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Fragment based discovery of Arginine isosteres through REPLACE: towards non-ATP competitive CDK inhibitors

In order to develop non-ATP competitive CDK2/cyclin A inhibitors, the REPLACE strategy has been applied to generate fragment alternatives for the N-terminal tetrapeptide of the cyclin binding motif (HAKRRLIF) involved in substrate recruitment prior to phosphotransfer. The docking approach used for t...

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Main Authors: Premnath, Padmavathy Nandha, Liu, Shu, Perkins, Tracy, Abbott, Jennifer, Anderson, Erin, McInnes, Campbell
格式: Artigo
語言:Inglês
出版: 2013
主題:
在線閱讀:https://ncbi.nlm.nih.gov/pmc/articles/PMC3917480/
https://ncbi.nlm.nih.gov/pubmed/24286762
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.bmc.2013.10.039
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