Terbinafine Hydrochloride

Terbinafine Hydrochloride

Catalog Number:
PB01342444TOK
Mfr. No.:
TOK-T142-1G
Price:
$185
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      • Overview
        • Terbinafine Hydrochloride (Terbinafine HCl) belongs to the allylamine class of antifungals. It is active against fungi and yeast. It is used in studies of adsorption and stability. It is used against the dematophytic fungi. It has anti-cancer properties.
          Terbinafine HCl is soluble in methanol.

          Please contact us at for specific academic pricing.

          Background

          Terbinafine inhibits squalene monooxygenase thus blocking ergosteriol biosynthesis, an essential component of fungal cell membranes. Inhibition results in squalene accumulation. It is lipophylic. The compound can also reduce the fungi's ability to generate reactive oxygen species.
          This product is considered a dangerous good. Quantities above 1 g may be subject to additional shipping fees. Please contact us for details.

      • Properties
        • CAS Number
          78628-80-5
          Molecular Formula
          C21H25N · HCl
          Molecular Weight
          327.89
          Solubility
          Soluble in methanol
          Other Properties
          Source: Synthetic
          Storage
          <30°C

          * For research use only

      • Applications
        • Application Description
          Spectrum: Terbinafine HCl is active against fungi and yeast, specifically against dermatophytes. It is fungistatic against Candida albicans.

          Microbiology Applications: Terbinafine can suppress cell proliferation in vitro via inhibition of DNA synthesis and apoptosis activation (Ho et al, 2004).

          Eukaryotic Cell Culture Applications: Terbinafine dose-dependently decreased cell number in cultured human umbilical vascular endothelial cells (HUVEC). It was not cytotoxic at 120 mM. studies have demonstrated that Terbinafine can inhibit angiogenesis (Ho et al, 2004).

          Cancer Applications: Terbinafine inhibits oral squamous cell carsinoma growth in a concentration-dependent way via anti-cancer cell proliferation and anti-angiogenesis (Chien et al, 2011).

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