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Terbinafine-d3 (hydrochloride) (Synonyms: TDT 067-d3 hydrochloride)

Katalog-Nr.GC48144

An internal standard for the quantification of terbinafine

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Terbinafine-d3 (hydrochloride) Chemische Struktur

Cas No.: 1310012-15-7

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500 μg
121,00 $
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1 mg
216,00 $
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5 mg
960,00 $
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Sample solution is provided at 25 µL, 10mM.

Description Chemical Properties Product Documents

Terbinafine-d3 is intended for use as an internal standard for the quantification of terbinafine by GC- or LC-MS. Terbinafine is a broad-spectrum antifungal agent that has activity against T. rubrum, T. mentagrophytes, T. verrucosum, E. floccosum, M. canis, A. fumigatus, and S. schenckii (MIC50s = 0.003-0.8 μg/ml).1 It selectively inhibits C. albicans squalene epoxidase over rat liver epoxidase (IC50s = 0.03 and 77 μM, respectively).2 Terbinafine (90-120 µM) induces cell cycle arrest at the G0/G1 phase in COLO 205 tumor cells and human umbilical vein endothelial cells (HUVECs).3,4 Formulations containing terbinafine have been used in the treatment of nail and skin fungal infections.

1.Petranyi, G., Meingassner, J.G., and Mieth, H.Antifungal activity of the allylamine derivative terbinafine in vitroAntimicrob. Agents Chemother.31(9)1365-1368(1987) 2.Ryder, N.S., and Dupont, M.C.Inhibition of squalene epoxidase by allylamine antimycotic compounds. A comparative study of the fungal and mammalian enzymesBiochem. J.230(3)765-770(1985) 3.Lee, W.S., Chen, R.J., Wang, Y.J., et al.In vitro and in vivo studies of the anticancer action of terbinafine in human cancer cell lines: G0/G1 p53-associated cell cycle arrestInternational Journal of Cancer106125-137(2003) 4.Ho, P.Y., Liang, Y.C., Ho, Y.S., et al.Inhibition of human vascular endothelial cells proliferation by terbinafineInternational Journal of Cancer11151-59(2004)

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