Chemical Structure : SCH 58261
CAS No.: 160098-96-4
货号: PC-45642Not For Human Use, Lab Use Only.
SCH 58261 is a potent and selective, competitive A2A adenosine receptor antagonist with Ki of 2.3 nM and 2.0 nM in rat and bovine brain, respectively.
规格 | 价格 | 库存 | 数量 |
---|---|---|---|
5 mg | ¥780 | In stock | |
10 mg | ¥1180 | In stock | |
25 mg | ¥1980 | In stock | |
50 mg | ¥3480 | In stock | |
100 mg | Get quote |
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SCH 58261 is a potent and selective, competitive A2A adenosine receptor antagonist with Ki of 2.3 nM and 2.0 nM in rat and bovine brain, respectively.
SCH 58261 displays 323-, 53- and 100-fold selectivity over A1, A2B and A3 receptors, respectively.
SCH 58261 reverses reperfusion injury (IR) increased hippocampal Glu, GABA, glycine and aspartate, MPO, TNF-α, nitric oxide, and PGE in Male Wistar rats.
分子量 | 345.358 | |
分子式 | C18H15N7O | |
外观性状 | Solid | |
储存条件 |
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Solubility |
DMSO: ≥ 34 mg/mL |
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Chemical Name/SMILES |
7H-Pyrazolo[4,3-e][1,2,4]triazolo[1,5-c]pyrimidin-5-amine, 2-(2-furanyl)-7-(2-phenylethyl)- |
1. Zocchi C, et al. J Pharmacol Exp Ther. 1996 Feb;276(2):398-404.
2. Beavis PA, et al. Proc Natl Acad Sci U S A. 2013 Sep 3;110(36):14711-6.
3. Mohamed RA, et al. Neurochem Res. 2012 Mar;37(3):538-47.
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