FG 7142
CAS No. 78538-74-6
FG 7142 ( ZK 39106,LSU-65 )
产品货号. M22444 CAS No. 78538-74-6
FG 7142 还可调节表达 α1 亚基的 GABAA 受体上 GABA 诱导的氯离子通量 (EC50= 137 nM)。 FG 7142 可增加酪氨酸羟基化并导致小鼠大脑皮层 β-肾上腺素受体上调。 FG 7142 是一种非选择性苯二氮卓反向激动剂,对含有 α1 亚基的 GABAA 受体具有高亲和力 (Ki=91 nM)。
纯度: >98% (HPLC)
COA
Datasheet
HNMR
HPLC
MSDS
Handing Instructions
| 规格 | 价格/人民币 | 库存 | 数量 |
| 2MG | ¥381 | 有现货 |
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| 5MG | ¥786 | 有现货 |
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| 10MG | ¥1320 | 有现货 |
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| 25MG | ¥2155 | 有现货 |
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| 50MG | ¥3200 | 有现货 |
|
| 100MG | ¥4763 | 有现货 |
|
| 500MG | ¥10206 | 有现货 |
|
| 1G | 获取报价 | 有现货 |
|
生物学信息
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产品名称FG 7142
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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FG 7142 还可调节表达 α1 亚基的 GABAA 受体上 GABA 诱导的氯离子通量 (EC50= 137 nM)。 FG 7142 可增加酪氨酸羟基化并导致小鼠大脑皮层 β-肾上腺素受体上调。 FG 7142 是一种非选择性苯二氮卓反向激动剂,对含有 α1 亚基的 GABAA 受体具有高亲和力 (Ki=91 nM)。
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产品描述FG 7142?also modulates GABA-induced chloride flux at GABAA receptors expressing the α1 subunit (EC50= 137 nM).?FG 7142?can increase tyrosine hydroxylation and cause upregulation of β-adrenoceptors in mouse cerebral cortex.?FG 7142 , a non-selectively benzodiazepine inverse agonist, has high affinity for the α1 subunit-containing GABAA receptor (Ki=91 nM).?FG-7142 has a high efficacy in modulating GABA-induced chloride flux at GABAA receptors expressing the α1 subunit (EC50 = 137 nM) as compared to the other α subunits.FG-7142 has affinity for those expressing the α subunit, the Ki values are 91 nM; 330 nM; 492 nM and 2.150 μM for α1, α2,α3 and α5 subunits, respectively.?FG-7142 (intraperitoneal injection;?15 mg/kg) increases tyrosine hydroxylase activity and dopamine turnover in the medial prefrontal cortex and ventral tegmentum in vivo, but effects are not detected in mesolimbic or nigrostriatal areas.FG-7142 (intraperitoneal injection; 15-30 mg/kg) activates mesolimbocortical dopaminergic projections, leading to increases in dopamine in the prefrontal cortex and the nucleus accumbens in rats.
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体外实验FG-7142 has affinity for those expressing the α subunit, the Ki values are 91 nM; 330 nM; 492 nM and 2.150 μM for α1, α2,α3 and α5 subunits, respectively.FG-7142 has a high efficacy in modulating GABA-induced chloride flux at GABAA receptors expressing the α1 subunit (EC50 = 137 nM) as compared to the other α subunits (EC50: α2= 507 nM,α3=1.021μM , α5=1.439 μM).
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体内实验FG-7142 (intraperitoneal?injection; 15-30 mg/kg) activates mesolimbocortical dopaminergic projections, leading to increases in dopamine in the prefrontal cortexandthe nucleus accumbens in rats. FG-7142 (intraperitoneal?injection; 15 mg/kg) increases tyrosine hydroxylase activity and dopamine turnover in the medial prefrontal cortex and ventral tegmentum in vivo, but effects are not detected in mesolimbic or nigrostriatal areas.
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同义词ZK 39106,LSU-65
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通路Others
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靶点Other Targets
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受体GABAA receptor
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研究领域——
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适应症——
化学信息
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CAS Number78538-74-6
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分子量225.25
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分子式C13H11N3O
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纯度>98% (HPLC)
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溶解度In Vitro:?DMSO : 100 mg/mL (443.95 mM)
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SMILESCNC(=O)c1cc2c(cn1)[nH]c1ccccc21
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化学全称——
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
1. Cottone P, et al. FG 7142 specifically reduces meal size and the rate and regularity of sustained feeding in female rats: evidence that benzodiazepine inverse agonists reduce food palatability.Neuropsychopharmacology. 2007 May;32(5):1069-81. Epub 2006 Nov 1.
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