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Oleoyl Ethanolamide

CAS No.
111-58-0
Chemical Name:
Oleoyl Ethanolamide
Synonyms
ODA;OLEOYL ETHANOLAMIDE;OEA;N-(2-Hydroxyethyl)oleamide;Oleoylethanolamide(OEA);N-(Hydroxyethyl)oleamide;AM-3101;OLEAMIDE MEA;UNII-1HI5J9N8E6;C18:1 anandamide
CBNumber:
CB1708480
Molecular Formula:
C20H39NO2
Molecular Weight:
325.53
MDL Number:
MFCD00045972
MOL File:
111-58-0.mol
MSDS File:
SDS
Last updated:2024-04-12 23:00:59

Oleoyl Ethanolamide Properties

Melting point 63-64 °C
Boiling point 496.4±38.0 °C(Predicted)
Density 0.915±0.06 g/cm3(Predicted)
storage temp. -20°C
solubility Soluble in DMSO (up to 25 mg/ml) or in Ethanol (up to 35 mg/ml)
pka 14.49±0.10(Predicted)
form White solid
color White
Stability Stable for 2 years from date of purchase as supplied. Solutions in DMSO or ethanol may be stored at -20°C for up to 1 month.
InChI InChI=1S/C20H39NO2/c1-2-3-4-5-6-7-8-9-10-11-12-13-14-15-16-17-20(23)21-18-19-22/h9-10,22H,2-8,11-19H2,1H3,(H,21,23)/b10-9-
InChIKey BOWVQLFMWHZBEF-KTKRTIGZSA-N
SMILES C(NCCO)(=O)CCCCCCC/C=C\CCCCCCCC
LogP 6.406 (est)
CAS DataBase Reference 111-58-0(CAS DataBase Reference)
EWG's Food Scores 1-4
FDA UNII 1HI5J9N8E6
EPA Substance Registry System 9-Octadecenamide, N-(2-hydroxyethyl)-, (9Z)- (111-58-0)

SAFETY

Risk and Safety Statements

Symbol(GHS)  GHS hazard pictogramsGHS hazard pictograms
GHS09,GHS05
Signal word  Danger
Hazard statements  H315-H411-H318
Precautionary statements  P264-P280-P302+P352-P321-P332+P313-P362-P280-P305+P351+P338-P310
Hazard Codes  Xi
Risk Statements  36/37/38
Safety Statements  26-36
WGK Germany  2
HazardClass  IRRITANT
NFPA 704
0
3 0

Oleoyl Ethanolamide price More Price(30)

Manufacturer Product number Product description CAS number Packaging Price Updated Buy
Sigma-Aldrich O0383 N-Oleoyl Ethanolamine ~98% (TLC) 111-58-0 10mg $257 2024-03-01 Buy
Cayman Chemical 90265 Oleoyl Ethanolamide ≥98% 111-58-0 500 mg $67 2024-03-01 Buy
Cayman Chemical 90265 Oleoyl Ethanolamide ≥98% 111-58-0 1 g $92 2024-03-01 Buy
Cayman Chemical 90265 Oleoyl Ethanolamide ≥98% 111-58-0 5mg $28 2022-04-27 Buy
Cayman Chemical 90265 Oleoyl Ethanolamide ≥98% 111-58-0 10mg $53 2022-04-27 Buy
Product number Packaging Price Buy
O0383 10mg $257 Buy
90265 500 mg $67 Buy
90265 1 g $92 Buy
90265 5mg $28 Buy
90265 10mg $53 Buy

Oleoyl Ethanolamide Chemical Properties,Uses,Production

Description

Oleoyl ethanolamide (OEA) is an analog of the endocannabinoid AEA found in brain tissue and in chocolate. It is one of the long chain fatty acid ethanolamides that accumulates rapidly in infarcted tissue, but its biosynthesis is reduced in the intestine of rats following food deprivation. OEA is an endogenous, potent agonist for PPARα, exhibiting an EC50 value of 120 nM in a transactivation assay. Systemic administration of OEA suppresses food intake and reduces weight gain in rats (10 mg/kg intraperitoneally) and PPARα wild-type mice, but not in PPARα knockout mice. These data indicate that OEA regulates food intake by a PPARα-mediated mechanism.

Uses

N-Oleoyl Ethanolamide is an agonist of peroxisome proliferator-activated receptor-α (PPAR-α). N-Oleoyl Ethanolamide generates an intestinal signal that stimulates central dopamine activity establishing a link between caloric-homeostatic and hedonic-homeostatic controllers. Oleoyl Ethanolamide has been implicated as the molecular mechanism associated with gastric bypass success. N-Oleoyl Ethanolamide is a selective GPR55 agonist.

Definition

ChEBI: Oleoyl ethanolamide is an N-(long-chain-acyl)ethanolamine that is the ethanolamide of oleic acid. The monounsaturated analogue of the endocannabinoid anandamide. It has a role as a PPARalpha agonist, an EC 3.5.1.23 (ceramidase) inhibitor and a geroprotector. It is a N-(long-chain-acyl)ethanolamine, an endocannabinoid and a N-acylethanolamine 18:1. It is functionally related to an oleic acid.

Application

N-Oleoyl Ethanolamide has been used to study its effects on glucagon-like peptide (GLP)-1RA-mediated anorectic signaling and weight loss.

Biosynthesis

Oleoylethanolamide (OEA) is produced by the small intestine following feeding in two steps. First an N-acyl transferase (NAT) activity joins the free amino terminus of phosphatidylethanolamine (PE) to the oleoyl group (one variety of acyl group) derived from sn-1-oleoyl-phosphatidylcholine, which contains the fatty acid oleic acid at the sn-1 position. This produces an N-acylphosphatidylethanolamine, which is then split (hydrolyzed) by N-acyl phosphatidylethanolamine-specific phospholipase D (NAPE-PLD) into phosphatidic acid and OEA. The biosynthesis of OEA and other bioactive lipid amides is modulated by bile acids.

Biological Functions

N-Oleoyl Ethanolamide is also a predominant NAE species in the injured rat brain, and it has also been found to be the major NAE species in a human brain that has suffered a hemispheric stroke. As early as 1975, N-Oleoyl Ethanolamide was synthesized as an inhibitor of ceramidase, the enzyme that degrades ceramide. Ceramide is involved in the regulation of apoptosis and cell proliferation. Cannabinoid-induced apoptosis in glioma cells is mediated via formation of ceramide. On a tentative basis, it can be suggested that anandamide-induced apoptosis may be aggravated by the presence of N-Oleoyl Ethanolamide because this leads to increased formation of ceramide. There are numerous studies in which N-Oleoyl Ethanolamide has been shown to facilitate the apoptosis-inducing effect of different compounds mediated via increased ceramide levels. However, it has also been reported that N-Oleoyl Ethanolamide decreases ceramide levels in JB6 P+ cells by an unknown mechanism. Recently, N-Oleoyl Ethanolamide has been shown to have a CB1-receptor-independent anorexic effect by inhibiting some intestinal neuronal functions in the rat, and it also causes vasodilation in rat mesenteric arterial segments by an unknown receptor mechanism. Whether these recently discovered biological effects of N-Oleoyl Ethanolamide are of significance for neuroprotection is not known, but it indicates that nonendocannabinoid NAEs are also bioactive molecules with potential for cerebral actions.

General Description

Oleoylethanolamide (OEA) is an endogenous fatty acid ethanolamine. Small intestine cells, adipose tissues, neurons and astrocytes produces OEA.

Biological Activity

Lipid mediator and analog of anandamide (N-(2-Hydroxyethyl)-5Z,8Z,11Z,14Z-eicosatetraenamide ) that is involved in peripheral regulation of feeding. Selective GPR55 agonist (EC 50 values are 0.44, >30 and >30 μ M at GPR55, CB 1 and CB 2 respectively) and PPAR α agonist (EC 50 = 120 nM). Induces satiety through activation of PPAR α and is also a ceramidase inhibitor. Also endogenous agonist at the GPR119 receptor.

Biochem/physiol Actions

Oleoylethanolamide (OEA) is a lipid mediator, which helps to control various biological functions, like food intake. It modulates the gene expression in the small intestine. OEA has the ability to initiate several receptors, such as cannabinoid receptor type 1 (CB1), peroxisome proliferator-activated receptors (PPARs) and G protein-coupled receptor 119 (GPR119).

Enzyme inhibitor

This endocannabinoid-related metabolite (N-Oleoyl Ethanolamide; FW = 325.54 g/mol; CAS 111- 58-0; Symbol: NOE and OEA; Soluble in Ethanol, Chloroform, or Methanol) is widely employed to inhibit acid and neutral ceramidases (IC50 ~ 500 μM) that cleave fatty acids from ceramide, producing sphingosine (SPH), which is then enzymatically phosphorylated to form the receptorsensed metabolite, sphingosine-1-phosphate, or S1P. NOE also inhibits the glucosylation of naturally occurring ceramides. In CHP-100 neuroepithelioma cells treated with N-hexanoylsphingosine (C6-Cer; 30 μM), NOE affected only marginally short-chain glucocerebroside accumulation, but markedly decreased accumulation of glucocerebrosides originating from glucosylation of a long-chain ceramide (Lc-Cer) produced upon C6-Cer treatment. NOE also inhibits fatty acid hydrolase (or FAAH), an integral membrane hydrolase possessing an unusual catalytic triad Ser-Ser-Lys.
N-Oleoyl Ethanolamide is also an effective inhibitor of mitochondrial swelling, but does not inhibit phospholipase A2 or ruthenium red-induced Ca2+ release. Moreover, among naturally occurring Nacylethanolamines, only NOE (at 10 μM) inhibits the accumulation of Narachidonoylethanolamine (or Anandamide, AEA), a putative endogenous ligand of the cannabinoid receptor, into cerebellar granule cells occurs by means of facilitated diffusion.

storage

Store at +4°C

References

1) Lo Verme et al. (2005), Regulation of food intake by oleoylethanolamide; Cell Mol. Life Sci. 62 708
2) Magotti et al. (2015), Structure of human N-acylphosphatidylethanolamine-hydrolyzing phospholipase D: regulation of fatty acid ethanolamide biosynthesis by bile acids; Structure 23 598
3) Overton et al. (2006), Deorphanization of a G protein-coupled receptor for oleoylethanolamide and its use in the discovery of small-molecules hypophagic agents; Cell Metab. 3 167
4) Brown (2007), Novel cannabinoid receptors; Br. J. Pharmacol. 152 567
5) Nielson et al. (2004), Food intake is inhibited by oral oleoylethanolamide; J. Lipid Res. 45 1027
6) Folick et al. (2015), Aging. Lysosomal signaling molecules regulate longevity in Caenorhabditis elegans; Science 347 83

Oleoyl Ethanolamide Preparation Products And Raw materials

Raw materials

Preparation Products

Global( 236)Suppliers
Supplier Tel Email Country ProdList Advantage
PNP Biotech Co. Ltd
+8618516098983 sales@pnpbiotech.com China 1001 58
GIHI CHEMICALS CO.,LIMITED
+8618058761490 info@gihichemicals.com China 49999 58
Hebei Yanxi Chemical Co., Ltd.
+8617531190177 peter@yan-xi.com China 5993 58
Shandong Juchuang Chemical Co., LTD
+86-18885615001 +86-18885615001 admin@juchuangchem.com China 387 58
airuikechemical co., ltd.
+undefined86-15315557071 sales02@airuikechemical.com China 994 58
CONTIDE BIOTECH CO.,LTD
+85253358525 xena@healthtide-api.com China 525 58
BINBO BIOLOGICAL CO.,LTD
+8618629063126 info@binbobiological.com China 224 58
Henan Tianfu Chemical Co.,Ltd.
+86-0371-55170693 +86-19937530512 info@tianfuchem.com China 21695 55
Hangzhou FandaChem Co.,Ltd.
008657128800458; +8615858145714 fandachem@gmail.com China 9352 55
Shanghai Zheyan Biotech Co., Ltd.
18017610038 zheyansh@163.com CHINA 3620 58

View Lastest Price from Oleoyl Ethanolamide manufacturers

Image Update time Product Price Min. Order Purity Supply Ability Manufacturer
Oleoyl Ethanolamide pictures 2024-04-19 Oleoyl Ethanolamide
111-58-0
US $0.00 / G 1G 99% 20 CONTIDE BIOTECH CO.,LTD
Oleoyl Ethanolamide pictures 2024-04-11 Oleoyl Ethanolamide
111-58-0
US $0.00 / kg 1kg 99.8% 1000 kg BINBO BIOLOGICAL CO.,LTD
N-oleoyl ethanolamine pictures 2024-04-07 N-oleoyl ethanolamine
111-58-0
US $0.00-0.00 / Kg 1Kg 99.9% 200tons airuikechemical co., ltd.

Oleoyl Ethanolamide Spectrum

N-(2-hydroxyethyl)-,(Z)-9-Octadecenamide OLEIC ACID-2,6-DIISOPROPYL ANILIDE N-[2,6-BIS(1-METHYLETHYL)PHENYL]-9Z-OCTADECENAMIDE N-Oleoylethanolamine, ~98% 9Z-OCTADECENOYLETHANOLAMIDE;C18:1 ANANDAMIDE C18:1 anandamide Oleoylmonoethanolamide Oleyl monoethanolamide N-(cis-9-Octadecenoyl)ethanolamine N-Oleoylethanolamine 9-Octadecenamide, N-(2-hydroxyethyl)-, (9Z)- (Z)-N-(2-hydroxyethyl)octadec-9-enamide LSUREMONOETHANOLAMID OLEAMIDE MEA N-(cis-9-Octadecenoyl)ethanolamine, N-(Hydroxyethyl)oleamide, OEA, oleoylethanolamide (Z)-N-(2-Hydroxyethyl)-9-octadecenamide AM-3101 N-(2-Hydroxyethyl)oleic amide OEA, oleoylethanolamide N-OleoylethanolaMide [n-(2-hydroxyethyl)oleaMide 9Z-octadecenoylethanolaMide Oleoyl ethanolaMine N-Oleoyl Ethanolamide (OEA) 9-Octadecenamide, N-(2-hydroxyethyl)- Monoethanolamine oleic acid amide UNII-1HI5J9N8E6 N-Oleoyl Ethanolamine - CAS 111-58-0 - Calbiochem N-Oleoylethanolamine ISO 9001:2015 REACH OEA Synonyms: Oleoylethanolamide N-Oleoylethanolamine 111-58-0 N-Oleylethanolamide ODA Oleoylethanolamide(OEA) N-(2-Hydroxyethyl)oleamide OEA N-(Hydroxyethyl)oleamide N-OLEOYLETHANOLAMIDE OLEOYL ETHANOLAMIDE Supply manufacturer Oleoylethanolamine(OEA 99%)111-58-0 Oleyl ethanolamine 111-58-0 C20H39NO2 C30H51NO A to C BioChemical Biochemicals and Reagents Ceramidase Enzyme Inhibitors by Enzyme Enzymes, Inhibitors, and Substrates Enzyme Inhibitors Intracellular receptor Fluorobenzene