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Isradipine(PN 200-110)
本半岛bd体育手机客户端 不向个人销售,仅用作科学研究,不用于任何人体实验及非科研性质的动物实验。
Isradipine(PN 200-110)图片
CAS NO: 75695-93-1
规格: ≥98%
包装与价格:
包装 价格(元)
5mg 电议
10mg 电议
25mg 电议
50mg 电议
100mg 电议
250mg 电议
500mg 电议

半岛bd体育手机客户端 介绍
理化性质和储存条件
Molecular Weight (MW) 371.39
Formula C19H21N3O5
CAS No. 75695-93-1
Storage -20℃ for 3 years in powder form
-80℃ for 2 years in solvent
Solubility(In vitro) DMSO: 74 mg/mL (199.3 mM)
Water: <1 mg/mL
Ethanol: 74 mg/mL (199.3 mM)
Solubility(In vivo) 2% DMSO+Corn oil: 10mg/mL
Synonyms PN 200-110; DynaCirc, Prescal, Lomir, PN-200-110, PN-205-033, PN-205-034
实验参考方法
In Vitro

In vitroactivity: Isradipine produces inhibition of both growth cultures and oxygen consumption on epimastigotes of Trypanosoma cruzi Tulahuen strain, at micromolar concentrations. Isradipine is found to be the most potent derivative in both, in growth cultures (I50 = 20.8 mM) and in vivo oxygen uptake (I50 = 31.1 mM).

In Vivo Isradipine reduces hypoxia-induced activation of calcium dependent xanthine oxidases, monoamine oxidases, cytosolic phospholipase A(2) and cyclooxygenases (COX-2) along with concomitant decrease in free radical generation and cytochrome c release. Isradipine prevents hypobaric hypoxia along with augmented neurodegeneration and memory impairment induced increased expression of calpain and caspase 3. Isradipine (at the dose of 1 mg/kg three times a day) reduces ethanol intake by over 70% in ethanol-preferring rats, the reduction in ethanol intake is compensated by a proportional increase in water consumption and the inhibitory effect persisted throughout the 5 days of treatment. Isradipine significantly reduces the arterial wall collagen contents in both strains, with marked increases in the elastin content in the carotid but not in the aortic wall in spontaneously hypertensive rats. Isradipine suppresses the reinforcing properties of morphine and cocaine and may be an effective pharmacotherapy for treatment of cocaine and heroin abuse in mice.
Animal model Mice
Formulation & Dosage 1 mg/kg
References

Gen Pharmacol. 1998 Jan;30(1):85-7; Neurobiol Dis. 2009 May;34(2):230-44.

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