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Molecule
ID:72857
Structure
Similarity
Functional Group
Text
General Information
Structure
Molecular Formula
C₂₁H₂₁BrF₂N₄O
Molecular Mass
463.3184464
Exact Mass
462.08667975
Charge
0
InChI
InChI=1S/C21H21BrF2N4O/c1-2-9-27(11-16-3-5-17(22)6-4-16)12-21(29,13-28-15-25-14-26-28)19-8-7-18(23)10-20(19)24/h2-8,10,14-15,29H,1,9,11-13H2
InChIKey
JBOSAXVFTHRCCQ-UHFFFAOYSA-N
Canonic Smiles
C=CCN(CC(c1ccc(cc1F)F)(Cn1ncnc1)O)Cc1ccc(cc1)Br
Isomeric Smiles
c1cc(cc(c1C(Cn1ncnc1)(CN(Cc1ccc(cc1)Br)CC=C)O)F)F
Calculated Properties
JChem
Acid pKa
12.856438
H Acceptors
4
H Donor
1
LogD (pH = 5.5)
1.6374968
LogD (pH = 7.4)
3.4117599
Log P
4.261017
Molar Refractivity
124.4502
Polarizability
42.3202
Polar Surface Area
54.18
Rotatable Bonds
9
Lipinski's Rule of Five
true
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Data Source
Commercial Catalog
Selleck Chemicals
S2143
Academic Data
PubChem
42631373
Names and Identifiers
IUPAC Traditional name
1-{[(4-bromophenyl)methyl](prop-2-en-1-yl)amino}-2-(2,4-difluorophenyl)-3-(1,2,4-triazol-1-yl)propan-2-ol
Synonyms
Cytochrome P450 14a-demethylase inhibitor 1i
IUPAC name
1-{[(4-bromophenyl)methyl](prop-2-en-1-yl)amino}-2-(2,4-difluorophenyl)-3-(1H-1,2,4-triazol-1-yl)propan-2-ol
Registration numbers
CAS Number
1155361-07-1
PubChem SID
162037778
PubChem CID
42631373
Properties
Pharmacology Properties
Target
p450
Source
Safety Information
Storage Condition
-20°C
Source
Product Information
Salt Data
Free Base
Source
Molecule Details
Selleck Chemicals
S2143
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