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Glimepiride - ≥99%, high purity , CAS No.93479-97-1

  • Moligand™
  • ≥99%
Item Number
G129354
Grouped product items
SKUSizeAvailabilityPrice Qty
G129354-1g
1g
Available within 4-8 weeks(?)
Items will be manufactured post-order and can take 4-8 weeks. Thank you for your patience!
$105.90
G129354-5g
5g
In stock
$462.90
G129354-25g
25g
In stock
$2,083.90

Potent cardiac K ATP channel blocker

View related series
Pharmaceutical ingredients

Basic Description

Synonymsglimepiride|93479-97-1|Amaryl|Amarel|Glimepirid|Glimepirida|Glimepiridum|cis-Glimepiride|Hoe-490|684286-46-2|Glimepride|HOE 490|Glimepiride, cis-|GLIMPERIDE|Glimepiride Impurity A|CHEBI:5383|1-((p-(2-(3-Ethyl-4-methyl-2-oxo-3-pyrroline-1-carboxamido)ethyl
Specifications & Purity≥99%
Storage TempStore at -20°C
Shipped InDry ice
GradeMoligand™
Product Description

Glimepiride is a third generation sulfonylurea compound, which increases the release of insulin from pancreatic beta cells. 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. 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.
A third generation sulfonylurea compound that induces the PI3K and Akt pathway

Associated Targets

CYP2C9 Tchem Cytochrome P450 2C9 0 Activities

Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)

Names and Identifiers

IUPAC Name 4-ethyl-3-methyl-N-[2-[4-[(4-methylcyclohexyl)carbamoylsulfamoyl]phenyl]ethyl]-5-oxo-2H-pyrrole-1-carboxamide
INCHI InChI=1S/C24H34N4O5S/c1-4-21-17(3)15-28(22(21)29)24(31)25-14-13-18-7-11-20(12-8-18)34(32,33)27-23(30)26-19-9-5-16(2)6-10-19/h7-8,11-12,16,19H,4-6,9-10,13-15H2,1-3H3,(H,25,31)(H2,26,27,30)
InChi Key WIGIZIANZCJQQY-UHFFFAOYSA-N
Canonical SMILES CCC1=C(CN(C1=O)C(=O)NCCC2=CC=C(C=C2)S(=O)(=O)NC(=O)NC3CCC(CC3)C)C
Isomeric SMILES CCC1=C(CN(C1=O)C(=O)NCCC2=CC=C(C=C2)S(=O)(=O)NC(=O)NC3CCC(CC3)C)C
WGK Germany 3
RTECS UX9363950
PubChem CID 3476
Molecular Weight 490.62
Reaxy-Rn 7731873

Certificates

Certificate of Analysis(COA)

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2 results found

Lot NumberCertificate TypeDateItem
K1901132Certificate of AnalysisJun 07, 2023 G129354
I1424185Certificate of AnalysisMay 07, 2022 G129354

Chemical and Physical Properties

SolubilitySoluble in DMSO (>10 mg/ml), water (<1 mg/ml at 25 °C), and ethanol (<1 mg/ml at 25 °C).
Melt Point(°C)204 °C

Safety and Hazards(GHS)

Pictogram(s) GHS06,   GHS08,   GHS07
Signal Danger
Hazard Statements

H315:Causes skin irritation

H319:Causes serious eye irritation

H301:Toxic if swallowed

H331:Toxic if inhaled

H361:Suspected of damaging fertility or the unborn child

Precautionary Statements

P261:Avoid breathing dust/fume/gas/mist/vapors/spray.

P305+P351+P338:IF IN EYES: Rinse cautiously with water for several minutes. Remove contact lenses if present and easy to do - continue rinsing.

P280:Wear protective gloves/protective clothing/eye protection/face protection.

P302+P352:IF ON SKIN: wash with plenty of water.

P321:Specific treatment (see ... on this label).

P405:Store locked up.

P501:Dispose of contents/container to ...

P264:Wash hands [and …] thoroughly after handling.

P271:Use only outdoors or in a well-ventilated area.

P270:Do not eat, drink or smoke when using this product.

P304+P340:IF INHALED: Remove person to fresh air and keep comfortable for breathing.

P403+P233:Store in a well-ventilated place. Keep container tightly closed.

P362+P364:Take off contaminated clothing and wash it before reuse.

P330:Rinse mouth.

P203:Obtain, read and follow all safety instructions before use.

P264+P265:Wash hands [and …] thoroughly after handling. Do not touch eyes.

P301+P316:IF SWALLOWED: Get emergency medical help immediately.

P318:if exposed or concerned, get medical advice.

P337+P317:If eye irritation persists: Get medical help.

P332+P317:If skin irritation occurs: Get medical help.

P316:Get emergency medical help immediately.

WGK Germany 3
RTECS UX9363950
Reaxy-Rn 7731873
Merck Index 4440

Related Documents

References

1. Miki T, Nagashima K, Seino S.  (1999)  The structure and function of the ATP-sensitive K+ channel in insulin-secreting pancreatic beta-cells..  J Mol Endocrinol,  22  (2): (113-23).  [PMID:10194514]
2. Rehmann H.  (2012)  Epac2: a sulfonylurea receptor?.  Biochem Soc Trans,  40  (1): (6-10).  [PMID:22260657]
3. Inagaki N, Gonoi T, Clement 4th JP, Namba N, Inazawa J, Gonzalez G, Aguilar-Bryan L, Seino S, Bryan J.  (1995)  Reconstitution of IKATP: an inward rectifier subunit plus the sulfonylurea receptor..  Science,  270  (5239): (1166-70).  [PMID:7502040]

Solution Calculators