S85678 |
UF010 |
源叶(MedMol) | 98% |
- 提示:详情请下载说明书。
- 产品描述: UF010是I类HDAC选择性抑制剂,对HDAC1、HDAC2、HDAC3、HDAC8、HDAC6和HDAC10的IC50值分别为0.5 nM、0.1 nM、0.06 nM、1.5 nM、9.1 nM和15.3 nM
- 靶点: HDAC3(Cell-free assay):0.06 nM; HDAC2(Cell-free assay):0.1 nM; HDAC1(Cell-free assay):0.5 nM; HDAC8(Cell-free assay):1.5 nM; HDAC6(Cell-free assay):9.1 nM; HDAC10:15.3 nM;HDAC
- 体外研究:
In Cell-cycle analysis using MDA-MB-231 cells, UF010 mainly blocks G1/S transition with an increased G1 cell population and a reduced cell population in the S phase in a dose-dependent manner. UF010 has a half-life of 15.8 hr in cell culture medium containing 10% fetal bovine serum
- 细胞实验: Cell lines: HCT116 cells and A549 cells Concentrations: 2 μM Incubation Time: 1 h Method: HCT116 and A549 cells are exposed to DMSO or etoposide (Etop, 10 μM) for 6 hr. TSA (0.2 μM), MS-275, and UF010 (2 μM) are added 1 hr before cell lysis. The total cell lysates are subject to western blotting with antibodies to the indicated proteins. PCNA is detected as a loading control.
- 参考文献:
1. Wang Y, et al. Identification of histone deacetylase inhibitors with benzoylhydrazide scaffold that selectively inhibit class I histone deacetylases. Chem Biol. 2015, 22(2):273-84.
- 溶解性: Soluble in DMSO、Ethanol
- 保存条件: -20℃
- 配置溶液浓度参考:
1mg 5mg 10mg 1 mM 3.688 ml 18.44 ml 36.879 ml 5 mM 0.738 ml 3.688 ml 7.376 ml 10 mM 0.369 ml 1.844 ml 3.688 ml 50 mM 0.074 ml 0.369 ml 0.738 ml
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质量 (mg) = 浓度 (mM) x 体积 (mL) x 分子摩尔量 (g/mol)