名称:
Design and synthesis of enediyne–peptide conjugates and their inhibiting activity against chymotrypsin
摘要:
Novel enediyne-amino acid conjugates 1-4 have been synthesized. All of these effectively target the enzyme chymotrypsin inhibiting its proteolytic activity. The conjugate with a directly linked phenyl alanine is the most effective inhibitor with a K-i of 3 mu M. The mode of inhibition is mostly competitive or of a mixed type depending on the nature of the inhibitor. (C) 2009 Elsevier Ltd. All rights reserved.
DOI:
10.1016/j.bmc.2009.04.019