Matsumoto M - Search Results

1

Biological activities and quantitative structure-activity relationships of spiro[imidazolidine-4,4'(1'H)-quinazoline]-2,2',5(3'H)-triones as aldose reductase inhibitors.

Yamagishi M, Yamada Y, Ozaki K, Asao M, Shimizu R, Suzuki M, Matsumoto M, Matsuoka Y, Matsumoto K. Yamagishi M, et al. Among authors: matsumoto k, matsumoto m. J Med Chem. 1992 May 29;35(11):2085-94. doi: 10.1021/jm00089a021. J Med Chem. 1992. PMID: 1597858

2

Effects of methyl (+)(3S)-1,2,3,4-tetrahydro-3-hydroxy-methyl-beta-carboline-2- carbodithioate (THC), a new hepatoprotective agent, on acute liver injuries induced by various hepatotoxic substances in mice and rats.

Matsumoto M, Matsuoka Y, Saiga Y, Iijima I. Matsumoto M, et al. J Pharmacobiodyn. 1987 Nov;10(11):599-607. doi: 10.1248/bpb1978.10.599. J Pharmacobiodyn. 1987. PMID: 3446768

3

Na(+)-glucose cotransporter (SGLT) inhibitors as antidiabetic agents. 4. Synthesis and pharmacological properties of 4'-dehydroxyphlorizin derivatives substituted on the B ring.

Tsujihara K, Hongu M, Saito K, Kawanishi H, Kuriyama K, Matsumoto M, Oku A, Ueta K, Tsuda M, Saito A. Tsujihara K, et al. Among authors: matsumoto m. J Med Chem. 1999 Dec 30;42(26):5311-24. doi: 10.1021/jm990175n. J Med Chem. 1999. PMID: 10639275

4

Structure-activity relationships of quinazoline derivatives: dual-acting compounds with inhibitory activities toward both TNF-alpha production and T cell proliferation.

Tobe M, Isobe Y, Tomizawa H, Matsumoto M, Obara F, Nagasaki T, Hayashi H. Tobe M, et al. Among authors: matsumoto m. Bioorg Med Chem Lett. 2001 Feb 26;11(4):545-8. doi: 10.1016/s0960-894x(00)00718-6. Bioorg Med Chem Lett. 2001. PMID: 11229767

5

Isolation and characterization of thioxamycin.

Matsumoto M, Kawamura Y, Yasuda Y, Tanimoto T, Matsumoto K, Yoshida T, Shoji J. Matsumoto M, et al. Among authors: matsumoto k. J Antibiot (Tokyo). 1989 Oct;42(10):1465-9. doi: 10.7164/antibiotics.42.1465. J Antibiot (Tokyo). 1989. PMID: 2808134 Free article.

6

Depudecin: a novel compound inducing the flat phenotype of NIH3T3 cells doubly transformed by ras- and src-oncogene, produced by Alternaria brassicicola.

Matsumoto M, Matsutani S, Sugita K, Yoshida H, Hayashi F, Terui Y, Nakai H, Uotani N, Kawamura Y, Matsumoto K, et al. Matsumoto M, et al. Among authors: matsumoto k. J Antibiot (Tokyo). 1992 Jun;45(6):879-85. doi: 10.7164/antibiotics.45.879. J Antibiot (Tokyo). 1992. PMID: 1500354 Free article.

7

Synthesis and structure-activity relationships of cephalosporins, 2-isocephems, and 2-oxaisocephems with C-3' or C-7 catechol or related aromatics.

Tsuji K, Tsubouchi H, Yasumura K, Matsumoto M, Ishikawa H. Tsuji K, et al. Among authors: matsumoto m. Bioorg Med Chem. 1996 Dec;4(12):2135-49. doi: 10.1016/s0968-0896(96)00217-9. Bioorg Med Chem. 1996. PMID: 9022977

8

New gamma-fluoromethotrexates modified in the pteridine ring: synthesis and in vitro immunosuppressive activity.

Kokuryo Y, Nakatani T, Kakinuma M, Kabaki M, Kawata K, Kugimiya A, Kawada K, Matsumoto M, Suzuki R, Ohtani M. Kokuryo Y, et al. Among authors: matsumoto m. Eur J Med Chem. 2000 May;35(5):529-34. doi: 10.1016/s0223-5234(00)00147-1. Eur J Med Chem. 2000. PMID: 10889331

9

Dopamine D3 and D4 receptor antagonists: synthesis and structure--activity relationships of (S)-(+)-N-(1-Benzyl-3-pyrrolidinyl)-5-chloro-4- [(cyclopropylcarbonyl) amino]-2-methoxybenzamide (YM-43611) and related compounds.

Ohmori J, Maeno K, Hidaka K, Nakato K, Matsumoto M, Tada S, Hattori H, Sakamoto S, Tsukamoto S, Usuda S, Mase T. Ohmori J, et al. Among authors: matsumoto m. J Med Chem. 1996 Jul 5;39(14):2764-72. doi: 10.1021/jm9601720. J Med Chem. 1996. PMID: 8709107

10

Na(+)-glucose cotransporter inhibitors as antidiabetic agents. II. Synthesis and structure-activity relationships of 4'-dehydroxyphlorizin derivatives.

Hongu M, Tanaka T, Funami N, Saito K, Arakawa K, Matsumoto M, Tsujihara K. Hongu M, et al. Among authors: matsumoto m. Chem Pharm Bull (Tokyo). 1998 Jan;46(1):22-33. doi: 10.1248/cpb.46.22. Chem Pharm Bull (Tokyo). 1998. PMID: 9468634

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