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C646

    
99.99%

C646

源叶(MedMol)
S80643 一键复制产品信息
328968-36-1
C24H19N3O6
445.42
4-[4-[[5-(4,5-二甲基-2-硝基苯基)-2-呋喃基]亚甲基]-4,5-二氢-3-甲基-5-氧代-1H-吡唑-1-基]-苯甲酸
货号 规格 价格 上海 北京 珠海 重庆 武汉 购买数量
S80643-2mg买3赠1
99.99%

¥232.00 ¥200.00

3 - - - -
S80643-5mg买3赠1
≥98%

¥360.00 ¥320.00

货期:2-3天 - - - -
S80643-10mg买3赠1
99.99%

¥640.00 ¥570.00

4 - - - -
S80643-25mg买3赠1
99.99%

¥1560.00 ¥1400.00

7 - - - -
S80643-50mg买3赠1
99.99%

¥2480.00 ¥2230.00

1 - - - -
S80643-100mg买3赠1
≥98%

¥4560.00 ¥4100.00

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: C646 is a selective and competitive histone acetyltransferase p300 inhibitor with Ki of 400 nM, and is less potent for other acetyltransferases
靶点: Ki: 400 nM (histone acetyltransferase p300);Apoptosis;EpigeneticReaderDomain;HistoneAcetyltransferase;Autophagy
体内研究: Suppression of P300 by c646 (intraperitoneally injected, 30 nmol/g/d for 2 weeks) dramatically reduces the level of blood glucose in db/db mice
参考文献: 1. Bowers EM, et al. Virtual ligand screening of the p300/CBP histone acetyltransferase: identification of a selective small molecule inhibitor. Chem Biol. 2010 May 28;17(5):471-82. 2. Oike T, et al. C646, a selective small molecule inhibitor of histone acetyltransferase p300, radiosensitizes lung cancer cells by enhancing mitotic catastrophe. Radiother Oncol. 2014 May;111(2):222-7. 3. Zheng WW, et al. EDAG positively regulates erythroid differentiation and modifies GATA1 acetylation through recruiting p300. Stem Cells. 2014 Aug;32(8):2278-89. 4. Zhen Fan, et al. Type 2 diabetes-induced overactivation of P300 contributes to skeletal muscle atrophy by inhibiting autophagic flux. Life Sci. 2020 Aug 10;258:118243.
溶解性: DMSO  :  16.67  mg/mL  (37.43  mM;  Need  ultrasonic)
保存条件: 2-8℃
配置溶液浓度参考:
1mg 5mg 10mg
1 mM 2.245 ml 11.225 ml 22.451 ml
5 mM 0.449 ml 2.245 ml 4.49 ml
10 mM 0.225 ml 1.123 ml 2.245 ml
50 mM 0.045 ml 0.225 ml 0.449 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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