马尼地平 T6577
品牌 | 厂商性质 | 产地 | 货期 |
---|---|---|---|
TargetMol | 生产商 | 美国 | 现货 |
性能特点
生化试剂,可用于动物细胞实验
规格 | CAS号 | 价格 | 操作 |
---|---|---|---|
200 mg | 89226-50-6 | ¥3,950.00 | 询底价 |
50 mg | 89226-50-6 | ¥1,850.00 | 询底价 |
25 mg | 89226-50-6 | ¥1,250.00 | 询底价 |
500 mg | 89226-50-6 | ¥6,330.00 | 询底价 |
1 mL | 89226-50-6 | ¥688.00 | 询底价 |
5 mg | 89226-50-6 | ¥512.00 | 询底价 |
10 mg | 89226-50-6 | ¥748.00 | 询底价 |
100 mg | 89226-50-6 | ¥2,760.00 | 询底价 |
1 mg | 89226-50-6 | ¥223.00 | 询底价 |
Product Introduction
Bioactivity
英文名: Manidipine
描述: Manidipine (Iperten) 是一种二氢吡啶类钙通道阻滞剂,有降压作用。
体外活性: Manidipine, a Ca(2+)-channel blocker, at concentrations that lower elevated blood pressure, modulates the transcription rates of cytokine genes in the mesangial cells of humans that had been stimulated with platelet-derived growth factor BB isomer. [1] Manidipine inhibits the ET-1-induced [Ca2+]i increase by reducing both the transient and sustained Ca2+ increments in A7r5 cells and glomerular mesangial cells (MCs). Manidipine (10(-5) mol/L) potentiates ET-1-induced c-fos and c-jun expression in A7r5 cells. Manidipine is a potent inhibitor for ET-1-induced [Ca2+]i signaling and that Manidipine has multiple effects on ET-1-induced signaling, including potentiating the immediate-early gene response. [2]
体内活性: Manidipine reduces systolic blood pressure with a slight sympathetic reflex increase in heart rate, and increases plasma nitrite/nitrates in perfused rat heart from ischemia-reperfusion damage. Manidipine combined with Simvastatin reduces creatine kinase, lactate dehydrogenase and tumor necrosis factor-alpha, and enhancement of 6-keto-PGF(1alpha) during reperfusion. [3] Manidipine hydrochloride prevents isoproterenol-induced left ventricular hypertrophy and expression of mRNA of ANP, collagen types I and type III, and fibronectin in rats with isoproterenol-induced cardiac hypertrophy. [4] Manidipine HCl increases renal blood flow (RBF) by dilating the afferent arterioles and improves glomerular hypertension by dilating the efferent arterioles in hypertensive rats. [5]
存储条件: Powder: -20°C for 3 years | In solvent: -80°C for 1 year
溶解度: DMSO : 113 mg/mL (185 mM)
Ethanol : 3 mg/mL (4.91 mM)
H2O : < 1 mg/mL (insoluble or slightly soluble)
关键字: Calcium Channel | Inhibitor | inhibit | Ca channels | Manidipine | Ca2+ channels
相关产品: ω-Conotoxin Bu8 | SB-237376 | SERCA2a activator 1 | Dantrolene sodium | Astragaloside A | Fargesone B | L-Ascorbic acid sodium salt | Dronedarone | Nisoldipine | Tiapamil hydrochloride
相关库: Drug Repurposing Compound Library | Anti-COVID-19 Compound Library | Anti-Cancer Compound Library | Anti-Cancer Drug Library | Membrane Protein-targeted Compound Library | Bioactive Compounds Library Max | Anti-Cancer Clinical Compound Library | Anti-Cancer Approved Drug Library | Autophagy Compound Library | NO PAINS Compound Library
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注:该产品未在中华人民共和国食品药品监督管理部门申请医疗器械注册和备案,不可用于临床诊断或治疗等相关用途