| 名称 | Amlodipine Besylate |
| 描述 | Amlodipine Besylate(Amlodipine benzenesulfonate) is a long-lasting calcium channel blocker. |
| 体外活性 | Amlodipine is a safe and effective oral medication for treating systemic hypertension in cats. In swine coronary arteries with intact endothelium, Amlodipine notably reduces mean indirect systolic pressure, from 198 mmHg to 155 mmHg. |
| 体内活性 | In mice infused with angiotensin II, Amlodipine significantly reduced systolic blood pressure, LOX-1 expression, endothelial dysfunction, aortic hypertrophy, and the production of aortic O2(-) and ONOO(-), alongside a decrease in plasma levels of free 8-F(2)α-isoprostanes. In isolated pre-contracted endothelium-intact porcine coronary arteries, Amlodipine induced NO-mediated relaxation, resulting in a leftward shift of the concentration-relaxation curve toward bradykinin. Electron spin resonance spectroscopy in native endothelial cells revealed that Amlodipine increased NO production and stimulated an 8-fold rise in endothelial cyclic GMP levels. Furthermore, Amlodipine induced NO-mediated relaxation in isolated rat aortic rings, leading to downregulation of B2 receptor expression. In endothelial cells, Amlodipine time-dependently attenuated protein kinase C phosphorylation, similar to endothelial nitric oxide synthase phosphorylation, and also prevented phorbol-12-myristate-13-acetate-induced PKC activation. Amlodipine besylate reduced p85αPI3K, phosphorylated GSK-3β, phosphorylated Akt, Bcl-2, and heat shock transcription factor 1 induced H2O2 content, and inhibited Cyclooxygenase-2, cytosolic cytochrome c, cleaved caspase9, and the increase of cleaved caspase3 in neuronal cell apoptosis. |
| 存储条件 | Powder: -20°C for 3 years | In solvent: -80°C for 1 year | Shipping with blue ice. |
| 溶解度 | H2O : 5.7 mg/mL (10 mM)
DMSO : 50 mg/mL (88.18 mM)
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| 关键字 | Inhibitor | hypertension | antianginal | Amlodipine | Amlodipine Besylate | Calcium Channel | Ca channels | dihydropyridine | inhibit | oral | Ca2+ channels |
| 相关产品 | Nisoldipine | Nimodipine | 2,5-Di-tert-butylhydroquinone | Diltiazem hydrochloride | Levetiracetam | L-Ascorbic acid | Lanthanum(III) chloride heptahydrate | Ethyl cinnamate | 1-Octanol | Otilonium bromide |
| 相关库 | 疼痛相关化合物库 | 经典已知活性库 | 膜蛋白靶向化合物库 | 抗癌临床化合物库 | 药物功能重定位化合物库 | 抑制剂库 | FDA 上市药物库 | 已知活性化合物库 | 离子通道库 | 抗癌活性化合物库 |
United States
