Basic information Safety Supplier Related
ChemicalBook >  Product Catalog >  Biochemical Engineering >  Biochemical Reagents >  Agonist Inhibitors >  Imeglimin

Imeglimin

Basic information Safety Supplier Related

Imeglimin Basic information

Product Name:
Imeglimin
Synonyms:
  • 1,3,5-Triazine-2,4-diamine,1,6-dihydro-N,N,6-trimethyl-,(+)-(9CI)
  • IMegliMin
  • EMD 387008
  • R-IMegliMin
  • EMD 387008/R-Imeglimin
  • EMD 387008 (R-IMEGLIMIN) HCL
  • 1,3,5-Triazine-2,4-diamine, 3,6-dihydro-N2,N2,6-trimethyl-, (6R)-
  • Emd 387008 hcl
CAS:
775351-65-0
MF:
C6H13N5
MW:
155.2
Product Categories:
  • AMINETERTIARY
  • METHYL
Mol File:
775351-65-0.mol
More
Less

Imeglimin Chemical Properties

Boiling point:
239.9±23.0 °C(Predicted)
Density 
1.29±0.1 g/cm3(Predicted)
storage temp. 
Store at -20°C
solubility 
Soluble in DMSO
pka
11.65±0.40(Predicted)
More
Less

Imeglimin Usage And Synthesis

Description

Imeglimin is an oral anti-diabetic drug discovered by Poxel and co-developed with Sumitomo Dainippon Pharma. In 2021, Imeglimin was approved in Japan for the treatment of type 2 diabetes (T2D).

Uses

Imeglimin (EMD 387008) is an oral glucose-lowering agent. Imeglimin improves insulin sensitivity. Imeglimin also reduces reactive oxygen species (ROS) production, increases mitochondrial DNA and improves mitochondrial function[1].

brand name

Twymeeg

Mechanism of action

Imeglimin belongs to a class of tetrahydrotriazines called “glimins” and works through a different mechanism than existing antidiabetic drugs. It is thought to protect mitochondria from oxidative stress, thereby significantly reducing blood glucose levels, restoring glucose tolerance, and improving insulin sensitivity in a high-fat, high-sucrose diet mouse model. In addition, Imeglimin increases glucose uptake in skeletal muscle and inhibits hepatic gluconeogenesis like metformin.

Synthesis

Synthesis of Imeglimin: Metformin hydrochloride (23.1) is treated with acetaldehyde diethyl acetal (23.2) under reflux conditions of isobutanol and catalytic acid to obtain a racemic crude product 23.3. After concentration, the crude product 23.3 is treated with triethylamine and L-(+)-tartaric acid. After crystallization, the diastereomeric pure tartrate 23.4 is obtained in two steps with a yield of 40-45%. Treatment of 23.4 with ethanolic hydrochloric acid can achieve double decomposition of the salt. After crystallization from cold EtOH, the product 23 is obtained with an enantiomeric purity of 50-55%.

in vivo

Imeglimin (200 mg/kg b.i.d. by oral gavage during the last 6 weeks of HFHSD feeding) significantly decreases hyperglycemia, restores normal glucose tolerance, and improves insulin sensitivity[1].

Animal Model:Male C57BL/6JOlaHsd mice (4 weeks old)[1]
Dosage:200 mg/kg
Administration:Oral gavage; b.i.d.; 6 weeks
Result:A slight decrease in body weight and food intake associated with some diarrhea was observed but only during the first few days of treatment.

References

[1] Vial G, et al. Imeglimin normalizes glucose tolerance and insulin sensitivity and improves mitochondrialfunction in liver of a high-fat, high-sucrose diet mice model. Diabetes. 2015 Jun;64(6):2254-64. DOI:10.2337/db14-1220
[2] Detaille D, et al. Imeglimin prevents human endothelial cell death by inhibiting mitochondrial permeability transition without inhibiting mitochondrial respiration. Cell Death Discov. 2016 Jan 18;2:15072. DOI:10.1038/cddiscovery.2015.72

ImegliminSupplier

Anhui Lianchuang Biological Medicine Co.,Ltd
Tel
0551-68779238 18056025720
Email
sales3@lcywhx.com
Artis Chemistry (Shanghai) Co. Ltd.
Tel
86-21-60936353
Shanghai Topbiochem Technology Co., Ltd
Tel
+86-21-60341587
Email
sales@topbiochem.com
Shanghai Jiyi Biological Technology Co., LTD
Tel
021-54135696 18516235431
Email
shgegenetech@163.com
MedChemexpress LLC
Tel
021-58955995
Email
sales@medchemexpress.cn