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Scientific Reports|July 29, 2017
In silico, in vitro, X-ray crystallography, and integrated strategies for discovering spermidine synthase inhibitors for Chagas diseaseRyunosuke Yoshino, Nobuaki Yasuo, Yohsuke Hagiwara, 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.
International Journal of Oncology|February 23, 2008
YM753, a novel histone deacetylase inhibitor, exhibits antitumor activity with selective, sustained accumulation of acetylated histones in tumors in the WiDr xenograft modelNobuaki Shindoh, Masamichi Mori, Yoh Terada, et al.
Biochemical and Biophysical Research Communications|December 7, 2010
Unique "delta lock" structure of telmisartan is involved in its strongest binding affinity to angiotensin II type 1 receptorKazuki Ohno, Yasushi Amano, Hirotoshi Kakuta, et al.
Plos One|May 12, 2015
Pharmacophore modeling for anti-Chagas drug design using the fragment molecular orbital methodRyunosuke Yoshino, Nobuaki Yasuo, Daniel Ken Inaoka, et al.
Bioorganic & Medicinal Chemistry|November 18, 2005
Synthesis and biological activity of novel 4,4-difluorobenzazepine derivatives as non-peptide antagonists of the arginine vasopressin V1A receptorYoshiaki Shimada, Nobuaki Taniguchi, Akira Matsuhisa, 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 Letters|July 18, 2009
Discovery of highly potent and selective biphenylacylsulfonamide-based beta3-adrenergic receptor agonists and molecular modeling based on the solved X-ray structure of the beta2-adrenergic receptor: part 6Kouji Hattori, Masaya Orita, Susumu Toda, 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.
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