Sato N - Search Results

1

Discovery of novel phenylpyridone derivatives as potent and selective MCH1R antagonists.

Haga Y, Mizutani S, Naya A, Kishino H, Iwaasa H, Ito M, Ito J, Moriya M, Sato N, Takenaga N, Ishihara A, Tokita S, Kanatani A, Ohtake N. Haga Y, et al. Among authors: sato n. Bioorg Med Chem. 2011 Jan 15;19(2):883-93. doi: 10.1016/j.bmc.2010.12.002. Epub 2010 Dec 6. Bioorg Med Chem. 2011. PMID: 21190859

2

Design and synthesis of the potent, orally available, brain-penetrable arylpyrazole class of neuropeptide Y5 receptor antagonists.

Sato N, Takahashi T, Shibata T, Haga Y, Sakuraba A, Hirose M, Sato M, Nonoshita K, Koike Y, Kitazawa H, Fujino N, Ishii Y, Ishihara A, Kanatani A, Fukami T. Sato N, et al. Among authors: sato m. J Med Chem. 2003 Feb 27;46(5):666-9. doi: 10.1021/jm025513q. J Med Chem. 2003. PMID: 12593644

3

Synthesis and evaluation of substituted 4-alkoxy-2-aminopyridines as novel neuropeptide Y1 receptor antagonists.

Sato N, Shibata T, Jitsuoka M, Ohno T, Takahashi T, Hirohashi T, Kanno T, Iwaasa H, Kanatani A, Fukami T. Sato N, et al. Bioorg Med Chem Lett. 2004 Apr 5;14(7):1761-4. doi: 10.1016/j.bmcl.2004.01.049. Bioorg Med Chem Lett. 2004. PMID: 15026066

4

Novel potent neuropeptide Y Y5 receptor antagonists: synthesis and structure-activity relationships of phenylpiperazine derivatives.

Takahashi T, Sakuraba A, Hirohashi T, Shibata T, Hirose M, Haga Y, Nonoshita K, Kanno T, Ito J, Iwaasa H, Kanatani A, Fukami T, Sato N. Takahashi T, et al. Among authors: sato n. Bioorg Med Chem. 2006 Nov 15;14(22):7501-11. doi: 10.1016/j.bmc.2006.07.023. Epub 2006 Aug 17. Bioorg Med Chem. 2006. PMID: 16919461

5

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

Nagase T, Mizutani T, Ishikawa S, Sekino E, Sasaki T, Fujimura T, Ito S, Mitobe Y, Miyamoto Y, Yoshimoto R, Tanaka T, Ishihara A, Takenaga N, Tokita S, Fukami T, Sato N. Nagase T, et al. Among authors: sato n. J Med Chem. 2008 Aug 14;51(15):4780-9. doi: 10.1021/jm8003834. Epub 2008 Jul 4. J Med Chem. 2008. PMID: 18598020

6

(9S)-9-(2-hydroxy-4,4-dimethyl-6-oxo-1-cyclohexen-1-yl)-3,3-dimethyl-2,3,4,9-tetrahydro-1H-xanthen-1-one, a selective and orally active neuropeptide Y Y5 receptor antagonist.

Sato N, Jitsuoka M, Shibata T, Hirohashi T, Nonoshita K, Moriya M, Haga Y, Sakuraba A, Ando M, Ohe T, Iwaasa H, Gomori A, Ishihara A, Kanatani A, Fukami T. Sato N, et al. J Med Chem. 2008 Aug 14;51(15):4765-70. doi: 10.1021/jm8003587. Epub 2008 Jul 19. J Med Chem. 2008. PMID: 18637668

7

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

Jitsuoka M, Tsukahara D, Ito S, Tanaka T, Takenaga N, Tokita S, Sato N. Jitsuoka M, et al. Among authors: sato n. Bioorg Med Chem Lett. 2008 Sep 15;18(18):5101-6. doi: 10.1016/j.bmcl.2008.07.125. Epub 2008 Aug 5. Bioorg Med Chem Lett. 2008. PMID: 18768318

8

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

Nagase T, Mizutani T, Sekino E, Ishikawa S, Ito S, Mitobe Y, Miyamoto Y, Yoshimoto R, Tanaka T, Ishihara A, Takenaga N, Tokita S, Sato N. Nagase T, et al. Among authors: sato n. J Med Chem. 2008 Nov 13;51(21):6889-901. doi: 10.1021/jm800569w. Epub 2008 Oct 8. J Med Chem. 2008. PMID: 18841880

9

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

Mizutani T, Nagase T, Ito S, Miyamoto Y, Tanaka T, Takenaga N, Tokita S, Sato N. Mizutani T, et al. Among authors: sato n. Bioorg Med Chem Lett. 2008 Dec 1;18(23):6041-5. doi: 10.1016/j.bmcl.2008.10.034. Epub 2008 Oct 11. Bioorg Med Chem Lett. 2008. PMID: 18952421

10

Discovery of substituted 2,4,4-triarylimidazoline derivatives as potent and selective neuropeptide Y Y5 receptor antagonists.

Sato N, Jitsuoka M, Ishikawa S, Nagai K, Tsuge H, Ando M, Okamoto O, Iwaasa H, Gomori A, Ishihara A, Kanatani A, Fukami T. Sato N, et al. Bioorg Med Chem Lett. 2009 Mar 15;19(6):1670-4. doi: 10.1016/j.bmcl.2009.01.101. Epub 2009 Feb 4. Bioorg Med Chem Lett. 2009. PMID: 19233647

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