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Isoform-Selective Enzyme Inhibitors by Exploring Pocket Size According to the Lock-and-Key Principle

In the design of high-affinity and enzyme isoform-selective inhibitors, we applied an approach of augmenting the substituents attached to the benzenesulfonamide scaffold in three ways, namely, substitutions at the 3,5- or 2,4,6-positions or expansion of the condensed ring system. The increased size...

詳細記述

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書誌詳細
出版年:Biophys J
主要な著者: Dudutienė, Virginija, Zubrienė, Asta, Kairys, Visvaldas, Smirnov, Alexey, Smirnovienė, Joana, Leitans, Janis, Kazaks, Andris, Tars, Kaspars, Manakova, Lena, Gražulis, Saulius, Matulis, Daumantas
フォーマット: Artigo
言語:Inglês
出版事項: The Biophysical Society 2020
主題:
オンライン・アクセス:https://ncbi.nlm.nih.gov/pmc/articles/PMC7642266/
https://ncbi.nlm.nih.gov/pubmed/32971003
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.bpj.2020.08.037
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