| Literature DB >> 29326083 |
Wei Li1, Iok-Hou Pang2, Mario Thiego F Pacheco3, Hong Tian4.
Abstract
As productivity of pharmaceutical research and development (R&D) for small-molecule drugs declines, the trend in drug discovery strategies is shifting towards biologics, which predominantly target secreted or cell surface proteins. Receptors and ligands are the most-valuable drug targets. In contrast to conventional approaches of discovering one ligand at a time, the emerging technology of ligandomics can systematically map disease-selective cellular ligands in the absence of molecular probes. Biologics targeting these ligands with disease selectivity have the advantages of high efficacy, minimal adverse effects, wide therapeutic indices, and low safety-related attrition rates. Therefore, ligandomics represents a paradigm shift to address the bottleneck of target discovery for biologics development.Entities:
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Year: 2018 PMID: 29326083 PMCID: PMC5849512 DOI: 10.1016/j.drudis.2018.01.013
Source DB: PubMed Journal: Drug Discov Today ISSN: 1359-6446 Impact factor: 7.851