Metabolite 12-Hydroxynevirapine

Name
12-Hydroxynevirapine
Description
Not Available
Structure
Synonyms
Not Available
UNII
Y6L0287CM4
CAS number
Not Available
Weight
Average: 282.2973
Monoisotopic: 282.111675712
Chemical Formula
C15H14N4O2
InChI Key
SEBABOMFNCVZGF-UHFFFAOYSA-N
InChI
InChI=1S/C15H14N4O2/c20-8-9-5-7-17-14-12(9)18-15(21)11-2-1-6-16-13(11)19(14)10-3-4-10/h1-2,5-7,10,20H,3-4,8H2,(H,18,21)
IUPAC Name
2-cyclopropyl-7-(hydroxymethyl)-2,4,9,15-tetraazatricyclo[9.4.0.0^{3,8}]pentadeca-1(11),3,5,7,9,12,14-heptaen-10-ol
SMILES
OCC1=C2N=C(O)C3=C(N=CC=C3)N(C3CC3)C2=NC=C1
Reactions
Spectra
SpectrumSpectrum TypeSplash Key
Predicted GC-MS Spectrum - GC-MSPredicted GC-MSsplash10-0il3-0690000000-89fefc747b118bc98b55
Predicted MS/MS Spectrum - 10V, Positive (Annotated)Predicted LC-MS/MSsplash10-001i-0090000000-6c39f0d212d73c7d7ee0
Predicted MS/MS Spectrum - 10V, Negative (Annotated)Predicted LC-MS/MSsplash10-001i-0090000000-97ef875ce4fac4e81300
Predicted MS/MS Spectrum - 20V, Positive (Annotated)Predicted LC-MS/MSsplash10-001i-0090000000-2063123693619e509314
Predicted MS/MS Spectrum - 20V, Negative (Annotated)Predicted LC-MS/MSsplash10-001i-0090000000-2bec5b20b4471e87d61a
Predicted MS/MS Spectrum - 40V, Positive (Annotated)Predicted LC-MS/MSsplash10-004i-0290000000-8d4dd9f64650b04c70a6
Predicted MS/MS Spectrum - 40V, Negative (Annotated)Predicted LC-MS/MSsplash10-00di-0190000000-7fdccf5807ec5919a165
Chromatographic Properties
Collision Cross Sections (CCS)
AdductCCS Value (Å2)Source typeSource
[M-H]-170.9351913
predicted
DarkChem Lite v0.1.0
[M-H]-170.8914913
predicted
DarkChem Lite v0.1.0
[M-H]-170.73808
predicted
DeepCCS 1.0 (2019)
[M+H]+171.0405913
predicted
DarkChem Lite v0.1.0
[M+H]+170.9346913
predicted
DarkChem Lite v0.1.0
[M+H]+173.09608
predicted
DeepCCS 1.0 (2019)
[M+Na]+170.7170913
predicted
DarkChem Lite v0.1.0
[M+Na]+179.60036
predicted
DeepCCS 1.0 (2019)
Human Metabolome Database
HMDB0013911
ChemSpider
399285
BindingDB
1577
ChEBI
145206
ChEMBL
CHEMBL39343
Predicted Properties
PropertyValueSource
Water Solubility0.426 mg/mLALOGPS
logP0.9ALOGPS
logP1.93Chemaxon
logS-2.8ALOGPS
pKa (Strongest Acidic)4.3Chemaxon
pKa (Strongest Basic)1.87Chemaxon
Physiological Charge0Chemaxon
Hydrogen Acceptor Count6Chemaxon
Hydrogen Donor Count2Chemaxon
Polar Surface Area81.84 Å2Chemaxon
Rotatable Bond Count2Chemaxon
Refractivity80.01 m3·mol-1Chemaxon
Polarizability28.9 Å3Chemaxon
Number of Rings4Chemaxon
Bioavailability1Chemaxon
Rule of FiveYesChemaxon
Ghose FilterYesChemaxon
Veber's RuleNoChemaxon
MDDR-like RuleNoChemaxon