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Glimepiride, Thermo Scientific Chemicals
A sulfonylurea hypoglecemic agent and potent potassium channel blocker
$155.22 - $675.68
Chemical Identifiers
| CAS | 93479-97-1 |
|---|---|
| Molecular Formula | C24H34N4O5S |
| Molecular Weight (g/mol) | 490.62 |
| MDL Number | MFCD00878417 |
| InChI Key | WIGIZIANZCJQQY-UHFFFAOYSA-N |
| Synonym | glimepiride, amaryl, glimepiridum, glimepirida, amarel, glimepirid, glimepride, endial, roname, glimepiridum latin |
| PubChem CID | 3476 |
| IUPAC Name | 3-ethyl-4-methyl-N-{2-[4-({[(4-methylcyclohexyl)carbamoyl]amino}sulfonyl)phenyl]ethyl}-2-oxo-2,5-dihydro-1H-pyrrole-1-carboxamide |
| SMILES | CCC1=C(C)CN(C(=O)NCCC2=CC=C(C=C2)S(=O)(=O)NC(=O)NC2CCC(C)CC2)C1=O |
| Catalog Number | Mfr. No. | Quantity | Price | Quantity | |||||
|---|---|---|---|---|---|---|---|---|---|
| Catalog Number | Mfr. No. | Quantity | Price | Quantity | |||||
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AAJ62032MC
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Thermo Scientific Chemicals
J62032MC |
100 mg |
Each for $155.22
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AAJ6203203
|
Thermo Scientific Chemicals
J6203203 |
1 g |
Each for $675.68
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Description
Glimepiride induces the PI3 kinase (PI3K) and Akt pathway, along with insulin receptor substrate-1/2 and endothelial nitric oxide synthase. Glimepiride also increases osteoblast proliferation and differentiation, which is thought to be related to its ability to activate the PI3K and Akt pathway. Furthermore, Glimepiride enhances intrinsic peroxisome proliferator-activated receptor γ activity. Glimepiride also increases protein expression of glucose transports 1 and 4, and is a potent KIR channel blocker. Potent Kir6 (KATP) channel blocker and anti-diabetic agent. Inhibits pinacidil-activated cardiac Kir6 channels with an IC50 of 6.8 nM.
This Thermo Scientific Chemicals brand product was originally part of the Alfa Aesar product portfolio. Some documentation and label information may refer to the legacy brand. The original Alfa Aesar product / item code or SKU reference has not changed as a part of the brand transition to Thermo Scientific Chemicals.
ApplicationsGlimepiride induces the PI3 kinase (PI3K) and Akt pathway, along with insulin receptor substrate-1/2 and endothelial nitric oxide synthase. Glimepiride also increases osteoblast proliferation and differentiation, which is thought to be related to its ability to activate the PI3K and Akt pathway. Furthermore, Glimepiride enhances intrinsic peroxisome proliferator-activated receptor γ activity. Glimepiride also increases protein expression of glucose transports 1 and 4, and is a potent KIR channel blocker. Potent Kir6 (KATP) channel blocker and anti-diabetic agent. Inhibits pinacidil-activated cardiac Kir6 channels with an IC50 of 6.8 nM.
Solubility
Soluble in DMSO
Notes
Store in cool place. Keep container tightly closed in a dry and well-ventilated place. Keep away from strong oxidizing agents.
Chemical Identifiers
| 93479-97-1 | |
| 490.62 | |
| WIGIZIANZCJQQY-UHFFFAOYSA-N | |
| 3476 | |
| CCC1=C(C)CN(C(=O)NCCC2=CC=C(C=C2)S(=O)(=O)NC(=O)NC2CCC(C)CC2)C1=O |
| C24H34N4O5S | |
| MFCD00878417 | |
| glimepiride, amaryl, glimepiridum, glimepirida, amarel, glimepirid, glimepride, endial, roname, glimepiridum latin | |
| 3-ethyl-4-methyl-N-{2-[4-({[(4-methylcyclohexyl)carbamoyl]amino}sulfonyl)phenyl]ethyl}-2-oxo-2,5-dihydro-1H-pyrrole-1-carboxamide |
Specifications
| 93479-97-1 | |
| White | |
| MFCD00878417 | |
| 14,4440 | |
| Soluble in DMSO | |
| CCC1=C(C)CN(C(=O)NCCC2=CC=C(C=C2)S(=O)(=O)NC(=O)NC2CCC(C)CC2)C1=O | |
| 490.62 | |
| 490.62 | |
| Glimepiride |
| 212°C to 215°C | |
| C24H34N4O5S | |
| 100 mg | |
| glimepiride, amaryl, glimepiridum, glimepirida, amarel, glimepirid, glimepride, endial, roname, glimepiridum latin | |
| WIGIZIANZCJQQY-UHFFFAOYSA-N | |
| 3-ethyl-4-methyl-N-{2-[4-({[(4-methylcyclohexyl)carbamoyl]amino}sulfonyl)phenyl]ethyl}-2-oxo-2,5-dihydro-1H-pyrrole-1-carboxamide | |
| 3476 | |
| Powder |
Safety and Handling
RTECSNumber : UX9363950
TSCA : No
Recommended Storage : Ambient temperatures
RUO – Research Use Only