H. Kanno

发表

Orally active zwitterionic factor Xa inhibitors with long duration of action.

Makoto Suzuki, D. Takano, A. Mochizuki, 2011, Bioorganic & medicinal chemistry letters.

Design, synthesis and SAR of novel ethylenediamine and phenylenediamine derivatives as factor Xa inhibitors.

K. Uoto, Makoto Suzuki, A. Mochizuki, 2011, Bioorganic & medicinal chemistry letters.

Potent inhibitors of neutral endopeptidase. 2-Biphenyl- methylglutaric acid amide derivatives

Yoshifumi Watanabe, H. Kanno, T. Furugohri, 1996 .

Cycloalkanediamine derivatives as novel blood coagulation factor Xa inhibitors.

N. Haginoya, Tsutomu Nagata, H. Kanno, 2007, Bioorganic & medicinal chemistry letters.

Stereoselective synthesis and biological evaluation of 3,4-diaminocyclohexanecarboxylic acid derivatives as factor Xa inhibitors.

Tsutomu Nagata, H. Kanno, T. Yoshino, 2008, Bioorganic & Medicinal Chemistry Letters.

2-aminomethylphenylamine as a novel scaffold for factor Xa inhibitor.

Makoto Suzuki, A. Mochizuki, Tsutomu Nagata, 2011, Bioorganic & medicinal chemistry.

Discovery of N-[(1R,2S,5S)-2-{[(5-chloroindol-2-yl)carbonyl]amino}-5-(dimethylcarbamoyl)cyclohexyl]-5-methyl-4,5,6,7-tetrahydrothiazolo[5,4-c]pyridine-2-carboxamide hydrochloride: a novel, potent and orally active direct inhibitor of factor Xa.

N. Haginoya, Makoto Suzuki, Tsutomu Nagata, 2009, Bioorganic & medicinal chemistry.

Aryloxyacetic acid diuretics with uricosuric activity. II. Substituted [(4-oxo-4H-1-benzopyran-7-yl)oxy]acetic acids and the related compounds.

M. Tanaka, K. Yamamoto, H. Kanno, 1991, Chemical & pharmaceutical bulletin.

A Reagent, Ethyl 2-(2-tert-Butyl-2H-tetrazol-5-yl)-3-(dimethylamino)acrylate (DMTE), for Facile Synthesis of 2, 3-(Ring Fused)-5-(5-tetratzolyl)-4H-pyrimidin-4-one Derivatives

H. Kanno, H. Yamaguchi, S. Isoda, 1991 .

Design, synthesis, and SAR of cis-1,2-diaminocyclohexane derivatives as potent factor Xa inhibitors. Part I: exploration of 5-6 fused rings as alternative S1 moieties.

Hiroyuki Naito, Tsutomu Nagata, Kengo Watanabe, 2009, Bioorganic & medicinal chemistry.

Diastereoselective addition-elimination reactions of lithium enolates of chiral N-acyloxazolidinones with 2-methylene-3-phenoxyalkanoates

H. Kanno, K. Osanai, 1995 .

Synthesis and antiallergy activity of [1,3,4]thiadiazolo[3,2-a]-1,2,3-triazolo[4,5-d]pyrimidin-9 (3H)-one derivatives. I.

H. Kanno, H. Takamori, W. Tsukada, 1992, Chemical & pharmaceutical bulletin.

Facile Methods for Preparation of Thiazolopyridine and Tetrahydro-thiazolopyridine Derivatives

N. Haginoya, Tsutomu Nagata, H. Kanno, 2004 .

Facile Methods for Preparation of Thiazolopyridine and Tetrahydrothiazolopyridine Derivatives.

N. Haginoya, Tsutomu Nagata, H. Kanno, 2004 .

Thromboxane A2 synthetase inhibitors. I. Syntheses and activities of various N-heteroaromatic derivatives.

S. Ashida, Y. Watanabe, H. Kanno, 1988, Chemical & pharmaceutical bulletin.

Diastereoselective palladium(0)-catalyzed reactions of lithium enolates of chiral N-acyloxazolidinones. Asymmetric synthesis of 2-substituted (E)-4-alkylidenepentanedioates

H. Kanno, K. Osanai, 1995 .

Thromboxane A2 synthetase inhibitors. 2. Syntheses and activities of tetrahydronaphthalene and indan derivatives.

J. Saegusa, S. Ashida, Y. Watanabe, 1989, Journal of medicinal chemistry.