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Life Sciences | 1993

Inhibition of hepatic cholesterol biosynthesis by a 3-hydroxy-3-methylglutaryl coenzyme a synthase inhibitor, 1233A, in mice

Hajime Nagashima; Hidetoshi Kumagai; Hiroshi Tomoda; Satoshi Ōmura

We have studied the in vivo inhibition of hepatic sterol biosynthesis by 1233A, a specific inhibitor of the enzyme 3-hydroxy-3-methylglutaryl coenzyme A (HMG-CoA) synthase. Administration of the compound orally to mice resulted in a dose-dependent inhibition of [14C]acetate incorporation into sterols in liver, but did not exert any significant effect on [14C]mevalonate incorporation. The results indicate that the in vivo inhibition of sterol synthesis occurs only at pre-mevalonate enzymatic steps in the sterol biosynthetic pathway, thus being compatible with the presumed site of inhibition, HMG-CoA synthase. Moreover, owing to irreversible inactivation of the enzyme by 1233A, it was possible to detect in vivo effect on the enzyme by assays of its activity in cell-free extracts from livers; the drug-treatment also resulted in a similarly dose-dependent inhibition of HMG-CoA synthase activity. In contrast, acetoacetyl-CoA thiolase and HMG-CoA reductase, the enzymes also responsible for mevalonate synthesis in the pathway, did not show any significant change in activity. These results clearly demonstrate that the inhibition of hepatic sterol synthesis caused by 1233A is indeed due to selective inhibition of HMG-CoA synthase in the tissues.


The Journal of Antibiotics | 1987

Potent inhibitory effect of antibiotic 1233A on cholesterol biosynthesis which specifically blocks 3-hydroxy-3-methylglutaryl coenzyme A synthase

Satoshi Omura; Hiroshi Tomoda; Hidetoshi Kumagai; Michael D. Greenspan; Joel B. Yodkovitz; Julie S. Chen; Alfred W. Alberts; Isobel Martin; Sagrario Mochales; Richard L. Monaghan; John C. Chabala; Robert E. Schwartz; Arthur A. Patchett


The Journal of Antibiotics | 1988

Atpenins, new antifungal antibiotics produced by Penicillium sp. Production, isolation, physico-chemical and biological properties.

Satoshi Omura; Hiroshi Tomoda; Keiko Kimura; D.-Z. Zhent; Hidetoshi Kumagai; Kazuaki Igarashi; Nobutaka Imamura; Yoko Takahashi; Yoshitake Tanaka; Yuzuru Iwai


The Journal of Antibiotics | 1988

F-244 (1233A), a specific inhibitor of 3-hydroxy-3-methylglutaryl coenzyme A synthase: taxonomy of producing strain, fermentation, isolation and biological properties.

Hiroshi Tomoda; Hidetoshi Kumagai; Yoko Takahashi; Yoshitake Tanaka; Yuzuru Iwai; Satoshi Omura


The Journal of Antibiotics | 1990

The structures of atpenins A4, A5 and B, new antifungal antibiotics produced by Penicillium sp.

Hidetoshi Kumagai; Hiroyuki Nishida; Nobutaka Imamura; Hiroshi Tomoda; Satoshi Omura; Jon Bordner


The Journal of Antibiotics | 1990

Mechanism of action of atpenin b on raji cells.

Kazushi Oshino; Hidetoshi Kumagai; Hiroshi Tomoda; Satoshi Omura


The Journal of Antibiotics | 1990

Method of search for microbial inhibitors of mevalonate biosynthesis using animal cells.

Hidetoshi Kumagai; Hiroshi Tomoda; Satoshi Omura


The Journal of Antibiotics | 1992

SYNTHESIS OF 1233A ANALOGS AND THEIR INHIBITORY ACTIVITY AGAINST HYDROXYMETHYLGLUTARYL COENZYME A SYNTHASE

Toshiaki Sunazuka; Kazuo Tsuzuki; Hidetoshi Kumagai; Hiroshi Tomoda; Haruo Tanaka; Hajime Nagashima; Hirokazu Hashizume; Satoshi Omura


Biochemical and Biophysical Research Communications | 1999

Differential Inhibition of HMG-CoA Synthase and Pancreatic Lipase by the Specific Chiral Isomers of β-Lactone DU-6622 ☆

Hiroshi Tomoda; Naomi Ohbayashi; Hidetoshi Kumagai; Hirokazu Hashizume; Toshiaki Sunazuka; Satoshi Ōmura


Journal of Organic Chemistry | 1997

SYNTHESIS OF FOUR CHIRAL ISOMERS OF BETA -LACTONE DU-6622 AND INHIBITION OF HMG-COA SYNTHASE BY THE SPECIFIC (2R,3R)-ISOMER

Hiroshi Tomoda; Hidetoshi Kumagai; Y. Ogawa; Toshiaki Sunazuka; H. Hashizume; H. Nagashima; Satoshi Omura

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