T. Terasawa

发表

Inhibitors of acyl-CoA:cholesterol O-acyltransferase (ACAT). Part 1: identification and structure-activity relationships of a novel series of substituted N-alkyl-N-biphenylylmethyl-N'-arylureas.

H. Tanaka, A. Tanaka, H. Takasugi, 1998, Bioorganic & medicinal chemistry.

Antinociceptive Effects of AS1892802, a Novel Rho Kinase Inhibitor, in Rat Models of Inflammatory and Noninflammatory Arthritis

A. Iwashita, Y. Shimizu, N. Ishii, 2010, Journal of Pharmacology and Experimental Therapeutics.

Orally active cephalosporins. Part 2: synthesis, structure-activity relationships and oral absorption of cephalosporins having a C-3 pyridyl side chain.

Y. Matsumoto, S. Matsumoto, K. Kawabata, 2000, Bioorganic & medicinal chemistry.

A Concise, Practical Synthesis of the Pyrido[3,2,1-i,j]Cinnoline Ring System of Potent DNA Gyrase Inhibitors

H. Sasaki, D. Barrett, T. Terasawa, 1995 .

A Concise, Practical Synthesis of the Pyrido(3.2.1-ij)cinnoline Ring System of Potent DNA Gyrase Inhibitors.

H. Sasaki, D. Barrett, T. Terasawa, 2010 .

Studies on beta-lactam antibiotics. Synthesis and antibacterial activity of novel C-3 alkyne-substituted cephalosporins.

T. Kamimura, N. Yasuda, T. Takaya, 1997, The Journal of antibiotics.

Stereocontrolled Synthesis of Petrosterol

N. Ikekawa, Y. Fujimoto, T. Terasawa, 1985 .

Orally active cephalosporins. Part 3: synthesis, structure-activity relationships and oral absorption of novel C-3 heteroarylmethylthio cephalosporins.

H. Tanaka, Y. Matsumoto, S. Matsumoto, 2001, Bioorganic & medicinal chemistry.

Patch esophagoplasty using an in-body-tissue-engineered collagenous connective tissue membrane.

Y. Nakayama, Y. Takama, H. Okuyama, 2017, Journal of pediatric surgery.

Synthesis and antibacterial activity of novel 4-pyrrolidinylthio carbapenems Part IV. 2-Alkyl substituents containing cationic heteroaromatics linked via a C-C bond.

M. Sakurai, D. Barrett, A. Tanaka, 2001, Bioorganic & medicinal chemistry.

Inhibitors of acyl-CoA:cholesterol O-acyltransferase. 2. Identification and structure-activity relationships of a novel series of N-alkyl-N-(heteroaryl-substituted benzyl)-N'-arylureas.

H. Tanaka, A. Tanaka, H. Takasugi, 1998, Journal of medicinal chemistry.

Synthesis, X-ray crystal structure, and biological activity of FR186054, a novel, potent, orally active inhibitor of acyl-CoA:cholesterol O-acyltransferase (ACAT) bearing a pyrazole ring.

T. Kinoshita, H. Tanaka, A. Tanaka, 1998, Bioorganic & medicinal chemistry letters.

Orally active cephalosporins: synthesis, structure-activity relationships and oral absorption of 3-[(E) and (Z)-2-substituted vinyl]-cephalosporins.

A. Ohki, Y. Matsumoto, S. Matsumoto, 2000, Bioorganic & medicinal chemistry.

PHOTOCHEMICAL REACTION OF CHOLESTEROL ANALOGS WITH A CARBENE-GENERATING SUBSTITUMENT ON THE SIDE CHAIN

N. Ikekawa, M. Morisaki, T. Terasawa, 1986 .

Stereocontrolled synthesis and determination of the c-24 and 25 stereochemistry of glaucasterol

N. Ikekawa, Y. Fujimoto, T. Terasawa, 1984 .

Stereocontrolled synthesis of gorgosterol

N. Ikekawa, Y. Fujimoto, Y. Hirano, 1984 .

Patch esophagoplasty using an in-body-tissue-engineered collagenous connective tissue membrane.

Y. Nakayama, Y. Takama, H. Okuyama, 2017, Journal of pediatric surgery.

Design, synthesis, and pharmacological evaluation of N-(3-carbamoyl-1H-pyrazol-4-yl)-1,3-oxazole-4-carboxamide derivatives as interleukin-1 receptor-associated kinase 4 inhibitors with reduced potential for cytochrome P450 1A2 induction.

T. Kontani, E. Imamura, T. Ishikawa, 2023, Bioorganic & medicinal chemistry.