870432P
Avanti
C18:1 anandamide
Avanti Research™ - A Croda Brand 870432P, powder
Synonym(s):
9Z-octadecenoylethanolamide
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About This Item
Recommended Products
form
powder
packaging
pkg of 1 × 5 mg (870432P-5mg)
manufacturer/tradename
Avanti Research™ - A Croda Brand 870432P
lipid type
bioactive lipids
shipped in
dry ice
storage temp.
−20°C
SMILES string
O=C(CCCCCCC/C=C\CCCCCCCC)NCCO
General description
Anandamide is an endocannabinoid. It acts as a ligand for cannabinoid (CB) receptors CB1 and CB2 in the brain and peripheral tissues. It is synthesized from glycerophospho-N-arachidonoylethanolamine (GP-NArE) precursor by the reaction catalyzed by glycerophosphodiesterase 1.
Biochem/physiol Actions
Anandamide plays a vital role in various processes including inflammation, pain, and appetite.
Packaging
5 mL Clear Glass Sealed Ampule (870432P-5mg)
Legal Information
Avanti Research is a trademark of Avanti Polar Lipids, LLC
Storage Class Code
11 - Combustible Solids
WGK
WGK 2
Flash Point(F)
Not applicable
Flash Point(C)
Not applicable
Certificates of Analysis (COA)
Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.
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Selective blockade of 2-arachidonoylglycerol hydrolysis produces cannabinoid behavioral effects
Nature Chemical Biology, 5(1), 37-37 (2009)
Identification of biosynthetic precursors for the endocannabinoid anandamide in the rat brain
Journal of Lipid Research, 49(1), 48-57 (2008)
Langmuir : the ACS journal of surfaces and colloids, 32(35), 8942-8950 (2016-08-16)
Oleoylethanolamide (OEA) is an endogenous lipid with neuroprotective properties and the fortification of its concentration in the brain can be beneficial in the treatment of many neurodegenerative disorders. However, OEA is rapidly eliminated by hydrolysis in vivo, limiting its therapeutic
Frontiers in neuroscience, 10, 620-620 (2017-01-31)
Brain μ-opioid receptors (MORs) stimulate high-fat (HF) feeding and have been implicated in the distinct long term outcomes on body weight of bariatric surgery and dieting. Whether alterations in fat appetite specifically following these disparate weight loss interventions relate to
The Journal of biological chemistry, 283(14), 9341-9349 (2008-01-30)
Anandamide (AEA) is an endogenous ligand of cannabinoid receptors and a well characterized mediator of many physiological processes including inflammation, pain, and appetite. The biosynthetic pathway(s) for anandamide and its N-acyl ethanolamine (NAE) congeners remain enigmatic. Previously, we proposed an
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