Case study 1. Practical considerations with experimental design and interpretation.
暂无分享,去创建一个
[1] A. Galetin,et al. Human udp-glucuronosyltransferases: isoform selectivity and kinetics of 4-methylumbelliferone and 1-naphthol glucuronidation, effects of organic solvents, and inhibition by diclofenac and probenecid. , 2004, Drug metabolism and disposition: the biological fate of chemicals.
[2] Donglu Zhang,et al. IN VITRO INHIBITION OF UDP GLUCURONOSYLTRANSFERASES BY ATAZANAVIR AND OTHER HIV PROTEASE INHIBITORS AND THE RELATIONSHIP OF THIS PROPERTY TO IN VIVO BILIRUBIN GLUCURONIDATION , 2005, Drug Metabolism and Disposition.
[3] A. Li,et al. Effects of organic solvents on the activities of cytochrome P450 isoforms, UDP-dependent glucuronyl transferase, and phenol sulfotransferase in human hepatocytes. , 2001, Drug metabolism and disposition: the biological fate of chemicals.
[4] N. Chauret,et al. Effect of common organic solvents on in vitro cytochrome P450-mediated metabolic activities in human liver microsomes. , 1998, Drug metabolism and disposition: the biological fate of chemicals.
[5] H. Yamazaki,et al. Effects of freezing, thawing, and storage of human liver samples on the microsomal contents and activities of cytochrome P450 enzymes. , 1997, Drug metabolism and disposition: the biological fate of chemicals.
[6] W. Busby,et al. Effect of methanol, ethanol, dimethyl sulfoxide, and acetonitrile on in vitro activities of cDNA-expressed human cytochromes P-450. , 1999, Drug metabolism and disposition: the biological fate of chemicals.
[7] B. Ma,et al. Solvent effect on cDNA-expressed human sulfotransferase (SULT) activities in vitro. , 2003, Drug metabolism and disposition: the biological fate of chemicals.
[8] P. Marathe,et al. Effect of Commonly Used Organic Solvents on the Kinetics of Cytochrome P450 2B6- and 2C8-Dependent Activity in Human Liver Microsomes , 2007, Drug Metabolism and Disposition.
[9] Yong-long Han,et al. Effect of Regular Organic Solvents on Cytochrome P450-Mediated Metabolic Activities in Rat Liver Microsomes , 2010, Drug Metabolism and Disposition.
[10] R. Obach,et al. Human Liver Aldehyde Oxidase: Inhibition by 239 Drugs , 2004, Journal of clinical pharmacology.
[11] L. Wienkers,et al. Impact of Organic Solvents on Cytochrome P450 Probe Reactions: Filling the Gap with (S)-Warfarin and Midazolam Hydroxylation , 2012, Drug Metabolism and Disposition.
[12] A. Parkinson,et al. Effects of freezing, thawing, and storing human liver microsomes on cytochrome P450 activity. , 1996, Archives of biochemistry and biophysics.
[13] K. Korzekwa,et al. Cytochromes P450 Expression Systems , 1995 .
[14] Jeffrey P. Jones,et al. Inhibition of Human Liver Aldehyde Oxidase: Implications for Potential Drug-Drug Interactions , 2011, Drug Metabolism and Disposition.