1022895-48-2Relevant academic research and scientific papers
Design and synthesis of 4″,6″-unsaturated cyclic ADP-carbocyclic ribose as a Ca2+-mobilizing agent
Kudoh, Takashi,Weber, Karin,Guse, Andreas H.,Potter, Barry V.L.,Hashii, Minako,Higashida, Haruhiro,Arisawa, Mitsuhiro,Matsuda, Akira,Shuto, Satoshi
, p. 3976 - 3979 (2008)
4″,6″-Didehydro-cADPcR (3), an unsaturated carbocyclic ribose analog of a Ca2+-mobilizing second messenger cyclic ADP-ribose (cADPR), was designed and successfully synthesized using a key intramolecular condensation reaction forming the 18-memb
Design and synthesis of 4″,6″-unsaturated cyclic ADP-carbocyclic-ribose, a Ca2+-mobilizing agent selectively active in T cells
Kudoh, Takashi,Murayama, Takashi,Hashii, Minako,Higashida, Haruhiro,Sakurai, Takashi,Maechling, Clarisse,Spiess, Bernard,Weber, Karin,Guse, Andreas H.,Potter, Barry V.L.,Arisawa, Mitsuhiro,Matsuda, Akira,Shuto, Satoshi
, p. 9754 - 9765 (2008/12/22)
We previously developed cyclic ADP-carbocyclic-ribose (cADPcR, 3a) as a stable mimic of cyclic ADP-ribose (cADPR, 1), a Ca2+-mobilizing second messenger. The unsaturated carbocyclic-ribose analogs of cADPR, i.e., 4″,6″-didehydro-cADPcR (8a) and
