Research Topics
Species | Jinghai J XuSummaryAffiliation: Pfizer Global Research and Development Country: USA Publications
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Detail Information
Publications
The role of absorption, distribution, metabolism, excretion and toxicity in drug discoveryJing Lin
Pharmacokinetics, Dynamics and Metabolism, Pfizer Global Research and Development, Groton Laboratories, CT 06340, USA
Curr Top Med Chem 3:1125-54. 2003..Fundamental concepts, key tools, reagents and experimental approaches used by the drug metabolism scientist to aid a modern project team in predicting human pharmacokinetics and assessing the "drug-like" molecule are discussed...
Applications of cytotoxicity assays and pre-lethal mechanistic assays for assessment of human hepatotoxicity potentialJinghai J Xu
Exploratory Medicinal Sciences, Pfizer Global Research and Development, Bldg 118W, Rm W127, Pfizer Groton Labs, Eastern Point Rd, Groton, CT 06340, USA
Chem Biol Interact 150:115-28. 2004....
Role of hepatic transporters in the disposition and hepatotoxicity of a HER2 tyrosine kinase inhibitor CP-724,714Bo Feng
Pharmacokinetics, Dynamics, and Metabolism Department, Pfizer Global Research and Development, Groton, CT 06340
Toxicol Sci 108:492-500. 2009..This study provides likely explanations for clinically observed adverse liver effects of CP-724,714...
Multiple effects of acetaminophen and p38 inhibitors: towards pathway toxicologyJinghai J Xu
Systems Biology, Pfizer Research Technology Center, 620 Memorial Drive, Cambridge, MA 02139, United States
FEBS Lett 582:1276-82. 2008..The advancement of pathway toxicology will be dependent on integrated applications of techniques from basic sciences and a fundamental understanding of the interdependence of multiple biological pathways in living organisms...
Cellular imaging predictions of clinical drug-induced liver injuryJinghai J Xu
Predictive Toxicology, Pfizer Research Technology Center, Pfizer Global Research and Development, Cambridge, Massachussetts 01239, USA
Toxicol Sci 105:97-105. 2008..Our findings provide insight to key DILI mechanisms, and suggest a new approach in hepatotoxicity testing of pharmaceuticals...
Inhibition of human organic anion transporting polypeptide OATP 1B1 as a mechanism of drug-induced hyperbilirubinemiaScott D Campbell
Pharmacokinetics, Dynamics and Metabolism, Pfizer Global Research and Development, Groton Laboratory, Eastern Point Road, MS 8118W 131, Groton, CT 06340, USA
Chem Biol Interact 150:179-87. 2004..Inhibition of OATPs may be an important mechanism in drug-drug and drug-endogenous substance interactions...
Differential interaction of 3-hydroxy-3-methylglutaryl-coa reductase inhibitors with ABCB1, ABCC2, and OATP1B1Cuiping Chen
Pharmacokinetics, Dynamics and Metabolism, Pfizer Global Research and Development, MS4044, Eastern Point Rd, Groton, CT 06340, USA
Drug Metab Dispos 33:537-46. 2005....
In vitro assessment of mitochondrial dysfunction and cytotoxicity of nefazodone, trazodone, and buspironeJames A Dykens
Drug Safety Research and Development, Pfizer, Inc, Sandwich CT139NJ, UK
Toxicol Sci 103:335-45. 2008..Our results suggest that the mitochondrial impairment imposed by nefazodone is profound and likely contributes to its hepatotoxicity, especially in patients cotreated with other drugs with mitochondrial liabilities...
