产品描述: | ACSS2 inhibitor 是有效的、特异性的乙酰辅酶A合成酶2 (ACSS2)抑制剂。ACSS2 inhibitor 还可抑制呼吸道合胞体病毒(RSV) |
靶点: |
ACSS2(Cell-free assay):~0.6 μM;RSV;FattyAcidSynthase |
体外研究: |
ACSS2 inhibitor抑制HepG2细胞将[14C]acetate整合入脂质中,IC50为6.8 μM。它能够抑制HepG2细胞利用[14C]acetate进行组蛋白乙酰化,IC50为5.5 μM |
细胞实验: |
Cell lines: MDA-MB-231-R cells Concentrations: 10 uM Incubation Time: 6 h Method: 10 µM of ACSS2 inhibitor was added in flag-WT or KR-STAT3 expressing MDA-MB-231-R cells and incubated for 6 h. |
动物实验: |
Animal Models: Female C57BL/6J mice Dosages: 15 mg/kg Administration: i.p. |
参考文献: |
1. Comerford SA, et al. Acetate dependence of tumors. Cell. 2014, 159(7):1591-602. 2. Li YJ, et al. Fatty acid oxidation protects cancer cells from apoptosis by increasing mitochondrial membrane lipids. Cell Rep. 2022 May 31;39(9):110870. 3. Hao F, et al. Butyrate enhances CPT1A activity to promote fatty acid oxidation and iTreg differentiation. Proc Natl Acad Sci U S A. 2021 Jun 1;118(22):e2014681118. |
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 |
2.436 ml |
12.18 ml |
24.36 ml |
5 mM |
0.487 ml |
2.436 ml |
4.872 ml |
10 mM |
0.244 ml |
1.218 ml |
2.436 ml |
50 mM |
0.049 ml |
0.244 ml |
0.487 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。 |