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• W2057995901 abstract "Treating tropical diseases: Structure-based design afforded highly active triazine nitrile inhibitors of the protozoan cysteine proteases falcipain-2 and rhodesain. Optimization of the occupancy of the S1, S2, and S3 pockets of these enzymes yielded inhibitory constants in the low nanomolar activity range. The new ligands are selective against other related proteases and exhibit in vitro activities against the protozoan parasites. Detailed facts of importance to specialist readers are published as ”Supporting Information”. Such documents are peer-reviewed, but not copy-edited or typeset. They are made available as submitted by the authors. Please note: The publisher is not responsible for the content or functionality of any supporting information supplied by the authors. Any queries (other than missing content) should be directed to the corresponding author for the article." @default.
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• W2057995901 date "2010-11-25" @default.
• W2057995901 modified "2023-10-16" @default.
• W2057995901 title "Potent and Selective Inhibition of Cysteine Proteases from<i>Plasmodium falciparum</i>and<i>Trypanosoma brucei</i>" @default.
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• W2057995901 doi "https://doi.org/10.1002/cmdc.201000449" @default.
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