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Literature summary for 3.4.22.56 extracted from

  • Schrieber, S.J.; Wen, Z.; Vourvahis, M.; Smith, P.C.; Fried, M.W.; Kashuba, A.D.; Hawke, R.L.
    The pharmacokinetics of silymarin is altered in patients with hepatitis C virus and nonalcoholic fatty liver disease and correlates with plasma caspase-3/7 activity (2008), Drug Metab. Dispos., 36, 1909-1916.
    View publication on PubMed

Application

Application Comment Organism
diagnostics a simple biochemical assay of caspase-3 activity in blood, may be useful for predicting the disposition of drugs that undergo extensive conjugation and biliary elimination like silymarin in patients with liver disease, caspase-3 activity correlates with the amount of silymarin conjugates, e.g. silychristin and silybin A and B, and is 5fold higher in the HCV cirrhosis cohort, overview Homo sapiens

Organism

Organism UniProt Comment Textmining
Homo sapiens
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Source Tissue

Source Tissue Comment Organism Textmining
liver the caspase-3 activity is about 2.4, 3.3, and 4.7fold higher in hepatitis C virus noncirrhosis, nonalcoholic fatty liver disease, and HCV cirrhosis cohorts, respectively, compared to healthy volunteers Homo sapiens
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