Mitiglinide calcium

本公司产品仅用于科研实验，不得用于人体或动物的临床与诊断

通过关闭胰腺 β 细胞中 ATP 敏感的钾 KATP 通道来刺激胰岛素分泌。

An insulin secretion stimulator by closing the ATP-sensitive potassium KATP channels in pancreatic β cells; has potent hypoglycemic effects.Diabetes Approved.

Mitiglinide Calcium inhibits the Kir6.2/SUR1 channel currents in a dose-dependent manner (IC50 value, 100 nM) but does not significantly inhibit either Kir6.2/SUR2A or Kir6.2/SUR2B channel currents even at high doses (more than 10 μM) in COS-1 cells.

Mitiglinide Calcium (1-3 mg/kg; p.o.) suppresses the increase in plasma glucose levels seen after a meal load and the area under the curve for plasma glucose levels (AUCglucose) up to 5 h after the meal load. Animal Model:Pregnant Wistar rats (12 weeks) Dosage:0.3 mg/kg, 1 mg/kg, 3 mg/kg Administration:Oral administration Result:Dose-dependently suppressed AUC glucose levels.

KAD-1229 | S-21403

Cell Cycle/DNA Damage

Potassium Channel

ATP-sensitiveK+channels

Metabolic Disease

Diabetes

145525-41-3

334.44

C19H24NO3Ca0.5

>98% (HPLC)

10 mM in DMSO

C1CCC2CN(CC2C1)C(=O)CC(CC3=CC=CC=C3)C(=O)[O-].C1CCC2CN(CC2C1)C(=O)CC(CC3=CC=CC=C3)C(=O)[O-].[Ca+2]

2H-Isoindole-2-butanoic acid, octahydro-γ-oxo-α-(phenylmethyl)-, calcium salt (2:1), (αS,3aR,7aS)-

(-20℃)

With Ice Pack

≥ 2 years