M. Nakano

发表

Enantiomer-enantiomer interaction of a uricosuric antihypertensive diuretic (DBCA) in renal tubular secretion and stereoselective inhibition by probenecid in the cynomolgus monkey.

K. Higaki, M. Nakano, S. Kawahara, 1993, Xenobiotica; the fate of foreign compounds in biological systems.

High-performance liquid chromatographic method for simultaneous determination of enantiomers of 5-dimethylsulphamoyl-6,7-dichloro-2-dihydrobenzofuran-2, carboxylic acid and its N-monodemethyl metabolite in monkey plasma and urine after chiral derivatization.

M. Nakano, S. Kawahara, 1991, Journal of chromatography.

Synthesis of a Homostatine-Containing Renin Inhibitor Which Incorporates a Sulfonemethylene Isostere at Its N-Terminus

H. Funabashi, M. Ohkubo, H. Morishima, 1990 .

Synthesis of Renin Inhibitors Containing a Sulfonemethylene Isostere at Their N-Terminals

H. Funabashi, M. Ohkubo, H. Morishima, 1990 .

A stereospecific synthesis of a renin inhibitor (BW-175) which incorporates a sulfonemethylene isostere and a dihydroxyethylene isostere.

H. Funabashi, H. Morishima, Seiichi Tanaka, 1990 .

Quaternary ammonium glucuronide of croconazole in rabbits.

K. Mizojiri, Y. Terui, Y. Nakagawa, 1989, Xenobiotica; the fate of foreign compounds in biological systems.

Design and effective synthesis of novel templates, 3,7-diphenyl-4-amino-thieno and furo-[3,2-c]pyridines as protein kinase inhibitors and in vitro evaluation targeting angiogenetic kinases.

J. D. Stuart, A. Truesdale, Laurie S. Kane-Carson, 2007, Bioorganic & medicinal chemistry letters.

Ruthenium-catalysed disproportionation between vinylsilanes and mono-substituted alkenes via silyl group transfer

H. Yamazaki, Yasuhiro Yamamoto, Y. Wakatsuki, 1991 .

Knowledge-based design of 7-azaindoles as selective B-Raf inhibitors.

K. Lackey, Hideyuki Sato, S. Dickerson, 2008, Bioorganic & medicinal chemistry letters.

Novel High Performance ansa-Zirconocene Catalysts for Isospecific Polymerization of Propylene

H. Yamazaki, Keisuke Kimura, M. Nakano, 1999 .

4-Acylamino-6-arylfuro[2,3-d]pyrimidines: potent and selective glycogen synthase kinase-3 inhibitors.

A. Truesdale, Y. Maeda, Hideyuki Sato, 2004, Bioorganic & medicinal chemistry letters.

Synthesis of NB-506, A new anticancer agent

H. Kawamoto, M. Ohkubo, H. Morishima, 1997 .

Rational design of 4-amino-5,6-diaryl-furo[2,3-d]pyrimidines as potent glycogen synthase kinase-3 inhibitors.

Y. Maeda, Hideyuki Sato, G. Mellor, 2008, Bioorganic & medicinal chemistry letters.

Lipase-catalyzed kinetic resolution of ethyl 3-aryl-3-hydroxypropionate: preparation of the side chain of a novel carbapenem, J-114,870

H. Morishima, Koji Yamada, Y. Sugimoto, 2000 .

Novel dithiocarbamate carbapenems with anti-MRSA activity.

H. Satō, N. Ohtake, M. Moriya, 1997, Bioorganic & medicinal chemistry.

Discovery of novel trans-3,5-disubstituted pyrrolidinylthio-1beta-methylcarbapenems.

Y. Tsuchiya, S. Sakuraba, H. Satō, 2000, Bioorganic & medicinal chemistry.

Total Synthesis of Brevisamide Using an Oxiranyl Anion Strategy.

Takeo Sakai, Y. Mori, M. Nakano, 2016, The Journal of organic chemistry.

Syntheses of methyl 6-deoxy-6-hydroxyamino-α-d-glucopyranoside, 6′-N-hydroxykanamycin A, and 6′-N-hydroxydibekacin

T. Torii, Yukiko Suzuki, S. Umezawa, 1985 .

Synthesis of μ-Oxo Complexes of Group 4 Bridged-Metallocenes: A Convenient Separation of meso and racemo Isomers

H. Yamazaki, Keisuke Kimura, M. Nakano, 1998 .

Croconazole metabolism in rats.

K. Mizojiri, M. Takeuchi, M. Nakano, 1990, Xenobiotica; the fate of foreign compounds in biological systems.

Metabolism of the antimycotic agent, croconazole, in rabbits.

Y. Nakagawa, Y. Nakajima, K. Sugeno, 1989, Drug metabolism and disposition: the biological fate of chemicals.

Novel 4-amino-furo[2,3-d]pyrimidines as Tie-2 and VEGFR2 dual inhibitors.

Yutaka Maeda, Wei Liu, Megumi Shibahara, 2005, Bioorganic & medicinal chemistry letters.

Deimidazolation of antimycotic croconazole through epoxide formation in rabbit liver microsomes.

K. Mizojiri, M. Nakano, 1989, Drug metabolism and disposition: the biological fate of chemicals.

An efficient enantioselective preparation of 2-substituted-3-hydroxypropionic acids via chemo-enzymatic reaction

H. Funabashi, M. Ohkubo, H. Morishima, 1990 .

An Efficient Enantioselective Preparation of 2‐Substituted 3‐Hydroxypropionic Acids via Chemoenzymatic Reaction.

H. Funabashi, M. Ohkubo, H. Morishima, 1990 .

A novel nonpeptidic, orally active renin inhibitor.

Y. Sawasaki, H. Funabashi, H. Morishima, 1989, Biochemical and biophysical research communications.

Trehalase: stereocomplementary hydrolytic and glucosyl transfer reactions with alpha- and beta-D-glucosyl fluoride.

E. Hehre, T. Sawai, C. Brewer, 1982, Biochemistry.

Steric course of the hydrolysis of α,α-trehalose and α-d-glucosyl fluoride catalyzed by pig kidney trehalase☆

E. Hehre, T. Kasumi, C. Brewer, 1989 .

A New Approach to the Stereospecific Synthesis of a Dihydroxyehylene Isostere

H. Funabashi, H. Morishima, Seiichi Tanaka, 1990 .

Synthesis and biological activities of NB-506 analogues modified at the glucose group.

T. Honma, S. Nishimura, H. Suda, 2000, Bioorganic & medicinal chemistry letters.

Orally active 4-amino-5-diarylurea-furo[2,3-d]pyrimidine derivatives as anti-angiogenic agent inhibiting VEGFR2 and Tie-2.

Liping Wang, R. Nolte, A. Truesdale, 2007, Bioorganic & medicinal chemistry letters.

Stereospecific Synthesis of a Dihydroxyethylene Isostere of Cyclohexylalanine Amide, (2S,3R,4S)-4-Amino-5-Cyclohexyl-1-Morpholino-2,3-Pentanediol(ACMP) from a Protected Sugar

H. Morishima, M. Nakano, S. Atsuumi, 1990 .

Rational design of 4-amino-5,6-diaryl-furo[2,3-d]pyrimidines as potent glycogen synthase kinase-3 inhibitors.

Y. Maeda, Hideyuki Sato, G. Mellor, 2008, Bioorganic & medicinal chemistry letters.

Renal trehalase: two subsites at the substrate-binding site.

B. Sacktor, M. Nakano, 1984, Biochimica et biophysica acta.

Total Synthesis of Brevisamide Using an Oxiranyl Anion Strategy.

Takeo Sakai, Y. Mori, M. Nakano, 2016, The Journal of organic chemistry.

In vivo screening of oral formulations using rats: Effects of ingested water volume on oral absorption of BCS class I and III drugs from immediate-release formulations

M. Kataoka, S. Yamashita, Takuya Nagato, 2020 .