Skip to Content
Merck
CN
All Photos(1)

Key Documents

870819P

Avanti

N-oleoylglycine

powder

Synonym(s):

Glycine, N-[(9Z)-1-oxo-9-octadecen-1-yl]- (ACI)

Sign Into View Organizational & Contract Pricing


About This Item

Empirical Formula (Hill Notation):
C20H37NO3
CAS Number:
Molecular Weight:
339.51
UNSPSC Code:
12352211

form

powder

packaging

pkg of 1 × 10 mg (870819P-10mg)

manufacturer/tradename

Avanti Research - A Croda Brand 870819P

lipid type

neutral glycerides
neutral lipids

shipped in

dry ice

storage temp.

−20°C

SMILES string

CCCCCCCC/C=C\CCCCCCCC(NCC(O)=O)=O

InChI

1S/C20H37NO3/c1-2-3-4-5-6-7-8-9-10-11-12-13-14-15-16-17-19(22)21-18-20(23)24/h9-10H,2-8,11-18H2,1H3,(H,21,22)(H,23,24)/b10-9-

InChI key

HPFXACZRFJDURI-KTKRTIGZSA-N

General description

N-oleoylglycine is an endogenous lipid containing glycine moiety in the head group. N-oleoylglycine structure contains an oleic acid, which is amide linked to glycine.

Application

N-oleoylglycine has been used as a related endogenous compound to investigate the nature of the lipid head group required for OLCarn activity at GlyT2 (glycine transporter 2).

Biochem/physiol Actions

N-oleoylglycine acts as a substrate for peptidylglycine α amidating monooxygenase (PAM) for synthesis of oleoylamide. It is also involved in activation of G?protein?coupled receptor GPR132.

Packaging

5 mL Amber Glass Screw Cap Vial (870819P-10mg)

Legal Information

Avanti Research is a trademark of Avanti Polar Lipids, LLC

Storage Class Code

11 - Combustible Solids

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable


Choose from one of the most recent versions:

Certificates of Analysis (COA)

Lot/Batch Number

Sorry, we don't have COAs for this product available online at this time.

If you need assistance, please contact Customer Support.

Already Own This Product?

Find documentation for the products that you have recently purchased in the Document Library.

Visit the Document Library

Shalini Chaturvedi et al.
Prostaglandins & other lipid mediators, 81(3-4), 136-149 (2006-11-07)
Oleamide (cis-9-octadecenamide) is a member of an emerging class of lipid-signaling molecules, the primary fatty acid amides. A growing body of evidence indicates that oleamide mediates fundamental neurochemical processes including sleep, thermoregulation, and nociception. Nevertheless, the mechanism for oleamide biosynthesis
James R Foster et al.
Pharmacology research & perspectives, 7(6), e00542-e00542 (2019-11-27)
The G-protein-coupled receptor GPR132, also known as G2A, is activated by 9-hydroxyoctadecadienoic acid (9-HODE) and other oxidized fatty acids. Other suggested GPR132 agonists including lysophosphatidylcholine (LPC) have not been readily reproduced. Here, we identify N-acylamides in particular N-acylglycines, as lipid
Heather B Bradshaw et al.
Vitamins and hormones, 81, 191-205 (2009-08-04)
Discovery of the endogenous cannabinoid and N-acyl amide, anandamide (N-arachidonoyl ethanolamine), paved the way for lipidomics discoveries in the growing family of N-acyl amides. Lipidomics is a field that is broadening our view of the molecular world to include a
J E Carland et al.
British journal of pharmacology, 168(4), 891-902 (2012-09-18)
Concentrations of extracellular glycine in the CNS are regulated by two Na(+)/Cl(-) -dependent glycine transporters, GlyT1 and GlyT2. Selective inhibitors of GlyT1 have been developed for the treatment of schizophrenia, whilst selective inhibitors of GlyT2 are analgesic in animal models
D J Merkler et al.
Archives of biochemistry and biophysics, 330(2), 430-434 (1996-06-15)
Fatty acid primary amides have recently been recognized as mammalian hormones [Cravatt et al. (1995) Science 268, 1506-1509]. The route to their biosynthesis is unknown. Many mammalian peptide hormones also possess a C-terminal alpha-amide moiety that arises from the posttranslational

Our team of scientists has experience in all areas of research including Life Science, Material Science, Chemical Synthesis, Chromatography, Analytical and many others.

Contact Technical Service