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Benzophenone-4-maleimide

Figure 5.34 Benzophenone-4-maleimide can couple to thiol-containing molecules to form stable thioether bonds. Exposure of the benzophenone group to UV light causes transition to a triplet-state ketone of high reactivity for insertion into C—H or N—H bonds. Figure 5.34 Benzophenone-4-maleimide can couple to thiol-containing molecules to form stable thioether bonds. Exposure of the benzophenone group to UV light causes transition to a triplet-state ketone of high reactivity for insertion into C—H or N—H bonds.
Tao, T., Lamkin, M., and Schemer, C. (1984) Studies on the proximity relationships between thin filament proteins using benzophenone-4-maleimide as a site-specific photoreactive crosslinker. Biophys. J. 45,261. [Pg.1120]

Benzophenone-4-maleimide is a heterobifunctional photoreactive cross-linker that has sulfhydryl reactivity similar to benzophenone-4-iodoacetamide discussed in the... [Pg.300]

See other pages where Benzophenone-4-maleimide is mentioned: [Pg.330]    [Pg.330]    [Pg.330]    [Pg.330]    [Pg.300]    [Pg.301]    [Pg.302]    [Pg.280]    [Pg.281]    [Pg.282]   


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Maleimides

Reaction benzophenone-4-maleimide

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