- Synthesis of 5 ''-branched derivatives of cyclic ADP-carbocyclic-ribose, a potent Ca2+-mobilizing agent: The first antagonists modified at the N1-ribose moiety
[作者:Sakaguchi, N; Kudoh, T; Tsuzuki, T; Murayama, T; Sakurai, T; Matsuda, A; Arisawa, M; Shuto, S,期刊:Bioorganic & Medicinal Chemistry Letters, 页码:3814-3818 , 文章类型: Article,,卷期:2008年18-13]
- The 5 ''-branched cyclic ADP-carbocyclic-ribose derivatives were designed and synthesized. These target compounds were identified as the first antagonists of cADPR without a substituent at the adenine 8-position, and wer...
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