Chemical Structure : LY2584702
CAS No.: 1082949-67-4
货号: PC-43058Not For Human Use, Lab Use Only.
LY2584702 is a potent, selective, ATP-competitive inhibitor of P70 S6 kinase-1 (p70S6K1) with IC50 of 4 nM.
| 规格 | 价格 | 库存 | 数量 |
|---|---|---|---|
| 5 mg | ¥780 | In stock | |
| 10 mg | ¥1180 | In stock | |
| 25 mg | ¥2180 | In stock | |
| 50 mg | Get quote | ||
| 100 mg | Get quote |
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LY2584702 is a potent, selective, ATP-competitive inhibitor of P70 S6 kinase-1 (p70S6K1) with IC50 of 4 nM.
LY2584702 blocks phosphorylation of p70S6K in primary rat hepatocytes without affecting the phosphorylation of other signaling kinases, including GSK-3β and ERK1/2.
LY2584702 inhibits phosphorylation of p70S6K in HCT116 colon cancer cells with IC50 of 0.1-0.24 uM, demonstrates significant antitumor efficacy in both U87MG glioblastoma and HCT116 colon carcinoma xenograft models.
| 分子量 | 445.4161 | |
| 分子式 | C21H19F4N7 | |
| 外观性状 | Solid | |
| 储存条件 |
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| Solubility |
DMSO: ≥ 4.5 mg/mL |
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| Chemical Name/SMILES |
1H-Pyrazolo[3,4-d]pyrimidine, 4-[4-[4-[4-fluoro-3-(trifluoromethyl)phenyl]-1-methyl-1H-imidazol-2-yl]-1-piperidinyl]- |
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1. Estridge TB, et al. J Pharmacol Exp Ther. 2017 Jul;362(1):108-118.
2. Tolcher A, et al. Eur J Cancer. 2014 Mar;50(5):867-75.
3. Hollebecque A, et al. Eur J Cancer. 2014 Mar;50(5):876-84.
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