2-Arachidonoylglycerol

CAS No. 53847-30-6

2-Arachidonoylglycerol ( —— )

Catalog No. M26591 CAS No. 53847-30-6

2-Arachidonoylglycerol activates neuronal cannabinoid receptors as a full agonist, and prevents the induction of long-term potentiation at CA3–CA1 synapses.

Purity : >98% (HPLC)

COA Datasheet HNMR HPLC MSDS Handing Instructions
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Biological Information

  • Product Name
    2-Arachidonoylglycerol
  • Note
    Research use only, not for human use.
  • Brief Description
    2-Arachidonoylglycerol activates neuronal cannabinoid receptors as a full agonist, and prevents the induction of long-term potentiation at CA3–CA1 synapses.
  • Description
    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).
  • Synonyms
    ——
  • Pathway
    GPCR/G Protein
  • Target
    Cannabinoid Receptor
  • Recptor
    DNA/RNA Synthesis
  • Research Area
    ——
  • Indication
    ——

Chemical Information

  • CAS Number
    53847-30-6
  • Formula Weight
    378.6
  • Molecular Formula
    C23H38O4
  • Purity
    >98% (HPLC)
  • Solubility
    ——
  • SMILES
    CCCCC\C=C/C\C=C/C\C=C/C\C=C/CCCC(=O)OC(CO)CO
  • Chemical Name
    ——

Shipping & Storage Information

  • Storage
    (-20℃)
  • Shipping
    With Ice Pack
  • Stability
    ≥ 2 years

Reference

1.Koolen HH, et al. An antimicrobial diketopiperazine alkaloid and co-metabolites from an endophytic strain of Gliocladium isolated from Strychnos cf. toxifera. Nat Prod Res. 2012 Nov;26(21):2013-9.
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