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(+)-假木贼碱 /Anabasine {[allProObj[0].p_purity_real_show]}

货号:A857821 同义名: (-)-假木贼碱 / (S)-Anabasine;(+)-Anabasine

Anabasine是一种源自烟草的生物碱,作为烟碱乙酰胆碱受体 (nAChRs) 的全激动剂,能够诱导 TE671 细胞的去极化,EC50 为 0.7 µM。它作为一种植物性杀虫剂,广泛应用于农业和生物防治研究。

Anabasine 化学结构 CAS号:494-52-0
Anabasine 化学结构
CAS号:494-52-0
Anabasine 3D分子结构
CAS号:494-52-0
Anabasine 化学结构 CAS号:494-52-0
Anabasine 3D分子结构 CAS号:494-52-0
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Anabasine 纯度/质量文件 产品仅供科研

货号:A857821 标准纯度: {[allProObj[0].p_purity_real_show]}
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产品名称 AChE AChR mAChR nAChR 其他靶点 纯度
Donepezil +++

bAChE, IC50: 8.12 nM

hAChE, IC50: 11.6 nM

98%
Loganin ++

AChE, IC50: 3.95 μM

99%+
topride HCl ++

AChE, IC50: 2.04 μM

98%
Dehydroevodiamine HCl 99%+
Jatrorrhizine ++

AChE, IC50: 872 nM

99%+
Palmatine ++

AChE, IC50: 0.51 μM

98%
(-)-Huperzine A ++++

AChE (G4 form), Ki: 7 nM

98%
Galanthamine HBr ++

AChE, IC50: 0.35 μM

98%
Trospium chloride 99%
Tiotropium Bromide Monohydrate 98+%
Gallamine Triethiodide +

AChR, IC50: 68.0 μM

98%
Hexamethonium Bromide 99%
Pancuronium dibromide 98%
Neostigmine bromide 98%
Orphenadrine citrate 98%
Oxybutynin 98%
Irsogladine PDE 98%
Pyridostigmine bromide 99+%
Rivastigmine +

AChR, IC50: 5.5 μM

98%
Paroxetine hydrochloride 97%
Rocuronium Bromide 98%
Tropicamide +++

M4 mAChR, IC50: 8 nM

98%
Diphenmanil methylsulfate 98%
Umeclidinium bromide 95%
Otilonium bromide 98%
Flavoxate HCl +

mAChR, IC50: 12.2 μM

98%
Ipratropium bromide 98%
Diphenidol HCl 98%
Darifenacin hydrobromide ++++

M3 mAChR, pKi: 8.9

98%
Aclidinium Bromide ++++

M4 mAChR, Ki: 0.21 nM

M2 mAChR, Ki: 0.1 nM

98%
Oxybutynin chloride 99%
Pentoxyverine citrate 98%
Solifenacin 98%
Catharanthine 98%
Benzethonium chloride +++

α4β2 nAChRs, IC50: 49 nM

α7 nAChRs, IC50: 122 nM

99+%
Vinblastine sulfate +

nAChR, IC50: 8.9 μM

99%
PNU-120596 ++

α7 nAChR, EC50: 216 nM

99+%
1. 鼠标悬停在“+”上可以显示相关IC50的具体数值。"+"越多,抑制作用越强。2. "✔"表示该化合物对相应的亚型有抑制作用,但抑制强度暂时没有相关数据。

Anabasine 生物活性

描述 ((S)-Anabasine) is a minor alkaloidal component in tobacco (Nicotiana) and functions as a full agonist at nicotinic acetylcholine receptors (nAChRs). It triggers depolarization in TE671 cells, which naturally express human fetal muscle-type nAChRs, with an EC50 value of 0.7 µM[1].[2].
体内研究

At dosages of 0.2 mg/kg (p<0.05) and 2 mg/kg (p<0.025), Anabasine notably mitigates impairment. However, Anabasine alone does not significantly affect response latency. At a dose of 0.06 mg/kg, Anabasine significantly (p<0.05) worsens the impairment caused by dizocilpine. On its own, none of the Anabasine dosages influence choice accuracy. Notably, combining 0.06 mg/kg Anabasine with dizocilpine leads to a significant (p<0.05) increase in non-response trials compared to dizocilpine alone (6.7±2.6 vs. 2.1±0.8)[1].

Anabasine 参考文献

[1]Levin ED, et al. Effects of tobacco smoke constituents, anabasine and anatabine, on memory and attention in female rats. J Psychopharmacol. 2014 Oct;28(10):915-22.

[2]Benedict T Green, et al. Actions of piperidine alkaloid teratogens at fetal nicotinic acetylcholine receptors. Neurotoxicol Teratol. May-Jun 2010;32(3):383-90.

Anabasine 实验方案

计算器
存储液制备 1mg 5mg 10mg

1 mM

5 mM

10 mM

6.16mL

1.23mL

0.62mL

30.82mL

6.16mL

3.08mL

61.64mL

12.33mL

6.16mL

Anabasine 技术信息

CAS号494-52-0
分子式C10H14N2
分子量 162.232
别名 (-)-假木贼碱 ;(S)-Anabasine;(+)-Anabasine;Anabazin
运输蓝冰
存储条件

液体 -20°C:3-6个月-80°C:12个月

溶解度

DMSO: 105 mg/mL(647.22 mM),配合低频超声助溶,注意:DMSO长时间开封后,会吸水并导致溶解能力下降,请避免使用长期开封的DMSO

动物实验配方
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