Ro60-0175,99.98%

产品编号:Bellancom-123838| CAS NO:169675-08-5| 分子式:C11H12ClFN2| 分子量:226.68

本网站销售的所有产品仅用于工业应用或者科学研究等非医疗目的,不可用于人类或动物的临床诊断或者治疗,非药用,非食用,

货号 包装 价格 库存与货期 购买量 操作
Bellancom-123838
3200.00 杭州 北京(现货)
Bellancom-123838
5100.00 杭州 北京(现货)
Bellancom-123838
10500.00 杭州 北京(现货)

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Ro60-0175

产品介绍 Ro60-0175 是一种有效的选择性 5-HT2C 受体激动剂。Ro60-0175 降低了成瘾性。
生物活性

Ro60-0175 is a potent and selective agonist of 5-HT2C receptor. Ro60-0175 reduces self-administration.

体外研究
体内研究

Ro60-0175(1 mg/kg;皮下注射)保留了在药物治疗组的对照动物中观察到的规律性反应,但药物治疗的动物更早达到它们的转折点
Ro60-0175(0.3、1 和 3 mg/kg;皮下注射)显着降低恢复组对主动杠杆的响应
Ro60-0175(0.5mg/kg SB242084;1mg/kg Ro60-0175;皮下注射)与恢复组中的载体相比降低了反应,并且通过 SB242084 预处理可以防止这种效应。对于对非活动杠杆的响应,没有显着的主效应或交互作用

西域 has not independently confirmed the accuracy of these methods. They are for reference only.

Animal Model: Adult male Sprague-Dawley rats (280-320 g)
Dosage: 1 mg/kg
Administration: s.c.
Result: Preserved the regularity of responding seen in control animals in drug-treated group, but drug-treated animals reached their break-points earlier.
Animal Model: Adult male Sprague-Dawley rats (280-320 g)
Dosage: 0.5 mg/kg (SB242084), 1 mg/kg (Ro60-0175)
Administration: s.c. (Ro60-0175), i.p. (SB242084)
Result: Reduced responding for cocaine and effect was reversed by SB242084.
Animal Model: Adult male Sprague-Dawley rats (280-320 g)
Dosage: 0.3, 1, and 3 mg/kg (Ro60-0175), 1 mg/kg (yohimbine)
Administration: s.c. (Ro60-0175), i.p. (yohimbine)
Result: Showed yohimbine treatment alone increased responding relative to vehicle injection, and the response was attenuated dose dependently by Ro60-0175.
Animal Model: Adult male Sprague-Dawley rats (280-320 g)
Dosage: 0.5 mg/kg (SB242084), 1 mg/kg (Ro60-0175), 1 mg/kg (yohimbine)
Administration: s.c. (Ro60-0175), i.p. (yohimbine), i.p. (SB242084)
Result: Ro60-0175 reduced responding and that this effect was prevented by SB242084 pretreatment.
体内研究

Ro60-0175(1 mg/kg;皮下注射)保留了在药物治疗组的对照动物中观察到的规律性反应,但药物治疗的动物更早达到它们的转折点
Ro60-0175(0.3、1 和 3 mg/kg;皮下注射)显着降低恢复组对主动杠杆的响应
Ro60-0175(0.5mg/kg SB242084;1mg/kg Ro60-0175;皮下注射)与恢复组中的载体相比降低了反应,并且通过 SB242084 预处理可以防止这种效应。对于对非活动杠杆的响应,没有显着的主效应或交互作用

西域 has not independently confirmed the accuracy of these methods. They are for reference only.

Animal Model: Adult male Sprague-Dawley rats (280-320 g)
Dosage: 1 mg/kg
Administration: s.c.
Result: Preserved the regularity of responding seen in control animals in drug-treated group, but drug-treated animals reached their break-points earlier.
Animal Model: Adult male Sprague-Dawley rats (280-320 g)
Dosage: 0.5 mg/kg (SB242084), 1 mg/kg (Ro60-0175)
Administration: s.c. (Ro60-0175), i.p. (SB242084)
Result: Reduced responding for cocaine and effect was reversed by SB242084.
Animal Model: Adult male Sprague-Dawley rats (280-320 g)
Dosage: 0.3, 1, and 3 mg/kg (Ro60-0175), 1 mg/kg (yohimbine)
Administration: s.c. (Ro60-0175), i.p. (yohimbine)
Result: Showed yohimbine treatment alone increased responding relative to vehicle injection, and the response was attenuated dose dependently by Ro60-0175.
Animal Model: Adult male Sprague-Dawley rats (280-320 g)
Dosage: 0.5 mg/kg (SB242084), 1 mg/kg (Ro60-0175), 1 mg/kg (yohimbine)
Administration: s.c. (Ro60-0175), i.p. (yohimbine), i.p. (SB242084)
Result: Ro60-0175 reduced responding and that this effect was prevented by SB242084 pretreatment.
性状Solid
溶解性数据
In Vitro: 

DMSO : 125 mg/mL (551.44 mM; Need ultrasonic)

配制储备液
浓度 溶剂体积 质量 1 mg 5 mg 10 mg
1 mM 4.4115 mL 22.0575 mL 44.1151 mL
5 mM 0.8823 mL 4.4115 mL 8.8230 mL
10 mM 0.4412 mL 2.2058 mL 4.4115 mL
*

请根据产品在不同溶剂中的溶解度选择合适的溶剂配制储备液;一旦配成溶液,请分装保存,避免反复冻融造成的产品失效
储备液的保存方式和期限:-80°C, 6 months; -20°C, 1 month (protect from light)。-80°C 储存时,请在 6 个月内使用,-20°C 储存时,请在 1 个月内使用。

In Vivo:

请根据您的实验动物和给药方式选择适当的溶解方案。以下溶解方案都请先按照 In Vitro 方式配制澄清的储备液,再依次添加助溶剂:

——为保证实验结果的可靠性,澄清的储备液可以根据储存条件,适当保存;体内实验的工作液,建议您现用现配,当天使用; 以下溶剂前显示的百
分比是指该溶剂在您配制终溶液中的体积占比;如在配制过程中出现沉淀、析出现象,可以通过加热和/或超声的方式助溶

  • 1.

    请依序添加每种溶剂: 10% DMSO    40% PEG300    5% Tween-80    45% saline

    Solubility: ≥ 2.08 mg/mL (9.18 mM); Clear solution

    此方案可获得 ≥ 2.08 mg/mL (9.18 mM,饱和度未知) 的澄清溶液。

    以 1 mL 工作液为例,取 100 μL 20.8 mg/mL 的澄清 DMSO 储备液加到 400 μL PEG300 中,混合均匀;向上述体系中加入50 μL Tween-80,混合均匀;然后继续加入 450 μL生理盐水定容至 1 mL。

    将 0.9 g 氯化钠,完全溶解于 100 mL ddH₂O 中,得到澄清透明的生理盐水溶液
  • 2.

    请依序添加每种溶剂: 10% DMSO    90% (20% SBE-β-CD in saline)

    Solubility: ≥ 2.08 mg/mL (9.18 mM); Clear solution

    此方案可获得 ≥ 2.08 mg/mL (9.18 mM,饱和度未知) 的澄清溶液。

    以 1 mL 工作液为例,取 100 μL 20.8 mg/mL 的澄清 DMSO 储备液加到 900 μL 20% 的 SBE-β-CD 生理盐水水溶液中,混合均匀。

    将 2 g 磺丁基醚 β-环糊精加入 5 mL 生理盐水中,再用生理盐水定容至 10 mL,完全溶解,澄清透明
  • 3.

    请依序添加每种溶剂: 10% DMSO    90% corn oil

    Solubility: ≥ 2.08 mg/mL (9.18 mM); Clear solution

    此方案可获得 ≥ 2.08 mg/mL (9.18 mM,饱和度未知) 的澄清溶液,此方案不适用于实验周期在半个月以上的实验。

    以 1 mL 工作液为例,取 100 μL 20.8 mg/mL 的澄清 DMSO 储备液加到 900 μL玉米油中,混合均匀。

*以上所有助溶剂都可在 西域 网站选购。
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

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