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


ABSTRACT: Identification of highly selective type II kinase inhibitors is described. Two different chiral peptidomimetic scaffolds were introduced on the tail region of non-selective type II kinase inhibitor GNF-7 to enhance the selectivity. Kinome-wide selectivity profiling analysis showed that type II kinase inhibitor 7a potently inhibited Lck kinase with great selectivity (IC50 of 23.0 nM). It was found that 7a and its derivatives possessed high selectivity for Lck over even structurally conserved all Src family kinases. We also observed that 7a inhibited Lck activation in Jurkat T cells. Moreover, 7a was found to alleviate clinical symptoms in DSS-induced colitis mice. This study provides a novel insight into the design of selective type II kinase inhibitors by adopting chiral peptidomimetic moieties on the tail region.

SUBMITTER: Han SJ 

PROVIDER: S-EPMC9067983 | biostudies-literature | 2022 Dec

REPOSITORIES: biostudies-literature

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

Han Seo-Jung SJ   Jung Jae Eun JE   Oh Do Hee DH   Kim Minsup M   Kim Jae-Min JM   Chung Kyung-Sook KS   Han Hee-Soo HS   Lee Jeong-Hun JH   Lee Kyung-Tae KT   Jeong Hee Jin HJ   Park In Ho IH   Jeon Eunkyeong E   Shin Jeon-Soo JS   Hwang Dongkeun D   Cho Art E AE   Lee Duck-Hyung DH   Sim Taebo T  

Journal of enzyme inhibition and medicinal chemistry 20221201 1


Identification of highly selective type II kinase inhibitors is described. Two different chiral peptidomimetic scaffolds were introduced on the tail region of non-selective type II kinase inhibitor GNF-7 to enhance the selectivity. Kinome-wide selectivity profiling analysis showed that type II kinase inhibitor <b>7a</b> potently inhibited Lck kinase with great selectivity (IC<sub>50</sub> of 23.0 nM). It was found that <b>7a</b> and its derivatives possessed high selectivity for Lck over even st  ...[more]

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