Yasuo Sato

发表

Antitubercular Activity of Disulfiram, an Antialcoholism Drug, against Multidrug- and Extensively Drug-Resistant Mycobacterium tuberculosis Isolates

L. Kremer, K. Onozaki, N. Fujiwara, 2012, Antimicrobial Agents and Chemotherapy.

Role of hydrophobic substituents on the terminal nitrogen of histamine in receptor binding and agonist activity: development of an orally active histamine type 3 receptor agonist and evaluation of its antistress activity in mice.

M. Ishikawa, Fumikazu Yokoyama, R. Shinei, 2010, Journal of medicinal chemistry.

Regulatory molecules for the 5-HT3 receptor ion channel gating system.

Takashi Watanabe, Yasuo Sato, S. Yoshida, 2007, Bioorganic & medicinal chemistry.

Synthesis and structure-activity relationships of N-aryl-piperidine derivatives as potent (partial) agonists for human histamine H3 receptor.

M. Ishikawa, Fumikazu Yokoyama, T. Furuuchi, 2010, Bioorganic & medicinal chemistry.

Orally active benzoxazole derivative as 5-HT3 receptor partial agonist for treatment of diarrhea-predominant irritable bowel syndrome.

Tomoko Ito, K. Kawano, Yasuo Sato, 2005, Journal of medicinal chemistry.

A Novel Human Serum Lectin with Collagen- and Fibrinogen-like Domains That Functions as an Opsonin (*)

T. Fujita, M. Matsushita, Y. Endo, 1996, The Journal of Biological Chemistry.

Synthesis and evaluation of anti-tubercular activity of new dithiocarbamate sugar derivatives.

L. Kremer, K. Onozaki, T. Takii, 2011, Bioorganic & medicinal chemistry letters.

Anxiolytic-like profiles of histamine H3 receptor agonists in animal models of anxiety: a comparative study with antidepressants and benzodiazepine anxiolytic

M. Ishikawa, Fumikazu Yokoyama, R. Shinei, 2009, Psychopharmacology.

Synthesis and SARs of novel lincomycin derivatives Part 5: optimization of lincomycin analogs exhibiting potent antibacterial activities by chemical modification at the 6- and 7-positions

Y. Hayashi, K. Ajito, Yoshinari Wakiyama, 2017, The Journal of Antibiotics.

Synthesis and structure–activity relationships of novel lincomycin derivatives part 3: discovery of the 4-(pyrimidin-5-yl)phenyl group in synthesis of 7(S)-thiolincomycin analogs

K. Ajito, Yoshinari Wakiyama, K. Kumura, 2016, The Journal of Antibiotics.

Investigation of the histamine H3 receptor binding site. Design and synthesis of hybrid agonists with a lipophilic side chain.

T. Kudo, M. Ishikawa, Fumikazu Yokoyama, 2010, Journal of medicinal chemistry.