| Literature DB >> 31550151 |
Debasmita Saha1, Anupreet Kharbanda1, Wei Yan1, Naga Rajiv Lakkaniga1, Brendan Frett1, Hong-Yu Li1.
Abstract
Chirality is important in drug discovery because stereoselective drugs can ameliorate therapeutic difficulties including adverse toxicity and poor pharmacokinetic profiles. The human kinome, a major druggable enzyme class has been exploited to treat a wide range of diseases. However, many kinase inhibitors are planar and overlap in chemical space, which leads to selectivity and toxicity issues. By exploring chirality within the kinome, a new iteration of kinase inhibitors is being developed to better utilize the three-dimensional nature of the kinase active site. Exploration into novel chemical space, in turn, will also improve drug solubility and pharmacokinetic profiles. This perspective explores the role of chirality to improve kinome druggability and will serve as a resource for pioneering kinase inhibitor development to address current therapeutic needs.Entities:
Year: 2019 PMID: 31550151 DOI: 10.1021/acs.jmedchem.9b00640
Source DB: PubMed Journal: J Med Chem ISSN: 0022-2623 Impact factor: 7.446