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首页-小分子抑制剂&激动剂-GPCR-Adenosine Receptor-Preladenant
Preladenant

Chemical Structure : Preladenant

CAS No.: 377727-87-2

Preladenant (SCH-420814;SCH 420814;SCH420814)

货号: PC-42729Not For Human Use, Lab Use Only.

Preladenant (SCH420814) is a potent and highly selective adenosine A2A receptor competitive antagonist with Ki of 1.1 nM.

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纯度 & COA & 质检文件 纯度: >98% (HPLC) Select Batch:

生物&药学活性

Preladenant (SCH420814) is a potent and highly selective adenosine A2A receptor competitive antagonist with Ki of 1.1 nM.
Preladenant (SCH420814) has >1000-fold selectivity over all other adenosine receptors.
Preladenant (SCH420814) attenuates hypolocomotion induced by the A2AR agonist CGS-21680.
Preladenant (SCH420814) potentiates L-Dopa -induced contralateral rotations after 6-hydroxydopamine lesions in the medial forebrain bundle in rats (0.1-1 mg/kg); orally active.

物理化学性质&存储条件

分子量 503.5563
分子式 C25H29N9O3
外观性状 Solid
CAS No.
储存条件
固体粉末
-20 °C 12 个月; 4°C 6 个月
配置液
-80 °C 6 个月; -20°C 6 个月
Shipping
Solubility

DMSO

Chemical Name/SMILES

7H-Pyrazolo[4,3-e][1,2,4]triazolo[1,5-c]pyrimidin-5-amine, 2-(2-furanyl)-7-[2-[4-[4-(2-methoxyethoxy)phenyl]-1-piperazinyl]ethyl]-

参考文献

1. Neustadt BR, et al. Bioorg Med Chem Lett. 2009 Feb 1;19(3):967-71.

2. Hodgson RA, et al. J Pharmacol Exp Ther. 2009 Jul;330(1):294-303.

3. Hodgson RA, et al. Exp Neurol. 2010 Oct;225(2):384-90.

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