Tomishima Y - Search Results

1

Sulfonamide derivatives as new potent and selective CB2 cannabinoid receptor agonists.

Ohta H, Ishizaka T, Yoshinaga M, Morita A, Tomishima Y, Toda Y, Saito S. Ohta H, et al. Among authors: tomishima y. Bioorg Med Chem Lett. 2007 Sep 15;17(18):5133-5. doi: 10.1016/j.bmcl.2007.07.005. Epub 2007 Jul 10. Bioorg Med Chem Lett. 2007. PMID: 17643986

2

N-Alkylidenearylcarboxamides as new potent and selective CB(2) cannabinoid receptor agonists with good oral bioavailability.

Ohta H, Ishizaka T, Tatsuzuki M, Yoshinaga M, Iida I, Tomishima Y, Toda Y, Saito S. Ohta H, et al. Among authors: tomishima y. Bioorg Med Chem Lett. 2007 Nov 15;17(22):6299-304. doi: 10.1016/j.bmcl.2007.09.004. Epub 2007 Sep 7. Bioorg Med Chem Lett. 2007. PMID: 17884496

3

Imine derivatives as new potent and selective CB2 cannabinoid receptor agonists with an analgesic action.

Ohta H, Ishizaka T, Tatsuzuki M, Yoshinaga M, Iida I, Yamaguchi T, Tomishima Y, Futaki N, Toda Y, Saito S. Ohta H, et al. Among authors: tomishima y. Bioorg Med Chem. 2008 Feb 1;16(3):1111-24. doi: 10.1016/j.bmc.2007.10.087. Epub 2007 Nov 1. Bioorg Med Chem. 2008. PMID: 18006322

4

Design and synthesis of 1-(4-benzoylphenyl)imidazole derivatives as new potent 20-HETE synthase inhibitors.

Nakamura T, Ishii T, Miyata N, Taniguchi K, Tomishima Y, Ueki T, Sato M. Nakamura T, et al. Among authors: tomishima y. Bioorg Med Chem Lett. 2004 Nov 1;14(21):5305-8. doi: 10.1016/j.bmcl.2004.08.025. Bioorg Med Chem Lett. 2004. PMID: 15454216

5

Sphingomyelin analogues as inhibitors of sphingomyelinase.

Taguchi M, Sugimoto K, Goda K, Akama T, Yamamoto K, Suzuki T, Tomishima Y, Nishiguchi M, Arai K, Takahashi K, Kobori T. Taguchi M, et al. Among authors: tomishima y. Bioorg Med Chem Lett. 2003 Jun 16;13(12):1963-6. doi: 10.1016/s0960-894x(03)00360-3. Bioorg Med Chem Lett. 2003. PMID: 12781174

6

Biological evaluation of sphingomyelin analogues as inhibitors of sphingomyelinase.

Taguchi M, Goda K, Sugimoto K, Akama T, Yamamoto K, Suzuki T, Tomishima Y, Nishiguchi M, Arai K, Takahashi K, Kobori T. Taguchi M, et al. Among authors: tomishima y. Bioorg Med Chem Lett. 2003 Nov 3;13(21):3681-4. doi: 10.1016/j.bmcl.2003.08.020. Bioorg Med Chem Lett. 2003. PMID: 14552757

7

A Novel Potent and Selective Histamine H₃ Receptor Antagonist Enerisant: In Vitro Profiles, In Vivo Receptor Occupancy, and Wake-Promoting and Procognitive Effects in Rodents.

Hino N, Marumo T, Kotani M, Shimazaki T, Kaku-Fukumoto A, Hikichi H, Karasawa JI, Tomishima Y, Komiyama H, Tatsuda E, Nozawa D, Nakamura T, Chaki S. Hino N, et al. Among authors: tomishima y. J Pharmacol Exp Ther. 2020 Nov;375(2):276-285. doi: 10.1124/jpet.120.000185. Epub 2020 Aug 29. J Pharmacol Exp Ther. 2020. PMID: 32862143

8

HET0016, a potent and selective inhibitor of 20-HETE synthesizing enzyme.

Miyata N, Taniguchi K, Seki T, Ishimoto T, Sato-Watanabe M, Yasuda Y, Doi M, Kametani S, Tomishima Y, Ueki T, Sato M, Kameo K. Miyata N, et al. Among authors: tomishima y. Br J Pharmacol. 2001 Jun;133(3):325-9. doi: 10.1038/sj.bjp.0704101. Br J Pharmacol. 2001. PMID: 11375247 Free PMC article.

9

Neurophysiologic and antipsychotic profiles of TASP0433864, a novel positive allosteric modulator of metabotropic glutamate 2 receptor.

Hiyoshi T, Marumo T, Hikichi H, Tomishima Y, Urabe H, Tamita T, Iida I, Yasuhara A, Karasawa J, Chaki S. Hiyoshi T, et al. Among authors: tomishima y. J Pharmacol Exp Ther. 2014 Dec;351(3):642-53. doi: 10.1124/jpet.114.218651. Epub 2014 Oct 2. J Pharmacol Exp Ther. 2014. PMID: 25277141

10

Antipsychotic profiles of TASP0443294, a novel and orally active positive allosteric modulator of metabotropic glutamate 2 receptor.

Hikichi H, Hiyoshi T, Marumo T, Tomishima Y, Kaku A, Iida I, Urabe H, Tamita T, Yasuhara A, Karasawa J, Chaki S. Hikichi H, et al. Among authors: tomishima y. J Pharmacol Sci. 2015 Mar;127(3):352-61. doi: 10.1016/j.jphs.2015.02.004. Epub 2015 Feb 9. J Pharmacol Sci. 2015. PMID: 25837934 Free article.

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