Studies on antidiabetic agents. II. Synthesis of 5-(4-(1-methylcyclohexylmethoxy)-benzyl)thiazolidine-2,4-dione (ADD-3878) and its derivatives.

Takashi Sohda(Takeda (Japan)), Katsutoshi Mizuno(Takeda (Japan)), Eiko Imamiya(Takeda (Japan)), Yasuo Sugiyama(Takeda (Japan)), Takeshi Fujita(Takeda (Japan)), Y. Kawamatsu(Takeda (Japan))
Chemical and Pharmaceutical Bulletin
January 1, 1982
Cited by 167Open Access
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Abstract

More than 100 5-substituted thiazolidine-2, 4-diones were prepared and their hypoglycemic and hypolipidemic activities were evaluated with genetically obese and diabetic mice, yellow KK. The structure-activity relationship study showed that the 5-(4-oxybenzyl) moiety is essential for substantial activity. Among these compounds, 5-(4-cyclohexylmethoxy) benzylthiazolidine-2, 4-dione (47), 5-[4-(1-methylcyclohexylmethoxy) benzyl]-thiazolidine-2, 4-dione (49, ADD-3878) and 5-{4-[2-(3-pyridyl) ethoxy] benzyl} thiazolidine-2, 4-dione (59) exhibited the most favorable properties in terms of activity and toxicity.


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