天堂网亚洲,天天操天天搞,91视频高清,菠萝蜜视频在线观看入口,美女视频性感美女视频,95丝袜美女视频国产,超高清美女视频图片

返回ChemicalBook首頁>CAS數(shù)據(jù)庫列表>796888-12-5

796888-12-5

中文名稱 LCH-7749944
英文名稱 LCH-7749944
CAS 796888-12-5
分子式 C20H22N4O2
分子量 350.41
MOL 文件 796888-12-5.mol
更新日期 2024/12/15 19:35:17
796888-12-5 結(jié)構(gòu)式 796888-12-5 結(jié)構(gòu)式

基本信息

中文別名
化合物L(fēng)CH-7749944
英文別名
GNF-PF-2356
LCH-7749944
LCH-7749944, GNF-PF-2356
2,4-Quinazolinediamine, N2-(3-methoxyphenyl)-N4-[(tetrahydro-2-furanyl)methyl]-

物理化學(xué)性質(zhì)

沸點(diǎn)580.0±58.0 °C(Predicted)
密度1.272±0.06 g/cm3(Predicted)
儲(chǔ)存條件Keep in dark place,Sealed in dry,2-8°C
溶解度DMSO: 250 mg/mL (713.45 mM)
酸度系數(shù)(pKa)7.68±0.30(Predicted)
形態(tài)Solid
顏色White to off-white
LCH-7749944價(jià)格(試劑級(jí))
報(bào)價(jià)日期產(chǎn)品編號(hào)產(chǎn)品名稱CAS號(hào)包裝價(jià)格
2024/11/08HY-125035LCH-7749944
LCH-7749944
796888-12-55mg1980元
2024/11/08HY-125035LCH-7749944
LCH-7749944
796888-12-510mM * 1mLin DMSO2178元
2024/11/08HY-125035LCH-7749944
LCH-7749944
796888-12-510mg2873元

常見問題列表

生物活性
LCH-7749944 (GNF-PF-2356) 是一種有效的 PAK4 抑制劑,IC50 為 14.93 μM。LCH-7749944通過下調(diào) PAK4/c-Src/EGFR/cyclin D1 途徑有效抑制人胃癌細(xì)胞的增殖,并誘導(dǎo)凋亡 (apoptosis)。
靶點(diǎn)

PAK4

14.93 μM (IC 50 )

體外研究

LCH-7749944 (GNF-PF-2356; 5-50 μM; 24 hours) inhibits the proliferation of MKN-1, BGC823, SGC7901 and MGC803 cells in a concentration dependent manner.
LCH-7749944 (5-20 μM; 12-48 hours) induces apoptosis of SGC7901 cells.
LCH-7749944 (5-20 μM; 12-48 hours) prominently induces a dose-dependent increase in the percentage of cells in G1 phase and decrease in S phase.
LCH-7749944 (5-30 μM; 24 hours) dramatically decreases levels of phosphoPAK4, phospho-c-Src, phospho-EGFR and cyclin D1 protein expression in a dose-dependent manner.

Cell Proliferation Assay

Cell Line: MKN-1, BGC823, SGC7901 and MGC803 human gastric cancer cells
Concentration: 5, 10, 15, 20, 25, 30, 35, 40, 45, 50 μM
Incubation Time: 24 hours
Result: Inhibited the proliferation of MKN-1, BGC823, SGC7901 and MGC803 cells in a concentration dependent manner.

Apoptosis Analysis

Cell Line: SGC7901 cells
Concentration: 5, 10, 20 μM
Incubation Time: 12, 24, 48 hours
Result: Induced apoptosis of SGC7901 cells.

Cell Cycle Analysis

Cell Line: SGC7901 cells
Concentration: 5, 10, 20 μM
Incubation Time: 12, 24, 48 hours
Result: Prominently induced a dose-dependent increase in the percentage of cells in G1 phase and decrease in S phase.

Western Blot Analysis

Cell Line: SGC7901 cells
Concentration: 5, 10, 20, 30 μM
Incubation Time: 24 hours
Result: Dramatically decreased levels of phosphoPAK4, phospho-c-Src, phospho-EGFR and cyclin D1 protein expression in a dose-dependent manner.
"796888-12-5" 相關(guān)產(chǎn)品信息