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 |
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| 10MG | ¥430 | 有现货 |
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| 25MG | ¥768 | 有现货 |
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| 50MG | ¥1386 | 有现货 |
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| 100MG | ¥1872 | 有现货 |
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| 200MG | ¥2664 | 有现货 |
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| 500MG | 获取报价 | 有现货 |
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| 1G | 获取报价 | 有现货 |
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| 1 mL x 10 mM in DMSO | ¥291 | 有现货 |
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生物学信息
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产品名称F-11440
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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
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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。
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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.
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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.
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体内实验——
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同义词Eptapirone
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通路GPCR/G Protein
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靶点5-HT Receptor
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受体5-HT1A
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研究领域Neurological Disease
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适应症Anxiety
化学信息
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CAS Number179756-58-2
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分子量345.3995
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分子式C16H23N7O2
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纯度>98% (HPLC)
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溶解度DMSO: 6 mg/mL (Need ultrasonic)
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SMILESO=C(N1C)N(CCCCN2CCN(C3=NC=CC=N3)CC2)N=CC1=O
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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
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储存条件(-20℃)
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运输条件With Ice Pack
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稳定性≥ 2 years
参考文献
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Sumatriptan
Sumatriptan (GR 43175) 是一种具有口服活性的 5-HT1 受体 激动剂,对 5-HT1D、5-HT1B 和 5-HT1F 受体的 IC50 分别为 7.3 nm、9.3nm 和 17.8 nm。Sumatriptan 可用于偏头痛研究。
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DA-6886
DA-6886 is an agonist 5-Hydroxytryptamine receptor 4 (5-HT4). DA-6886 induced relaxation of the rat oesophagus preparation in a 5-HT4 receptor antagonist-sensitive manner. The evaluation of DA-6886 in CHO cells expressing hERG channels revealed that it inhibited hERG channel current with an pIC50 value of 4.3, indicating that the compound was 1000-fold more selective for the 5-HT4 receptor over hERG channels.
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p-MPPF
p-MPPF is a selective 5-HT antagonist that dose-dependently antagonizes hypothermia induced by 8-hydroxy-2-(di-n-propylamino)tetralin (8-OH-DPAT) and can be used to study neurological diseases.
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