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其他生物化学试剂

坎地沙坦 T1461

英文名称:Candesartan
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

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产品参数
规格 CAS号 价格 操作
25 mg 139481-59-7 ¥977.00 询底价
100 mg 139481-59-7 ¥2,490.00 询底价
50 mg 139481-59-7 ¥1,650.00 询底价
1 mL 139481-59-7 ¥397.00 询底价
5 mg 139481-59-7 ¥315.00 询底价
10 mg 139481-59-7 ¥492.00 询底价
1 mg 139481-59-7 ¥176.00 询底价
产品介绍

Product Introduction
Bioactivity


英文名: Candesartan

描述: Candesartan (CV 11974) 是一种血管紧张素II 受体拮抗剂(IC50:0.26 nM)。

细胞实验: KU-19-19 cells are seeded at a cell density of 2 × 104 per well in 96-well plates and allowed to grow overnight. Then the cells are treated with various concentrations of Candesartan for various periods of time. Cell viability is determined by the Alamar Blue assay to examine the cytotoxicity and antiproliferative effect of candesartan. The absorbance value of each well is determined in a microplate reade(Only for Reference)

激酶实验: Binding assay: Cells are plated in 24-well plates and cultured until confluence. Before the experiment, the cells are washed three times with 0.5 mL per well of DMEM at room temperature. After removal of the medium, 400 μL binding DMEM is added and the plate is then left for 15 min at 37 ℃. For saturation binding assays cells are incubated with increasing concentrations [3H]Candesartan (final concentrations between 0.15 nM and 15 nM) in a final volume of 0.5 mL at 37 ℃ for 5 min to 180 min. For competition binding assays 50 μL of buffer or 50 μL of buffer containing increasing concentrations of unlabelled Candesartan is added. After 30 min, 50 μL of buffer containing [3H]Candesartan (final concentration 1.1 nM) or [3H]Candesartan (final concentration 1.0 nM) is added, and the cells are further incubated for 30 min at 37 ℃.

体外活性: 在处理携带KU-19-19移植瘤的小鼠中,Candesartan(10 mg/kg)能够降低微血管密度和VEGF的表达,抑制肿瘤细胞生长.在WKY大鼠中,Candesartan(0.5 mg/kg )能够降低血压,抑制AT1在穹窿下器,下丘脑室旁核,孤束核,和极后区的结合.在成年自发性高血压大鼠中,Candesartan(0.3 mg/kg)能够减少梗死区域,减少在缺血周边区域和皮层下严重缺血性病变区域,减低脑部血流量的减少.

体内活性: 在CHO-AT1细胞中,Candesartan 能够高选择性地与血管紧张素II AT1 受体结合。Candesartan(0.1 nM)能够降低对于血管紧张素II的最大收缩反应。在 KU-19-19细胞中,加入Candesartan,能够上调VEGF和和白细胞介素-8的表达,同时不影响细胞增殖。

存储条件: Powder: -20°C for 3 years | In solvent: -80°C for 1 year

溶解度: DMSO : 4.5 mg/mL (100 mM)
Ethanol : 0.4 mg/mL (10 mM))


关键字: inhibit | angiotensin II AT1-Receptor | hypertension | hronic heart failure (CHF) | antihypertensive | oral | CV-11974 | Angiotensin Receptor | Traumatic brain injury (TBI) | PPAR-γ | Candesartan | CV11974 | Inhibitor

相关产品: Zofenopril calcium | ANGIOTENSIN IV TFA(12676-15-2(free base)) | DX600 TFA | Allisartan Isoproxil | Angiotensin III, human, mouse | Moveltipril | ZD 7155 hydrochloride | Araloside A | Remodelin hydrobromide | Buloxibutid

相关库: Drug Repurposing Compound Library | Anti-Hypertension Compound Library | FDA-Approved & Pharmacopeia Drug Library | Angiogenesis related Compound Library | Membrane Protein-targeted Compound Library | Human Metabolite Library | CNS-Penetrant Compound Library | Inhibitor Library | Endocrinology-Hormone Compound Library | Bioactive 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

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