NOLADIN ETHER Struktur

NOLADIN ETHER

Bezeichnung:NOLADIN ETHER

CAS-Nr222723-55-9

Englisch Name:NOLADIN ETHER

CBNumberCB8350967

SummenformelC23H40O3

Molgewicht364.56

MOL-Datei222723-55-9.mol

NOLADIN ETHER physikalisch-chemischer Eigenschaften

Siedepunkt	488.9±45.0 °C(Predicted)
Dichte	0.948±0.06 g/cm3(Predicted)
Flammpunkt	14℃
storage temp.	Desiccate at -20°C
Löslichkeit	DMF: 20 mg/ml; DMSO: 15 mg/ml; Ethanol: 25 mg/ml; Ethanol:PBS(pH 7.2) (1:1): 500 μg/ml
pka	13.92±0.10(Predicted)
Aggregatzustand	ethanol solution (10 mg/mL (1% w/v))
Farbe	colorless to light yellow

Sicherheit

Kennzeichnung gefährlicher	F
R-Sätze:	11
S-Sätze:	7-16
RIDADR	UN1170 - class 3 - PG 2 - Ethanol, solution
WGK Germany	2

Gefahreninformationscode (GHS)

NOLADIN ETHER Chemische Eigenschaften,Einsatz,Produktion Methoden

Beschreibung
2-Arachidonyl glycerol ether (2-AG ether) selectively binds to cannabinoid (CB) receptor 1 (K_is = 21.2 and >3,000 nM for CB₁ and CB₂, respectively, in a radioligand binding assay). It is a potent and selective agonist of CB₁ and GPR55 with EC₅₀ values of 10, 37, and >30,000 nM for CB₁, GPR55, and CB₂, respectively. 2-AG ether displays the typical tetrad of CB activities in mice. It is more chemically stable than 2-AG , with an endogenous half-life of hours rather than minutes. However, it is at least 10-fold less potent than 2-AG in eliciting typical CB₁-mediated responses. 2-AG ether elicits modest reductions in intraocular pressure in rabbits when administered at doses exceeding 50 μg per eye. It increases aqueous humor outflow via the CB₁ receptor in the trabecular meshwork. Administration of 2-AG ether to the nucleus accumbens (0.0625-1 μg) increases dietary intake and enhances fat consumption in rats given access to both high-carbohydrate and high-fat diets.
Verwenden
HU 310 is an endogenous GPR55 and CB1 receptors agonist. HU 310 has been shown to induce hyperglycia in rats. HU 310 can be used to investigate the biological roles of GPR55 and CB1 receptors.
Definition
ChEBI: A monoalkylglycerol that is the 2-O-arachidonyl derivative of glycerol.
Biologische Aktivität
Endogenous agonist for the GPR55 and CB 1 receptors (EC 50 values are 10 and 37 nM respectively) that displays selectivity over CB 2 receptors (K i values are 21.2 nM and > 3mM at CB 1 and CB 2 respectively). Causes sedation, hypothermia, intestinal immobility and mild antinociception in vivo . Attenuates sensory neurotransmission in rat mesenteric arteries via GPR55. Also available as part of the Endocannabinoid Tocriset™ .

NOLADIN ETHER Anbieter Lieferant Produzent Hersteller Vertrieb Händler.

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