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ChemicalBook--->CAS DataBase List--->52169-36-5

52169-36-5

52169-36-5 Structure

52169-36-5 Structure
IdentificationBack Directory
[Name]

Glyburide (potassium salt)
[CAS]

52169-36-5
[Synonyms]

Glyburide Potassium
Glyburide (potassium salt)
KAJMFLAYIQKSQT-UHFFFAOYSA-N
[Molecular Formula]

C23H27ClKN3O5S
[MOL File]

52169-36-5.mol
[Molecular Weight]

532.094
Chemical PropertiesBack Directory
[storage temp. ]

Store at -20°C
[solubility ]

DMF: 2 mg/ml; DMSO: 10 mg/ml; DMSO:PBS (pH 7.2) (1:1): 0.5 mg/ml
[form ]

A crystalline solid
Safety DataBack Directory
[Symbol(GHS) ]


GHS07
[Signal word ]

Warning
[Hazard statements ]

H413-H302
[Precautionary statements ]

P264-P270-P301+P312-P330-P501
Hazard InformationBack Directory
[Description]

Glyburide is a sulfonylurea and an inhibitor of sulfonylurea receptor 1 (SUR1) linked to ATP-sensitive potassium channel Kir6.2 (IC50 = 4.3 nM).1 It binds to microsomes derived from RINm5F pancreatic β-cells (Kd = 0.3 nM) and inhibits 86Rb+ efflux from intact RINm5 cells with a half-maximal inhibition (K0.5) value of 0.06 nM.2 Glyburide (5 mg/kg) reduces blood glucose levels and increases the activity of hepatic glutathione-S-transferase (GST) and glucose-6-phosphate dehydrogenase (G6PDH) in a rat model of diabetes induced by streptozotocin (STZ; ).3 It inhibits ATP-induced increases in caspase-1 activation and IL-1β and IL-18 secretion in a concentration-dependent manner in LPS-primed bone marrow-derived macrophages (BMDMs).4 Glyburide (80 mg/ml) also reduces lesion growth in mice infected with L. mexicana.5 Formulations containing glyburide have been used in the treatment of type 2 diabetes.
[Uses]

Glibenclamide (Glyburide) potassium is a potassium salt of Glibenclamide (HY-15206). Glibenclamid potassium exists in anhydrous and hydrate forms, with higher solubility compared to pure Glibenclamide[1].
[References]

1. Coghlan, M.J., Carroll, W.A., and Gopalakrishnan, M. Recent developments in the biology and medicinal chemistry of potassium channel modulators: Update from a decade of progress J. Med. Chem. 44(11),1627-1653(2001).
2. Schmid-Antomarchi, H., De Weille, J., Fosset, M., et al. The receptor for antidiabetic sulfonylureas controls the activity of the ATP-modulated K+ channel in insulin-secreting cells J. Biol. Chem. 262(33),15840-15844(1987).
3. Bugdayci, G., Altan, N., Sancak, B., et al. The effect of the sulfonylurea glyburide on glutathione-S-transferase and glucose-6-phosphate dehydrogenase in streptozotocin-induced diabetic rat liver Acta. Diabetol. 43(4),131-134(2006).
4. Lamkanfi, M., Mueller, J.L., Vitari, A.C., et al. Glyburide inhibits the Cryopyrin/Nalp3 inflammasome J. Cell Biol. 187(1),61-70(2009).
5. Serrano-Martín, X., Payares, G., and Mendoza-León, A. Glibenclamide, a blocker of K+ATP channels, shows antileishmanial activity in experimental murine cutaneous leishmaniasis Antimicrob. Agents Chemother. 50(12),4214-4216(2006).
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