4°C, sealed storage and away from moisture;*In solvent : -80°C, 6 months; -20°C, 1 month (sealed storage and away from moisture);
生物活性
Galanthamine hydrobromide (Galantamine hydrobromide) is a selective, reversible, competitive, alkaloid AChE inhibitor, with an IC50 of 0.35 μM. Galanthamine hydrobromide is a potent allosteric potentiating ligand (APL) of human α3β4, α4β2, α6β4 nicotinic receptors ( nAChRs). Galanthamine hydrobromide is developed for the research of Alzheimers disease (AD).
性状
Solid
IC50 & Target[1][2]
IC50: 0.35 μM (AChE)
体外研究(In Vitro)
Galanthamine hydrobromide is 53-fold selectivity for AChE over butyrylcholinesterase.Galanthamine hydrobromide (25-1000 μM) inhibits both Aβ 1-40 (50 μM) and Aβ 1-42 (50 μM) aggregation.Galanthamine hydrobromide (25-1000 μM) protects against Aβ(1-40) and Aβ(1-42) toxicity in SH-SY5Y cells.Galanthamine hydrobromide also dramatically reduces Aβ(1-40)-induced cellular apoptosis.Medlife has not independently confirmed the accuracy of these methods. They are for reference only.
体内研究(In Vivo)
Galanthamine hydrobromide (1.25-2.5 mg/kg; i.p. ) reduces cognitive deficits in APP23 mice.Galanthamine hydrobromide (10 mg/kg; i.g.) displays short elimination half-life of approximately 2 h in wild-type mice.Medlife has not independently confirmed the accuracy of these methods. They are for reference only.Animal Mode
运输条件
Room temperature or refrigerated transport.
储存方式
4°C, sealed storage and away from moisture;*In solvent : -80°C, 6 months; -20°C, 1 month (sealed storage and away from moisture);
ClinicalTrial
结构分类
AlkaloidsOther A
来源
PlantsAmaryllida
溶解度数据
体外研究:H2O : 16.67 mg/mL(45.27 mM;ultrasonic and warming and heat to 80°C)DMSO : 12.5 mg/mL(33.94 mM;ultrasonic and warming and heat to 60°C)