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Satoshi Shuto

Showing results (61-70 of 182) with videos related to

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Chembiochem : a European Journal of Chemical Biology|June 3, 2016
Highly Sensitive Measurement of Inositol 1,4,5-Trisphosphate by Using a New Fluorescent Ligand and Ligand Binding Domain CombinationTai Oura, Kaori Murata, Takao Morita, et al.
Bioorganic & Medicinal Chemistry|November 5, 2002
Synthesis of derivatives of (1S,2R)-1-phenyl-2-[(S)-1-aminopropyl]-N,N-diethylcyclopropanecarboxamide (PPDC) modified at the 1-aromatic moiety as novel NMDA receptor antagonists: the aromatic group is essential for the activityYuji Kazuta, Ryuichi Tsujita, Kanako Yamashita, et al.
Biochemistry|January 29, 2003
The immunosuppressive agent mizoribine monophosphate forms a transition state analogue complex with inosine monophosphate dehydrogenaseLu Gan, Mohammad R Seyedsayamdost, Satoshi Shuto, et al.
Anticancer Research|May 6, 2021
Structure-activity Relationship of Indomethacin Derivatives as IDO1 InhibitorsTohru Obata, Sara Shiratani, Tomomi Nada, et al.
The Journal of Organic Chemistry|June 16, 2015
Synthesis of 7-Deaza-cyclic Adenosine-5'-diphosphate-carbocyclic-ribose and Its 7-Bromo Derivative as Intracellular Ca(2+)-Mobilizing AgentsSatoshi Takano, Takayoshi Tsuzuki, Takashi Murayama, et al.
Journal of Medicinal Chemistry|December 4, 2003
A method for designing conformationally restricted analogues based on allylic strain: synthesis of a novel class of noncompetitive NMDA receptor antagonists having the acrylamide structureYutaka Ohmori, Akitake Yamashita, Ryuichi Tsujita, et al.
Prostaglandins & Other Lipid Mediators|June 16, 2023
Individual resolvin E family members work distinctly and in a coordinated manner in the resolution of inflammationAyaka Hamaguchi, Hayato Fukuda, Koichi Fujiwara, et al.
Bioorganic & Medicinal Chemistry Letters|September 5, 2018
Design and synthesis of cyclopropane-based conformationally restricted GABA analogues as selective inhibitors for betaine/GABA transporter 1Akihiro Suemasa, Mizuki Watanabe, Takaaki Kobayashi, et al.
Bioorganic & Medicinal Chemistry Letters|November 3, 2018
Design and synthesis of histamine H<sub>3</sub>/H<sub>4</sub> receptor ligands with a cyclopropane scaffoldMizuki Watanabe, Takaaki Kobayashi, Yoshihiko Ito, et al.
The Journal of Organic Chemistry|November 12, 2013
Preparation of chiral bromomethylenecyclopropane and its use in Suzuki-Miyaura coupling: synthesis of the arylmethyl-(Z)-cyclopropane structure coreMakoto Tanabe, Mizuki Watanabe, Naoyuki Hoshiya, et al.
Pageof 19

Showing results (61-70 of 182) with videos related to

Sort By:
Pageof 19
Chembiochem : a European Journal of Chemical Biology|June 3, 2016
Highly Sensitive Measurement of Inositol 1,4,5-Trisphosphate by Using a New Fluorescent Ligand and Ligand Binding Domain CombinationTai Oura, Kaori Murata, Takao Morita, et al.
Bioorganic & Medicinal Chemistry|November 5, 2002
Synthesis of derivatives of (1S,2R)-1-phenyl-2-[(S)-1-aminopropyl]-N,N-diethylcyclopropanecarboxamide (PPDC) modified at the 1-aromatic moiety as novel NMDA receptor antagonists: the aromatic group is essential for the activityYuji Kazuta, Ryuichi Tsujita, Kanako Yamashita, et al.
Biochemistry|January 29, 2003
The immunosuppressive agent mizoribine monophosphate forms a transition state analogue complex with inosine monophosphate dehydrogenaseLu Gan, Mohammad R Seyedsayamdost, Satoshi Shuto, et al.
Anticancer Research|May 6, 2021
Structure-activity Relationship of Indomethacin Derivatives as IDO1 InhibitorsTohru Obata, Sara Shiratani, Tomomi Nada, et al.
The Journal of Organic Chemistry|June 16, 2015
Synthesis of 7-Deaza-cyclic Adenosine-5'-diphosphate-carbocyclic-ribose and Its 7-Bromo Derivative as Intracellular Ca(2+)-Mobilizing AgentsSatoshi Takano, Takayoshi Tsuzuki, Takashi Murayama, et al.
Journal of Medicinal Chemistry|December 4, 2003
A method for designing conformationally restricted analogues based on allylic strain: synthesis of a novel class of noncompetitive NMDA receptor antagonists having the acrylamide structureYutaka Ohmori, Akitake Yamashita, Ryuichi Tsujita, et al.
Prostaglandins & Other Lipid Mediators|June 16, 2023
Individual resolvin E family members work distinctly and in a coordinated manner in the resolution of inflammationAyaka Hamaguchi, Hayato Fukuda, Koichi Fujiwara, et al.
Bioorganic & Medicinal Chemistry Letters|September 5, 2018
Design and synthesis of cyclopropane-based conformationally restricted GABA analogues as selective inhibitors for betaine/GABA transporter 1Akihiro Suemasa, Mizuki Watanabe, Takaaki Kobayashi, et al.
Bioorganic & Medicinal Chemistry Letters|November 3, 2018
Design and synthesis of histamine H<sub>3</sub>/H<sub>4</sub> receptor ligands with a cyclopropane scaffoldMizuki Watanabe, Takaaki Kobayashi, Yoshihiko Ito, et al.
The Journal of Organic Chemistry|November 12, 2013
Preparation of chiral bromomethylenecyclopropane and its use in Suzuki-Miyaura coupling: synthesis of the arylmethyl-(Z)-cyclopropane structure coreMakoto Tanabe, Mizuki Watanabe, Naoyuki Hoshiya, et al.
Pageof 19