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Yusuke Kamada

Showing results (21-30 of 23) with videos related to

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Journal of Medicinal Chemistry|July 30, 2021
Design and Synthesis of Novel Spiro Derivatives as Potent and Reversible Monoacylglycerol Lipase (MAGL) Inhibitors: Bioisosteric Transformation from 3-Oxo-3,4-dihydro-2<i>H</i>-benzo[<i>b</i>][1,4]oxazin-6-yl MoietyShuhei Ikeda, Hideyuki Sugiyama, Hidekazu Tokuhara, et al.
Journal of Medicinal Chemistry|May 23, 2014
A fragment-based approach to identifying S-adenosyl-l-methionine -competitive inhibitors of catechol O-methyl transferase (COMT)Marion Lanier, Geza Ambrus, Derek C Cole, et al.
Molecular Cancer Therapeutics|December 2, 2016
A Novel LSD1 Inhibitor T-3775440 Disrupts GFI1B-Containing Complex Leading to Transdifferentiation and Impaired Growth of AML CellsYoshinori Ishikawa, Kanae Gamo, Masato Yabuki, et al.
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Showing results (21-30 of 23) with videos related to

Sort By:
Pageof 3
You have reached the last page of results.This site can display upto 23 results.
Journal of Medicinal Chemistry|July 30, 2021
Design and Synthesis of Novel Spiro Derivatives as Potent and Reversible Monoacylglycerol Lipase (MAGL) Inhibitors: Bioisosteric Transformation from 3-Oxo-3,4-dihydro-2<i>H</i>-benzo[<i>b</i>][1,4]oxazin-6-yl MoietyShuhei Ikeda, Hideyuki Sugiyama, Hidekazu Tokuhara, et al.
Journal of Medicinal Chemistry|May 23, 2014
A fragment-based approach to identifying S-adenosyl-l-methionine -competitive inhibitors of catechol O-methyl transferase (COMT)Marion Lanier, Geza Ambrus, Derek C Cole, et al.
Molecular Cancer Therapeutics|December 2, 2016
A Novel LSD1 Inhibitor T-3775440 Disrupts GFI1B-Containing Complex Leading to Transdifferentiation and Impaired Growth of AML CellsYoshinori Ishikawa, Kanae Gamo, Masato Yabuki, et al.
Pageof 3