HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
2-Arachidonylglycerol
2-ARACHIDONOYLGLYCEROL · 2-ARACHIDONYLGLYCEROL · (5Z,8Z,11Z,14Z)-1,3-Dihydroxypropan-2-yl icosa-5,8,11,14-tetraenoate · 2-AG · NOLADIN · 2-Ara-gl · 2-Monoarachidonin · 2-Monoarachidonoylglycerol

Identifikatoren & physikalische Daten
| CAS No. | 53847-30-6 |
|---|---|
| Summenformel | C23H38O4 |
| Durchschnittliche Molmasse | 378,5 g/mol |
| Monoisotopische Masse | 378,2770097 g/mol |
| SMILES | CCCCC/C=C\C/C=C\C/C=C\C/C=C\CCCC(=O)OC(CO)CO |
| InChIKey | RCRCTBLIHCHWDZ-DOFZRALJSA-N |
| PubChem CID | 5282280 |
| ChEMBL | CHEMBL122972 |
| ChEBI | CHEBI:52392 |
| DTXSID | DTXSID001017454 |
Chemische & physikalische Eigenschaften
| XLogP | 5,3 |
|---|---|
| Polarare Oberfläche (TPSA) | 66,8 |
| H-Brücken-Donoren | 2 |
| H-Brücken-Akzeptoren | 4 |
| Frei drehbare Bindungen | 18 |
| Schwere Atome | 27 |
| Formalladung | 0 |
| Komplexität | 445 |
| Lipide | Lipids -> Glycerolipids [GL] -> Monoradylglycerols [GL01] -> Monoacylglycerols [GL0101] |
| Physical Description | Solid |
| Siedepunkt | 508.6±50.0 °C(Predicted) |
| Dichte | 0.992±0.06 g/cm3(Predicted) |
| Flammpunkt | 2 °C |
| Lagerbedingungen | -20°C |
| Löslichkeit | DMSO: 10 mg/mlEthanol: MisciblePBS (pH 7.2): ~150 μg/ml |
| Aggregatzustand | acetonitrile solution |
| pKa (Säurekonstante) | 13.54±0.10(Predicted) |
| Farbe | Colorless to light yellow |
| InChIKey | RCRCTBLIHCHWDZ-DOFZRALJSA-N |
| SMILES | [H]C(CO)(OC(CCC/C=C\C/C=C\C/C=C\C/C=C\CCCCC)=O)CO |
| CAS Datenbank | 53847-30-6(CAS DataBase Reference) |
Sicherheit & Vorschriften
| Wassergefährdungsklasse (WGK) | 2 |
|---|---|
| UN-Transportnummer | UN 1648 3/PG 2 |
| R-Sätze (R) | 11-20/21/22-36 |
| Gefahrensymbole | F,Xn |
| Sicherheitshinweise (S) | 26-36/37-16 |
| Lagerklasse | 12 - Non Combustible Liquids |
Anwendungen & Verwendung
Verwenden
2-Arachidonoylglycerol is a major endocannabinoid, which can inhibit synaptic transmission by presynaptic cannabinoid CB1 receptors. It plays an inhibitory role in the bombesin-induced activation of central adrenomedullary outflow in rats.