Fujimoto M - Search Results

1

Synthesis and structure-activity relationships of potent and orally active sulfonamide ETB selective antagonists.

Kanda Y, Kawanishi Y, Oda K, Sakata T, Mihara SI, Asakura K, Kanemasa T, Ninomiya M, Fujimoto M, Konoike T. Kanda Y, et al. Among authors: fujimoto m. Bioorg Med Chem. 2001 Apr;9(4):897-907. doi: 10.1016/s0968-0896(00)00305-9. Bioorg Med Chem. 2001. PMID: 11354672

2

Structure-activity relationships of an endothelin ETA receptor antagonist, 50-235, and its derivatives.

Mihara S, Sakurai K, Nakamura M, Konoike T, Fujimoto M. Mihara S, et al. Among authors: fujimoto m. Eur J Pharmacol. 1993 Oct 15;247(2):219-21. doi: 10.1016/0922-4106(93)90081-j. Eur J Pharmacol. 1993. PMID: 8282010

3

1,3-Disubstituted benzazepines as novel, potent, selective neuropeptide Y Y1 receptor antagonists.

Murakami Y, Hara H, Okada T, Hashizume H, Kii M, Ishihara Y, Ishikawa M, Shimamura M, Mihara S, Kato G, Hanasaki K, Hagishita S, Fujimoto M. Murakami Y, et al. Among authors: fujimoto m. J Med Chem. 1999 Jul 15;42(14):2621-32. doi: 10.1021/jm990044m. J Med Chem. 1999. PMID: 10411482

4

Discovery and synthesis of a potent sulfonamide ET(B) selective antagonist.

Kanda Y, Takahashi T, Araki Y, Konoike T, Mihara S, Fujimoto M. Kanda Y, et al. Among authors: fujimoto m. Bioorg Med Chem Lett. 2000 Aug 21;10(16):1875-8. doi: 10.1016/s0960-894x(00)00366-8. Bioorg Med Chem Lett. 2000. PMID: 10969989

5

Effect of S-312, a new calcium channel blocker, on the 1,4-dihydropyridine binding sites in porcine basilar blood vessels and rat aortic smooth muscle cells.

Mihara S, Fujimoto M. Mihara S, et al. Among authors: fujimoto m. Jpn J Pharmacol. 1991 Jul;56(3):249-59. doi: 10.1254/jjp.56.249. Jpn J Pharmacol. 1991. PMID: 1832726 Free article.

6

Interaction of lipocortin I with peripheral-type benzodiazepine binding sites.

Mihara S, Sakata T, Fujimoto M. Mihara S, et al. Among authors: fujimoto m. Eur J Pharmacol. 1990 Sep 18;189(2-3):233-6. doi: 10.1016/0922-4106(90)90028-v. Eur J Pharmacol. 1990. PMID: 2174791

7

High-affinity binding sites for PK 11195, but not for RO5-4864, in porcine aortic smooth muscle.

Mihara S, Fujimoto M. Mihara S, et al. Among authors: fujimoto m. Life Sci. 1989;44(22):1713-20. doi: 10.1016/0024-3205(89)90488-8. Life Sci. 1989. PMID: 2733549

8

The endothelin ETA receptor-specific effect of 50-235, a nonpeptide endothelin antagonist.

Mihara S, Fujimoto M. Mihara S, et al. Among authors: fujimoto m. Eur J Pharmacol. 1993 Jun 15;246(1):33-8. doi: 10.1016/0922-4106(93)90006-u. Eur J Pharmacol. 1993. PMID: 8354341

9

Endothelin receptor antagonist triterpenoid, myriceric acid A, isolated from Myrica cerifera, and structure activity relationships of its derivatives.

Sakurawi K, Yasuda F, Tozyo T, Nakamura M, Sato T, Kikuchi J, Terui Y, Ikenishi Y, Iwata T, Takahashi K, Konoike T, Mihara S, Fujimoto M. Sakurawi K, et al. Among authors: fujimoto m. Chem Pharm Bull (Tokyo). 1996 Feb;44(2):343-51. doi: 10.1248/cpb.44.343. Chem Pharm Bull (Tokyo). 1996. PMID: 8998841

10

Binding characterization of [3H]S-0139, an antagonist of the endothelin ET(A) receptor subtype.

Mihara S, Tozawa F, Itazaki K, Fujimoto M. Mihara S, et al. Among authors: fujimoto m. Eur J Pharmacol. 1998 Jan 26;342(2-3):319-24. doi: 10.1016/s0014-2999(97)01479-9. Eur J Pharmacol. 1998. PMID: 9548403

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