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SR18662

    
99.80%

(E)-3-(3,4-dichlorophenyl)-N-(2-(4-(methylsulfonyl)piperazin-1-yl)-2-oxoethyl)acrylamide

源叶(MedMol)
S89294 一键复制产品信息
2505001-62-5
C16H19Cl2N3O4S
420.31
货号 规格 价格 上海 北京 珠海 重庆 武汉 购买数量
S89294-5mg买3赠1
99.80%

¥360.00

6 - - - -
S89294-10mg买3赠1
99.80%

¥640.00

6 - - - -
S89294-25mg促销
99.80%

¥1160.00 ¥928.00

5 - - - -
S89294-100mg促销
≥98%

¥2870.00 ¥2290.00

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: SR18662 是一种基于ML264的优化化合物,可抑制 Krüppel-like factor 5 (KLF5) 对应的IC50值为4.4 nM。SR18662 可降低多种结直肠癌细胞系的生存能力并诱导凋亡
靶点: KLF5(Cell-free assay):4.4 nM
体内研究: A significant dose-dependent inhibition of xenograft growth in mice is observed following SR18662 treatment that exceeds the effect of ML264 at equivalent doses. SR18662 is potential for colorectal cancer therapy.
细胞实验: Cell lines: DLD-1, HCT116, HT29 and SW620 colorectal cancer cell lines Concentrations: 0.001 μM-20 μM Incubation Time: 24 h Method: KLF5 promoter activity assay: DLD-1/pGL4.18hKLF5p cells are seeded in 96 well plate format and treated with DMSO or with SR18662 dissolved in DMSO in the range of 0.001 to 20 μM final concentration for 24 h and the human KLF5 promoter activity is determined with the ONE-Glo luciferase assay system using a SpectramMax M3 plate reader.
动物实验: Animal Models: 7-week-old male NuJ/Foxn1nu mice with DLD-1 human colorectal cells injected Dosages: 5 mg/kg, 10 mg/kg, 25 mg/kg Administration: IP
参考文献: 1. Julie Kim, et al. Mol Cancer Ther. 2019 Nov;18(11):1973-1984.
溶解性: Soluble  in  DMSO
保存条件: 2-8℃
配置溶液浓度参考:
1mg 5mg 10mg
1 mM 2.379 ml 11.896 ml 23.792 ml
5 mM 0.476 ml 2.379 ml 4.758 ml
10 mM 0.238 ml 1.19 ml 2.379 ml
50 mM 0.048 ml 0.238 ml 0.476 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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