Nomura E - Search Results

1

Synthesis of amide compounds of ferulic acid, and their stimulatory effects on insulin secretion in vitro.

Nomura E, Kashiwada A, Hosoda A, Nakamura K, Morishita H, Tsuno T, Taniguchi H. Nomura E, et al. Bioorg Med Chem. 2003 Aug 15;11(17):3807-13. doi: 10.1016/s0968-0896(03)00280-3. Bioorg Med Chem. 2003. PMID: 12901926

2

Synthesis of novel polyphenols consisted of ferulic and gallic acids, and their inhibitory effects on phorbol ester-induced Epstein-Barr virus activation and superoxide generation.

Nomura E, Hosoda A, Morishita H, Murakami A, Koshimizu K, Ohigashi H, Taniguchi H. Nomura E, et al. Bioorg Med Chem. 2002 Apr;10(4):1069-75. doi: 10.1016/s0968-0896(01)00361-3. Bioorg Med Chem. 2002. PMID: 11836117

3

Syntheses of ferulic acid derivatives and their suppressive effects on cyclooxygenase-2 promoter activity.

Hosoda A, Ozaki Y, Kashiwada A, Mutoh M, Wakabayashi K, Mizuno K, Nomura E, Taniguchi H. Hosoda A, et al. Among authors: nomura e. Bioorg Med Chem. 2002 Apr;10(4):1189-96. doi: 10.1016/s0968-0896(01)00386-8. Bioorg Med Chem. 2002. PMID: 11836130

4

Synthesis of feruloyl-myo-insitol derivatives and their inhibitory effects on phorbol ester-induced superoxide generation and Esptein-Barr virus activation.

Hosoda A, Nomura E, Murakami A, Koshimizu K, Ohigashi H, Mizuno K, Taniguchi H. Hosoda A, et al. Among authors: nomura e. Bioorg Med Chem. 2002 Jun;10(6):1855-63. doi: 10.1016/s0968-0896(02)00010-x. Bioorg Med Chem. 2002. PMID: 11937343

5

Preparation of ferulic acid and its application for the synthesis of cancer chemopreventive agents.

Taniguchi H, Hosoda A, Tsuno T, Maruta Y, Nomura E. Taniguchi H, et al. Among authors: nomura e. Anticancer Res. 1999 Sep-Oct;19(5A):3757-61. Anticancer Res. 1999. PMID: 10625954

6

Synthesis of feruloyl-myo-inositols and their inhibitory effects on superoxide generation.

Hosoda A, Nomura E, Murakami A, Koshimizu K, Ohigashi H, Mizuno K, Taniguchi H. Hosoda A, et al. Among authors: nomura e. Bioorg Med Chem Lett. 2000 Jul 3;10(13):1439-42. doi: 10.1016/s0960-894x(00)00252-3. Bioorg Med Chem Lett. 2000. PMID: 10888327

7

Preparation of a (+/-)-1,6-di-O-feruloyl-myo-inositol derivative: an efficient method for introduction of ferulic acid to 1,6-vicinal hydroxyl groups of myo-inositol.

Hosoda A, Nomura E, Mizuno K, Taniguchi H. Hosoda A, et al. Among authors: nomura e. J Org Chem. 2001 Oct 19;66(21):7199-201. doi: 10.1021/jo015629e. J Org Chem. 2001. PMID: 11597252 No abstract available.

8

A novel molecular assembly mode of ferulic acid derivatives.

Miyake Y, Hosoda A, Takagaki M, Nomura E, Taniguchi H. Miyake Y, et al. Among authors: nomura e. Chem Commun (Camb). 2002 Jan 21;(2):132-3. doi: 10.1039/b107785f. Chem Commun (Camb). 2002. PMID: 12120338

9

FA15, a hydrophobic derivative of ferulic acid, suppresses inflammatory responses and skin tumor promotion: comparison with ferulic acid.

Murakami A, Nakamura Y, Koshimizu K, Takahashi D, Matsumoto K, Hagihara K, Taniguchi H, Nomura E, Hosoda A, Tsuno T, Maruta Y, Kim HW, Kawabata K, Ohigashi H. Murakami A, et al. Among authors: nomura e. Cancer Lett. 2002 Jun 28;180(2):121-9. doi: 10.1016/s0304-3835(01)00858-8. Cancer Lett. 2002. PMID: 12175542

10

A novel geranylated derivative, ethyl 3-(4'-geranyloxy-3'-methoxyphenyl)-2-propenoate, synthesized from ferulic acid suppresses carcinogenesis and inducible nitric oxide synthase in rat tongue.

Tanaka T, Kohno H, Nomura E, Taniguchi H, Tsuno T, Tsuda H. Tanaka T, et al. Among authors: nomura e. Oncology. 2003;64(2):166-75. doi: 10.1159/000067764. Oncology. 2003. PMID: 12566915

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