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ECB-ART-39598
Nucleosides Nucleotides Nucleic Acids 2005 Jan 01;245-7:655-8. doi: 10.1081/ncn-200060167.
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Synthesis and biological activity of cyclic ADP-carbocyclic-ribose analogs: structure-activity relationship and conformational analysis of N-1-carbocyclic-ribose moiety.

Kudoh T , Fukuoka M , Shuto S , Matsuda A .


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Several cyclic ADP-carbocyclic-ribose analogs 3-10 modified in the N-1-carbocyclic-ribose moiety were synthesized. Their Ca2+-releasing activity was estimated in sea urchin eggs to show that the 3"-deoxy analog 6 shows 5 times more potent activity than cADPcR, but the 2",3"-didieoxy-2",3"-unsunsaturated analog 3 has very weak activity. We also calculated their stable conformation and found that 3 and 6 were significantly different in their stable conformation.

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Genes referenced: LOC100887844