| CAS: | 35920-39-9 | ||||||||
| 分子式: | C12H16N6O4 | ||||||||
| 分子量: | 308.29 | ||||||||
| 英文名称: |
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| 用途: | NECA is a nonselective adenosine receptor agonist. |
| 货号 | 品牌 | 产品名称 | 规格 | 包装、参考价格 | |||||||||||||||||||||||||||||||||||||||||||||||||||
| N911309 | MACKLIN | 5'-N-Ethylcarboxamidoadenosine (NECA) | 98% | 499元/5mg; 1385元/25mg; | 咨询 | ||||||||||||||||||||||||||||||||||||||||||||||||||
储存:-20°C,密闭,干燥 | |||||||||||||||||||||||||||||||||||||||||||||||||||||||
| N793107 | MACKLIN | 5'-N-Ethylcarboxamidoadenosine (NECA) | 10mM in DMSO | 410元/1ml; | 咨询 | ||||||||||||||||||||||||||||||||||||||||||||||||||
储存:-20°C | |||||||||||||||||||||||||||||||||||||||||||||||||||||||
| 528753 | J&K | 5'-Ethylcarboxamidoadenosine | 98% | 1596元/25MG; 4522元/100MG; | 咨询 | ||||||||||||||||||||||||||||||||||||||||||||||||||
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| E2387 | Sigma-Aldrich | 5′-(N-Ethylcarboxamido)adenosine | powder | 2684.1元/50 MG; | 咨询 | ||||||||||||||||||||||||||||||||||||||||||||||||||
产品说明 一般描述 5′-(N-乙基酰胺基)腺苷通过 A2-腺苷受体激活刺激肺循环中的血管舒张。 应用 5′-(N-乙基酰胺基)腺苷用于:
包装 50 mg in poly bottle 生化/生理作用 强效腺苷受体激动剂与 A 1 和 A 2 受体的亲和力几乎相等。 特点和优势 该化合物已被列于《受体分类和信号转导手册》的腺苷受体页面中。 若要浏览手册其他页面,请单击此处。 基本信息
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| 119140 | Sigma-Aldrich | Adenosine Receptor Agonist, NECA-CAS 35920-39-9-Calbiochem | 837.5元/10 MG; | 咨询 | |||||||||||||||||||||||||||||||||||||||||||||||||||
产品说明 一般描述 A cell-permeable adenosine analog that acts a potent non-selective agonist of adenosine receptors (Ki = 14 nM, 20 nM, 2.4 µM and 6.2 nM for A1, A2A, A2B, A3, respectively). Increases intracellular cAMP production (EC50 = 3.1 µM in A2B expressing CHO cells). Shown to increase glucagon release in a dose-dependent manner and inhibit insulin release at low concentrations. Although at higher concentration some insulin release is observed. Also, displays a wide range adenosine-dependent effects, such as blocking platelet aggregation and inhibiting DNA synthesis. When administered at reperfusion, it is shown reduce infarction and block the formation of the mitochondrial permeability transition pore by activating p70S6 kinase. 包装 10 mg in Glass bottle 生化/生理作用 Reversible: yes 警告 Toxicity: Standard Handling (A) 重悬 Following reconstitution, aliquot and freeze (-20°C). Stock solutions are stable for up to 3 months at -20°C. 其他说明 Forster, K., et al. 2006. Basic Res. Cardiol.101, 319. 法律信息 CALBIOCHEM is a registered trademark of Merck KGaA, Darmstadt, Germany 基本信息
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