Title : Organic azide inhibitors of cysteine proteases.

Pub. Date : 2006 Sep 27

PMID : 16984172






1 Functional Relationships(s)
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1 This new approach resulted in potent, reversible, competitive inhibitors of caspase-1 (IC50 < 10 nM), with significant advantages over aldehydes such as high stability in vitro to thiols (10 mM dithiothreitol (pH 7.2), 20 mM glutathione (pH 7.2, 9, 11)) and aqueous media, as well as some highly desirable druglike features. Sulfhydryl Compounds caspase 1 Homo sapiens