1266664-85-0Relevant academic research and scientific papers
Reversible protein affinity-labelling using bromomaleimide-based reagents
Nathani, Ramiz I.,Chudasama, Vijay,Ryan, Chris P.,Moody, Paul R.,Morgan, Rachel E.,Fitzmaurice, Richard J.,Smith, Mark E. B.,Baker, James R.,Caddick, Stephen
, p. 2408 - 2411 (2013)
Reversible protein biotinylation is readily affected via conjugation with a bromomaleimide-based reagent followed by reductive cleavage. The intermediate biotinylated protein constructs are stable at physiological temperature and pH 8.0. Quantitative reve
A mild synthesis of N-functionalised bromomaleimides, thiomaleimides and bromopyridazinediones
Casta?eda, Lourdes,Wright, Zo? V.F.,Marculescu, Cristina,Tran, Trang M.,Chudasama, Vijay,Maruani, Antoine,Hull, Elizabeth A.,Nunes, Jo?o P.M.,Fitzmaurice, Richard J.,Smith, Mark E.B.,Jones, Lyn H.,Caddick, Stephen,Baker, James R.
supporting information, p. 3493 - 3495 (2013/07/05)
Bromomaleimides are useful building blocks in synthesis and powerful reagents for the selective chemical modification of proteins. A mild new synthesis of these reagents is described, along with the convenient transferability of the approach to dithiomale
Photocycloadditions of thiomaleimides
Tedaldi, Lauren M.,Aliev, Abil E.,Baker, James R.
supporting information; experimental part, p. 4725 - 4727 (2012/06/01)
Thiomaleimides, generated by the addition of bromomaleimides to thiols including cysteine, undergo highly efficient [2+2] photocycloadditions.
