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358721-70-7

中文名稱 UBCS039
英文名稱 UBCS039
CAS 358721-70-7
分子式 C16H13N3
分子量 247.29
MOL 文件 358721-70-7.mol
更新日期 2024/04/02 15:36:40
358721-70-7 結構式 358721-70-7 結構式

基本信息

中文別名
化合物UBCS039
4-(吡啶-3-基)-4,5-二氫吡咯并[1,2-A]喹喔啉
英文別名
UBCS039
Pyrrolo[1,2-a]quinoxaline, 4,5-dihydro-4-(3-pyridinyl)-
所屬類別
有機原料:雜環(huán)化合物

物理化學性質

沸點453.9±45.0 °C(Predicted)
密度1.25±0.1 g/cm3(Predicted)
儲存條件Sealed in dry,2-8°C
溶解度DMSO : 125 mg/mL (505.48 mM)
酸度系數(pKa)4.66±0.12(Predicted)
形態(tài)Solid
顏色Light yellow to yellow

安全數據

危險性符號(GHS)GHS hazard pictograms
GHS07
警示詞警告
危險性描述H302-H315-H319-H335

常見問題列表

生物活性
UBCS039是第一個合成的SIRT6激活劑,EC50為38 μM,在多種人類腫瘤細胞系中均可誘導自噬的時間依賴性激活。
靶點
TargetValue
SIRT6
(Cell-free assay)
38 μM(EC50)
體外研究

UBCS039 (75 μM, 48 or 72 hours) induces deacetylation of SIRT6-targeted histone H3 sites in human cancer cells.
UBCS039 leads to autophagosome accumulation in human cancer cells.
UBCS039 induces autophagy via AMP-activated protein kinase (AMPK) signaling pathway activation.

Western Blot Analysis

Cell Line: Human H1299 cells.
Concentration: 75 μM.
Incubation Time: 48 and 72 hours.
Result: Induced deacetylation of SIRT6-targeted histone H3 sites in human H1299 cells.

Western Blot Analysis

Cell Line: Human H1299 cells.
Concentration: 75 μM.
Incubation Time: 48 and 72 hours.
Result: Induced deacetylation of SIRT6-targeted histone H3 sites in human H1299 cells.

Cell Proliferation Assay

Cell Line: Human H1299 cells.
Concentration: 100 μM.
Incubation Time: 48 and 72 hours.
Result: Led to a strong decrease of cell proliferation in a dose-dependent manner when compared with control or DMSO-treated cells, starting from day 3 of growth (48 h after treatment) in both H1299 and HeLa cell lines.
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