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Satoshi Shuto

Showing results (111-120 of 182) with videos related to

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Biochemistry|July 9, 2004
Oligodeoxynucleotides having a loop consisting of 3'-deoxy-4'-C-(2-hydroxyethyl)thymidines form stable hairpinsYuji Yamamoto, Satoshi Shuto, Yutaka Tamura, et al.
Organic & Biomolecular Chemistry|July 11, 2009
Three-dimensional structure-activity relationship study of belactosin A and its stereo- and regioisomers: development of potent proteasome inhibitors by a stereochemical diversity-oriented strategyKeisuke Yoshida, Kazuya Yamaguchi, Akira Mizuno, et al.
The Journal of Organic Chemistry|July 14, 2018
Synthesis of Chiral cis-Cyclopropane Bearing Indole and Chromone as Potential TNFα InhibitorsRyutaro Kanada, Makoto Tanabe, Ryuta Muromoto, et al.
Journal of Medicinal Chemistry|April 4, 2013
Potent proteasome inhibitors derived from the unnatural cis-cyclopropane isomer of Belactosin A: synthesis, biological activity, and mode of actionShuhei Kawamura, Yuka Unno, Anja List, et al.
Journal of Medicinal Chemistry|July 9, 2016
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 MessengerTakatoshi Sato, Mizuki Watanabe, Takayoshi Tsuzuki, et al.
ACS Medicinal Chemistry Letters|February 19, 2021
Synthesis of Resolvin E1 and Its Conformationally Restricted Cyclopropane Congeners with Potent Anti-Inflammatory EffectKohei Ishimura, Hayato Fukuda, Koichi Fujiwara, et al.
Journal of Medicinal Chemistry|January 17, 2022
Discovery of Gut-Restricted Small-Molecule Inhibitors of Intestinal Sodium-Dependent Phosphate Transport Protein 2b (NaPi2b) for the Treatment of HyperphosphatemiaMichihiro Maemoto, Yuuki Hirata, Shintaro Hosoe, et al.
Bioorganic & Medicinal Chemistry|June 24, 2019
Synthesis of oxytocin derivatives lipidated via a carbonate or carbamate linkage as a long-acting therapeutic agent for social impairment-like behaviorsStanislav M Cherepanov, Risako Miura, Anna A Shabalova, et al.
Journal of Medicinal Chemistry|April 20, 2010
Investigation of the bioactive conformation of histamine H3 receptor antagonists by the cyclopropylic strain-based conformational restriction strategyMizuki Watanabe, Takatsugu Hirokawa, Takaaki Kobayashi, et al.
Journal of Medicinal Chemistry|July 11, 2013
Investigation of the noncovalent binding mode of covalent proteasome inhibitors around the transition state by combined use of cyclopropylic strain-based conformational restriction and computational modelingShuhei Kawamura, Yuka Unno, Motohiro Tanaka, et al.
Pageof 19

Showing results (111-120 of 182) with videos related to

Sort By:
Pageof 19
Biochemistry|July 9, 2004
Oligodeoxynucleotides having a loop consisting of 3'-deoxy-4'-C-(2-hydroxyethyl)thymidines form stable hairpinsYuji Yamamoto, Satoshi Shuto, Yutaka Tamura, et al.
Organic & Biomolecular Chemistry|July 11, 2009
Three-dimensional structure-activity relationship study of belactosin A and its stereo- and regioisomers: development of potent proteasome inhibitors by a stereochemical diversity-oriented strategyKeisuke Yoshida, Kazuya Yamaguchi, Akira Mizuno, et al.
The Journal of Organic Chemistry|July 14, 2018
Synthesis of Chiral cis-Cyclopropane Bearing Indole and Chromone as Potential TNFα InhibitorsRyutaro Kanada, Makoto Tanabe, Ryuta Muromoto, et al.
Journal of Medicinal Chemistry|April 4, 2013
Potent proteasome inhibitors derived from the unnatural cis-cyclopropane isomer of Belactosin A: synthesis, biological activity, and mode of actionShuhei Kawamura, Yuka Unno, Anja List, et al.
Journal of Medicinal Chemistry|July 9, 2016
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 MessengerTakatoshi Sato, Mizuki Watanabe, Takayoshi Tsuzuki, et al.
ACS Medicinal Chemistry Letters|February 19, 2021
Synthesis of Resolvin E1 and Its Conformationally Restricted Cyclopropane Congeners with Potent Anti-Inflammatory EffectKohei Ishimura, Hayato Fukuda, Koichi Fujiwara, et al.
Journal of Medicinal Chemistry|January 17, 2022
Discovery of Gut-Restricted Small-Molecule Inhibitors of Intestinal Sodium-Dependent Phosphate Transport Protein 2b (NaPi2b) for the Treatment of HyperphosphatemiaMichihiro Maemoto, Yuuki Hirata, Shintaro Hosoe, et al.
Bioorganic & Medicinal Chemistry|June 24, 2019
Synthesis of oxytocin derivatives lipidated via a carbonate or carbamate linkage as a long-acting therapeutic agent for social impairment-like behaviorsStanislav M Cherepanov, Risako Miura, Anna A Shabalova, et al.
Journal of Medicinal Chemistry|April 20, 2010
Investigation of the bioactive conformation of histamine H3 receptor antagonists by the cyclopropylic strain-based conformational restriction strategyMizuki Watanabe, Takatsugu Hirokawa, Takaaki Kobayashi, et al.
Journal of Medicinal Chemistry|July 11, 2013
Investigation of the noncovalent binding mode of covalent proteasome inhibitors around the transition state by combined use of cyclopropylic strain-based conformational restriction and computational modelingShuhei Kawamura, Yuka Unno, Motohiro Tanaka, et al.
Pageof 19