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Submit Review6140 has been discontinued.
α7 nAChR agonist at human and rat receptors (EC50 of 0.72 and 0.88 μM respectively). Stimulates α7 nAChR induced ERK phosphorylation in vitro and enhances avoidance learning in mice. Also evokes Ca2+ transients in IMR-32 neuroblastoma cells, with similar potency to PNU 282987 (Cat.No. 2303).
分子量 | 306.79 |
公式 | C15H18N4O.HCl |
储存 | Store at +4°C |
纯度 | ≥98% (HPLC) |
PubChem ID | 132470911 |
InChI Key | SLZGVSXFCPFOOO-UHFFFAOYSA-N |
Smiles | N12CCC(N(C3=NN=C(C4=CC=CC=C4)O3)CC2)CC1.Cl |
上方提供的技术数据仅供参考。批次相关数据请参见分析证书。
Tocris products are intended for laboratory research use only, unless stated otherwise.
参考文献是支持产品生物活性的出版物。
Kouhen et al (2009) Pharmacology of α7 nicotinic acetylcholine receptor mediated extracellular signal-regulatedkinase signalling in PC12 cells. Br.J.Pharmacol. 156 638 PMID: 19226255
Briggs et al (2009) Role of channel activation in cognitive enhancement mediated by α7 nicotinic acetylcholine receptors. Br.J.Pharmacol. 158 1486 PMID: 19845675
Ween et al (2010) α3* and α7 nAChR-mediated Ca2+ transient generation in IMR-32 neuroblastoma cells. Neurochem.Int. 57 269 PMID: 20558224
关键词: NS 6784 hydrochloride, NS 6784 hydrochloride supplier, NS6784, HCl, 677723-97-6, alpha, 7, nicotinic, acetylcholine, receptors, activators, activates, agonists, nAChRs, Nicotinic, (a7), Receptors, 6140, Tocris Bioscience
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