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GNE-274

    
≥98%

源叶(MedMol)
V48061 一键复制产品信息
2369048-69-9
C29H31NO4
457.57
货号 规格 价格 上海 北京 珠海 重庆 武汉 购买数量
V48061-1mg
≥98%

¥2990.00

货期:3-5天 - - - -
V48061-5mg
≥98%

¥6630.00

货期:3-5天 - - - -
产品介绍 参考文献 质检证书(COA) 摩尔浓度计算器 相关产品
产品描述: GNE-274 is a structural analog of the ER degrader GDC-0927 and is a non-degrader. GNE-274 does not induce conversion of ER in breast cancer cell lines and functions as a partial ER agonist (partial ER agonist). GNE-274 increases the chromatin accessibility of ER-DNA binding sites, whereas GDC-0927 does not. GNE-274 is an effective ER ligand binding domain (LBD) inhibitor. GNE-274 can be used in cancer research.
体外研究: GNE-274 (0.1 nM-1000 nM; 4 hours) fails to trigger increased ER turnover in MCF7, MD-134, HCC1500 and CAMA cells.
GNE-274 (1-1000 nM; 7-10 days) potently inhibits cellular proliferation, exhibiting greater potency than fulvestrant, 4-OHT, AZD9496, and GDC-0810 in E2-stimulated ER+ breast cancer cell lines.
In transposaseaccessible chromatin sequencing (ATAC-seq) assay, GNE-274 increase chromatin accessibility at ER-DNA binding sites, it significantly alters chromatin accessibility at 594 sites. But GDC-0927 has considerably less impact on chromatin accessibility.
保存条件: 2-8°C, 避光, 氮气保存
配置溶液浓度参考:
1mg 5mg 10mg
1 mM 2.185 ml 10.927 ml 21.855 ml
5 mM 0.437 ml 2.185 ml 4.371 ml
10 mM 0.219 ml 1.093 ml 2.185 ml
50 mM 0.044 ml 0.219 ml 0.437 ml
注意: 部分产品我司仅能提供部分信息,我司不保证所提供信息的权威性,仅供客户参考交流研究之用。

参考文献

质检证书(COA)

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摩尔浓度计算器

质量 (mg) = 浓度 (mM) x 体积 (mL) x 分子摩尔量 (g/mol)

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