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• W2054313211 abstract "A series of 15 cinnamoyl triazole derivatives was prepared by Cu(I)-catalyzed azide/alkyne [3+2]-cycloaddition reactions and examined as inhibitors of guinea-pig liver transglutaminase. Several compounds exhibited activity as reversible inhibitors that were competitive with acyl donor transglutaminase substrates. For example, triazole 4d has a K(i) value of 174 nM and represents one of the most potent reversible transglutaminase inhibitors reported to date." @default.
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• W2054313211 date "2008-09-01" @default.
• W2054313211 modified "2023-09-30" @default.
• W2054313211 title "Reversible and Competitive Cinnamoyl Triazole Inhibitors of Tissue Transglutaminase" @default.
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• W2054313211 doi "https://doi.org/10.1111/j.1747-0285.2008.00696.x" @default.
• W2054313211 hasPubMedId "https://pubmed.ncbi.nlm.nih.gov/18715232" @default.
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