Sayaka Ito

发表

Development of a selective and potent radioactive ligand for histamine H(3) receptors: A compound potentially useful for receptor occupancy studies.

Y. Mitobe, Sayaka Ito, Takashi Mizutani, 2009, Bioorganic & medicinal chemistry letters.

Synthesis, structure-activity relationships, and biological profiles of a dihydrobenzoxathiin class of histamine H(3) receptor inverse agonists.

R. Yoshimoto, Y. Mitobe, Sayaka Ito, 2009, Bioorganic & medicinal chemistry letters.

Development of novel 2-[4-(aminoalkoxy)phenyl]-4(3H)-quinazolinone derivatives as potent and selective histamine H3 receptor inverse agonists.

Sayaka Ito, Takashi Mizutani, T. Nagase, 2008, Bioorganic & medicinal chemistry letters.

Synthesis and evaluation of a spiro-isobenzofuranone class of histamine H3 receptor inverse agonists.

Sayaka Ito, N. Sato, S. Tokita, 2008, Bioorganic & Medicinal Chemistry Letters.

Synthesis and evaluation of a series of 2,4-diaminopyridine derivatives as potential positron emission tomography tracers for neuropeptide Y Y1 receptors.

Tomoki Suzuki, M. Kameda, M. Ando, 2009, Bioorganic & medicinal chemistry letters.

Detailed pharmacological characterization of GT-2331 for the rat histamine H3 receptor.

D. Macneil, R. Yoshimoto, Takao Nakamura, 2006, European journal of pharmacology.

Synthesis, structure-activity relationships, and biological profiles of a quinazolinone class of histamine H3 receptor inverse agonists.

R. Yoshimoto, T. Fukami, Y. Mitobe, 2008, Journal of medicinal chemistry.

Tunneling splittings in the S1 electronic states of symmetrically substituted 3,7‐dichlorotropolone, 3,5,7‐trichlorotropolone, and 3,7‐dibromotropolone

T. Tsuji, A. Mori, H. Sekiya, 1994 .

Proton tunneling in tropolone—Rg (Rg Ar, Kr, Xe) van der Waals complexes

T. Tsuji, H. Sekiya, Y. Nishimura, 1993 .

Synthesis and evaluation of structurally constrained quinazolinone derivatives as potent and selective histamine H3 receptor inverse agonists.

Shigeru Tokita, Shiho Ishikawa, Akane Ishihara, 2008, Journal of medicinal chemistry.

Electronic spectra of jet‐cooled 3‐ and 4‐chlorotropolones in the S1–S0 region. Inhibition of proton tunneling by asymmetric substitution

T. Tsuji, A. Mori, H. Sekiya, 1993 .

Characteristics of Lipids in Pork Fed Diets Containing Food By-products

Keiichi Suzuki, Sayaka Ito, Mitsuharu Ishida, 2004 .

Optimization of a series of 2,4-diaminopyridines as neuropeptide Y Y1 receptor antagonists with reduced hERG activity.

Tomoki Suzuki, M. Kameda, M. Ando, 2009, Bioorganic & medicinal chemistry letters.

Synthesis, structure-activity relationships, and biological profiles of a quinazolinone class of histamine H3 receptor inverse agonists.

R. Yoshimoto, T. Fukami, Sayaka Ito, 2008, Journal of medicinal chemistry.

Design, synthesis and evaluation of a novel cyclohexanamine class of neuropeptide Y Y1 receptor antagonists.

Tomoki Suzuki, M. Ando, Kensuke Kobayashi, 2009, Bioorganic & medicinal chemistry letters.