Seno K - Search Results

1

Cytosolic phospholipase A2 alpha inhibitor, pyrroxyphene, displays anti-arthritic and anti-bone destructive action in a murine arthritis model.

Tai N, Kuwabara K, Kobayashi M, Yamada K, Ono T, Seno K, Gahara Y, Ishizaki J, Hori Y. Tai N, et al. Among authors: seno k. Inflamm Res. 2010 Jan;59(1):53-62. doi: 10.1007/s00011-009-0069-8. Epub 2009 Aug 5. Inflamm Res. 2010. PMID: 19655230

2

Characterization of a novel inhibitor of cytosolic phospholipase A2alpha, pyrrophenone.

Ono T, Yamada K, Chikazawa Y, Ueno M, Nakamoto S, Okuno T, Seno K. Ono T, et al. Among authors: seno k. Biochem J. 2002 May 1;363(Pt 3):727-35. doi: 10.1042/0264-6021:3630727. Biochem J. 2002. PMID: 11964173 Free PMC article.

3

Group X secretory phospholipase A2 can induce arachidonic acid release and eicosanoid production without activation of cytosolic phospholipase A2 alpha.

Saiga A, Uozumi N, Ono T, Seno K, Ishimoto Y, Arita H, Shimizu T, Hanasaki K. Saiga A, et al. Among authors: seno k. Prostaglandins Other Lipid Mediat. 2005 Jan;75(1-4):79-89. doi: 10.1016/j.prostaglandins.2004.10.001. Prostaglandins Other Lipid Mediat. 2005. PMID: 15789617

4

Pyrrolidine inhibitors of human cytosolic phospholipase A(2).

Seno K, Okuno T, Nishi K, Murakami Y, Watanabe F, Matsuura T, Wada M, Fujii Y, Yamada M, Ogawa T, Okada T, Hashizume H, Kii M, Hara S, Hagishita S, Nakamoto S, Yamada K, Chikazawa Y, Ueno M, Teshirogi I, Ono T, Ohtani M. Seno K, et al. J Med Chem. 2000 Mar 23;43(6):1041-4. doi: 10.1021/jm9905155. J Med Chem. 2000. PMID: 10737736 No abstract available.

5

Pyrrolidine inhibitors of human cytosolic phospholipase A2. Part 2: synthesis of potent and crystallized 4-triphenylmethylthio derivative 'pyrrophenone'.

Seno K, Okuno T, Nishi K, Murakami Y, Yamada K, Nakamoto S, Ono T. Seno K, et al. Bioorg Med Chem Lett. 2001 Feb 26;11(4):587-90. doi: 10.1016/s0960-894x(01)00003-8. Bioorg Med Chem Lett. 2001. PMID: 11229777

6

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: seno k. Bioorg Med Chem. 1997 Aug;5(8):1695-714. doi: 10.1016/s0968-0896(97)00104-1. Bioorg Med Chem. 1997. PMID: 9313871

7

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: seno k. Bioorg Med Chem. 1997 Jul;5(7):1411-23. doi: 10.1016/s0968-0896(97)00075-8. Bioorg Med Chem. 1997. PMID: 9377101

8

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: seno k. Bioorg Med Chem. 1997 Jul;5(7):1433-46. doi: 10.1016/s0968-0896(97)00083-7. Bioorg Med Chem. 1997. PMID: 9377103

9

Thromboxane A2 receptor antagonists. I. Synthesis and pharmacological activity of 7-oxabicyclo-[2.2.1]heptane derivatives with the benzenesulfonylamino group.

Hagishita S, Seno K. Hagishita S, et al. Among authors: seno k. Chem Pharm Bull (Tokyo). 1989 Feb;37(2):327-35. doi: 10.1248/cpb.37.327. Chem Pharm Bull (Tokyo). 1989. PMID: 2525965

10

Thromboxane A2 receptor antagonists. III. Synthesis and pharmacological activity of 6,6-dimethylbicyclo[3.1.1]heptane derivatives with a substituted sulfonylamino group at C-2.

Seno K, Hagishita S. Seno K, et al. Chem Pharm Bull (Tokyo). 1989 Jun;37(6):1524-33. doi: 10.1248/cpb.37.1524. Chem Pharm Bull (Tokyo). 1989. PMID: 2528414

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