布鲁顿酪氨酸激酶
停留时间(流体动力学)
酪氨酸激酶
体内
化学
半胱氨酸
住所
药理学
生物化学
共价键
酶
受体
医学
生物
遗传学
有机化学
人口学
社会学
岩土工程
工程类
作者
J. Michael Bradshaw,Jesse M. McFarland,Ville O. Paavilainen,Angelina Bisconte,Danny Tam,Vernon T. Phan,Sergei Romanov,David Finkle,Jin Shu,Vaishali Patel,Tony Ton,Xiaoyan Li,David G. Loughhead,Philip A. Nunn,Dane E. Karr,Mary E. Gerritsen,Jens Oliver Funk,Timothy D. Owens,Erik Verner,Ken A. Brameld
标识
DOI:10.1038/nchembio.1817
摘要
Drugs with prolonged on-target residence times often show superior efficacy, yet general strategies for optimizing drug-target residence time are lacking. Here we made progress toward this elusive goal by targeting a noncatalytic cysteine in Bruton's tyrosine kinase (BTK) with reversible covalent inhibitors. Using an inverted orientation of the cysteine-reactive cyanoacrylamide electrophile, we identified potent and selective BTK inhibitors that demonstrated biochemical residence times spanning from minutes to 7 d. An inverted cyanoacrylamide with prolonged residence time in vivo remained bound to BTK for more than 18 h after clearance from the circulation. The inverted cyanoacrylamide strategy was further used to discover fibroblast growth factor receptor (FGFR) kinase inhibitors with residence times of several days, demonstrating the generalizability of the approach. Targeting of noncatalytic cysteines with inverted cyanoacrylamides may serve as a broadly applicable platform that facilitates 'residence time by design', the ability to modulate and improve the duration of target engagement in vivo.
科研通智能强力驱动
Strongly Powered by AbleSci AI