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Bioorganic & Medicinal Chemistry|April 25, 2008
Synthesis of 5-chloro-N-aryl-1H-indole-2-carboxamide derivatives as inhibitors of human liver glycogen phosphorylase aKenichi Onda, Takayuki Suzuki, Ryota Shiraki, et al.
Bioorganic & Medicinal Chemistry|July 2, 2005
Synthetic studies on novel Syk inhibitors. Part 1: Synthesis and structure-activity relationships of pyrimidine-5-carboxamide derivativesHiroyuki Hisamichi, Ryo Naito, Akira Toyoshima, et al.
Journal of Medicinal Chemistry|April 10, 2013
4-Hydroxypyridazin-3(2H)-one derivatives as novel D-amino acid oxidase inhibitorsTakeshi Hondo, Masaichi Warizaya, Tatsuya Niimi, et al.
Bioorganic & Medicinal Chemistry|August 13, 2008
Potent CCR4 antagonists: synthesis, evaluation, and docking study of 2,4-diaminoquinazolinesKazuhiro Yokoyama, Noriko Ishikawa, Susumu Igarashi, et al.
Bioorganic & Medicinal Chemistry|April 10, 2007
Prodrug-based design, synthesis, and biological evaluation of N-benzenesulfonylpiperidine derivatives as novel, orally active factor Xa inhibitorsTsukasa Ishihara, Norio Seki, Fukushi Hirayama, et al.
Antiviral Chemistry & Chemotherapy|November 26, 2008
Binding modes of two novel non-nucleoside reverse transcriptase inhibitors, YM-215389 and YM-228855, to HIV type-1 reverse transcriptaseEiichi Kodama, Masaya Orita, Naoyuki Masuda, et al.
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