(+)-假木贼碱,Anabasine,99.87%
产品编号:Bellancom-B1532| CAS NO:494-52-0| 分子式:C10H14N2| 分子量:162.23
Anabasine 是一种烟碱受体激动剂。
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(+)-假木贼碱
| 产品介绍 | Anabasine ((S)-Anabasine) 是一种生物碱,烟草中的一种成分。Anabasine 是一种植物性杀虫剂,作为烟碱乙酰胆碱受体的全激动剂 (nAChRs)。Anabasine 诱导内源表达人肌型 nAChRs 的 TE671 细胞去极化 (EC50=0.7 µM)。 | ||||||||||||||||
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| 生物活性 | Anabasine ((S)-Anabasine) is an alkaloid that found as a minor component in tobacco (Nicotiana). Anabasine is a botanical pesticide nicotine, acts as a full agonist of nicotinic acetylcholine receptors (nAChRs). Anabasine induces depolarization of TE671 cells endogenously expressing human fetal muscle-type nAChRs (EC50=0.7 µM). | ||||||||||||||||
| 体外研究 | |||||||||||||||||
| 体内研究 |
Anabasine significantly reverses the impairment at the 0.2 mg/kg (p<0.05) and 2 mg/kg doses (p<0.025). Anabasine does not have any significant effects on response latency when administered alone. The 0.06 mg/kg Anabasine dose, in fact, significantly (p<0.05) exacerbates the dizocilpine-induced impairment. None of these Anabasine doses affects choice accuracy on their own. Individual dose comparisons show that the 0.06 mg/kg Anabasine dose plus dizocilpine (6.7±2.6) causes a significant (p<0.05) increase in non-response trials compare with dizocilpine alone (2.1±0.8). 西域 has not independently confirmed the accuracy of these methods. They are for reference only. | ||||||||||||||||
| 体内研究 |
Anabasine significantly reverses the impairment at the 0.2 mg/kg (p<0.05) and 2 mg/kg doses (p<0.025). Anabasine does not have any significant effects on response latency when administered alone. The 0.06 mg/kg Anabasine dose, in fact, significantly (p<0.05) exacerbates the dizocilpine-induced impairment. None of these Anabasine doses affects choice accuracy on their own. Individual dose comparisons show that the 0.06 mg/kg Anabasine dose plus dizocilpine (6.7±2.6) causes a significant (p<0.05) increase in non-response trials compare with dizocilpine alone (2.1±0.8). 西域 has not independently confirmed the accuracy of these methods. They are for reference only. | ||||||||||||||||
| 性状 | Liquid | ||||||||||||||||
| 溶解性数据 |
In Vitro:
DMSO : 100 mg/mL (616.41 mM; Need ultrasonic) 配制储备液
*
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。 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
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| 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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| 危害码 (欧洲) | T:Toxic |
|---|---|
| 风险声明 (欧洲) | R23/24/25 |
| 安全声明 (欧洲) | S28-S36/37-S45-S61 |
| 危险品运输编码 | 3140 |
| RTECS号 | BV4375000 |
| 包装等级 | I |
| 危险类别 | 6.1 |
| 上游产品 8 | |
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| 下游产品 10 | |
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