Sakamoto S - Search Results

1

Synthesis and structure-activity relationships of 6-{4-[(3-fluorobenzyl)oxy]phenoxy}nicotinamide derivatives as a novel class of NCX inhibitors: a QSAR study.

Kuramochi T, Kakefuda A, Sato I, Tsukamoto I, Taguchi T, Sakamoto S. Kuramochi T, et al. Among authors: sakamoto s. Bioorg Med Chem. 2005 Feb 1;13(3):717-24. doi: 10.1016/j.bmc.2004.10.047. Bioorg Med Chem. 2005. PMID: 15653339

2

Discovery of 4,5-diphenyl-1,2,4-triazole derivatives as a novel class of selective antagonists for the human V(1A) receptor.

Kakefuda A, Suzuki T, Tobe T, Tahara A, Sakamoto S, Tsukamoto Si. Kakefuda A, et al. Among authors: sakamoto s. Bioorg Med Chem. 2002 Jun;10(6):1905-12. doi: 10.1016/s0968-0896(02)00009-3. Bioorg Med Chem. 2002. PMID: 11937348

3

Synthesis and pharmacological evaluation of 5-(4-biphenyl)-3-methyl-4-phenyl-1,2,4-triazole derivatives as a novel class of selective antagonists for the human vasopressin V(1A) receptor.

Kakefuda A, Suzuki T, Tobe T, Tsukada J, Tahara A, Sakamoto S, Tsukamoto S. Kakefuda A, et al. Among authors: sakamoto s. J Med Chem. 2002 Jun 6;45(12):2589-98. doi: 10.1021/jm010544r. J Med Chem. 2002. PMID: 12036368

4

Design, synthesis and biological activity of YM-60828 derivatives: potent and orally-bioavailable factor Xa inhibitors based on naphthoanilide and naphthalensulfonanilide templates.

Hirayama F, Koshio H, Ishihara T, Watanuki S, Hachiya S, Kaizawa H, Kuramochi T, Katayama N, Kurihara H, Taniuchi Y, Sato K, Sakai-Moritani Y, Kaku S, Kawasaki T, Matsumoto Y, Sakamoto S, Tsukamoto S. Hirayama F, et al. Among authors: sakamoto s. Bioorg Med Chem. 2002 Aug;10(8):2597-610. doi: 10.1016/s0968-0896(02)00106-2. Bioorg Med Chem. 2002. PMID: 12057649

5

Synthesis and pharmacological evaluation of 1-oxo-2-(3-piperidyl)-1,2,3,4- tetrahydroisoquinolines and related analogues as a new class of specific bradycardic agents possessing I(f) channel inhibitory activity.

Kubota H, Kakefuda A, Watanabe T, Ishii N, Wada K, Masuda N, Sakamoto S, Tsukamoto S. Kubota H, et al. Among authors: sakamoto s. J Med Chem. 2003 Oct 23;46(22):4728-40. doi: 10.1021/jm0301742. J Med Chem. 2003. PMID: 14561092

6

Synthesis and pharmacological evaluation of N-acyl-1,2,3,4-tetrahydroisoquinoline derivatives as novel specific bradycardic agents.

Kubota H, Watanabe T, Kakefuda A, Masuda N, Wada K, Ishii N, Sakamoto S, Tsukamoto S. Kubota H, et al. Among authors: sakamoto s. Bioorg Med Chem. 2004 Mar 1;12(5):871-82. doi: 10.1016/j.bmc.2003.12.032. Bioorg Med Chem. 2004. PMID: 14980599

7

Synthesis and pharmacological evaluation of piperidinoalkanoyl-1,2,3,4-tetrahydroisoquinoline derivatives as novel specific bradycardic agents.

Kubota H, Watanabe T, Kakefuda A, Masuda N, Wada K, Ishii N, Sakamoto S, Tsukamoto S. Kubota H, et al. Among authors: sakamoto s. Bioorg Med Chem Lett. 2004 Jun 21;14(12):3049-52. doi: 10.1016/j.bmcl.2004.04.031. Bioorg Med Chem Lett. 2004. PMID: 15149642

8

Synthesis and structure-activity relationships of phenoxypyridine derivatives as novel inhibitors of the sodium-calcium exchanger.

Kuramochi T, Kakefuda A, Yamada H, Sato I, Taguchi T, Sakamoto S. Kuramochi T, et al. Among authors: sakamoto s. Bioorg Med Chem. 2004 Oct 1;12(19):5039-56. doi: 10.1016/j.bmc.2004.07.038. Bioorg Med Chem. 2004. PMID: 15351388

9

Synthesis and structure-activity relationships of benzyloxyphenyl derivatives as a novel class of NCX inhibitors: effects on heart failure.

Kuramochi T, Kakefuda A, Yamada H, Ogiyama T, Taguchi T, Sakamoto S. Kuramochi T, et al. Among authors: sakamoto s. Bioorg Med Chem. 2005 Feb 1;13(3):725-34. doi: 10.1016/j.bmc.2004.10.048. Bioorg Med Chem. 2005. PMID: 15653340

10

Discovery of an N-(2-aminopyridin-4-ylmethyl)nicotinamide derivative: a potent and orally bioavailable NCX inhibitor.

Kuramochi T, Kakefuda A, Yamada H, Tsukamoto I, Taguchi T, Sakamoto S. Kuramochi T, et al. Among authors: sakamoto s. Bioorg Med Chem. 2005 Jun 2;13(12):4022-36. doi: 10.1016/j.bmc.2005.03.052. Epub 2005 Apr 25. Bioorg Med Chem. 2005. PMID: 15911315

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