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TrkA-IN-6
MCE 国际站:TrkA-IN-6
产品活性:TrkA-IN-6 (compound R48) 是原肌球蛋白激酶 A 型受体激酶 (TrkA) 的腙类、选择性抑制剂。TrkA-IN-6 对 U87 GBM 细胞表现出比 Temozolomide (HY-17364) 更高的细胞毒性作用,IC50 为 68.99 μM。
研究领域:Neuronal Signaling | Protein Tyrosine Kinase/RTK
作用靶点:Trk Receptor
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文献和实验Network-Based Analysis of Multivariate Gene Expression Data
procedures that do not use the pathway information, with similar observed false discovery rates. We applied the proposed methods for analysis of a microarray time course gene expression study of TrkA- and TrkB-transfected neuroblastoma cell lines
The Neurotrophin Family of Neurotrophic Factors: An Overview
. Biological effects of each of the four mammalian neurotrophins are mediated through activation of one or more of the three members of the tropomyosin-related kinase (Trk) family of receptor tyrosine kinases (TrkA, TrkB, and TrkC). In addition
痛敏。最近研究已经显示,ERK级联反应发生于肾上腺素引发的痛敏,Ras-MEK-ERK-CREB(cAMP反应元件结合蛋白)通路不依赖PKA或PKC而被激活。将NGF注入外周组织,能增加p-ERK(磷酸化的ERK)标记的酪氨酸(trkA)阳性DRG神经元。然而只有少数信号传导研究涉及到初级传入神经元的活动依赖性研究。已经证实,在外周组织的伤害性刺激或外周神经的电刺激过程中初级传入神经元(DRG神经元)中ERK的活动依赖性激活,一种MEK抑制剂U0126能剂量依赖性减轻辣椒素注射后的热痛
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