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- TP0903 1341200-45-0

- TP0903 1341200-45-0
TP0903 1341200-45-0
产品描述 描述 TP-0903 is a potent and selective Axl kinase inhibitor with IC50 of 27 nM.纯度 98%储存/保存方法 Store at -20℃ for one year(Powder);Store at 2-4℃ for two weeks;Store at -20℃ for six months after dissolution.基本信息 可溶性/溶解性 10 mM in DMSO生物活性 靶点 AxlIn vitro(体外研究) In pancreatic cancer cells (PSN-1), TP-0903 shows strong antiproliferative activity with IC50 of 6 M. TP-0903 also induces strong G2/M arrest by potently inhibiting Aurora A and B. In CLL B cells from all the patients with CLL, TP-0903 causes a dose-dependent induction of massive apoptosis by targeting phosphorylated Axl, and overcomes CLL BMSC-mediated protection of CLL B cells from apoptosis.In vivo(体内研究) In the adult rat hippocampus, the intracerebroventricular administration of SAG (2.5 nM) significantly increases the number of newly generated cells and extends survival of hippocampal cells. In mice, SAG (20 μg/g, i.p.) effectively prevents GC-induced neonatal cerebellar developmental abnormalities.参考文献 参考文献 1. Feneyrolles C, et al. Mol Cancer Ther. 2014 Sep;13(9):2141-8.
2. Mollard A, et al. ACS Med Chem Lett. 2011 Dec 8;2(12):907-912.
研究领域 研究领域 CancerCell cycleKinases/phosphatasesOtherCancerOncoproteins/suppressorsOncoproteinsSignal transducersCancerSignal transductionOtherCell CycleKinases/PhosphatasesOtherNeuroscienceProcessesSignal TransductionProtein PhosphorylationTyrosine KinasesReceptor Tyrosine KinasesTags & Cell MarkersCell Type MarkersTumor AssociatedDrug DiscoverySmall Molecule DrugLead Compound DiscoveryTP0903 1341200-45-0温馨提示:本产品仅作科研实验使用,不支持临床等研究
