General
Preferred name
TERBINAFINE
Synonyms
TERBINAFINE HYDROCHLORIDE ()
CPD000469152 ()
TDT 067 ()
SF 86-327 ()
Lamisil ()
Terbinex ()
TDT 067 hydrochloride ()
Terbinafine HCl ()
KWD 2019 ()
KWD 201,KWD 2019,TDT 067 hydrochloride ()
SF 86-327,TDT 067 ()
Terbine ()
Bramizil ()
Bramazil ()
Terbina ()
Muzonal ()
Athlete's Foot ()
Lamisil Once ()
Terbinafine (as hydrochloride) ()
NSC-759113 ()
Lamisil at ()
SF-86-327 ()
TDT-067 ()
Terbinafine (hydrochloride) ()
Terbinafine-d3 (hydrochloride) ()
P&D ID
PD009684
CAS
91161-71-6
78628-80-5
1310012-15-7
Tags
natural product
drug
available
Approved by
FDA
First approval
1992
Drug Status
investigational
approved
vet_approved
Drug indication
Antifungal
Fungal infection
Onychomycosis
Max Phase
Phase 4
Structure
Probe scores
P&D probe-likeness score
[[ v.score ]]%
Structure formats
[[ format ]]
[[ compound[format === 'MOL' ? 'molblock' : format.toLowerCase()] ]]
Description
(extracted from source data)
DESCRIPTION Selective, high affinity P2X3 and P2X2/3 receptor antagonist; antinociceptive (Tocris Bioactive Compound Library)
DESCRIPTION Terbinafine HCl inhibits squalene epoxidase, preventing biosynthesis of ergosterol. (BOC Sciences Bioactive Compounds)
Cell lines
1
Organisms
18
Compound Sets
29
AdooQ Bioactive Compound Library
Axon Medchem Screening Library
Bioprocess diversity set
BOC Sciences Bioactive Compounds
Cayman Chemical Bioactives
ChEMBL Approved Drugs
Drug Repurposing Hub
DrugBank
DrugBank Approved Drugs
DrugCentral
DrugCentral Approved Drugs
DrugMAP
DrugMAP Approved Drugs
Enamine BioReference Compounds
EU-OPENSCREEN Bioactive Compound Library
LSP-MoA library (Laboratory of Systems Pharmacology)
MedChem Express Bioactive Compound Library
NCATS Inxight Approved Drugs
NIH Clinical Collections (NCC)
NPC Screening Collection
Pandemic Response Box
Prestwick Chemical Library
ReFrame library
Selleckchem Bioactive Compound Library
TargetMol Bioactive Compound Library
The Spectrum Collection
Tocris Bioactive Compound Library
ZINC Tool Compounds
External IDs
65
Properties
(calculated by RDKit )
Molecular Weight
291.2
Hydrogen Bond Acceptors
1
Hydrogen Bond Donors
0
Rotatable Bonds
4
Ring Count
2
Aromatic Ring Count
2
cLogP
4.88
TPSA
3.24
Fraction CSP3
0.33
Chiral centers
0.0
Largest ring
6.0
QED
0.73
Structural alerts
0
No structural alerts detected
Custom attributes
(extracted from source data)
Biological process
Resipration, oxidative phosphorylation, & mitochondrial targeting
Pathway
Microbiology&virology
Anti-infection
Target
squalene epoxidase
SQLE
Antifungal agent
antibiotic
Bacterial
Fungal
Primary Target
Two-P Potassium Channels
MOA
Activator
fungal squalene epoxidase inhibitor
Indication
tinea pedis, tinea cruris, tinea corporis
Therapeutic Class
Antifungal Agents
Source data