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Bioorganic & Medicinal Chemistry|October 20, 2006
Synthesis and biological evaluation of imidazo[1,2-a]pyridine derivatives as novel PI3 kinase p110alpha inhibitorsMasahiko Hayakawa, Hiroyuki Kaizawa, Ken-Ichi Kawaguchi, et al.Bioorganic & Medicinal Chemistry|April 18, 2012
Discovery of Ipragliflozin (ASP1941): a novel C-glucoside with benzothiophene structure as a potent and selective sodium glucose co-transporter 2 (SGLT2) inhibitor for the treatment of type 2 diabetes mellitusMasakazu Imamura, Keita Nakanishi, Takayuki Suzuki, et al.Bioorganic & Medicinal Chemistry Letters|August 3, 2012
Orally available pyridinylpyrimidine derivatives as novel RANKL-induced osteoclastogenesis inhibitorsJunji Miyata, Chiyoshi Kasahara, Toru Asano, et al.Journal of Medicinal Chemistry|January 20, 2006
(+)-(2R,5S)-4-[4-cyano-3-(trifluoromethyl)phenyl]-2,5-dimethyl-N-[6-(trifluoromethyl)pyridin-3- yl]piperazine-1-carboxamide (YM580) as an orally potent and peripherally selective nonsteroidal androgen receptor antagonistIsao Kinoyama, Nobuaki Taniguchi, Akira Toyoshima, et al.Bioorganic & Medicinal Chemistry|September 15, 2009
Novel 7H-pyrrolo[2,3-d]pyrimidine derivatives as potent and orally active STAT6 inhibitorsShinya Nagashima, Takeshi Hondo, Hiroshi Nagata, et al.Bioorganic & Medicinal Chemistry|November 3, 2004
Studies of nonnucleoside HIV-1 reverse transcriptase inhibitors. Part 1: Design and synthesis of thiazolidenebenzenesulfonamidesNaoyuki Masuda, Osamu Yamamoto, Masahiro Fujii, et al.Bioorganic & Medicinal Chemistry|January 27, 2005
Studies of non-nucleoside HIV-1 reverse transcriptase inhibitors. Part 2: synthesis and structure-activity relationships of 2-cyano and 2-hydroxy thiazolidenebenzenesulfonamide derivativesNaoyuki Masuda, Osamu Yamamoto, Masahiro Fujii, et al.Pageof 8