| CAS: | 264622-53-9 | ||||||
| 分子式: | C27H29N5O5 | ||||||
| 分子量: | 503.55 | ||||||
| 英文名称: |
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| 用途: | MRS-1706 是一种有效选择的 A2B 腺苷受体的反向激动剂。MRS-1706 对人 A2B、A2A、A1 和 A3 受体的 Ki 值分别为 1.39、112、157 和 230 nM。 |
| 货号 | 品牌 | 产品名称 | 规格 | 包装、参考价格 | 详情 | ||||||||||||||||||||
| M879925 | MACKLIN | MRS-1706 | ≥98% | 750元/5mg; 1248元/10mg; | 展开 | ||||||||||||||||||||
储存:2-8℃ | |||||||||||||||||||||||||
| SML3089 | Sigma-Aldrich | MRS-1706 | ≥98% (HPLC) | 878.98元/5 MG; 3550.61元/25 MG; | 展开 | ||||||||||||||||||||
产品说明 生化/生理作用 MRS-1706 is a high-affinity, potent and selective adenosine 2B receptor (A2B) antagonist/inverse agonist (human A1/A2A/A2B/A3 Ki = 157/112/1.39/230 nM; rat A1/A2A Ki = 37.6/548 nM). MRS-1706 (20 nM), but not the A2A antagonist SCH 58261 (20 nM), completely blocks the enhancement of electrically evoked tritium overflow from isolated rat tail artery by 10 μM adenosine receptor agonist NECA in the presence of 30 nM A1 antagonist DPCPX. 基本信息
产品性质
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