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Molecule
ID:72851
Structure
Similarity
Functional Group
Text
General Information
Structure
Molecular Formula
C₂₁H₂₁F₃N₄O
Molecular Mass
402.4128496
Exact Mass
402.16674597
Charge
0
InChI
InChI=1S/C21H21F3N4O/c1-2-8-27(11-16-4-3-5-17(22)9-16)12-21(29,13-28-15-25-14-26-28)19-7-6-18(23)10-20(19)24/h2-7,9-10,14-15,29H,1,8,11-13H2
InChIKey
HVGVWTUVQVPWKH-UHFFFAOYSA-N
Canonic Smiles
C=CCN(CC(c1ccc(cc1F)F)(Cn1ncnc1)O)Cc1cccc(c1)F
Isomeric Smiles
c1cc(cc(c1C(Cn1ncnc1)(CN(Cc1cccc(c1)F)CC=C)O)F)F
Calculated Properties
JChem
Acid pKa
12.856366
H Acceptors
4
H Donor
1
LogD (pH = 5.5)
1.2147849
LogD (pH = 7.4)
2.9730058
Log P
3.6349664
Molar Refractivity
117.0438
Polarizability
39.202045
Polar Surface Area
54.18
Rotatable Bonds
9
Lipinski's Rule of Five
true
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Molecular Spectra
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Molecule Details
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Data Source
Commercial Catalog
Selleck Chemicals
S2137
Academic Data
PubChem
42631260
Names and Identifiers
IUPAC Traditional name
2-(2,4-difluorophenyl)-1-{[(3-fluorophenyl)methyl](prop-2-en-1-yl)amino}-3-(1,2,4-triazol-1-yl)propan-2-ol
IUPAC name
2-(2,4-difluorophenyl)-1-{[(3-fluorophenyl)methyl](prop-2-en-1-yl)amino}-3-(1H-1,2,4-triazol-1-yl)propan-2-ol
Synonyms
Cytochrome P450 14a-demethylase inhibitor 1c
Registration numbers
PubChem SID
162037772
PubChem CID
42631260
CAS Number
1155361-01-5
Properties
Pharmacology Properties
Target
p450
Source
Safety Information
Storage Condition
-20°C
Source
Product Information
Salt Data
Free Base
Source
Molecule Details
Selleck Chemicals
S2137
Related research area: Infection
References
PubChem Literature
From Data Sources
•
Chai X et al. Eur J Med Chem. 2009 May;44(5):1913-20
Bioactivity
PubChem BioAssay