2-Arachidonoylglycerol

本公司产品仅用于科研实验，不得用于人体或动物的临床与诊断

2-Arachidonoylglycerol 作为完全激动剂激活神经元大麻素受体，并防止 CA3-CA1 突触长期增强的诱导。

2-Arachidonoylglycerol activates neuronal cannabinoid receptors as a full agonist, and prevents the induction of long-term potentiation at CA3–CA1 synapses.(In Vitro):The CB1 receptor agonist WIN-55212-2 (3?μM) inhibited forskolin-induced cAMP accumulation, an effect that was reverted by the CB1 antagonist SR-141716 (1?μM) or by pertussis toxin. 2-Arachidonoylglycerol (10?μM) elicited a quantitatively similar inhibition which was also sensitive to SR-141716 and pertussis toxin. This effect occurred with a potency (IC50 = 0.8?μM) consistent with the affinity of 2-Arachidonoylglycerol for CB1 receptors (Ki = 0.7–2.4?μM) and comparable to the potency of anandamide (IC50 = 1.2?μM).

2-Arachidonylglycerol (2-AG) is a cannabinoid ligand isolated from intestinal tissue. 2-Arachidonoylglycerol activates neuronal cannabinoid receptors as a full agonist, and prevents the induction of long-term potentiation at CA3-CA1 synapses. 2-Arachidonoylglycerol binds to cannabinoid receptors and exerts several effects typical of cannabinoid drugs.

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GPCR/G Protein

Cannabinoid Receptor

DNA/RNA Synthesis

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53847-30-6

378.553

C23H38O4

>98% (HPLC)

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CCCCC\C=C/C\C=C/C\C=C/C\C=C/CCCC(=O)OC(CO)CO

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(-20℃)

With Ice Pack

≥ 2 years