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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: | , , , , , |
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格式: | Artigo |
語言: | Inglês |
出版: |
2013
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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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