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F-11440

CAS No. 179756-58-2

F-11440 ( Eptapirone )

产品货号. M12716 CAS No. 179756-58-2

一种有效的选择性 5-HT1A 受体激动剂,Ki 为 4.8 nM,pKi 为 8.33。

纯度: >98% (HPLC)

COA Datasheet HNMR HPLC MSDS Handing Instructions
规格 价格/人民币 库存 数量
5MG ¥265 有现货
10MG ¥430 有现货
25MG ¥768 有现货
50MG ¥1386 有现货
100MG ¥1872 有现货
200MG ¥2664 有现货
500MG 获取报价 有现货
1G 获取报价 有现货
1 mL x 10 mM in DMSO ¥291 有现货

生物学信息

  • 产品名称
    F-11440
  • 注意事项
    本公司产品仅用于科研实验,不得用于人体或动物的临床与诊断
  • 产品简述
    一种有效的选择性 5-HT1A 受体激动剂,Ki 为 4.8 nM,pKi 为 8.33。
  • 产品描述
    A potent, selective 5-HT1A receptor agonist with Ki of 4.8 nM, pKi of 8.33; shows ≥shows 100-fold higher affinity for the other serotonin receptor subtypes, and has no detectable antidopaminergic activity and antihistaminergic activity; decreases the forskolin-induced increase in AMP in HeLa cells expressing human 5-HT1A receptors; produces anxiolytic- and antidepressant-like effects in animal models.Anxiety Phase 1 Discontinued(In Vitro):The affinity of Eptapirone (F11440) for 5-HT1Abinding sites (pKi, 8.33) was higher than that of buspirone (pKi , 7.50), and somewhat lower than that of flesinoxan (pKi , 8.91).In vivo, Eptapirone (F11440) was 4- to 20-fold more potent than flesinoxan, and 30- to 60-fold more potent than buspirone, in exerting 5-HT1A agonist activity at pre- and postsynaptic receptors in rats (measured by, for example, its ability to decrease hippocampal extracellular serotonin (5-HT) levels and to increase plasma corticosterone levels, respectively). Eptapirone (F11440), shown here to be a potent, selective, high efficacy 5-HT1Areceptor agonist, appears to have the potential to exert marked anxiolytic and antidepressant activity in humans.
  • 体外实验
    The affinity of Eptapirone (F11440) for 5-HT1Abinding sites (pKi, 8.33) was higher than that of buspirone (pKi , 7.50), and somewhat lower than that of flesinoxan (pKi , 8.91).In vivo, Eptapirone (F11440) was 4- to 20-fold more potent than flesinoxan, and 30- to 60-fold more potent than buspirone, in exerting 5-HT1A agonist activity at pre- and postsynaptic receptors in rats (measured by, for example, its ability to decrease hippocampal extracellular serotonin (5-HT) levels and to increase plasma corticosterone levels, respectively). Eptapirone (F11440), shown here to be a potent, selective, high efficacy 5-HT1Areceptor agonist, appears to have the potential to exert marked anxiolytic and antidepressant activity in humans.
  • 体内实验
    ——
  • 同义词
    Eptapirone
  • 通路
    GPCR/G Protein
  • 靶点
    5-HT Receptor
  • 受体
    5-HT1A
  • 研究领域
    Neurological Disease
  • 适应症
    Anxiety

化学信息

  • CAS Number
    179756-58-2
  • 分子量
    345.3995
  • 分子式
    C16H23N7O2
  • 纯度
    >98% (HPLC)
  • 溶解度
    DMSO: 6 mg/mL (Need ultrasonic)
  • SMILES
    O=C(N1C)N(CCCCN2CCN(C3=NC=CC=N3)CC2)N=CC1=O
  • 化学全称
    1,2,4-Triazine-3,5(2H,4H)-dione, 4-methyl-2-[4-[4-(2-pyrimidinyl)-1-piperazinyl]butyl]-

运输与储存

  • 储存条件
    (-20℃)
  • 运输条件
    With Ice Pack
  • 稳定性
    ≥ 2 years

参考文献

1. Koek W, et al. J Pharmacol Exp Ther. 1998 Oct;287(1):266-83. 2. Prinssen EP, et al. Eur J Pharmacol. 2002 Oct 25;453(2-3):217-21. 3. Pauwels PJ, et al. J Pharmacol Exp Ther. 2003 Nov;307(2):608-14.
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