glucuronide 20V, Negative-QTOF	splash10-0540-1192400000-9809461a6cc5cd3e2d26	2021-10-12	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 3-Hydroxynevirapine glucuronide 40V, Negative-QTOF	splash10-000i-1090000000-66404caf8df43c572ef9	2021-10-12	Wishart Lab	View Spectrum

NMR Spectra

Spectrum Type	Description	Deposition Date	Source	View
Predicted 1D NMR	¹³C NMR Spectrum (1D, 100 MHz, D₂O, predicted)	2021-09-24	Wishart Lab	View Spectrum
Predicted 1D NMR	¹H NMR Spectrum (1D, 100 MHz, D₂O, predicted)	2021-09-24	Wishart Lab	View Spectrum
Predicted 1D NMR	¹³C NMR Spectrum (1D, 1000 MHz, D₂O, predicted)	2021-09-24	Wishart Lab	View Spectrum
Predicted 1D NMR	¹H NMR Spectrum (1D, 1000 MHz, D₂O, predicted)	2021-09-24	Wishart Lab	View Spectrum
Predicted 1D NMR	¹³C NMR Spectrum (1D, 200 MHz, D₂O, predicted)	2021-09-24	Wishart Lab	View Spectrum
Predicted 1D NMR	¹H NMR Spectrum (1D, 200 MHz, D₂O, predicted)	2021-09-24	Wishart Lab	View Spectrum
Predicted 1D NMR	¹³C NMR Spectrum (1D, 300 MHz, D₂O, predicted)	2021-09-24	Wishart Lab	View Spectrum
Predicted 1D NMR	¹H NMR Spectrum (1D, 300 MHz, D₂O, predicted)	2021-09-24	Wishart Lab	View Spectrum
Predicted 1D NMR	¹³C NMR Spectrum (1D, 400 MHz, D₂O, predicted)	2021-09-24	Wishart Lab	View Spectrum
Predicted 1D NMR	¹H NMR Spectrum (1D, 400 MHz, D₂O, predicted)	2021-09-24	Wishart Lab	View Spectrum
Predicted 1D NMR	¹³C NMR Spectrum (1D, 500 MHz, D₂O, predicted)	2021-09-24	Wishart Lab	View Spectrum
Predicted 1D NMR	¹H NMR Spectrum (1D, 500 MHz, D₂O, predicted)	2021-09-24	Wishart Lab	View Spectrum
Predicted 1D NMR	¹³C NMR Spectrum (1D, 600 MHz, D₂O, predicted)	2021-09-24	Wishart Lab	View Spectrum
Predicted 1D NMR	¹H NMR Spectrum (1D, 600 MHz, D₂O, predicted)	2021-09-24	Wishart Lab	View Spectrum
Predicted 1D NMR	¹³C NMR Spectrum (1D, 700 MHz, D₂O, predicted)	2021-09-24	Wishart Lab	View Spectrum
Predicted 1D NMR	¹H NMR Spectrum (1D, 700 MHz, D₂O, predicted)	2021-09-24	Wishart Lab	View Spectrum
Predicted 1D NMR	¹³C NMR Spectrum (1D, 800 MHz, D₂O, predicted)	2021-09-24	Wishart Lab	View Spectrum
Predicted 1D NMR	¹H NMR Spectrum (1D, 800 MHz, D₂O, predicted)	2021-09-24	Wishart Lab	View Spectrum
Predicted 1D NMR	¹³C NMR Spectrum (1D, 900 MHz, D₂O, predicted)	2021-09-24	Wishart Lab	View Spectrum
Predicted 1D NMR	¹H NMR Spectrum (1D, 900 MHz, D₂O, predicted)	2021-09-24	Wishart Lab	View Spectrum

Biological Properties

Cellular Locations

Cytoplasm

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	Normal	Not Available	details
Urine	Expected but not Quantified	Not Quantified	Not Available	Not Available	Normal	Not Available	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

35031776

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

131769937

PDB ID

Not Available

ChEBI ID

189987

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 3-Hydroxynevirapine glucuronide (HMDB0060743)

MOL for HMDB0060743 (3-Hydroxynevirapine glucuronide)

3D MOL for HMDB0060743 (3-Hydroxynevirapine glucuronide)

3D SDF for HMDB0060743 (3-Hydroxynevirapine glucuronide)

3D-SDF for HMDB0060743 (3-Hydroxynevirapine glucuronide)

PDB for HMDB0060743 (3-Hydroxynevirapine glucuronide)

3D PDB for HMDB0060743 (3-Hydroxynevirapine glucuronide)

SMILES for HMDB0060743 (3-Hydroxynevirapine glucuronide)

INCHI for HMDB0060743 (3-Hydroxynevirapine glucuronide)

Structure for HMDB0060743 (3-Hydroxynevirapine glucuronide)

3D Structure for HMDB0060743 (3-Hydroxynevirapine glucuronide)

Predicted Collision Cross Sections

Predicted Kovats Retention Indices

Underivatized

Derivatized

GC-MS Spectra

MS/MS Spectra

NMR Spectra