Satoshi Shuto
Faculty of Pharmaceutical Sciences
Hokkaido University
Kita-12
Nishi-6
Japan
Name/email consistency: high
- Design, synthesis, and biological activity of carbocyclic analogues of cyclic ADP-ribose, a Ca2+-mobilizing second messenger. Shuto, S. Nucleic. Acids. Symp. Ser. (Oxf) (2007)
- Chemistry of cyclic ADP-ribose and its analogs. Shuto, S., Matsuda, A. Curr. Med. Chem. (2004)
- Convergent synthesis and unexpected Ca(2+)-mobilizing activity of 8-substituted analogues of cyclic ADP-carbocyclic-ribose, a stable mimic of the Ca(2+)-mobilizing second messenger cyclic ADP-ribose. Shuto, S., Fukuoka, M., Kudoh, T., Garnham, C., Galione, A., Potter, B.V., Matsuda, A. J. Med. Chem. (2003)
- (1S,2R)-1-Phenyl-2-[(S)-1-aminopropyl]-N,N-diethylcyclopropanecarboxamide (PPDC), a new class of NMDA-receptor antagonist: molecular design by a novel conformational restriction strategy. Shuto, S., Yoshii, K., Matsuda, A. Jpn. J. Pharmacol. (2001)
- Total synthesis of cyclic ADP-carbocyclic-ribose, a stable mimic of Ca2+-mobilizing second messenger cyclic ADP-ribose. Shuto, S., Fukuoka, M., Manikowsky, A., Ueno, Y., Nakano, T., Kuroda, R., Kuroda, H., Matsuda, A. J. Am. Chem. Soc. (2001)
- Intracellular Ca(2+)-mobilizing adenine nucleotides. Synthesis and biological activity of cyclic ADP-carbocyclic-ribose and C-glycosidic analog of adenophostin A. Shuto, S., Fukuoka, M., Abe, H., Matsuda, A. Nucleosides. Nucleotides. Nucleic. Acids (2001)
