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FGFR1 inhibitor-6
本产品不向个人销售,仅用作科学研究,不用于任何人体实验及非科研性质的动物实验。
FGFR1 inhibitor-6图片

FGFR1 inhibitor-6 是一种有效的 FGFR1 抑制剂,IC50值为 16.31 nM。FGFR1 inhibitor-6 显示出细胞毒活性。FGFR1 inhibitor-6 诱导细胞凋亡 (apoptosis) 和细胞周期停滞在前 G1 和 G2/M 期。
生物活性

FGFR1inhibitor-6 is a potentFGFR1inhibitor with anIC50value of 16.31 nM.FGFR1inhibitor-6 shows cytotoxic activities.FGFR1inhibitor-6 inducesapoptosisand cell cycle arrest at pre-G1 and G2/M phase[1].

IC50& Target[1]

FGFR1

16.31 nM (IC50)

体外研究
(In Vitro)

FGFR1 inhibitor-6 (compound 3) (48 h) shows cytotoxic activities with IC50s of 2.06, 0.73, 97.2 μM for HepG-2, MCF-7, WI-38 cells, respectively[1].
FGFR1 inhibitor-6 (0.73 μM; 24 h) induces apoptosis and cell cycle arrest at pre-G1 and G2/M phase[1].
FGFR1 inhibitor-6 (0.73 μM; 24 h) increases the expression of caspase-3/7/9 protein levels in MCF-7 cells[1].

Cell Cytotoxicity Assay[1]

Cell Line:HepG-2, MCF-7, WI-38 cells
Concentration:
Incubation Time:48 h
Result:Showed cytotoxic activities with IC50s of 2.06, 0.73, 97.2 μM for HepG-2, MCF-7, WI-38 cells, respectively.

Cell Cycle Analysis[1]

Cell Line:MCF-7 cells
Concentration:0.73 μM
Incubation Time:24 h
Result:Induced pronounced increase in the cell percentages at pre-G1 and G2/M phase at 27.72% and 19.22%, respectively.

Apoptosis Analysis[1]

Cell Line:MCF-7 cells
Concentration:0.73 μM
Incubation Time:24 h
Result:Induced apoptosis with late apoptosis percentages are 11.24 % and the early apoptosis percentages from 1.59% to 5.07%.

Western Blot Analysis[1]

Cell Line:MCF-7 cells
Concentration:0.73 μM
Incubation Time:24 h
Result:Increased the expression of caspase-3/7/9 protein levels with the caspase-3, aspase-7, aspase-9 protein levels increased to 5.60, 11.62, 7.14 folds, respectively comparing with the untreated cells.
分子量

541.60

Formula

C27H19N5O4S2

运输条件

Room temperature in continental US; may vary elsewhere.

储存方式

Please store the product under the recommended conditions in the Certificate of Analysis.

 
 
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