Miyata K - Search Results

1

Characterization of [3H]YM060, a potent and selective 5-HT3 receptor radioligand, in the cerebral cortex of rats.

Akuzawa S, Miyata K, Fukutomi H. Akuzawa S, et al. Among authors: miyata k. Eur J Pharmacol. 1995 Jul 25;281(1):37-42. doi: 10.1016/0014-2999(95)00226-b. Eur J Pharmacol. 1995. PMID: 8566114

2

Comparative study of the affinities of the 5-HT3 receptor antagonists, YM060, YM114 (KAE-393), granisetron and ondansetron in rat vagus nerve and cerebral cortex.

Ito H, Akuzawa S, Tsutsumi R, Kiso T, Kamato T, Nishida A, Yamano M, Miyata K. Ito H, et al. Among authors: miyata k. Neuropharmacology. 1995 Jun;34(6):631-7. doi: 10.1016/0028-3908(95)00033-3. Neuropharmacology. 1995. PMID: 7566499

3

Effect of serotonin (5-HT)3-receptor antagonists YM060, YM114 (KAE-393), ondansetron and granisetron on 5-HT4 receptors and gastric emptying in rodents.

Miyata K, Yamano M, Kamato T, Akuzawa S. Miyata K, et al. Jpn J Pharmacol. 1995 Nov;69(3):205-14. doi: 10.1254/jjp.69.205. Jpn J Pharmacol. 1995. PMID: 8699628 Free article.

4

Comparison of [3H]YM060 binding to native and cloned rat 5-HT3 receptors.

Akuzawa S, Miyake A, Miyata K, Fukutomi H. Akuzawa S, et al. Among authors: miyata k. Eur J Pharmacol. 1996 Jan 25;296(2):227-30. doi: 10.1016/0014-2999(95)00798-9. Eur J Pharmacol. 1996. PMID: 8838461

5

YF476 is a new potent and selective gastrin/cholecystokinin-B receptor antagonist in vitro and in vivo.

Takinami Y, Yuki H, Nishida A, Akuzawa S, Uchida A, Takemoto Y, Ohta M, Satoh M, Semple G, Miyata K. Takinami Y, et al. Among authors: miyata k. Aliment Pharmacol Ther. 1997 Feb;11(1):113-20. doi: 10.1046/j.1365-2036.1997.110281000.x. Aliment Pharmacol Ther. 1997. PMID: 9042983 Free article.

6

Pharmacological properties of a novel gastrointestinal prokinetic benzamide selective for human 5-HT4 receptor versus human 5-HT3 receptor.

Nagakura Y, Akuzawa S, Miyata K, Kamato T, Suzuki T, Ito H, Yamaguchi T. Nagakura Y, et al. Among authors: miyata k. Pharmacol Res. 1999 May;39(5):375-82. doi: 10.1006/phrs.1998.0454. Pharmacol Res. 1999. PMID: 10328995

7

Pharmacological profile of YM-31636, a novel 5-HT3 receptor agonist, in vitro.

Ito H, Kiso T, Miyata K, Kamato T, Yuki H, Akuzawa S, Nagakura Y, Yamano M, Suzuki M, Naitoh Y, Sakai H, Iwaoka K, Yamaguchi T. Ito H, et al. Among authors: miyata k. Eur J Pharmacol. 2000 Dec 8;409(2):195-201. doi: 10.1016/s0014-2999(00)00851-7. Eur J Pharmacol. 2000. PMID: 11104834

8

Pharmacological profile of (R)-1-[2,3-dihydro-1-(2'-methylphenacyl)-2-oxo- 5-phenyl-1H-1,4-benzodiazepin-3-yl]-3-(3-methylphenyl)urea (YM022), a new potent and selective gastrin/cholecystokinin-B receptor antagonist, in vitro and in vivo.

Nishida A, Miyata K, Tsutsumi R, Yuki H, Akuzawa S, Kobayashi A, Kamato T, Ito H, Yamano M, Katuyama Y, et al. Nishida A, et al. Among authors: miyata k. J Pharmacol Exp Ther. 1994 May;269(2):725-31. J Pharmacol Exp Ther. 1994. PMID: 7910212

9

YM022 [(R)-1-[2,3-dihydro-1-(2'-methylphenacyl)-2-oxo-5-phenyl- 1H-1,4-benzodiazepin-3-yl]-3-(3-methylphenyl)urea], a potent and selective gastrin/cholecystokinin-B receptor antagonist, prevents gastric and duodenal lesions in rats.

Nishida A, Takinami Y, Yuki H, Kobayashi A, Akuzawa S, Kamato T, Ito H, Yamano M, Nagakura Y, Miyata K. Nishida A, et al. Among authors: miyata k. J Pharmacol Exp Ther. 1994 Sep;270(3):1256-61. J Pharmacol Exp Ther. 1994. PMID: 7932178

10

YM022, a potent and selective gastrin/CCK-B receptor antagonist, inhibits peptone meal-induced gastric acid secretion in Heidenhain pouch dogs.

Yuki H, Nishida A, Miyake A, Ito H, Akuzawa S, Takinami Y, Takemoto Y, Miyata K. Yuki H, et al. Among authors: miyata k. Dig Dis Sci. 1997 Apr;42(4):707-14. doi: 10.1023/a:1018887308280. Dig Dis Sci. 1997. PMID: 9125636

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