T. Miki

发表

Prevention of Chemically Induced Rat Carcinogenesis by Antioxidants: Focus on HTHQ

M. Hirose, T. Shirai, M. Futakuchi, 1997 .

Synthesis and anti lipid-peroxidation activity of hydroquinone monoalkyl ethers.

T. Satoh, H. Matsumoto, T. Miki, 1994, Chemical & pharmaceutical bulletin.

Prevention by synthetic phenolic antioxidants of 2-amino-3,8-dimethylimidazo[4,5-f]quinoxaline (MeIQx)- or activated MelQx-induced mutagenesis and MelQx-induced rat hepatocarcinogenesis, and role of antioxidant activity in the prevention of carcinogenesis

M. Hirose, T. Shirai, S. Takahashi, 1998, European journal of cancer prevention : the official journal of the European Cancer Prevention Organisation.

Inhibitory effects of 1-O-hexyl-2,3,5-trimethylhydroquinone (HTHQ), green tea catechins and other antioxidants on 2-amino-6-methyldipyrido[1,2-a:3',2'-d]imidazole (Glu-P-1)-induced rat hepatocarcinogenesis and dose-dependent inhibition by HTHQ of lesion induction by Glu-P-1 or 2-amino-3,8-dimethylim

K. Wakabayashi, M. Hirose, N. Ito, 1995, Carcinogenesis.

Stage and organ dependent effects of 1‐ O‐hexyl‐2,3,5‐trimethylhydroquinone, ascorbic acid derivatives, N‐heptadecane‐8,10‐dione and phenylethyl isothiocyanate in a rat multiorgan carcinogenesis model

M. Hirose, T. Shirai, P. Boonyaphiphat, 1998, International journal of cancer.

Effects of 1‐O‐hexyl‐2,3,5‐trimethylhydroquinone on carbon tetrachloride‐induced hepatic cirrhosis in rats

H. Goto, N. Ishikawa, S. Sugiyama, 2010, Hepatology research : the official journal of the Japan Society of Hepatology.

Effects of Antioxidant 1‐O‐Hexyl‐2,3,5‐trimethylhydroquinone or Ascorbic Acid on Carcinogenesis Induced by Administration of Aminopyrine and Sodium Nitrite in a Rat Multi‐organ Carcinogenesis Model

M. Hirose, Satoru Takahashi, T. Shirai, 2002, Japanese journal of cancer research : Gann.

HX‐1171, a Novel Nrf2 Activator, Induces NQO1 and HMOX1 Expression

Jae Wha Kim, T. Miki, Jong-koo Kang, 2017, Journal of cellular biochemistry.

Single and multiple dose pharmacokinetics and tolerability of HX-1171, a novel antioxidant, in healthy volunteers

Hyeong-Seok Lim, Kyoung-Goo Han, Yo Han Kim, 2015, Drug design, development and therapy.

Chemoprevention of acrylamide toxicity by antioxidative agents in rats—effective suppression of testicular toxicity by phenylethyl isothiocyanate

M. Hirose, M. Shibutani, Kyoung-youl Lee, 2005, Archives of Toxicology.

Protective effects of hydroxychalcones on free radical-induced cell damage.

H. Ueda, T. Satoh, H. Matsumoto, 1994, Biological & pharmaceutical bulletin.

Inhibition of DMBA-initiated rat mammary tumour development by 1-O-hexyl-2,3,5-trimethylhydroquinone, phenylethyl isothiocyanate, and novel synthetic ascorbic acid derivatives.

M. Hirose, T. Shirai, M. Futakuchi, 1998, European journal of cancer prevention : the official journal of the European Cancer Prevention Organisation.

3-O-alkylascorbic acids as free radical quenchers. 3. Protective effect on coronary occlusion-reperfusion induced arrhythmias in anesthetized rats.

T. Satoh, H. Matsumoto, T. Miki, 1992, Journal of medicinal chemistry.

3-O-alkylascorbic acids as free radical quenchers. II. Inhibitory effects on some lipid peroxidation models.

T. Satoh, H. Matsumoto, T. Miki, 1991, Chemical & pharmaceutical bulletin.

Dose Dependence of 1‐O‐Hexyl‐2,3,5‐trimethylhydroquinone Promotion of Forestomach Carcinogenesis in Rats Pretreated with N‐Ethylnitrosourethane

M. Hirose, T. Shirai, Y. Mizoguchi, 1998, Japanese journal of cancer research : Gann.

Prevention by antioxidants of heterocyclic amine-induced carcinogenesis in a rat medium-term liver bioassay: results of extended and combination treatment experiments.

M. Hirose, T. Shirai, M. Futakuchi, 1998, European journal of cancer prevention : the official journal of the European Cancer Prevention Organisation.

Chemoprevention of 2-amino-1-methyl-6-phenylimidazo- [4,5-b]pyridine-induced colon carcinogenesis by 1-O-hexyl-2,3,5-trimethylhydroquinone after initiation with 1,2-dimethylhydrazine in F344 rats.

K. Imaida, M. Hirose, Satoru Takahashi, 2002, Carcinogenesis.

1‐0‐Hexyl‐2,3,5‐trimethylhydroquinone inhibits IκB phosphorylation and degradation‐linked inducible nitric oxide synthase expression: beyond antioxidant function

W. Liu, M. Itoigawa, N. Ishikawa, 2002, The Journal of pharmacy and pharmacology.

Strong Inhibition of 2‐Amino‐6‐methyldipyrido[l,2‐a:3′,2′‐d]imidazole‐induced Mutagenesis and Hepatocarcinogenesis by 1‐O‐Hexyl‐2,3,5‐trimethylhydroquinone

T. Sugimura, M. Hirose, N. Ito, 1993, Japanese journal of cancer research : Gann.

3,4-Dihydroxychalcones as potent 5-lipoxygenase and cyclooxygenase inhibitors.

H. Ueda, T. Satoh, H. Matsumoto, 1993, Journal of medicinal chemistry.

Effects of 1-O-hexyl-2, 3, 5-trimethylhydroquinone in Carbon Tetrachloride-induced Hepatic Apoptosis with a Possible Relationship to Naofen

N. Ishikawa, S. Sugiyama, T. Nonami, 2012 .