1627710-50-2
中文名稱
2,6-二氟-4-[4-[4-(4-甲基-1-哌嗪基)苯基]-3-吡啶基]苯酚
英文名稱
1627710-50-2
CAS
1627710-50-2
分子式
C22H21F2N3O
分子量
381.42
MOL 文件
1627710-50-2.mol
更新日期
2025/02/05 16:39:32
1627710-50-2 結(jié)構(gòu)式
基本信息
中文別名
RSK抑制劑(LJH685)2,6-二氟-4-[4-[4-(4-甲基-1-哌嗪基)苯基]-3-吡啶基]苯酚
英文別名
LJH685CS-2182
LJH685(LJH-685)
LJH-685
LJH 685
LJH685
2,6-Difluoro-4-[4-[4-(4-methyl-1-piperazinyl)phenyl]-3-pyridinyl]phenol
Phenol, 2,6-difluoro-4-[4-[4-(4-methyl-1-piperazinyl)phenyl]-3-pyridinyl]-
所屬類別
生物化工：激動劑抑制劑物理化學性質(zhì)
沸點481.1±45.0 °C(Predicted)
密度1.257±0.06 g/cm3(Predicted)
儲存條件-20°C儲存
溶解度溶于二甲基亞砜
酸度系數(shù)(pKa)5.86±0.25(Predicted)
形態(tài)結(jié)晶固體
顏色White to off-white
2,6-二氟-4-[4-[4-(4-甲基-1-哌嗪基)苯基]-3-吡啶基]苯酚價格(試劑級)
| 報價日期 | 產(chǎn)品編號 | 產(chǎn)品名稱 | CAS號 | 包裝 | 價格 |
| 2025/02/08 | HY-19712 | 2,6-二氟-4-[4-[4-(4-甲基-1-哌嗪基)苯基]-3-吡啶基]苯酚 LJH685 | 1627710-50-2 | 1 mg | 431元 |
| 2025/02/08 | HY-19712 | 2,6-二氟-4-[4-[4-(4-甲基-1-哌嗪基)苯基]-3-吡啶基]苯酚 LJH685 | 1627710-50-2 | 5mg | 800元 |
| 2025/02/08 | HY-19712 | 2,6-二氟-4-[4-[4-(4-甲基-1-哌嗪基)苯基]-3-吡啶基]苯酚 LJH685 | 1627710-50-2 | 10mM * 1mLin DMSO | 880元 |
常見問題列表
生物活性
LJH685 是一種有效的選擇性，ATP-競爭性的 RSK 抑制劑, 抑制 RSK1/2/3 生物活性, IC50 為 6、5、4 nM。靶點
IC50: 6 nM (RSK1), 5 nM (RSK1), 4 nM (RSK1)
體外研究
LJH685 (0.01-100 μM; 72 hours) efficiently inhibits the growth of MDA-MB-231 and H358 cells in soft agar with EC 50 s of 0.73 and 0.79 μM, respectively. LJH685 (0.1-10 μM; 4 hours) efficiently reduces phosphorylation of YB1 at submicromolar concentrations and causes nearly complete inhibition at higher concentrations.
Cell Proliferation Assay
| Cell Line: | MDA-MB-231, H358 cells |
| Concentration: | 0.01, 0.1, 1, 10, 100 μM |
| Incubation Time: | 72 hours |
| Result: | The growth in soft agar was efficiently inhibited with EC 50 values of 0.73 and 0.79 μM in MDA-MB-231 and H358, respectively. |
Western Blot Analysis
| Cell Line: | MDA-MB-231, H358 cells |
| Concentration: | 0.1, 0.3, 1, 3, 10 μM |
| Incubation Time: | 4 hours |
| Result: | Efficiently reduced phosphorylation of YB1 at submicromolar concentrations and caused nearly complete inhibition at higher concentrations. |