N-Methylcytisine

本公司产品仅用于科研实验，不得用于人体或动物的临床与诊断

N-甲基金雀花碱和 N,N-二甲基金雀花碱在 0.1 mM 浓度下并未取代 14C-筒箭毒碱，金雀花碱是 14C-筒箭毒碱特异性结合的唯一有效抑制剂 (Ki=7 nM)。

N-Methylcytisine's nicotinic receptors have high affinity (KD = 5 nM)to nAChR from squid optical ganglia. N-Methylcytisine and N, N-dimethylcytisine did not displace 14C-tubocurarine at a concentration of .1 mM, cytisine was the only effective inhibitor of 14C-tubocurarine specific binding (Ki=7 nM).

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Caulophylline

JAK/STAT Signaling

STAT

Others

Others-Field

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486-86-2

204.27

C12H16N2O

>98% (HPLC)

In Vitro:?DMSO : 120 mg/mL (587.46 mM)

CN1CC2CC(C1)C3=CC=CC(=O)N3C2

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(-20℃)

With Ice Pack

≥ 2 years