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870439C

Avanti

C18:2 anandamide phosphate

Avanti Research™ - A Croda Brand 870439C

Synonym(s):

linoleoyl ethanolamide phosphate (sodium salt)

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About This Item

Empirical Formula (Hill Notation):
C20H37NO5PNa
CAS Number:
2260670-52-6
Molecular Weight:
425.48
UNSPSC Code:
12352211
NACRES:
NA.25

form

liquid

packaging

pkg of 1 × 1 mL (870439C-1mg)

manufacturer/tradename

Avanti Research™ - A Croda Brand 870439C

concentration

1 mg/mL (870439C-1mg)

lipid type

bioactive lipids

shipped in

dry ice

storage temp.

−20°C

SMILES string

O=C(CCCCCCC/C=C\C/C=C\CCCCC)NCCOP(O)([O-])=O.[Na+]

InChI key

PVAGBVTWXZTXFO-NBTZWHCOSA-M

General description

Anandamide is produced by the enzymatic hydrolysis of acyl phosphatidyl ethanolamides by phospholipase D.

Biochem/physiol Actions

Anandamide acts as a ligand for cannabinoid receptors. Anandamide possesses anti-inflammatory and analgesic properties. Its effect is regulated by cannabinoid CB1 and CB2 receptors.

Packaging

5 mL Amber Screw Cap Bottle with Foil Bag Argon Overseal (870439C-1mg)

Legal Information

Avanti Research is a trademark of Avanti Polar Lipids, LLC

pictograms

Skull and crossbonesHealth hazard
GHS06,GHS08

signalword

Danger

Hazard Classifications

Acute Tox. 3 Inhalation - Acute Tox. 4 Oral - Carc. 2 - Eye Irrit. 2 - Repr. 2 - Skin Irrit. 2 - STOT RE 1 - STOT SE 3

target_organs

Central nervous system

wgk_germany

WGK 3

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Synthesis of linoleoyl ethanolamide
Wang X, et al.
Journal of Oleo Science, 62(6), 427-433 (2013)
Protective role of palmitoylethanolamide in contact allergic dermatitis
Petrosino S, et al.
Allergy, 65(6), 698-711 (2010)
Ocular hypotensive effect of oral palmitoyl-ethanolamide: a clinical trial
Gagliano C, et al.
Investigative Ophthalmology & Visual Science, 52(9), 6096-6100 (2011)
Anandamide receptors
Di Marzo V, et al.
Prostaglandins, Leukotrienes, and Essential Fatty Acids, 66(2-3), 377-391 (2002)

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