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Current Topics in Medicinal Chemistry|December 17, 2008
Peroxisome proliferator-activated receptor gamma agonists as insulin sensitizers: from the discovery to recent progressNobuo Cho, Yu MomoseMethods in Enzymology|February 10, 2023
Synthesis of SNIPERs against BCR-ABL with kinase inhibitors and a method to evaluate their growth inhibitory activity derived from BCR-ABL degradationNobuo Cho, Mikihiko NaitoBioorganic & Medicinal Chemistry Letters|January 27, 2022
Development of a degrader against oncogenic fusion protein FGFR3-TACC3Norihito Shibata, Nobuo Cho, Hiroo Koyama, et al.Cancer Science|February 14, 2017
SNIPER(TACC3) induces cytoplasmic vacuolization and sensitizes cancer cells to BortezomibNobumichi Ohoka, Katsunori Nagai, Norihito Shibata, et al.The Journal of Clinical Endocrinology and Metabolism|April 8, 2003
Suppression of a pituitary-ovarian axis by chronic oral administration of a novel nonpeptide gonadotropin-releasing hormone antagonist, TAK-013, in cynomolgus monkeysTakahito Hara, Hideo Araki, Masami Kusaka, et al.JACS Au|February 27, 2026
Data-Driven Design of PROTAC Linkers to Improve PROTAC Cell Membrane PermeabilityYuki Murakami, Shoichi Ishida, Nobuo Cho, et al.Journal of Medicinal Chemistry|December 28, 2002
Discovery of a thieno[2,3-d]pyrimidine-2,4-dione bearing a p-methoxyureidophenyl moiety at the 6-position: a highly potent and orally bioavailable non-peptide antagonist for the human luteinizing hormone-releasing hormone receptorSatoshi Sasaki, Nobuo Cho, Yoshi Nara, et al.Chemical & Pharmaceutical Bulletin|October 30, 2018
Different Degradation Mechanisms of Inhibitor of Apoptosis Proteins (IAPs) by the Specific and Nongenetic IAP-Dependent Protein Eraser (SNIPER)Nobumichi Ohoka, Osamu Ujikawa, Kenichiro Shimokawa, et al.Bioorganic & Medicinal Chemistry|December 25, 2021
Discovery of phenylpyrrolidine derivatives as a novel class of retinol binding protein 4 (RBP4) reducersShinji Nakamura, Masahiro Kamaura, Yuichiro Akao, et al.Bioorganic & Medicinal Chemistry Letters|July 20, 2002
A new class of potent nonpeptide luteinizing hormone-releasing hormone (LHRH) antagonists: design and synthesis of 2-phenylimidazo[1,2-a]pyrimidin-5-onesSatoshi Sasaki, Toshihiro Imaeda, Yoji Hayase, et al.Pageof 3