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Bromoacetophenone-based photonucleases: photoinduced cleavage of DNA by 4'-bromoacetophenone-pyrrolecarboxamide conjugates.

Organic letters (2000-06-03)
P A Wender, R Jeon
RESUMEN

[formula: see text] 4'-Bromoacetophenone derivatives which upon excitation can generate monophenyl radicals capable of hydrogen atom abstraction were investigated as photoinducible DNA cleaving agents. Pyrrolecarboxamide-conjugated 4'-bromoacetophenones were synthesized, and their DNA cleaving activities and sequence selectivities were determined.

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Sigma-Aldrich
2-Bromoacetophenone, 98%
Supelco
2-Bromoacetophenone, for GC derivatization, LiChropur, ≥99.0%