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PKC-θ抑制剂

    
98%

PKC-theta inhibitor

源叶(MedMol)
S88708 一键复制产品信息
736048-65-0
C20H25F3N6O3
454.45
MDK-8650
货号 规格 价格 上海 北京 珠海 重庆 武汉 购买数量
S88708-2mg促销
98%

¥556.00 ¥500.00

10 - - - -
S88708-5mg促销
98%

¥1110.00 ¥999.00

10 2 - - -
S88708-10mg促销
98%

¥1850.00 ¥1660.00

10 2 - - -
S88708-25mg促销
98%

¥3700.00 ¥3330.00

10 - - - -
S88708-50mg促销
98%

¥5840.00 ¥5250.00

10 - - - -
S88708-100mg促销
98%

¥9260.00 ¥8340.00

6 - - - -
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: PKC-theta inhibitor (compound 20) 可抑制PKC-θ,IC50值为18 nM
靶点: PKCθ:18 nM;PKC
体外研究: PKC-theta inhibitor (compound 20) inhibits PKC-θ.
体内研究: Compound 20 is a potent inhibitor of Protein Kinase C θ (PKC-θ). It improves muscle performance in the mdx mice model of Duchenne muscular dystrophy.
细胞实验: Cell lines: MN9D cells Concentrations: 5 μM Incubation Time: 24 h Method: PKCθ inhibitor was dissolved in DMSO at 5 mM and diluted to the working concentration (5 μM) and cells were incubated with PKCθ inhibitor was 24 h.
动物实验: Animal Models: C57BL/6 mice Dosages: 10 mg/kg Administration: i.p.
参考文献: 1. Cywin CL, et al. Discovery of potent and selective PKC-theta inhibitors. Bioorg Med Chem Lett. 2007, 17(1):225-30. 2. Gong J, et al. 4,4'-Dimethoxychalcone regulates redox homeostasis by targeting riboflavin metabolism in Parkinson's disease therapy. Free Radic Biol Med. 2021 Oct;174:40-56. 3. Marroco V, et al. Pharmacological Inhibition of PKCθ Counteracts Muscle Disease in a Mouse Model of Duchenne Muscular Dystrophy. EBioMedicine. 2017 Feb;16:150-161.
溶解性: Soluble  in  DMSO、Ethanol
保存条件: -20°C
配置溶液浓度参考:
1mg 5mg 10mg
1 mM 2.2 ml 11.002 ml 22.005 ml
5 mM 0.44 ml 2.2 ml 4.401 ml
10 mM 0.22 ml 1.1 ml 2.2 ml
50 mM 0.044 ml 0.22 ml 0.44 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

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