Chemodex

Glimepiride

CHF 48.00
In stock
CDX-G0208-M250250 mgCHF 48.00
CDX-G0208-G0011 gCHF 150.00
More Information
Product Details
Synonyms trans-3-Ethyl-2,5-dihydro-4-methyl-N-[2-[4-[[[[trans-4-methylcyclohexyl)amino]carbonyl]amino]sulfonyl]phenyl]ethyl]-2-oxo-1H-pyrrole-1-carboxyamide; Amaryl; HOE 490
Product Type Chemical
Properties
Formula

C24H34N4O5S

MW 490.62
CAS 93479-97-1
RTECS UX9363950
Source/Host Chemicals Synthetic.
Purity Chemicals ≥98% (HPLC)
Appearance White solid.
Solubility Soluble in DMSO (10mg/ml) or DMF (10mg/ml).
Identity Determined by 1H-NMR.
Declaration Manufactured by Chemodex.
Other Product Data

Click here for Original Manufacturer Product Datasheet
Our product description may differ slightly from the original manufacturers product datasheet.

InChi Key WIGIZIANZCJQQY-RUCARUNLSA-N
Smiles O=C(N1C(C(CC)=C(C)C1)=O)NCCC2=CC=C(S(NC(N[C@H]3CC[C@H](C)CC3)=O)(=O)=O)C=C2
Shipping and Handling
Shipping AMBIENT
Short Term Storage +20°C
Long Term Storage +20°C
Handling Advice Protect from light and moisture.
Use/Stability Stable for at least 2 years after receipt when stored at RT.
Documents
MSDS Download PDF
Product Specification Sheet
Datasheet Download PDF
Description

Glimepiride is a long-acting sulfonylurea antidiabetic agent inhibiting ATP-sensitive potassium (KATP) channels in pancreatic β-cells, which leads to the release of insulin. In addition, Glimepiride increases the activity of intracellular insulin receptors. Studies conducted on adipocytes and skeletal muscle suggest that Glimepiride induces the PI3 kinase (PI3K) and Akt pathway, along with insulin receptor substrate-1/2 and endothelial nitric oxide synthase and stimulates glucose transporter 1 and 4 (GLUT1/4) expression. Glimepiride also increases osteoblast proliferation and differentiation, which is thought to be related to its ability to activate the PI3K and Akt pathway and exhibits neuroprotective benefit, decreasing expression and activity of BACE1 and amyloid-β (Aβ) in neurons in a PPARγ-dependent manner.

Product References

(1) W. Kramer, et al.; Horm. Metab. Res. 28, 464 (1996) | (2) G. Muller & K. Geisen; Horm. Metab. Res. 28, 469 (1996) | (3) D.K. Song & F.M. Ashcroft; Br. J. Pharmacol. 133, 193 (2001) | (4) M.L. Hribal, et al.; Mol. Pharmacol. 59, 322 (2001) | (5) C.L. Lawrence, et al.; Br. J. Pharmacol. 136, 746 (2002) | (6) K. Inukai, et al.; BBRC 328, 484 (2005) | (7) P. Ma, et al.; Metab. Clin. Exp. 59, 359 (2010) | (8) V.J. Briscoe, et al.; Expert Opin. Drug Metab. Toxicol. 6, 225 (2010) | (9) F. Liu, et al.; Neurosci. Lett. 557, 90 (2013)

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