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Droxinostat

    
99.70%

Droxinostat

源叶(MedMol)
S81186 一键复制产品信息
99873-43-5
C11H14ClNO3
243.69
MFCD01326592
4-(4-chloro-2-methylphenoxy)-N-hydroxybutanamide
货号 规格 价格 上海 北京 珠海 重庆 武汉 购买数量
S81186-5mg促销
99.70%

¥98.00 ¥78.00

6 - - - -
S81186-10mg促销
99.70%

¥180.00 ¥144.00

7 - - - -
S81186-25mg促销
99.70%

¥360.00 ¥288.00

5 - - - -
S81186-50mg促销
99.70%

¥560.00 ¥448.00

5 - - - -
S81186-100mg促销
≥98%

¥1070.00 ¥856.00

货期:2-3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: Droxinostat is a selective inhibitor of HDAC, mostly for HDACs 6 and 8 with IC50 of 2.47 μM and 1.46 μM, greater than 8-fold selective against HDAC3 and no inhibition to HDAC1, 2, 4, 5, 7, 9, and 10.
靶点: Apoptosis;HDAC;Apoptosis; HDAC
体内研究: In SCID mice models, Droxinostat (30 μM)-treated PPC-1 cells results in decreased distant tumor formation than untreated cells.
细胞实验: PPC-1 cells (1 × 104) are seeded overnight into 96-well flat-bottomed plates in 100 μL of medium containing 2.5% FCS. The next day, Droxinostat is added. CH-11 antibody (100 ng/mL) is then added and the cells are incubated for 24 hours before assessing cell viability by 3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyltetrazolium bromide (MTT) dye reduction assay.(Only for Reference)
参考文献: 1.Wood TE, et al. Mol Cancer Ther, 2010, 9(1), 246-256. 2.Bijangi-Vishehsaraei K, et al. Mol Cell Biochem, 2010, 342(1-2), 133-142. 3.Mawji IA, et al. J Natl Cancer Inst, 2007, 99(10), 811-822. 4.Schimmer AD, et al. Cancer Res, 2006, 66(4), 2367-2375.
溶解性: DMSO:46  mg/mL  (188.8  mM)    Ethanol:46  mg/mL  (188.8  mM)    H2O:<1  mg/mL
保存条件: -20℃
配置溶液浓度参考:
1mg 5mg 10mg
1 mM 4.104 ml 20.518 ml 41.036 ml
5 mM 0.821 ml 4.104 ml 8.207 ml
10 mM 0.41 ml 2.052 ml 4.104 ml
50 mM 0.082 ml 0.41 ml 0.821 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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