盐酸米那普仑
| CAS号 | 101152-94-7 | 货号 | BCP05817 |
| 中文名 | 盐酸米那普仑 | ||
| 英文名 | F2207 | ||
| 中文别名 | |||
| 英文别名 | F 2207;F-2207;Milnacipran hydrochloride;Dalcipran hydrochloride;Ixel hydrochloride;Savella hydrochloride;Toledomin hydrochloride; | ||
| 分子式 | C15H23ClN2O | 分子量 | 282.81 |
| 生物活性 | Milnacipran (Ixel, Savella, Dalcipran, Toledomin) is a serotonin-norepinephrine reuptake inhibitor (SNRI) used in the clinical treatment of fibromyalgia. It is not approved for the clinical treatment of major depressive disorder in the USA, but it is in other countries. Milnacipran inhibits the reuptake of serotonin and norepinephrine in an approximately 1:3 ratio, respectively; in practical use this means a relatively balanced action upon bothneurotransmitters. Increasing both neurotransmitters concentration simultaneously works synergistically to treat both depression and fibromyalgia. Milnacipran exerts no significant actions onH1, α1, D1, D2, and mACh receptors, as well as on benzodiazepine and opioid binding sites. Milnacipran is well absorbed after oral dosing and has a bioavailability of 85%. Meals do not have an influence on the rapidity and extent of absorption. Peak plasma concentrations are reached 2 hours after oral dosing. The elimination half-life of 8 hours is not increa | ||
| 信号通路 | Neuro Signaling Pathway GPCR/G Protein | ||
| 靶 点 | 5 HT Receptor/Serotonin Receptor SSRI | ||
结构式
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