Literature DB >> 29192286

Mechanistic enzymology in drug discovery: a fresh perspective.

Geoffrey A Holdgate1, Thomas D Meek2, Rachel L Grimley1.   

Abstract

Given the therapeutic and commercial success of small-molecule enzyme inhibitors, as exemplified by kinase inhibitors in oncology, a major focus of current drug-discovery and development efforts is on enzyme targets. Understanding the course of an enzyme-catalysed reaction can help to conceptualize different types of inhibitor and to inform the design of screens to identify desired mechanisms. Exploiting this information allows the thorough evaluation of diverse compounds, providing the knowledge required to efficiently optimize leads towards differentiated candidate drugs. This review highlights the rationale for conducting high-quality mechanistic enzymology studies and considers the added value in combining such studies with orthogonal biophysical methods.

Year:  2017        PMID: 29192286     DOI: 10.1038/nrd.2017.219

Source DB:  PubMed          Journal:  Nat Rev Drug Discov        ISSN: 1474-1776            Impact factor:   84.694


  121 in total

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5.  New substructure filters for removal of pan assay interference compounds (PAINS) from screening libraries and for their exclusion in bioassays.

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6.  A new class of angiotensin-converting enzyme inhibitors.

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7.  Potent inhibitors of HIV-1 integrase display a two-step, slow-binding inhibition mechanism which is absent in a drug-resistant T66I/M154I mutant.

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8.  Biophysical screening for the discovery of small-molecule ligands.

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9.  Chemical mechanism of a cysteine protease, cathepsin C, as revealed by integration of both steady-state and pre-steady-state solvent kinetic isotope effects.

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Journal:  Biochemistry       Date:  2008-07-26       Impact factor: 3.162

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  31 in total

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Review 3.  The Taxonomy of Covalent Inhibitors.

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Review 4.  The Continuing Challenge of Metallo-β-Lactamase Inhibition: Mechanism Matters.

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5.  Kinetic Tuning of HDAC Inhibitors Affords Potent Inducers of Progranulin Expression.

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6.  Heterologous expression of a papain-like protease inhibitor (SnuCalCpI17) in the E. coli and its mode of inhibition.

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7.  Insights into the product release mechanism of dengue virus NS3 helicase.

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8.  Validation of Human Sterol 14α-Demethylase (CYP51) Druggability: Structure-Guided Design, Synthesis, and Evaluation of Stoichiometric, Functionally Irreversible Inhibitors.

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