Title : In vitro evaluation of the interaction potential of irosustat with drug-metabolizing enzymes.

Pub. Date : 2012 Jul

PMID : 22451700






2 Functional Relationships(s)
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1 CYP1A2 inhibition by 667-coumarin was competitive, with a K(i) of 0.77 muM, a concentration exceeding by only 5-fold the maximal steady-state concentration of 667-coumarin in human plasma with the recommended dose of irosustat. coumarin latexin Homo sapiens
2 667-Coumarin also appeared to be a competitive inhibitor of CYP2C19 (K(i) = 5.8 muM) in human liver microsomes, and this inhibition increased with assessment in human hepatocytes. coumarin latexin Homo sapiens