Publication Date:
2012
abstract:
We describe a new class of NO-donor hypoglycemic products obtained by joining tolbutamide, a typical
hypoglycemic sulfonylurea, with a NO-donor moiety through a hard link. As NO-donors we chose either
furoxan (1,2,5-oxadiazole 2-oxide) derivatives or the classical nitrooxy function. A preliminary biological
characterization of these compounds, including stimulation of insulin release from cultured rat
pancreatic b-cells and in vitro vasodilator and anti-aggregatory activities, is reported.
hypoglycemic sulfonylurea, with a NO-donor moiety through a hard link. As NO-donors we chose either
furoxan (1,2,5-oxadiazole 2-oxide) derivatives or the classical nitrooxy function. A preliminary biological
characterization of these compounds, including stimulation of insulin release from cultured rat
pancreatic b-cells and in vitro vasodilator and anti-aggregatory activities, is reported.
Iris type:
01.01 Articolo in rivista
Keywords:
Diabetes mellitus; NO-donor; Multitarget drugs; Anti-aggregatory activity; Insulin release
List of contributors:
Beffy, PASCALE BRIGITTE
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