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Satoshi Shuto

Showing results (81-90 of 182) with videos related to

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ACS Medicinal Chemistry Letters|May 19, 2016
Identification of a Potent and Selective GPR4 Antagonist as a Drug Lead for the Treatment of Myocardial InfarctionHayato Fukuda, Saki Ito, Kenji Watari, et al.
Journal of the American Chemical Society|July 27, 2011
Synthesis and characterization of a series of highly fluorogenic substrates for glutathione transferases, a general strategyJie Zhang, Aya Shibata, Mika Ito, et al.
Journal of the American Chemical Society|September 11, 2013
Very rapid DNA-templated reaction for efficient signal amplification and its steady-state kinetic analysis of the turnover cycleAya Shibata, Takanori Uzawa, Yuko Nakashima, et al.
Cancer Science|February 26, 2008
Antineovascular therapy with angiogenic vessel-targeted polyethyleneglycol-shielded liposomal DPP-CNDACTomohiro Asai, Souichiro Miyazawa, Noriyuki Maeda, et al.
Bioorganic & Medicinal Chemistry Letters|June 7, 2008
Synthesis of 5''-branched derivatives of cyclic ADP-carbocyclic-ribose, a potent Ca2+-mobilizing agent: The first antagonists modified at the N1-ribose moietyNatsumi Sakaguchi, Takashi Kudoh, Takayoshi Tsuzuki, et al.
Journal of Medicinal Chemistry|October 17, 2003
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-riboseSatoshi Shuto, Masayoshi Fukuoka, Takashi Kudoh, et al.
Organic & Biomolecular Chemistry|March 24, 2005
Synthesis of 5'-methylenearisteromycin and its 2-fluoro derivative with potent antimalarial activity due to inhibition of the parasite S-adenosylhomocysteine hydrolaseChieko Takagi, Makoto Sukeda, Hye-Sook Kim, et al.
Organic Letters|March 28, 2006
Design and synthesis of 5'-deoxy-5'-phenyladenophostin A, a highly potent IP3 receptor ligandTetsuya Mochizuki, Yoshihiko Kondo, Hiroshi Abe, et al.
Journal of Medicinal Chemistry|March 24, 2016
Identification of Adenine and Benzimidazole Nucleosides as Potent Human Concentrative Nucleoside Transporter 2 Inhibitors: Potential Treatment for Hyperuricemia and GoutKazuya Tatani, Masahiro Hiratochi, Norihiko Kikuchi, et al.
Chemical Communications (Cambridge, England)|December 13, 2019
Intracellular build-up RNAi with single-strand circular RNAs as siRNA precursorsYasuaki Kimura, Zhaoma Shu, Mika Ito, et al.
Pageof 19

Showing results (81-90 of 182) with videos related to

Sort By:
Pageof 19
ACS Medicinal Chemistry Letters|May 19, 2016
Identification of a Potent and Selective GPR4 Antagonist as a Drug Lead for the Treatment of Myocardial InfarctionHayato Fukuda, Saki Ito, Kenji Watari, et al.
Journal of the American Chemical Society|July 27, 2011
Synthesis and characterization of a series of highly fluorogenic substrates for glutathione transferases, a general strategyJie Zhang, Aya Shibata, Mika Ito, et al.
Journal of the American Chemical Society|September 11, 2013
Very rapid DNA-templated reaction for efficient signal amplification and its steady-state kinetic analysis of the turnover cycleAya Shibata, Takanori Uzawa, Yuko Nakashima, et al.
Cancer Science|February 26, 2008
Antineovascular therapy with angiogenic vessel-targeted polyethyleneglycol-shielded liposomal DPP-CNDACTomohiro Asai, Souichiro Miyazawa, Noriyuki Maeda, et al.
Bioorganic & Medicinal Chemistry Letters|June 7, 2008
Synthesis of 5''-branched derivatives of cyclic ADP-carbocyclic-ribose, a potent Ca2+-mobilizing agent: The first antagonists modified at the N1-ribose moietyNatsumi Sakaguchi, Takashi Kudoh, Takayoshi Tsuzuki, et al.
Journal of Medicinal Chemistry|October 17, 2003
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-riboseSatoshi Shuto, Masayoshi Fukuoka, Takashi Kudoh, et al.
Organic & Biomolecular Chemistry|March 24, 2005
Synthesis of 5'-methylenearisteromycin and its 2-fluoro derivative with potent antimalarial activity due to inhibition of the parasite S-adenosylhomocysteine hydrolaseChieko Takagi, Makoto Sukeda, Hye-Sook Kim, et al.
Organic Letters|March 28, 2006
Design and synthesis of 5'-deoxy-5'-phenyladenophostin A, a highly potent IP3 receptor ligandTetsuya Mochizuki, Yoshihiko Kondo, Hiroshi Abe, et al.
Journal of Medicinal Chemistry|March 24, 2016
Identification of Adenine and Benzimidazole Nucleosides as Potent Human Concentrative Nucleoside Transporter 2 Inhibitors: Potential Treatment for Hyperuricemia and GoutKazuya Tatani, Masahiro Hiratochi, Norihiko Kikuchi, et al.
Chemical Communications (Cambridge, England)|December 13, 2019
Intracellular build-up RNAi with single-strand circular RNAs as siRNA precursorsYasuaki Kimura, Zhaoma Shu, Mika Ito, et al.
Pageof 19