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- Gemcitabine

- Gemcitabine
产品描述 描述 Gemcitabine is a nucleoside metabolic inhibitor in PANC1(IC50=50 nM), MIAPaCa2(IC50=40 nM), BxPC3(IC50=18 nM) and Capan2 cells(IC50=12 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 别名 吉西他滨;NSC 613327;LY188011外观 白色至浅黄色粉末可溶性/溶解性 DMSO : 15 mg/mL (56.99 mM)生物活性 靶点 DNA_RNA SynthesisIn vitro(体外研究) MTS assay demonstrates that Gemcitabine at 15 nM, indole-3-carbinol (I3C) at 50 μM and the combination does not affect hTERT-HPNE cell viability. However, treatment with Gemcitabine at 15 nM, I3C at 50 μM and the combination results in 31%, 19% and 72% cell death of BxPC-3 cells, respectively.In vivo(体内研究) Treatment of the LSL-KrasG12D/+; LSL-Trp53R172H; Pdx-1-Cre mice with either Gemcitabine (50 mg/kg, i.p.) or the combination DMAPT/Gemcitabine significantly increased the median survival time by more than 30 days compared to the placebo group (254.5 or 255 days vs. 217.5 days, respectively). Gemcitabine can be administered via endotracheal spray in rats without marked toxicity with a maximum tolerated dose of 4 mg/kg once a week for 9 weeks. The toxicity of Gemcitabine is lower via lung than oral administration at dosages of 2, 4, and 6 mg/kg.参考文献 参考文献 1. Hastak K, et al. Cancer Res. 2010 Aug 26.
2. Kunnumakkara AB, et al. Cancer Res, 2007, 67(8), 3853-3861.
3. Rosell R, et al. Oncology (Williston Park). 2004 Nov;18(13 Suppl 8):70-6.
4. Vernejoul F, et al. Mol Ther. 2006 Dec; 14(6):758-67.
5. Ledermann JA, et al. Clin Cancer Res. 2010 Aug 18.
研究领域 研究领域 CancerCancer MetabolismCancerTumor biomarkersCancerTumor immunologyDrug DiscoverySmall Molecule DrugLead Compound Discovery温馨提示:本产品仅作科研实验使用,不支持临床等研究
