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30 in total

1. Prediction of human metabolic clearance from in vitro systems: retrospective analysis and prospective view.

Authors: David Hallifax; Joanne A Foster; J Brian Houston
Journal: Pharm Res Date: 2010-07-27 Impact factor: 4.200

2. Structure-based prediction of the nonspecific binding of drugs to hepatic microsomes.

Authors: Haiyan Li; Jin Sun; Xiaofan Sui; Zhongtian Yan; Yinghua Sun; Xiaohong Liu; Yongjun Wang; Zhonggui He
Journal: AAPS J Date: 2009-05-14 Impact factor: 4.009

Review 3. In vitro evaluation of reversible and irreversible cytochrome P450 inhibition: current status on methodologies and their utility for predicting drug-drug interactions.

Authors: Stephen Fowler; Hongjian Zhang
Journal: AAPS J Date: 2008-08-07 Impact factor: 4.009

4. Physiologically based pharmacokinetic model of mechanism-based inhibition of CYP3A by clarithromycin.

Authors: Sara K Quinney; Xin Zhang; Aroonrut Lucksiri; J Christopher Gorski; Lang Li; Stephen D Hall
Journal: Drug Metab Dispos Date: 2009-11-02 Impact factor: 3.922

5. Consideration of the Unbound Drug Concentration in Enzyme Kinetics.

Authors: Nigel J Waters; R Scott Obach; Li Di
Journal: Methods Mol Biol Date: 2021

6. Glucuronidation of dihydrotestosterone and trans-androsterone by recombinant UDP-glucuronosyltransferase (UGT) 1A4: evidence for multiple UGT1A4 aglycone binding sites.

Authors: Jin Zhou; Timothy S Tracy; Rory P Remmel
Journal: Drug Metab Dispos Date: 2009-12-09 Impact factor: 3.922

10. Pharmacoepidemiologic and in vitro evaluation of potential drug-drug interactions of sulfonylureas with fibrates and statins.

Authors: H Schelleman; X Han; C M Brensinger; S K Quinney; W B Bilker; D A Flockhart; L Li; Sean Hennessy
Journal: Br J Clin Pharmacol Date: 2014-09 Impact factor: 4.335

Binding of drugs to hepatic microsomes: comment and assessment of current prediction methodology with recommendation for improvement.