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N-Arachidonylglycine-d8是经过氘代标记的N-Arachidonylglycine。N-Arachidonylglycine (NA-Gly) 是内源性大麻素anandamide (AEA)的羧基类似物,作为GPR18激动剂,其EC50值为44.5 nM。与AEA不同,NA-Gly在CB1和CB2受体上没有活性。它可抑制GLYT2,其IC50值为5.1 μM,并且是子宫内膜细胞迁移的有效激活剂。

N-Arachidonylglycine-d8是经过氘代标记的N-Arachidonylglycine。N-Arachidonylglycine (NA-Gly) 是内源性大麻素anandamide (AEA)的羧基类似物,作为GPR18激动剂,其EC50值为44.5 nM。与AEA不同,NA-Gly在CB1和CB2受体上没有活性。它可抑制GLYT2,其IC50值为5.1 μM,并且是子宫内膜细胞迁移的有效激活剂。
| 规格 | 价格 | 库存 | 数量 |
|---|---|---|---|
| 10 mg | 待询 | 待询 | |
| 50 mg | 待询 | 待询 |
| 产品描述 | N-Arachidonylglycine-d8 is the deuterium-labeled version of N-Arachidonylglycine. N-Arachidonylglycine (NA-Gly), a carboxylic analog of the endogenous cannabinoid anandamide (AEA), functions as a GPR18 agonist with an EC50 of 44.5 nM. Unlike AEA, it does not show activity at CB1 and CB2 receptors. It inhibits GLYT2 with an IC50 of 5.1 μM and is an effective stimulator of endometrial cell migration. |
| 体内活性 | N-Arachidonylglycine(10 mg/kg,口服)可使anandamide在血液中的浓度增加9倍。N-Arachidonylglycine(1.2 mg/kg,口服,一次)导致腹腔细胞显著减少70%。 |
| 分子量 | 369.57 |
| 分子式 | C22H35NO3 |
| CAS No. | 1159908-44-7 |
| Smiles | C(CCC(NCC(O)=O)=O)/C(=C(\C/C(=C(\C/C(=C(\C/C(=C(\CCCCC)/[2H])/[2H])/[2H])/[2H])/[2H])/[2H])/[2H])/[2H] |
| 存储 | Powder: -20°C for 3 years | In solvent: -80°C for 1 year | Shipping with blue ice/Shipping at ambient temperature.(实际储存温度请以该批次产品标识为准) |
对于不同动物的给药剂量换算,您也可以参考 更多