Description
Gliquidone is a second generation sulfonylurea that selectively inhibits ATP-sensitive potassium channel currents (IK
ATP) in pancreatic β-cells (IC
50s = 0.45, 119.1, and 149.7 μM for HIT-T15 cells, cardiomyocytes, and vascular smooth muscle cells, respectively).
1 It is also a peroxisome proliferator-activated receptor γ (PPARγ) agonist (EC
50 = 10 μM in a transactivation assay).
2 Gliquidone (0.2 nmol/g) decreases plasma levels of D-glucose and stimulates insulin release in anesthetized rats.
3 It decreases blood glucose levels, serum alkaline phosphatase (ALP), aspartate aminotransferase (AST), and alanine aminotransferase (ALT) activities, and hepatic lipid peroxidation and increases hepatic glutathione (GSH) levels in a rat model of diabetes induced by streptozotocin (STZ; Item No.
13104) when administered at a dose of 10 mg/kg.
4
Originator
Glurenorm,Thornae,W. Germany,1975
Definition
ChEBI: 1-cyclohexyl-3-[4-[2-(7-methoxy-4,4-dimethyl-1,3-dioxo-2-isoquinolinyl)ethyl]phenyl]sulfonylurea is a member of isoquinolines.
Manufacturing Process
A mixture consisting of 4 grams of 1,2,3,4-tetrahydro-4,4-dimethyl-7-
methoxy-isochromanedione-(1,3) (MP 95° to 97°C), 2.53 grams of 4-
aminosulfonyl-phenyl-(2)-ethylamine and 150 ml of xylene was heated for 2
hours at its boiling point in an apparatus provided with a water separator.
Thereafter, the reaction mixture was allowed to cool and was then vacuumfiltered, and the filter cake was recrystallized from n-propanol in the presence
of activated charcoal. 2.9 grams (58% of theory) of 1,2,3,4-tetrahydro-4,4-
dimethyl-2-[p-aminosulfonylphenyl-(2)-ethyl]-7-methoxy-isoquinolinedione-
(1,3), MP 203° to 205°C, of the formula below were obtained.
32.2 grams of 1,2,3,4-tetrahydro-4,4-dimethyl-2-[p-aminosulfonylphenyl-(2)-ethyl]-7-methoxy-isoquinolinedione-(1,3) were dissolved in 700 ml of
dimethylformamide, 9.1 grams of potassium tert-butylate were added to the
solution, and, while cooling the mixture with ice, 14.9 grams of cyclohexyl
isocyanate were added dropwise thereto.
Subsequently, the reaction mixture was stirred for 5 hours on an ice bath and
was then allowed to stand overnight at -2°C. Thereafter, the reaction solution
was admixed with water, the precipitate formed thereby was separated by
vacuum-filtration, the filtrate was admixed with more water, and the aqueous
solution was acidified with 2N hydrochloric acid. A greasy substance
precipitated out which crystallized after a brief period of contact with boiling
methanol. 2.6 grams (85% of theory) of 1,2,3,4-tetrahydro-2-[p-(N'-
cyclohexyl-ureido-N-sulfonyl)-phenethyl]-4,4-dimethyl-7-methoxyisoquinolinedione-(1,3), MP 180° to 182°C, were obtained.
References
[1]. oca?a m, del pozo e, baeyens jm. gliquidone, an atp-dependent k+ channel antagonist, antagonizes morphine-induced hypermotility. eur j pharmacol, 1993, 239(1-3): 253-255.
[2]. oca?a m, baeyens jm. role of atp-sensitive k+ channels in antinociception induced by r-pia, an adenosine a1 receptor agonist. naunyn schmiedebergs arch pharmacol, 1994, 350(1): 57-62.
[3]. von nicolai h, brickl r, eschey h, et al. duration of action and pharmacokinetics of the oral antidiabetic drug gliquidone in patients with non-insulin-dependent (type 2) diabetes mellitus. arzneimittelforschung, 1997, 47(3): 247-252.
[4]. tuerk tr, bandur s, nuernberger j, et al. gliquidone therapy of new-onset diabetes mellitus after kidney transplantation. clin nephrol, 2008, 70(1): 26-32.