
ARN-3236
CAS No. 1613710-01-2
ARN-3236 ( ARN3236 )
产品货号. M12345 CAS No. 1613710-01-2
ARN-3236 是一种新型有效、选择性、口服活性的 SIK2 抑制剂,IC50 小于 1 nM。
纯度: >98% (HPLC)






规格 | 价格/人民币 | 库存 | 数量 |
5MG | ¥1021 | 有现货 |
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25MG | ¥2916 | 有现货 |
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50MG | ¥3645 | 有现货 |
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100MG | ¥5613 | 有现货 |
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200MG | 获取报价 | 有现货 |
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500MG | 获取报价 | 有现货 |
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1G | 获取报价 | 有现货 |
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生物学信息
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产品名称ARN-3236
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注意事项本公司产品仅用于科研实验,不得用于人体或动物的临床与诊断
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产品简述ARN-3236 是一种新型有效、选择性、口服活性的 SIK2 抑制剂,IC50 小于 1 nM。
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产品描述ARN-3236 is a novel potent, selective, and orally active SIK2 inhibitor with IC50 of <1 nM; does not significantly inhibit SIK1 and SIK3, as well as other AMPK family members; inhibits the growth of 10 ovarian cancer cell lines with IC50 of 0.8-2.6 uM; increasess centrosome uncoupling from nucleus, and inhibits centrosome splitting in mitotic cells; induces cell cycle arrest, apoptosis and tetraploidy, also inhibits AKT phosphorylation and attenuates survivin expression; sensitizes ovarian cancer to paclitaxel in SKOv3ip xenograft model.
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体外实验ARN-3236 inhibits SIK2 activity with an IC50 <1 nM.ARN-3236 inhibits cell growth and increases NSC 125973 sensitivity in ovarian cancer cells. Cell Viability Assay Cell Line:HEY and A2780 human ovarian cancer cell lines.Concentration:0-10 μM.Incubation Time:24 hours.Result:Inhibited SIK2 activity with an IC50 <1 nM.
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体内实验ARN-3236 (60 mg/kg, orally) sensitizes ovarian cancer to NSC 125973 in vivo. Animal Model:SKOv3ip-bearing mice and OVCAR8-bearing mice.Dosage:60 mg/kg.Administration:Orally once daily for 3 weeks (SKOv3ip-bearing mice) and 4 weeks (OVCAR8-bearing mice).Result:Sensitized ovarian cancer to NSC 125973.
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同义词ARN3236
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通路Autophagy
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靶点SIK
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受体SIK
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研究领域——
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适应症——
化学信息
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CAS Number1613710-01-2
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分子量336.409
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分子式C19H16N2O2S
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纯度>98% (HPLC)
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溶解度DMSO : 130 mg/mL. 386.43 mM
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SMILESCOC1=CC=C(C2=CNC3=NC=CC(C4=CSC=C4)=C32)C(OC)=C1
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化学全称3-(2,4-Dimethoxyphenyl)-4-(3-thienyl)-1H-pyrrolo[2,3-b]pyridine
运输与储存
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储存条件(-20℃)
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运输条件With Ice Pack
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稳定性≥ 2 years
参考文献
1. Zhou J, et al. Clin Cancer Res. 2017 Apr 15;23(8):1945-1954.
2. Bon H, et al. Mol Cancer Res. 2015 Apr;13(4):620-635.
3. Lombardi MS, et al. J Leukoc Biol. 2016 May;99(5):711-21.