Mihara S - Search Results

1

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: mihara s. Chem Pharm Bull (Tokyo). 1996 Feb;44(2):343-51. doi: 10.1248/cpb.44.343. Chem Pharm Bull (Tokyo). 1996. PMID: 8998841

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. 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

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

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

4

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. 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

5

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: mihara s. 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

6

A novel non-peptide endothelin antagonist isolated from bayberry, Myrica cerifera.

Fujimoto M, Mihara S, Nakajima S, Ueda M, Nakamura M, Sakurai K. Fujimoto M, et al. Among authors: mihara s. FEBS Lett. 1992 Jun 22;305(1):41-4. doi: 10.1016/0014-5793(92)80651-v. FEBS Lett. 1992. PMID: 1321729 Free article.

7

Structure-activity relationships of a novel class of endothelin-A receptor antagonists and discovery of potent and selective receptor antagonist, 2-(benzo[1,3]dioxol-5-yl)-6-isopropyloxy-4-(4-methoxyphenyl)-2H-chromene-3-carboxylic acid (S-1255). 1. Study on structure-activity relationships and basic structure crucial for ET(A) antagonism.

Ishizuka N, Matsumura K, Sakai K, Fujimoto M, Mihara S, Yamamori T. Ishizuka N, et al. Among authors: mihara s. J Med Chem. 2002 May 9;45(10):2041-55. doi: 10.1021/jm010382z. J Med Chem. 2002. PMID: 11985472

8

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: mihara si. Bioorg Med Chem. 2001 Apr;9(4):897-907. doi: 10.1016/s0968-0896(00)00305-9. Bioorg Med Chem. 2001. PMID: 11354672

9

Two states of the L-type Ca2+ channel in PC12 cells: different sensitivity to 1,4-dihydropyridines.

Fujimoto M, Mihara S. Fujimoto M, et al. Among authors: mihara s. Neurosci Lett. 1991 Jan 14;122(1):9-12. doi: 10.1016/0304-3940(91)90180-2. Neurosci Lett. 1991. PMID: 1647507

10

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. Jpn J Pharmacol. 1991 Jul;56(3):249-59. doi: 10.1254/jjp.56.249. Jpn J Pharmacol. 1991. PMID: 1832726 Free article.

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