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首页-小分子抑制剂&激动剂-Membrane Transporter/Ion Channel-nAChR-ABT-418
ABT-418

Chemical Structure : ABT-418

CAS No.: 147402-53-7

ABT-418 (ABT418)

货号: PC-20544Not For Human Use, Lab Use Only.

ABT-418 (ABT418) is an analog of (-)-nicotine and cholinergic ligand (activator) of nAChRs, a potent inhibitor of [3H]-cytisine binding to nAChR in rat brain with Ki of 2 nM.

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纯度 & COA & 质检文件 纯度: >98% (HPLC)

生物&药学活性

ABT-418 (ABT418) is an analog of (-)-nicotine and cholinergic ligand (activator) of nAChRs, a potent inhibitor of [3H]-cytisine binding to nAChR in rat brain with Ki of 2 nM.
ABT-418 is inactive (Ki > 10,000 nM) in 37 other receptor/neurotransmitter-uptake/enzyme/transduction system binding assays.
ABT-418 is also approximately 10-fold less potent (EC50 value=380 nM) than (-)-nicotine (40 nM) in increasing [3H]-dopamine release from rat striatal slices.
ABT-418 (MED, 0.002 mumol/kg i.v.) is remarkably potent in enhancing basal forebrain-elicited increases in cortical cerebral blood flow in rats.
ABT-418 demonstrates potent cognitive-enhancing and anxiolytic properties in animal models without eliciting significant side effects.

物理化学性质&存储条件

分子量 166.22
分子式 C9H14N2O
外观性状 Solid
CAS No.
储存条件
固体粉末
-20°C 12 个月; 4°C 6 个月
配置液
-80°C 6 个月; -20°C 6 个月
Shipping
Solubility

10 mM in DMSO

Chemical Name/SMILES

CN1[C@H](C2=CC(C)=NO2)CCC1

参考文献

1. Arneric SP, et al. J Pharmacol Exp Ther. 1994 Jul;270(1):310-8.

2. Decker MW, et al. J Pharmacol Exp Ther. 1994 Jul;270(1):319-28.

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