Mitiglinide calcium
CAS No. 145525-41-3
Mitiglinide calcium ( KAD-1229;S-21403 )
Catalog No. M11966 CAS No. 145525-41-3
An insulin secretion stimulator by closing the ATP-sensitive potassium KATP channels in pancreatic β cells.
Purity : >98% (HPLC)
COA
Datasheet
HNMR
HPLC
MSDS
Handing Instructions
Size | Price / USD | Stock | Quantity |
100MG | 43 | Get Quote |
|
200MG | 61 | Get Quote |
|
500MG | Get Quote | Get Quote |
|
1G | Get Quote | Get Quote |
|
Biological Information
-
Product NameMitiglinide calcium
-
NoteResearch use only, not for human use.
-
Brief DescriptionAn insulin secretion stimulator by closing the ATP-sensitive potassium KATP channels in pancreatic β cells.
-
DescriptionAn insulin secretion stimulator by closing the ATP-sensitive potassium KATP channels in pancreatic β cells; has potent hypoglycemic effects.DiabetesApproved
-
SynonymsKAD-1229;S-21403
-
PathwayCell Cycle/DNA Damage
-
TargetPotassium Channel
-
RecptorATP-sensitiveK+channels
-
Research AreaMetabolic Disease
-
IndicationDiabetes
Chemical Information
-
CAS Number145525-41-3
-
Formula Weight334.44
-
Molecular FormulaC19H24NO3Ca0.5
-
Purity>98% (HPLC)
-
Solubility10 mM in DMSO
-
SMILESC1CCC2CN(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]
-
Chemical Name2H-Isoindole-2-butanoic acid, octahydro-γ-oxo-α-(phenylmethyl)-, calcium salt (2:1), (αS,3aR,7aS)-
Shipping & Storage Information
-
Storage(-20℃)
-
ShippingWith Ice Pack
-
Stability≥ 2 years
Reference
1. Ohnota H, et al. J Pharmacol Exp Ther. 1994 May;269(2):489-95.
2. Ohnota H, et al. Biochem Pharmacol. 1995 Jan 18;49(2):165-71.
3. Kinukawa M, et al. Br J Pharmacol. 1996 Apr;117(8):1702-6.
2. Ohnota H, et al. Biochem Pharmacol. 1995 Jan 18;49(2):165-71.
3. Kinukawa M, et al. Br J Pharmacol. 1996 Apr;117(8):1702-6.
molnova catalog
related products
-
Indapamide
Indapamide is a non-thiazide sulphonamide diuretic compound, generally used in the treatment of hypertension, as well as decompensated cardiac failure.
-
Lei-Dab 7
High affinity, selective KCa2.2 (SK2) channel blocker (Kd = 3.8 nM). Exhibits >200-fold selectivity for KCa2.2 over KCa2.1, KCa2.3, KCa3.1, IK, Kv and Kir2.1. Increases theta-burst responses and increases LTP in rat hippocampal slices in vitro. Convulsive in vivo.
-
A2764 dihydrochlorid...
A2764 dihydrochloride is a highly selective inhibitor of TRESK.