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Tritiated compounds Peptides

Several applications of photoreactive peptides require the presence of a radionuclide to allow specific and sensitive detection of the photo-cross-linked conjugates. In several cases, radioiodination of tyrosyl moieties and radiolabeled Bolton-Hunter reagents have been used. However, the presence of a radiolabel within the benzophenone photophore is desirable, particularly when the objective is to identify the site of photo-insertion of benzophenone. To this end some radiolabeled, benzophenone-based compounds have been developed and used in peptide synthesis, in particular tritiated Phe(4-Bz) (Scheme 24)J2161 [1-14C-carboxy]-4-benzoylbenzoic acid,1221 and 4-benzoyl-(2,3-3H2)-dihydrocinnamic acid.[154l In addition, 4-(4-hydroxybenzoyl)phenylalanine (Scheme 25) has been directly radioiodinated with Na125I and Chloramine-T)151 ... [Pg.125]


See other pages where Tritiated compounds Peptides is mentioned: [Pg.163]    [Pg.101]    [Pg.60]    [Pg.201]    [Pg.113]    [Pg.42]    [Pg.37]    [Pg.460]    [Pg.244]    [Pg.67]    [Pg.120]    [Pg.165]    [Pg.364]   
See also in sourсe #XX -- [ Pg.227 ]




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