Rational Tuning of Fluorobenzene Probes for Cysteine-Selective Protein Modification was written by Embaby, Ahmed M.;Schoffelen, Sanne;Kofoed, Christian;Meldal, Morten;Diness, Frederik. And the article was included in Angewandte Chemie, International Edition in 2018.Formula: C5F5N The following contents are mentioned in the article:
Fluorobenzene probes for protein profiling through selective cysteine labeling have been developed by rational reactivity tuning. Tuning was achieved by selecting an electron-withdrawing para substituent in combination with variation of the number of fluorine substituents. Optimized probes chemoselectively arylated cysteine residues in proteins under aqueous conditions. Probes linked to azide, biotin, or a fluorophore were applicable to labeling of eGFP and albumin. Selective inhibition of cysteine proteases was also demonstrated with the probes. Addnl., probes were tuned for site-selective labeling of cysteine residues and for activity-based protein profiling in cell lysates. This study involved multiple reactions and reactants, such as 2,3,4,5,6-Perfluoropyridine (cas: 700-16-3Formula: C5F5N).
2,3,4,5,6-Perfluoropyridine (cas: 700-16-3) belongs to pyridine derivatives. Pyridine has a conjugated system of six 蟺 electrons that are delocalized over the ring. The molecule is planar and, thus, follows the H眉ckel criteria for aromatic systems. Pyridine, its benzo and pyridine-based compounds play diverse roles in organic chemistry. Pyridine-based materials are valued for their optical and physical properties as well as their medical potential. Formula: C5F5N