M. Nomura

发表

Enantio-dependent binding and transactivation of optically active phenylpropanoic acid derivatives at human peroxisome proliferator-activated receptor alpha.

Masahiro Suzuki, H. Miyachi, K. Murakami, 2002, Bioorganic & medicinal chemistry letters.

Efficient asymmetric synthesis of (S)-2-ethylphenylpropanoic acid derivative, a selective agonist for human peroxisome proliferator-activated receptor alpha.

H. Miyachi, M. Nomura, T. Tanase, 2002, Bioorganic & medicinal chemistry letters.

Design, synthesis, and evaluation of substituted phenylpropanoic acid derivatives as human peroxisome proliferator activated receptor activators. Discovery of potent and human peroxisome proliferator activated receptor alpha subtype-selective activators.

Masahiro Suzuki, H. Miyachi, T. Ide, 2003, Journal of medicinal chemistry.

LpxC Inhibitors: Design, Synthesis, and Biological Evaluation of Oxazolidinones as Gram-negative Antibacterial Agents.

Y. Yamaguchi, K. Iwase, Y. Kohno, 2016, ACS medicinal chemistry letters.

Synthesis and structure-activity relationship of 4-quinolone-3-carboxylic acid based inhibitors of glycogen synthase kinase-3β.

J. Kozarich, J. Rosenblum, Qiang Li, 2011, Bioorganic & medicinal chemistry letters.

Oxazinomycin, a new carbon-linked nucleoside antibiotic.

T. Okazaki, T. Haneishi, C. Tamura, 1971, The Journal of antibiotics.

(3-substituted benzyl)thiazolidine-2,4-diones as structurally new antihyperglycemic agents.

M. Tsunoda, K. Murakami, K. Awano, 1999, Bioorganic & medicinal chemistry letters.

A New Method for the Stereoselective Synthesis of Nucleosides by Means of Sodium Borohydride Mediated Reductive C-C or C-N Bond Cleavage Reaction

Hiroshi Sato, N. Katagiri, C. Kaneko, 1992 .

Synthesis and anti-HIV activity of 9-[c-4,t-5-bis(hydroxymethyl)cyclopent-2-en-r-1-yl]-9H-adenine.

T. Tsuruo, H. Satō, K. Yusa, 1992, Journal of medicinal chemistry.

Synthesis of Nucleosides and Related Compounds. Part 23. Synthesis and Anti‐HIV Activity of 9‐(c‐4,t‐5‐Bis(hydroxymethyl)cyclopent‐2‐en‐r‐1‐ yl)‐9H‐adenine.

T. Tsuruo, K. Yusa, N. Katagiri, 1993 .

Synthesis of Carbocyclic Nucleosides from 2-Azabicyclo[2.2.1]hept-5-en-3-ones : Sodium Borohydride-Mediated Carbon : Nitrogen Bond Cleavage of Five- and Six-Membered Lactams

N. Katagiri, C. Kaneko, M. Nomura, 1991 .

Synthesis of nucleosides and related compounds. XXII: Carbocyclic analogues of thymidine and related compounds from 2-azabicyclo[2.2.1]hept-5-en-3-ones

N. Katagiri, C. Kaneko, M. Nomura, 1991 .

Synthesis of nucleosides and their related compounds. 15 dimethyl rel-(1S,2S,3R,4R)-2-(2,3-epoxy-4-hydroxymethylcyclopent-1-YL)malonate as a novel building block for carbocyclic arabinosyl nucleosides

N. Katagiri, C. Kaneko, M. Nomura, 1990 .

Synthesis of Nucleosides and Related Compounds. Part 20. Synthesis of Carbocyclic Nucleosides from 2-Azabicyclo(2.2.1)hept-5-en-3-ones: Sodium Borohydride Mediated Carbon-Nitrogen Bond Cleavage of Five- and Six-Membered Lactams.

N. Katagiri, C. Kaneko, M. Nomura, 2010 .

Design, synthesis and evaluation of substituted phenylpropanoic acid derivatives as peroxisome proliferator-activated receptor (PPAR) activators: novel human PPARalpha-selective activators.

H. Miyachi, T. Ide, M. Tsunoda, 2002, Bioorganic & Medicinal Chemistry Letters.

Antimicrobial activity of thiophenes and furans with d- and l-carvone residues

A. Yamamoto, M. Nomura, K. Kasemura, 2002 .

Synthesis and antimicrobial activity of furans and thiophenes with iononyl derivatives

A. Yamamoto, M. Nomura, K. Kasemura, 2001 .

Design, synthesis and evaluation of substituted phenylpropanoic acid derivatives as peroxisome proliferator-activated receptor (PPAR) activators: novel human PPARalpha-selective activators.

H. Miyachi, T. Ide, M. Tsunoda, 2002, Bioorganic & medicinal chemistry letters.

Discovery of cyclic amine-substituted benzoic acids as PPARα agonists.

Y. Takano, K. Murakami, M. Nomura, 2012, Bioorganic & medicinal chemistry letters.