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Tethered benzophenone reagents for the synthesis of photoactivatable ligands
J D Olszewski1, G Dormán, J T Elliott
1Department of Chemistry, University at Stony Brook, New York 11794-3400, USA.
Bioconjugate Chemistry
|July 1, 1995
Abstract:
A new radiolabeled, bifunctional photoaffinity cross-linking reagent, N-succinimidyl p-benzoyl-[2,3-3H2]dihydrocinnamate, has been synthesized in high yield and with high specific activity. This reagent can be used to append the benzophenone photophore to amino groups of small molecules, such as O-aminoalkylinositol polyphosphates and polypeptides. The resulting tritiated photoaffinity labels can be purified and manipulated in ambient light and can be activated at 360 nm.