3 Results for "

liver parenchymal necrosis

" in MedChemExpress (MCE) Product Catalog:
Products (3)

3 Results for "liver parenchymal necrosis" in MCE Product Catalog:

5
5 Cited Publications
Cat. No.: HY-Y0698
CAS No.: 62-55-5
Synonyms: Acetothioamide; TAA; Thiacetamide
Thioacetamide (TAA) is an indirect hepatotoxin and causes parenchymal cell necrosis. Thioacetamide requires metabolic activation by microsomal CYP2E1 to thioacetamide-S-oxide initially and then to thioacetamide-S-dioxide, which is a highly reactive metabolite, and its reactive metabolites covalently bind to proteins and lipids thereby causing oxidative stress and centrilobular necrosis. Thioacetamide can induce chronic liver fibrosis, encephalopathy and other events model .
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Cat. No.: HY-Y0698R
CAS No.: 62-55-5
Synonyms: Acetothioamide (Standard); TAA (Standard); Thiacetamide (Standard)
Research Areas:  

Inflammation/Immunology

Thioacetamide (Standard) is the analytical standard of Thioacetamide (HY-Y0698). This product is intended for research and analytical applications. Thioacetamide (TAA) is an indirect hepatotoxin and causes parenchymal cell necrosis. Thioacetamide requires metabolic activation by microsomal CYP2E1 to thioacetamide-S-oxide initially and then to thioacetamide-S-dioxide, which is a highly reactive metabolite, and its reactive metabolites covalently bind to proteins and lipids thereby causing oxidative stress and centrilobular necrosis. Thioacetamide can induce chronic liver fibrosis, encephalopathy and other events model .
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Cat. No.: HY-W982689
CAS No.: 6723-40-6
Research Areas:  

Metabolic Disease

Fluindarol is a phenylindandione derivative and an orally active anticoagulant. Fluindarol acts as a toxicant that induces organ and tissue haemorrhages and liver parenchymal necrosis in rats. Fluindarol exhibits acute and cumulative preclinical toxicity in rats, rabbits, and dogs, with higher toxicity in female rats than male rats. Fluindarol lacks analgesic action, produces only minor blood pressure effects, and does not alter circulation, respiration, CNS, or cardiac activity. Fluindarol is considered too toxic for clinical use based on preclinical data .
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