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Mechanism-Based Inhibitors of Serine Proteases with High Selectivity Through Optimization of S’ Subsite Binding

A series of mechanism-based inhibitors designed to interact with the S’ subsites of serine proteases was synthesized and their inhibitory activity toward the closely-related serine proteases human neutrophil elastase (HNE) and proteinase 3 (PR 3) was investigated. The compounds were found to be time...

Täydet tiedot

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Bibliografiset tiedot
Päätekijät: Li, Yi, Dou, Dengfeng, He, Guijia, Lushington, Gerald H., Groutas, William C.
Aineistotyyppi: Artigo
Kieli:Inglês
Julkaistu: 2009
Aiheet:
Linkit:https://ncbi.nlm.nih.gov/pmc/articles/PMC2853036/
https://ncbi.nlm.nih.gov/pubmed/19394830
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.bmc.2009.04.011
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