45280-17-9

Arachidonoyl-N,N-dimethyl amide Chemical Structure
45280-17-9

Chemical Structure

Arachidonoyl-N,N-dimethyl amide

Synonym(s): Arachidonic acid-N,N-dimethyl amide

  • CAS No.: 45280-17-9
  • Formula:C22H37NO
  • Molecular Weight:331.54

IUPAC Name: (5Z,8Z,11Z,14Z)-N,N-dimethylicosa-5,8,11,14-tetraenamide

InChIKey: FCHAVFLICKAOOF-GKFVBPDJSA-N

SMILES: CCCCC/C=C\C/C=C\C/C=C\C/C=C\CCCC(N(C)C)=O

Biological Activity: Anandamide (AEA) is an endogenous cannabinoid that binds to both central cannabinoid (CB1) and peripheral cannabinoid (CB2) receptors. The biological actions of AEA are terminated by cellular uptake and hydrolysis of the amide bond by the enzyme fatty acid amide hydrolase. Arachidonoyl-N,N-dimethyl amide is an analog of anandamide that exhibits weak or no binding to the human central cannabinoid (CB1) receptor (Ki >1 μM). It inhibits rat glial gap junction cell-cell communication 100% at a concentration of 50 μM.

Cat. No. Product Name Purity Description Pricing
HY-134055
Arachidonoyl-N,N-dimethyl amide 99.9% Anandamide (AEA) is an endogenous cannabinoid that binds to both central cannabinoid (CB1) and peripheral cannabinoid (CB2) receptors. The biological actions of AEA are terminated by cellular uptake and hydrolysis of the amide bond by the enzyme fatty acid amide hydrolase. Arachidonoyl-N,N-dimethyl amide is an analog of anandamide that exhibits weak or no binding to the human central cannabinoid (CB1) receptor (Ki >1 μM). It inhibits rat glial gap junction cell-cell communication 100% at a concentration of 50 μM.
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