O. Kanno

发表

A novel oral carbapenem CS-834: chemical stability of pivaloyloxymethyl esters of carbapenems and cephalosporins in phosphate buffer solution.

I. Kawamoto, M. Miyauchi, O. Kanno, 1997, The Journal of antibiotics.

Stereoselective Synthesis of Novel anti-MRSA Tricyclic Carbapenems (Trinems)

I. Kawamoto, O. Kanno, 2000 .

Synthesis and biological evaluation of novel tricyclic carbapenems (trinems).

I. Kawamoto, S. Ohya, O. Kanno, 2000, The Journal of antibiotics.

Regio- and enantioselective hydroamination of dienes by gold(I)/menthol cooperative catalysis.

F. Toste, Z. J. Wang, O. Kanno, 2011, Angewandte Chemie.

Chiral Brønsted acid from a cationic gold(I) complex: catalytic enantioselective protonation of silyl enol ethers of ketones.

F. Toste, C. Cheon, O. Kanno, 2011, Journal of the American Chemical Society.

Efficient Syntheses of(S)-4-Hydroxy-2-pyrrolidinone Derivatives

I. Kawamoto, M. Miyauchi, O. Kanno, 2000 .

Synthesis and structure-activity relationships of novel parenteral carbapenems, CS-023 (R-115685) and related compounds containing an amidine moiety.

I. Kawamoto, S. Ohya, K. Kojima, 2003, The Journal of antibiotics.

Synthesis and antibacterial activity of novel 1beta-methyl carbapenems with cycloalkylamine moiety at the C-2 position.

I. Kawamoto, R. Endo, S. Ohya, 2001, The Journal of antibiotics.

Synthesis and biological evaluation of new oral carbapenems with 1-methyl-5-oxopyrrolidin-3-ylthio moiety.

I. Kawamoto, S. Ohya, T. Shibayama, 1999, The Journal of antibiotics.

Stereoselective Synthesis of Novel anti-MRSA Tricyclic Carbapenems (Trinems)

I. Kawamoto, O. Kanno, 2000 .

Novel orally bioavailable EZH1/2 dual inhibitors with greater antitumor efficacy than an EZH2 selective inhibitor

T. Horiuchi, M. Hirasawa, T. Takizawa, 2017, Cancer science.

Chiral Broensted Acid from a Cationic Gold(I) Complex: Catalytic Enantioselective Protonation of Silyl Enol Ethers of Ketones.

F. Toste, C. Cheon, O. Kanno, 2012 .

Discovery of potent and orally active tricyclic-based FBPase inhibitors.

A. Okuno, Mizuki Takahashi, T. Nishi, 2010, Bioorganic & medicinal chemistry.

Structure-based drug design of tricyclic 8H-indeno[1,2-d][1,3]thiazoles as potent FBPase inhibitors.

Mizuki Takahashi, T. Nishi, Takahiro Yamane, 2010, Bioorganic & medicinal chemistry letters.

Synthesis, SAR, and X-ray structure of tricyclic compounds as potent FBPase inhibitors.

Mizuki Takahashi, T. Nishi, Takahiro Yamane, 2009, Bioorganic & medicinal chemistry letters.

Novel mouse model for evaluating in vivo efficacy of xCT inhibitor.

Hiroshi Yukiura, Yusuke Fujieda, Asako Nagahira, 2019, Journal of pharmacological sciences.