Radiolytic one-electron reduction characteristics of tyrosine derivative caged by 2-oxopropyl group

K Tanabe, M Ebihara, N Hirata, S Nishimoto

Index: Tanabe, Kazuhito; Ebihara, Masahiko; Hirata, Nao; Nishimoto, Sei-ichi Bioorganic and Medicinal Chemistry Letters, 2008 , vol. 18, # 23 p. 6126 - 6129

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Abstract

We employed X-irradiation to activate a caged amino acid with a 2-oxoalkyl group. We designed and synthesized tyrosine derivative caged by a 2-oxoalkyl group (Tyr (Oxo)) to evaluate its radiolytic one-electron reduction characteristics in aqueous solution. Upon hypoxic X-irradiation, Tyr (Oxo) released a 2-oxopropyl group to form the corresponding uncaged tyrosine. In addition, radiolysis of dipeptides containing Tyr (Oxo) revealed that ...