Design, Synthesis, and Identification of 4″α-Azidoethyl-cyclic ADP-Carbocyclic-ribose as a Highly Potent Analogue of Cyclic ADP-Ribose, a Ca(2+)-Mobilizing Second Messenger.

نویسندگان

  • Takatoshi Sato
  • Mizuki Watanabe
  • Takayoshi Tsuzuki
  • Satoshi Takano
  • Takashi Murayama
  • Takashi Sakurai
  • Tomoshi Kameda
  • Hayato Fukuda
  • Mitsuhiro Arisawa
  • Satoshi Shuto
چکیده

Cyclic adenosine diphosphate-carbocyclic-ribose (cADPcR, 2) is a stable equivalent of cyclic adenosine diphosphate-ribose (cADPR, 1), a Ca(2+)-mobilizing second messenger. On the basis of the structure-activity relationship of cADPR-related compounds and three-dimensional structural modeling of cADPcR, we designed and synthesized cyclic-ADP-4″α-azidoethyl carbocyclic-ribose (N3-cADPcR, 3) to demonstrate that it has a highly potent Ca(2+)-mobilizing activity (EC50 = 24 nM). N3-cADPcR will be a useful precursor for the preparation of biological tools effective to investigate cADPR-mediated signaling pathways.

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عنوان ژورنال:
  • Journal of medicinal chemistry

دوره 59 15  شماره 

صفحات  -

تاریخ انتشار 2016