Terbinafine [91161-71-6]

Cat# HY-17395A-100mg

Size : 100mg

Brand : MedChemExpress

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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.

IC50 & Target

Ki: 30 nM (squalene epoxidase)[1]

Cellular Effect
Cell Line Type Value Description References
J774 IC50
88 μM
Compound: Tbf
Cytotoxicity against mouse J774 cells after 48 hrs by MTT assay
Cytotoxicity against mouse J774 cells after 48 hrs by MTT assay
[PMID: 19110434]
J774 IC50
88 μM
Compound: Terbinafine, Tbf
Cytotoxicity against mouse J774 cells after 48 hrs by MTT assay
Cytotoxicity against mouse J774 cells after 48 hrs by MTT assay
[PMID: 18547811]
THP-1 IC50
329.3 μM
Compound: Tbf, Terbinafine
Cytotoxicity against human THP1 cells after 48 hrs
Cytotoxicity against human THP1 cells after 48 hrs
[PMID: 17960923]
THP-1 IC50
329.3 μM
Compound: Tbf, terbinafine
Cytotoxicity against human THP1 cells assessed as reduction of cell viability after 48 hrs
Cytotoxicity against human THP1 cells assessed as reduction of cell viability after 48 hrs
[PMID: 17287123]
Vero IC50
30.9 μg/mL
Compound: TRB
Cytotoxicity against african green monkey Vero cells after 48 hrs by MTT assay
Cytotoxicity against african green monkey Vero cells after 48 hrs by MTT assay
[PMID: 23831506]
In Vitro

Terbinafine has a primary fungicidal action in vitro against most fungal pathogens, including dermatophytes, and dimorphic and filamentous fungi. Terbinafine specifically inhibits fungal ergosterol biosynthesis at the point of squalene epoxidation. The treated fungal cells rapidly accumulate tlic intermediate squalene[1].

MedChemExpress (MCE) has not independently confirmed the accuracy of these methods. They are for reference only.

Solvent & Solubility
In Vitro: 

DMSO : mg/mL (343.14 mM; Hygroscopic DMSO has a significant impact on the solubility of product, please use newly opened DMSO)

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Preparing
Stock Solutions
Concentration Solvent Mass 1 mg 5 mg 10 mg
1 mM 3.4314 mL 17.1568 mL 34.3136 mL
5 mM 0.6863 mL 3.4314 mL 6.8627 mL
View the Complete Stock Solution Preparation Table

* Please refer to the solubility information to select the appropriate solvent. Once prepared, please aliquot and store the solution to prevent product inactivation from repeated freeze-thaw cycles.
Storage method and period of stock solution: -80 years; -20 year. When stored at -80 years. When stored at -20 year.

Mass (g) = Concentration (mol/L) × Volume (L) × Molecular Weight (g/mol)

Mass
=
Concentration
×
Volume
×
Molecular Weight *

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