Here, we show that functionalization of the 4-arylidene position of the fluorescent curcumin scaffold with an aryl nitrogen mustard provides a stable Hck inhibitor (Kd = 50 ± 10 nM). The mustard curcumin derivative preferentially interacts with the inactive conformation of Hck, similar to type-II kinase inhibitors that are less https://ekim-bonusu-veren-siteler.ktwiki.com/1234519/Смарт_трик_hãçķlnc_что_никто_не_обсуждает_вопрос