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首页-小分子抑制剂&激动剂-GPCR-Cannabinoid Receptor-BAY38-7271
BAY38-7271

Chemical Structure : BAY38-7271

CAS No.: 212188-60-8

BAY38-7271 (BAY 38-7271)

货号: PC-21983Not For Human Use, Lab Use Only.

BAY 38-7271 is selective, highly potent and cannabinoid CB1/CB2 receptor agonist with 0.46-1.85 nM for rat brain, human cortex, or recombinant human CB1 receptors.

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纯度 & COA & 质检文件 纯度: >98% (HPLC)

生物&药学活性

BAY 38-7271 is selective, highly potent and cannabinoid CB1/CB2 receptor agonist with 0.46-1.85 nM for rat brain, human cortex, or recombinant human CB1 receptors.
BAY 38-7271 shows high affinity to cannabinoid CB2 receptors (Ki=6 nM, recombinant human cannabinoid CB2 receptor).
BAY 38-7271 induced a dose-dependent reduction in body temperature (minimal effective dose = 6 μg/kg, i.v.) in rat hypothermia assays.
BAY 38-7271 demonstrated highly potent and efficient neuroprotective properties in rat traumatic brain injury model.
BAY 38-7271 shows pronounced neuroprotective properties that do not result from drug-induced hypothermia, devoid of typical cannabinoid-like side effects.

物理化学性质&存储条件

分子量 430.44
分子式 C20H21F3O5S
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

10 mM in DMSO

Chemical Name/SMILES

3-[[(2R)-2,3-Dihydro-2-(hydroxymethyl)-1H-inden-4-yl]oxy]phenyl 4,4,4-trifluoro-1-butanesulfonate

参考文献

1. Mauler F, et al. BAY 38-7271: a novel highly selective and highly potent cannabinoid receptor agonist for the treatment of traumatic brain injury. CNS Drug Rev. 2003 Winter;9(4):343-58.

2. Mauler F, et al. J Pharmacol Exp Ther. 2002 Jul;302(1):359-68.

3. De Vry J, et al. Eur J Pharmacol. 2002 Dec 20;457(2-3):147-52.

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