共价键
半胱氨酸
化学
组合化学
反应性(心理学)
电泳剂
亲核细胞
化学生物学
酶
氨基酸
立体化学
生物化学
有机化学
催化作用
病理
医学
替代医学
作者
László Petri,Péter Ábrányi‐Balogh,Tı́mea Imre,Gyula Pálfy,András Perczel,Damijan Knez,Martina Hrast,Martina Gobec,Izidor Sosič,Kinga Nyíri,Beáta G. Vértessy,Niklas Jänsch,Charlotte Desczyk,Franz‐Josef Meyer‐Almes,Iza Ogris,Simona Golič Grdadolnik,L.G. Iacovino,Claudia Binda,Stanislav Gobec,György M. Keserű
出处
期刊:ChemBioChem
[Wiley]
日期:2020-11-09
卷期号:22 (4): 743-753
被引量:19
标识
DOI:10.1002/cbic.202000700
摘要
Abstract Targeted covalent inhibition and the use of irreversible chemical probes are important strategies in chemical biology and drug discovery. To date, the availability and reactivity of cysteine residues amenable for covalent targeting have been evaluated by proteomic and computational tools. Herein, we present a toolbox of fragments containing a 3,5‐bis(trifluoromethyl)phenyl core that was equipped with chemically diverse electrophilic warheads showing a range of reactivities. We characterized the library members for their reactivity, aqueous stability and specificity for nucleophilic amino acids. By screening this library against a set of enzymes amenable for covalent inhibition, we showed that this approach experimentally characterized the accessibility and reactivity of targeted cysteines. Interesting covalent fragment hits were obtained for all investigated cysteine‐containing enzymes.
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