Information LJH685 LJH685 is a potent pan- RSK inhibitor with IC50 of 6 nM, 5 nM and 4 nM for RSK1, RSK2, and RSK3, respectively. Targets RSK3 (Cell-free assay); RSK2 (Cell-free assay); RSK1 (Cell-free assay) 4 nM; 5 nM; 6 nM In vitro LJH685 modulates YB1 phosphorylation by potently and selectively inhibiting RSK in cells. In MAPK pathway–dependent cancer cell lines, LJH685 shows antiproliferative effects, and causes cell-cycle regulation and apoptosis induction. Cell Research(from reference) Cell lines:Calu6, NCI-H2122, NCI-H358, NCI-H727, NCI-H2087, SW620, SW480, HT29, Capan-2, MiaPaCa2, SW1990, Panc02.03, MDA-MB-231, A375, G361, Colo205, Malme3M, WM1799, WM983B and WM266-4 cells Concentrations:~100 μM Incubation Time:72 h
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LJH685
CAS number:1627710-50-2 molecular formula:C22H21F2N3O
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| Chinese alias | - | ||
| English alias | CCG-268422 | AKOS030526619 | 2,6-difluoro-4-[4-[4-(4-methylpiperazin-1-yl)phenyl]-3-pyridyl]phenol | LJH 685 | Phenol, 2,6-difluoro-4-(4-(4-(4-methyl-1-piperazinyl)phenyl)-3-pyridinyl)- | MS-26250 | LJH685 | LJH-685 | F85376 | HY-19712 | Q27453129 | EX-A2 | ||
| CAS number | 1627710-50-2 | molecular formula | C22H21F2N3O |
| molecular weight | 381.42 g/mol | Exact mass | ≥98% |
| PSA | 39.600 Ų | logp | 3.900 |
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