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Covalent inhibitors in drug discovery: from accidental discoveries to avoided liabilities and designed therapies

Journal

DRUG DISCOVERY TODAY
Volume 20, Issue 9, Pages 1061-1073

Publisher

ELSEVIER SCI LTD
DOI: 10.1016/j.drudis.2015.05.005

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Drugs that covalently bond to their biological targets have a long history in drug discovery. A look at drug approvals in recent years suggests that covalent drugs will continue to make impacts on human health for years to come. Although fraught with concerns about toxicity, the high potencies and prolonged effects achievable with covalent drugs may result in less-frequent drug dosing and in wide therapeutic margins for patients. Covalent inhibition can also dissociate drug pharmacodynamics (PD) from pharmacokinetics (PK), which can result in desired drug efficacy for inhibitors that have short systemic exposure. Evidence suggests that there is a reduced risk for the development of resistance against covalent drugs, which is a major challenge in areas such as oncology and infectious disease.

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