G0639

Glybenclamide

≥99% (HPLC)

• Sinónimos: 5-Chloro-N-[4-(cyclohexylureidosulfonyl)phenethyl]-2-methoxybenzamide, Glyburide, N-p-[2-(5-Chloro-2-methoxybenzamido)ethyl]benzenesulfonyl-N′-cyclohexylurea
• Fórmula empírica (notación de Hill): C₂₃H₂₈ClN₃O₅S
• Número de CAS: 10238-21-8
• Peso molecular: 494.00
• Número CE: 233-570-6
• Número MDL: MFCD00056625
• Código UNSPSC: 12352200
• ID de la sustancia en PubChem: 57654199
• NACRES: NA.77

Propiedades

• Ensayo: ≥99% (HPLC)
• solubilidad: ethanol: 2 mg/mL; DMSO: soluble; H₂O: insoluble
• emisor: Roche
• temp. de almacenamiento: 2-8°C
• cadena SMILES: COc1ccc(Cl)cc1C(=O)NCCc2ccc(cc2)S(=O)(=O)NC(=O)NC3CCCCC3
• InChI: 1S/C23H28ClN3O5S/c1-32-21-12-9-17(24)15-20(21)22(28)25-14-13-16-7-10-19(11-8-16)33(30,31)27-23(29)26-18-5-3-2-4-6-18/h7-12,15,18H,2-6,13-14H2,1H3,(H,25,28)(H2,26,27,29)
• Clave InChI: ZNNLBTZKUZBEKO-UHFFFAOYSA-N
• Información sobre el gen: human ... ABCC8(6833) , KCNH2(3757) , KCNJ1(3758) , KCNJ11(3767) ; rat ... Kcnj1(24521)

Descripción

Aplicación

Glybenclamide has been used:

• as a positive control oral hypoglycemic drug to study the hypoglycemic effects of Chlorella in streptozotocin-induced diabetic mice[1]
• as a K+ATP channel antagonist in canine with induced acute hypoxia[2]
• as an inhibitor of cystic fibrosis transmembrane conductance regulator (CFTR) channel in fetal distal lung epithelial (FDLE) cells[3]

Acciones bioquímicas o fisiológicas

Glybenclamide is a sulfonylurea class of antidiabetic drug used in the treatment of type 2 diabetes mellitus. It has benzamide moiety and stimulates pancreatic β cells to produce insulin resulting in a hypoglycemic effect. It selectively blocks ATP-sensitive K⁺ channels in the brain with high-affinity binding sites and elicits cardiovascular effects.[4] It may be a potential therapeutic for thromboembolic disorders due to its in vivo antiplatelet functionality.[5] Glybenclamide traverses to the ischemic brain and provides neuroprotection especially during the early stages of stroke.[6]

Selectively blocks ATP-sensitive K⁺ channels; high affinity binding sites found in brain, pancreatic β cells, and cardiovascular system.

Características y beneficios

This compound is a featured product for ADME Tox research. Click here to discover more featured ADME Tox products. Learn more about bioactive small molecules for other areas of research at sigma.com/discover-bsm.

This compound is featured on the Chloride Channels and Potassium Channels pages of the Handbook of Receptor Classification and Signal Transduction. To browse other handbook pages, click here.

This compound was developed by Roche. To browse the list of other pharma-developed compounds and Approved Drugs/Drug Candidates, click here.

Información de seguridad

• Frases de peligro: H413
• Consejos de prudencia: P273 - P501
• Clasificaciones de peligro: Aquatic Chronic 4
• Código de clase de almacenamiento: 11 - Combustible Solids
• Clase de riesgo para el agua (WGK): WGK 2
• Punto de inflamabilidad (°F): Not applicable
• Punto de inflamabilidad (°C): Not applicable
• Equipo de protección personal: Eyeshields, Gloves, type N95 (US)