General
Preferred name
TERBINAFINE
Synonyms
TERBINAFINE HYDROCHLORIDE ()
CPD000469152 ()
Terbinex ()
SF 86-327 ()
Lamisil ()
TDT 067 ()
KWD 2019 ()
Terbinafine HCl ()
TDT 067 hydrochloride ()
KWD 201,KWD 2019,TDT 067 hydrochloride ()
SF 86-327,TDT 067 ()
Terbinafine (hydrochloride) ()
Terbine ()
Bramazil ()
Lamisil at ()
Lamisil Once ()
Terbina ()
Bramizil ()
Muzonal ()
Athlete's Foot ()
Terbinafine (as hydrochloride) ()
NSC-759113 ()
TDT-067 ()
Terbinafina ()
Lamasil ()
SF-86-327 ()
Terbinafine component of osurnia ()
Terbinafine-d3 (hydrochloride) ()
P&D ID
PD009684
CAS
91161-71-6
78628-80-5
1310012-15-7
Tags
available
drug
Approved by
FDA
First approval
1992
Drug indication
Onychomycosis
Fungal infection
Tinea pedis
Drug Status
vet_approved
approved
investigational
Max Phase
4.0
Probe control
Probe control not defined
Orthogonal probes
0
No orthogonal probes found
Similar probes
0
No structurally similar probes found
Structure formats
[[ format ]]
[[ compound[format === 'MOL' ? 'molblock' : format.toLowerCase()] ]]
Description
(extracted from source data)
DESCRIPTION
Terbinafine hydrochloride (TDT 067 hydrochloride) is an orally active and potent antifungal agent. Terbinafine hydrochloride is a potent non-competitive inhibitor of squalene epoxidase from Candida, with a Ki of 30 nM. Terbinafine hydrochloride also shows antibacterial activity against certain Gram-positive and Gram-negative bacteria[1][2][3]. Terbinafine hydrochloride is a click chemistry reagent, it contains an Alkyne group and can undergo copper-catalyzed azide-alkyne cycloaddition (CuAAc) with molecules containing Azide groups.
PRICE
29
DESCRIPTION
Terbinafine (TDT 067) is an orally active and potent antifungal agent. Terbinafine is a potent non-competitive inhibitor of squalene epoxidase from Candida, with a Ki of 30 nM. Terbinafine also shows antibacterial activity against certain Gram-positive and Gram-negative bacteria[1][2][3]. Terbinafine is a click chemistry reagent, it contains an Alkyne group and can undergo copper-catalyzed azide-alkyne cycloaddition (CuAAc) with molecules containing Azide groups.
PRICE
29
DESCRIPTION
Selective, high affinity P2X3 and P2X2/3 receptor antagonist; antinociceptive
(Tocris Bioactive Compound Library)
DESCRIPTION
Terbinafine hydrochloride (KWD 2019) is a synthetic allylamine derivative structurally related to naftifine. Terbinafine is active against dermatophytes.
(TargetMol Bioactive Compound Library)
DESCRIPTION
Terbinafine HCl inhibits squalene epoxidase, preventing biosynthesis of ergosterol.
(BOC Sciences Bioactive Compounds)
DESCRIPTION
Terbinafine is a synthetic allylamine antifungal. It is highly lipophilic in nature and tends to accumulate in skin, nails, and fatty tissues. Terbinafine inhibits ergosterol synthesis by inhibiting the fungal squalene monooxygenase, an enzyme that is part of the fungal cell wall synthesis pathway. It is used to treat dermatophyte infections of toenails and fingernails as well as other fungal skin infections.
(Enamine Bioactive Compounds)
DESCRIPTION
Terbinafine (TDT 067) is a synthetic allylamine derivative with antifungal activity. Terbinafine exerts its effect through inhibition of squalene epoxidase, thereby blocking the biosynthesis of ergosterol, an important component of fungal cell membranes. As a result, this agent disrupts fungal cell membrane synthesis and inhibits fungal growth.
(TargetMol Bioactive Compound Library)
[[ p.pathway_name ]]
[[ compound.targets[tid].gene_name ]]
Cell lines
1
Organisms
18
Compound Sets
30
AdooQ Bioactive Compound Library
Axon Medchem Screening Library
Bioprocess diversity set
BOC Sciences Bioactive Compounds
ChEMBL Approved Drugs
ChEMBL Drugs
Drug Repurposing Hub
DrugBank
DrugBank Approved Drugs
DrugCentral
DrugCentral Approved Drugs
DrugMAP
DrugMAP Approved Drugs
Enamine Bioactive Compounds
Enamine BioReference Compounds
EU-OPENSCREEN Bioactive Compound Library
LSP-MoA library (Laboratory of Systems Pharmacology)
NCATS Inxight Approved Drugs
NIH Clinical Collections (NCC)
NPC Screening Collection
Pandemic Response Box
Prestwick Chemical Library
ReFrame library
Selleckchem Bioactive Compound Library
The Spectrum Collection
Tocris Bioactive Compound Library
ZINC Tool Compounds
[[ a.name ]]
[[ ligand_id ]]
free of charge
External IDs
69
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
Primary Target
Two-P Potassium Channels
MOA
Activator
fungal squalene epoxidase inhibitor
Indication
tinea pedis, tinea cruris, tinea corporis
Target
SQLE
Antifungal agent
antibiotic
Bacterial
Fungal
squalene epoxidase
Therapeutic Class
Antifungal Agents
Source data

