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Journal of Medicinal Chemistry|May 8, 2009
Design, synthesis, and biological activity of boronic acid-based histone deacetylase inhibitorsNobuaki Suzuki, Takayoshi Suzuki, Yosuke Ota, et al.
American Journal of Physiology. Lung Cellular and Molecular Physiology|October 26, 2018
HDAC8 inhibition ameliorates pulmonary fibrosisShigeki Saito, Yan Zhuang, Takayoshi Suzuki, et al.
Bioorganic & Medicinal Chemistry|February 10, 2024
Design, synthesis, and biological evaluation of phenylcyclopropylamine-entinostat conjugates that selectively target cancer cellsYosuke Ota, Yukihiro Itoh, Yuri Takada, et al.
Chemmedchem|January 10, 2014
Design, synthesis, and biological activity of NCC149 derivatives as histone deacetylase 8-selective inhibitorsTakayoshi Suzuki, Nobusuke Muto, Masashige Bando, et al.
Chemical & Pharmaceutical Bulletin|September 2, 2009
Explorative study on isoform-selective histone deacetylase inhibitorsTakayoshi Suzuki
Organic & Biomolecular Chemistry|August 23, 2016
C-H activation enables a rapid structure-activity relationship study of arylcyclopropyl amines for potent and selective LSD1 inhibitorsShin Miyamura, Misaho Araki, Yosuke Ota, et al.
Bioorganic & Medicinal Chemistry|January 15, 2018
Design, synthesis and evaluation of γ-turn mimetics as LSD1-selective inhibitorsYosuke Ota, Shin Miyamura, Misaho Araki, et al.
Acta Crystallographica. Section E, Structure Reports Online|May 18, 2011
Bis[μ-2-(aminosulfanyl)pyridine(1-)]bis-[(η-penta-methyl-cyclo-penta-dien-yl)iridium(III)] diiodideYusuke Sekioka, Takayoshi Suzuki
Yakugaku Zasshi : Journal of the Pharmaceutical Society of Japan|March 3, 2017
"Drug" Discovery with the Help of Organic ChemistryYukihiro Itoh, Takayoshi Suzuki
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