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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.
Bioorganic & Medicinal Chemistry|September 1, 2006
Potent and selective TF/FVIIa inhibitors containing a neutral P1 ligandMasanori Miura, Norio Seki, Takanori Koike, et al.
Bioorganic & Medicinal Chemistry|July 22, 2009
Synthesis, biological evaluation, and metabolic stability of acrylamide derivatives as novel CCR3 antagonistsIppei Sato, Koichiro Morihira, Hiroshi Inami, et al.
Bioorganic & Medicinal Chemistry Letters|March 7, 2007
Synthesis and biological evaluation of pyrido[3',2':4,5]furo[3,2-d]pyrimidine derivatives as novel PI3 kinase p110alpha inhibitorsMasahiko Hayakawa, Hiroyuki Kaizawa, Hiroyuki Moritomo, et al.
Bioorganic & Medicinal Chemistry|December 17, 2008
Potent and orally bioavailable CCR4 antagonists: Synthesis and structure-activity relationship study of 2-aminoquinazolinesKazuhiro Yokoyama, Noriko Ishikawa, Susumu Igarashi, et al.
Bioorganic & Medicinal Chemistry|October 24, 2007
Synthesis and structure-activity relationships of N-{1-[(6-fluoro-2-naphthyl)methyl]piperidin-4-yl}benzamide derivatives as novel CCR3 antagonistsIppei Sato, Koichiro Morihira, Hiroshi Inami, et al.
Bioorganic & Medicinal Chemistry|October 28, 2008
Design, synthesis, and pharmacological evaluation of N-bicyclo-5-chloro-1H-indole-2-carboxamide derivatives as potent glycogen phosphorylase inhibitorsKenichi Onda, Ryota Shiraki, Takashi Ogiyama, et al.
Bioorganic & Medicinal Chemistry|July 3, 2007
Synthesis and biological evaluation of sulfonylhydrazone-substituted imidazo[1,2-a]pyridines as novel PI3 kinase p110alpha inhibitorsMasahiko Hayakawa, Ken-Ichi Kawaguchi, Hiroyuki Kaizawa, et al.
Bioorganic & Medicinal Chemistry|October 27, 2006
Design, synthesis and biological activity of selective and orally available TF/FVIIa complex inhibitors containing non-amidine P1 ligandsMasanori Miura, Norio Seki, Takanori Koike, et al.
Bioorganic & Medicinal Chemistry|May 9, 2013
Synthesis and biological evaluation of C-glucosides with azulene rings as selective SGLT2 inhibitors for the treatment of type 2 diabetes mellitus: discovery of YM543Kazuhiro Ikegai, Masakazu Imamura, Takayuki Suzuki, et al.
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