Pharmacokinetic and pharmacodynamic alterations of 3-hydroxy-3-methylglutaryl coenzyme A (HMG-CoA) reductase inhibitors: drug–drug interactions and …

Y Shitara, Y Sugiyama - Pharmacology & therapeutics, 2006 - Elsevier
3-Hydroxy-3-methylglutaryl coenzyme A (HMG-CoA) reductase inhibitors (statins) are widely
used for the treatment of hypercholesterolemia. Their efficacy in preventing cardiovascular …

Mechanism-based inhibition of cytochrome P450 3A4 by therapeutic drugs

S Zhou, SY Chan, BC Goh, E Chan, W Duan… - Clinical …, 2005 - Springer
Consistent with its highest abundance in humans, cytochrome P450 (CYP) 3A is responsible
for the metabolism of about 60% of currently known drugs. However, this unusual low …

Contribution of OATP2 (OATP1B1) and OATP8 (OATP1B3) to the hepatic uptake of pitavastatin in humans

M Hirano, K Maeda, Y Shitara, Y Sugiyama - Journal of Pharmacology and …, 2004 - ASPET
Pitavastatin, a novel potent 3-hydroxymethylglutaryl-CoA reductase inhibitor, is selectively
distributed to the liver in rats. However, the hepatic uptake mechanism of pitavastatin has not …

Toxicology and genetic toxicology in the new era of “toxicogenomics”: impact of “-omics” technologies

MJ Aardema, JT MacGregor - Toxicogenomics, 2003 - Springer
The unprecedented advances in molecular biology during the last two decades have
resulted in a dramatic increase in knowledge about gene structure and function, an …

Interactions of herbs with cytochrome P450

S Zhou, Y Gao, W Jiang, M Huang, A Xu… - Drug metabolism …, 2003 - Taylor & Francis
A resurgence in the use of medical herbs in the Western world, and the co-use of modern
and traditional therapies is becoming more common. Thus there is the potential for both …

Development of a substrate-activity based approach to identify the major human liver P-450 catalysts of cyclophosphamide and ifosfamide activation based on cDNA …

P Roy, JY Li, CL Crespi, DJ Waxman - Drug Metabolism and Disposition, 1999 - ASPET
The contributions of specific human liver cytochrome P-450 (CYP) enzymes to the activation,
via 4-hydroxylation, of the oxazaphosphorine anticancer prodrugs cyclophosphamide (CPA) …

Quality related safety issue-evidence-based validation of herbal medicine farm to pharma

PK Mukherjee, S Bahadur, SK Chaudhary, A Kar… - … -based validation of …, 2015 - Elsevier
Because of their unique effects and relatively low side effects, herbal medicine has been
gaining popularity all over the world. Quality control is a challenge to ensure safety, efficacy …

Human drug metabolism and the cytochromes P450: application and relevance of in vitro models

K Venkatakrishnan, LL von Moltke… - The Journal of …, 2001 - Wiley Online Library
The cytochromes P450 (CYPs) constitute a superfamily of hemoprotein enzymes that are
responsible for the biotransformation of numerous xenobiotics, including therapeutic agents …

PRL-3 and PRL-1 promote cell migration, invasion, and metastasis

Q Zeng, JM Dong, K Guo, J Li, HX Tan, V Koh… - Cancer research, 2003 - AACR
We demonstrate here that Chinese hamster ovary cells stably expressing PRL-3, a M r
20,000 prenylated protein tyrosine phosphatase, or its relative, PRL-1, exhibit enhanced …

Inhibition of cytochromes P450 by antifungal imidazole derivatives

W Zhang, Y Ramamoorthy, T Kilicarslan, H Nolte… - Drug Metabolism and …, 2002 - ASPET
The interactions of a panel of antifungal agents with cytochromes P450 (P450s), as a means
of predicting potential drug-drug interactions, have not yet been investigated. The objective …