thioacetamide


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thioacetamide

[¦thī·ō·ə′sed·ə·mīd]
(organic chemistry)
C2H5NS A crystalline compound with a melting point of 113-114°C; soluble in water and ethanol; used in laboratories in place of hydrogen sulfide.
References in periodicals archive ?
Effects of losartan and candesartan on the levels of: A, serum tumor necrosis factor-[alpha] (TNF-[alpha]), B, hepatic malondialdehyde (MDA), C, hepatic glutathione (GSH), and D, hepatic expression of TNF-[alpha] mRNA in thioacetamide (TAA)-induced chronic liver failure rats.
In this study, we investigated the effects of methylprednisolone (MP) on intestinal oxidative damage and bacterial translocation (BT) in thioacetamide (TAA)-induced liver failure in rats.
et al (2001) Epidermal growth factor reduces multiorgan failure induced by thioacetamide.
Protective effects of Rosmarinus tomentosus ethanol extract on thioacetamide induced liver cirrhosis in rats.
Necrogenic and regenerative responses of liver of newly weaned rats against a sublethal dose of thioacetamide.
Differential effect of thioacetamide on hepatic methionine adenosyltransferase expression in the rat.
ethionine, thioacetamide, coumarin, ethanol, 2-acetamidofluorene, AThitrosodiethylamine).
Depletion of kupffer cell function by gadoli- nium chloride attenuates thioacetamide induced he- patotoxicity.
against paracetamol and thioacetamide intoxication in albino rats.
In case of CdS nanoparticles prepared via cadmium acetate/ thioacetamide the absorption edge is located at about362 nm while the same prepared from cadmium chloride/ sodium sulfide shows it at 375nm.