Similar substrate specificity of cynomolgus monkey cytochrome P450 2C19 to reported human P450 2C counterpart enzymes by evaluation of 89 drug clearances

Author:

Hosaka Shinya12,Murayama Norie1,Satsukawa Masahiro2,Uehara Shotaro1,Shimizu Makiko1,Iwasaki Kazuhide3,Iwano Shunsuke14,Uno Yasuhiro3,Yamazaki Hiroshi1

Affiliation:

1. Showa Pharmaceutical University; Machida Tokyo 194-8543 Japan

2. Kaken Pharmaceutical Co., LTD.; Shizuoka 426-8646 Japan

3. Shin Nippon Biomedical Laboratories, Ltd; Kainan Wakayama 642-0017 Japan

4. Novartis Pharma K.K.; Tokyo 106-8618 Japan

Publisher

Wiley

Subject

Pharmacology (medical),Pharmaceutical Science,Pharmacology,General Medicine

Reference33 articles.

1. Interindividual variations in human liver cytochrome P-450 enzymes involved in the oxidation of drugs, carcinogens and toxic chemicals: studies with liver microsomes of 30 Japanese and 30 Caucasians;Shimada;J Pharmacol Exp Ther,1994

2. Clinical relevance of genetic polymorphisms in the human CYP2C subfamily;Goldstein;Br J Clin Pharmacol,2001

3. Macaque cytochromes P450: nomenclature, transcript, gene, genomic structure, and function;Uno;Drug Metab Rev,2011

4. CYP2C76, a novel cytochrome P450 in cynomolgus monkey, is a major CYP2C in liver, metabolizing tolbutamide and testosterone;Uno;Mol Pharmacol,2006

5. Identification and characterization of CYP2C18 in the cynomolgus macaque (Macaca fascicularis);Uno;J Vet Med Sci,2010

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