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[Studies for analyzing the prohibited ingredients such as acetohexamide in cosmetics] [Journal Article]
Kokuritsu Iyakuhin Shokuhin Eisei Kenkyusho Hokoku 2005; (123):19-22.
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| Imamura Y, Shimada H
Differential pharmacokinetics of acetohexamide in male Wistar-Imamichi and Sprague-Dawley rats: role of microsomal carbonyl reductase. [Journal Article]
Biol Pharm Bull 2005 Jan; 28(1):185-7.
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| Imamura Y, Shimada H
Strain- and sex-related differences of carbonyl reductase activities in kidney microsomes and cytosol of rats. [Journal Article]
J Appl Toxicol 2004 Nov-Dec; 24(6):437-41.
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| Imamura Y, Kaneko M, Takada H, et al.
Sex-dependent pharmacokinetics of S(-)-hydroxyhexamide, a pharmacologically active metabolite of acetohexamide, in rats. [Journal Article]
Comp Biochem Physiol C Toxicol Pharmacol 2002 Dec; 133(4):587-92.
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| Shimada H, Yamaguchi S, Murata H, et al.
Cadmium exposure decreases androgen-dependent metabolism of acetohexamide in liver microsomes of male rats through its testicular toxicity. [Journal Article]
Arch Toxicol 2002 Feb; 76(1):8-12.
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| Imamura Y, Sanai K, Seri K, et al.
Hypoglycemic effect of S(-)-hydroxyhexamide, a major metabolite of acetohexamide, and its enantiomer R(+)-hydroxyhexamide. [Journal Article]
Life Sci 2001 Sep 7; 69(16):1947-55.
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| Stephenson GA
Structure determination from conventional powder diffraction data: application to hydrates, hydrochloride salts, and metastable polymorphs. [Journal Article]
J Pharm Sci 2000 Jul; 89(7):958-66.
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| Imamura Y, Koga T, Uriu Y, et al.
Catalytic properties for naphthoquinones and partial primary structure of rabbit heart acetohexamide reductase. [Journal Article]
Biol Pharm Bull 2000 Feb; 23(2):155-8.
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| Seri K, Sanai K, Kurashima K, et al.
(R)-ACX is a novel sufonylurea compound with potent, quick and short-lasting hypoglycemic activity. [Journal Article]
Eur J Pharmacol 2000 Feb 18; 389(2-3):253-6.
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| Sabb PC, Allen JC
Acetohexamide-acetazolamide mix-up during emergency treatment. [Case Reports, Letter]
Am J Health Syst Pharm 1999 Dec 1; 56(23):2463.
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