Ro60-0175

目录号: PL09381 纯度: ≥99%
Ro60-0175 是一种有效的选择性 5-HT2C 受体激动剂。Ro60-0175 降低了可卡因的成瘾性以及可卡因在戒断反应消失后重新成瘾的可能性。
CAS No. :169675-08-5
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中文名称
Ro60-0175
英文名称
Ro60-0175
英文别名
(2S)-1-(6-chloro-5-fluoroindol-1-yl)propan-2-amine;(S)-1-(6-chloro-5-fluoro-1H-indol-1-yl)propan-2-amine;(S)-2-(6-chloro-5-fluoroindol-1-yl)-1-methylethylamine;(S)-2-(6-Chloro-5-fluoro-indol-1-yl)-1-methyl-ethylamine;GTPL166;BDBM50144841;BDBM50428891;ORG 35030;Ro600175;Q27088596;(2S)-1-(6-chloro-5-fluoroindol-1-yl)-propan-2-amine;(1S)-2-(6-chloro-5-fluoroindol-1-yl)-1-methylethylamine;(2S)-1-(6-chloro-5-fluoro-1H
Cas No.
169675-08-5
分子式
C11H12ClFN2
分子量
226.68
包装储存
4°C, protect from light In solvent : -80°C, 6 months; -20°C, 1 month (protect from light)
详情描述
Ro60-0175 是一种有效的选择性 5-HT2C 受体激动剂。Ro60-0175 降低了可卡因的成瘾性以及可卡因在戒断反应消失后重新成瘾的可能性。
产品详情
Ro60-0175 是一种有效的选择性 5-HT2C 受体激动剂。Ro60-0175 降低了可卡因的成瘾性以及可卡因在戒断反应消失后重新成瘾的可能性。
生物活性
Ro60-0175 is a potent and selective agonist of 5-HT 2C receptor. Ro60-0175 reduces cocaine self-administration, and the ability of cocaine to reinstate responding after extinction of drug-seeking behavior.
性状
Solid
IC50 & Target[1][2]
5-HT2C Receptor
体内研究(In Vivo)
Ro60-0175 (1 mg/kg; s.c.) preserves the regularity of responding seen in control animals in drug-treated group, but drug-treated animals reach their break-points earlier.
Ro60-0175 (0.5?mg/kg (SB242084); 1?mg/kg (Ro60-0175); s.c., i.p.) reduces responding for cocaine and effect is reversed by SB242084.
Ro60-0175 (0.3, 1, and?3 mg/kg (Ro60-0175); 1?mg/kg (yohimbine); s.c.; i.p.) dose dependently attenuates the response increased by the yohimbine treatment alone relative to vehicle injection.
Ro60-0175 (0.5 mg/kg (SB242084); 1?mg/kg (Ro60-0175); 1?mg/kg (yohimbine); s.c.; i.p.) reduces responding and that this effect is prevented by SB242084 pretreatment.
Ro60-0175 (0.3, 1, and?3 mg/kg; s.c.) significantly reduces responding on the active lever in the reinstatement group.
Ro60-0175 (0.5?mg/kg SB242084; 1?mg/kg Ro60-0175; s.c.; i.p.) reduces responding compare
运输条件
Room temperature in continental US; may vary elsewhere.
储存方式
4°C, protect from light In solvent : -80°C, 6 months; -20°C, 1 month (protect from light)
参考文献
[1]. Fletcher PJ, et al. The 5-HT2C receptor agonist Ro60-0175 reduces cocaine self-administration and reinstatement induced by the stressor yohimbine, and contextual cues. Neuropsychopharmacology. 2008;33(6):1402-1412.
溶解度数据
In Vitro: DMSO : 125 mg/mL (551.44 mM; Need ultrasonic)配制储备液
搜索质检报告(COA)
[1]. Fletcher PJ, et al. The 5-HT2C receptor agonist Ro60-0175 reduces cocaine self-administration and reinstatement induced by the stressor yohimbine, and contextual cues. Neuropsychopharmacology. 2008;33(6):1402-1412.

1:一般建议:溶解度为Medlife测试数据,可能与文献描述存在差异。这是由于生产工艺和批次不同产生的正常现象。为了使其更好的溶解,请用37℃加热试管并在超声波水浴中震动片刻。不同批次产品溶解度各有差异,仅做参考,具体以实验方案为准。

2:储存条件:粉末-20°C一般情况可以保存3年,溶于溶剂-80°C一般情况可以保存1年。不同产品及不同批次产品可能存在差异,请细致阅读产品信息,并辅助参考相关文献描述。

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