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ECB-ART-39858
Nucleosides Nucleotides Nucleic Acids 2006 Jan 01;254-6:583-99. doi: 10.1080/15257770600685867.
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Synthesis of cyclic ADP-carbocylcic-xylose and its 3"-O-methyl analogue as stable and potent Ca2+ -mobilizing agents.

Kudoh T , Matsuda A , Shuto S , Murayama T , Ogawa Y .


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We previously showed that 3"-deoxy-cyclic ADP-carbocyclic-ribose (3"-deoxy-cADPcR, 3) is a stable and highly potent analogue of cyclic ADP-ribose (cADPR, 1), a Ca2+ -mobilizing second messenger. From these results, we newly designed another 3"-modified analogues of cADPcR and identified the N1-"xylo"-type carbocyclic analogue, i.e., cADPcX (4), as one of the most potent cADPR-related compounds reported so far.

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