| CAS: | 124182-57-6 | |
| 分子式: | C23H29N7O6.HCl | |
| 分子量: | 535.98 | |
| 英文名称: |
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| 用途: | 腺苷受体激动剂,对 A 2 和 A 1 受体具有选择性。 |
| 货号 | 品牌 | 产品名称 | 规格 | 包装、参考价格 | |||||||||||||||||||||||||||||||||||||||||||||
| C920926 | MACKLIN | 2-p-(2-羧乙基)苯乙氨基-5′-N-乙基甲酰胺基腺苷 盐酸盐 水合物 | 98% (HPLC) | 990元/5mg; 3780元/25mg; | 咨询 | ||||||||||||||||||||||||||||||||||||||||||||
储存:−20°C 状态:白色固体 | |||||||||||||||||||||||||||||||||||||||||||||||||
| 119137 | Sigma-Aldrich | Adenosine A2A Receptor Agonist I, CGS 21680, Hydrochloride-CAS 124182-57-6-Calbiochem | 2345.3元/5 MG; | 咨询 | |||||||||||||||||||||||||||||||||||||||||||||
产品说明 一般描述 A xanthin derivative that acts as a potent agonist of adenosine A2A receptors (Ki = 27 nM). Exhibits reduced affinity for A2B receptors (Ki = 67 nM), but offers greater selectivity over A1R (Ki = 290 nM) and A3R (88.8 µM). Exerts an anti-inflammatory effect during chronic inflammation and ameliorates the tissue damage associated with collagen-induced arthritis. Also shown to reduce CCR7 Protein Expression in THP1 macrophages. Shown to delay the progressive deterioration of motor performance and prevent a reduction in brain weight in murine model of Huntington′s disease. Please note that the molecular weight for this compound is batch-specific due to variable water content. Please refer to the vial label or the certificate of analysis for the batch-specific molecular weight. The molecular weight provided represents the baseline molecular weight without water. 包装 5 mg in Glass bottle 警告 Toxicity: Standard Handling (A) 外形 Supplied as a hydrochloride salt. 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 Willians, A. J., et al. 2012. Inflammation.35, 614. 法律信息 CALBIOCHEM is a registered trademark of Merck KGaA, Darmstadt, Germany 基本信息
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| C141 | Sigma-Aldrich | CGS-21680 hydrochloride hydrate | solid | 2800.96元/5 MG; 4140.44元/10 MG; 10062元/25 MG; | 咨询 | ||||||||||||||||||||||||||||||||||||||||||||
产品说明 包装 5, 10, 25, 100 mg in glass bottle 生化/生理作用 腺苷受体激动剂,对 A 2 和 A 1 受体具有选择性。 注意 吸湿 基本信息
产品性质
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