Literature DB >> 31889388

New Promise and Opportunities for Allosteric Kinase Inhibitors.

Xiaoyun Lu1, Jeff B Smaill2, Ke Ding1.   

Abstract

Drugs that function through allosteric inhibition of kinase signaling represent a promising approach for the targeted discovery of therapeutics. The majority of developed allosteric kinase inhibitors are characterized as type III and IV inhibitors that show good kinome selectivity but generally lack the subtype selectivity of same kinase family. Recently allosteric inhibitors have been developed that bind outside the catalytic kinase domain with high selectivity for specific kinase subtypes. Allosteric inhibitors that bind to the pseudokinase domain of pseudokinase or the extracellular domain of receptor tyrosine kinases are reviewed. We also review recent developments in the field of allosteric kinase inhibitors including examples of proteolysis targeting chimeras, and highlight the unique binding modes for each type of inhibitors and address future opportunities in this area.
© 2019 Wiley-VCH Verlag GmbH & Co. KGaA, Weinheim.

Entities:  

Keywords:  allosteric kinase inhibitors; drug design; extracellular domain; kinase domain; pseudokinase domain

Year:  2020        PMID: 31889388     DOI: 10.1002/anie.201914525

Source DB:  PubMed          Journal:  Angew Chem Int Ed Engl        ISSN: 1433-7851            Impact factor:   15.336


  17 in total

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Review 6.  An overview of kinase downregulators and recent advances in discovery approaches.

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7.  Nanobodies as allosteric modulators of Parkinson's disease-associated LRRK2.

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Journal:  Proc Natl Acad Sci U S A       Date:  2022-03-01       Impact factor: 11.205

8.  Identification of highly selective type II kinase inhibitors with chiral peptidomimetic tails.

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9.  On the development of B-Raf inhibitors acting through innovative mechanisms.

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Journal:  F1000Res       Date:  2022-02-25

Review 10.  Pharmacological inhibition of NF-κB-inducing kinase (NIK) with small molecules for the treatment of human diseases.

Authors:  Jing Cheng; Xuexin Feng; Zhiqiang Li; Feilong Zhou; Jin-Ming Yang; Yujun Zhao
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