Drug-Target Residence Time Affects Target Occupancy through Multiple Pathways.

作者信息

Lee Kin Sing Stephen, Yang Jun, Niu Jun, Ng Connie J, Wagner Karen M, Dong Hua, Kodani Sean D, Wan Debin, Morisseau Christophe, Hammock Bruce D

机构信息

Department of Entomology and Nematology and UCD Comprehensive Cancer Center, University of California at Davis, One Shields Avenue, Davis, California 95616, United States.

Department of Pharmacology and Toxicology and Department of Chemistry, Michigan State University, 1355 Bogue Street, East Lansing, Michigan 48824, United States.

出版信息

ACS Cent Sci. 2019 Sep 25;5(9):1614-1624. doi: 10.1021/acscentsci.9b00770. Epub 2019 Sep 3.

Abstract

The drug discovery and development process is greatly hampered by difficulties in translating potency to efficacy. Recent studies suggest that the long-neglected drug-target residence time parameter complements classical drug affinity parameters ( , , IC, or EC) and is a better predictor of efficacy. Compounds with a long drug-target residence time are often more efficacious . The impact, however, of the drug-target residence time on efficacy remains controversial due to difficulties in experimentally determining the target occupancy during drug treatment. To tackle this problem, an displacement assay was developed using soluble epoxide hydrolase as a biological model. In this report, we experimentally demonstrated that drug-target residence time affects the duration of drug-target binding. In addition, the drug-target residence time plays an important role in modulating the rate of drug metabolism which also affects the efficacy of the drug.

摘要
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/73d6/6764161/91ec87ee966b/oc9b00770_0001.jpg

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