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折扣/货期| 货号：22233-1 mg | 规格：1 mg | 目录价：￥482 |
| 货号：22233-10 mg | 规格：10 mg | 目录价：￥3162 |
| 货号：22233-25 mg | 规格：25 mg | 目录价：￥7290 |
| 货号：22233-5 mg | 规格：5 mg | 目录价：￥1943 |
产品详情
* 以下信息仅供参考，详情请以原厂网站为准
产品名称:
SCH 442416
产品描述:
A potent, brain-permeable, and selective A2AR antagonist; selective for A2AR over A1R, A2BR, and A3R (Kis = 0.048, 1,111, >10,000, and >10,000 nM, respectively) using human recombinant receptors; selective for A2AR over A1R and A3R in rat cerebral membranes (Kis = 0.50, 1,815, and >10,000 nM, respectively); is taken up preferentially by liver, adrenal gland, kidney, and lungs, and by the striatum in the brain; attenuates adenosine-mediated and A2AR agonist-induced arteriole dilation at a concentration of 10 μM
保存温度:
-20
运输温度:
-20
预期分子量:
389.4
产品形式:
A crystalline solid
纯度:
≥98%
CAS号:
316173-57-6
分子式:
C20H19N7O2
促销活动
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