Ishikawa M - Search Results

1

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: ishikawa m. J Med Chem. 1999 Jul 15;42(14):2621-32. doi: 10.1021/jm990044m. J Med Chem. 1999. PMID: 10411482

2

A potent nonpeptide neuropeptide Y Y1 receptor antagonist, a benzodiazepine derivative.

Shigeri Y, Ishikawa M, Ishihara Y, Fujimoto M. Shigeri Y, et al. Among authors: ishikawa m. Life Sci. 1998;63(11):PL 151-60. doi: 10.1016/s0024-3205(98)00357-9. Life Sci. 1998. PMID: 9747900

3

Synthesis and pharmacological properties of ureidomethylcarbamoylphenylketone derivatives. A new potent and subtype-selective nonpeptide CCK-B/gastrin receptor antagonist, S-0509.

Hagishita S, Murakami Y, Seno K, Kamata S, Haga N, Konoike T, Kanda Y, Kiyama R, Shiota T, Ishihara Y, Ishikawa M, Shimamura M, Abe K, Yoshimura K. Hagishita S, et al. Among authors: ishikawa m. Bioorg Med Chem. 1997 Aug;5(8):1695-714. doi: 10.1016/s0968-0896(97)00104-1. Bioorg Med Chem. 1997. PMID: 9313871

4

Synthesis and structure-activity relationships of dual histamine H2 and gastrin receptor antagonists with decreased hydrophobicity.

Kawanishi Y, Ishihara S, Tsushima T, Hagishita S, Ishikawa M, Ishihara Y. Kawanishi Y, et al. Among authors: ishikawa m. Bioorg Med Chem. 1997 Jul;5(7):1401-9. doi: 10.1016/s0968-0896(97)00074-6. Bioorg Med Chem. 1997. PMID: 9377100

5

Synthesis and structure-activity relationships of dual histamine H2 and gastrin receptor antagonists with modified benzodiazepine skeletons.

Kawanishi Y, Ishihara S, Tsushima T, Seno K, Hagishita S, Ishikawa M, Ishihara Y. Kawanishi Y, et al. Among authors: ishikawa m. Bioorg Med Chem. 1997 Jul;5(7):1411-23. doi: 10.1016/s0968-0896(97)00075-8. Bioorg Med Chem. 1997. PMID: 9377101

6

Synthesis and structure-activity relationships of dual histamine H2 and gastrin receptor antagonists with noncyclic gastrin receptor antagonistic moieties.

Kawanishi Y, Ishihara S, Kiyama R, Hagishita S, Tsushima T, Ishikawa M, Ishihara Y. Kawanishi Y, et al. Among authors: ishikawa m. Bioorg Med Chem. 1997 Jul;5(7):1425-31. doi: 10.1016/s0968-0896(97)00076-x. Bioorg Med Chem. 1997. PMID: 9377102

7

Potent and subtype-selective CCK-B/gastrin receptor antagonists: 2,4-dioxo-1,5-benzodiazepines with a plane of symmetry.

Hagishita S, Seno K, Kamata S, Haga N, Ishihara Y, Ishikawa M, Shimamura M. Hagishita S, et al. Among authors: ishikawa m. Bioorg Med Chem. 1997 Jul;5(7):1433-46. doi: 10.1016/s0968-0896(97)00083-7. Bioorg Med Chem. 1997. PMID: 9377103

8

Synthesis and biological evaluation of a new reversely linked type of dual histamine H2 and gastrin receptor antagonist.

Kawanishi Y, Ishihara S, Takahashi K, Tsushima T, Hagishita S, Ishikawa M, Ishihara Y. Kawanishi Y, et al. Among authors: ishikawa m. Chem Pharm Bull (Tokyo). 1997 Jan;45(1):116-24. doi: 10.1248/cpb.45.116. Chem Pharm Bull (Tokyo). 1997. PMID: 9023973

9

Effects of S-0509, a novel CCKB/gastrin receptor antagonist, on acid secretion and experimental duodenal ulcers in rats.

Takeuchi K, Hirata T, Yamamoto H, Kunikata T, Ishikawa M, Ishihara Y. Takeuchi K, et al. Among authors: ishikawa m. Aliment Pharmacol Ther. 1999 Jan;13(1):87-96. doi: 10.1046/j.1365-2036.1999.00439.x. Aliment Pharmacol Ther. 1999. PMID: 9892884

10

Discovery of a novel CCR3 selective antagonist.

Naya A, Kobayashi K, Ishikawa M, Ohwaki K, Saeki T, Noguchi K, Ohtake N. Naya A, et al. Among authors: ishikawa m. Bioorg Med Chem Lett. 2001 May 7;11(9):1219-23. doi: 10.1016/s0960-894x(01)00176-7. Bioorg Med Chem Lett. 2001. PMID: 11354381

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