TETHERED BENZOPHENONE REAGENTS FOR THE SYNTHESIS OF PHOTOACTIVATABLE LIGANDS

Citation
Jd. Olszewski et al., TETHERED BENZOPHENONE REAGENTS FOR THE SYNTHESIS OF PHOTOACTIVATABLE LIGANDS, Bioconjugate chemistry, 6(4), 1995, pp. 395-400
Citations number
38
Categorie Soggetti
Biology,Chemistry,"Biochemical Research Methods
Journal title
ISSN journal
10431802
Volume
6
Issue
4
Year of publication
1995
Pages
395 - 400
Database
ISI
SICI code
1043-1802(1995)6:4<395:TBRFTS>2.0.ZU;2-F
Abstract
A new radiolabeled, bifunctional photoaffinity cross-linking reagent, N-succinimidyl p-benzoyl-[2,3-H-3(2)]dihydrocinnamate, has been synthe sized 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 polypeptid es. The resulting tritiated photoaffinity labels can be purified and m anipulated in ambient light and can be activated at 360 nm.