应用 |
A highly potent and selective serotonin (5-HT) uptake inhibitor |
产品介绍 |
Paroxetine HCl, a phenylpiperidine derivative, is a highly potent and selective ST (serotonin transporter/5-HT) uptake inhibitor. It acts by binding to ST (serotonin transporter/SERT) with high affinity (Ki = 05 nM). In vitro paroxetine competitively inhibits the uptake of 5-HT by rat hypothalamic and cortical synaptosomes with only very weak inhibitory effects on SLC6A2 (noradrenaline) uptake and DAT (dopamine) uptake. Paroxetine HCl has also displayed a high affinity for muscarinic acetylcholine receptors. Other experiments have shown Paroxetine HCl to inhibit NOS (nitric oxide synthase) and also to be both a substrate and an inhibitor of CYP2D6 (cytochrome isoenzyme P450 2D6). |
备注 |
Paroxetine is an antidepressant drug of the SSRI type. |
生化机理 |
Paroxetine hydrochloride hemihydrate is one of the most potent and selective of the selective serotonin reuptake inhibitors (SSRI); antidepressant. |
别名 |
(3S,4R)-(-)-3-[(1,3-苯并二恶茂-5-基氧)甲基]-4-(4-氟苯基)哌啶盐酸盐;盐酸帕罗西汀半水合物;(3S,4R)-(-)-3-[(1,3-Benzodioxol-5-yloxy)methyl]-4-(4-fluorophenyl)piperidine Hydrochloride Hemihydrate;Paxil; Seroxat; BRL29060 hydrochloride hemihydrate; BRL29060A hemihydrate |