YK-4-279
CAS No. 1037184-44-3
YK-4-279 ( YK-4-279 | YK4-279 | YK 4-279 | YK 4279 )
产品货号. M17770 CAS No. 1037184-44-3
YK 4-279 是一种 RNA 解旋酶 A (RHA) 抑制剂,可与致癌转录因子 EWS-FLI1 结合。
纯度: >98% (HPLC)
COA
Datasheet
HNMR
HPLC
MSDS
Handing Instructions
规格 | 价格/人民币 | 库存 | 数量 |
5MG | ¥437 | 有现货 |
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10MG | ¥640 | 有现货 |
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25MG | ¥1199 | 有现货 |
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50MG | ¥2244 | 有现货 |
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100MG | ¥3977 | 有现货 |
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200MG | ¥6083 | 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YK-4-279
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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YK 4-279 是一种 RNA 解旋酶 A (RHA) 抑制剂,可与致癌转录因子 EWS-FLI1 结合。
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产品描述YK-4-279 is a ETV1 inhibitor, which inhibitor protein-protein interactions between ES-FLI1 and RHA.YK-4-279 effectively antagonizes EWS-FLI1 induced leukemia in a transgenic mouse model. YK-4-279 demonstrates specificity in targeting the oncogene EWS-FLI1. YK-4-279, prevents prostate cancer growth and metastasis in a mouse xenograft model.(In Vitro):YK-4-279 (3-30 μM; overight) dissociates EWS-FLI1 from RHA in Ewing’s sarcoma family tumor (ESFT) cells.YK-4-279 (3-30 μM; 14 h) nearly eliminates cyclin D1 in TC32 cells.YK-4-279 (3-30 μM; 72 h) potently and specifically inhibits ESFTs.YK-4-279 (50 μM; 6 h) induces substantial apoptosis of ESFT cells.YK-4-279 (0.1-30 μM; 72 h) inhibits the growth of ESFT, prostate, breast and pancreatic cancer cells.(In Vivo):YK-4-279 (1.5 mg; i.p. once) inhibited ESFT tumor growth.
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体外实验Cell Viability Assay Cell Line:TC32, ES925, GUES1, TC71, A673, A4573, CHP100, PANC1, ASP1, MCF-7, MDA-MB-231, PC-3, HFK and HEC cell lines Concentration:3-30 μM Incubation Time:72 h Result:Inhibited cell growth with IC50s of 900 nM, 1 μM and 8 μM for TC32, ES925 and GUES1 cells, respectively.Apoptosis Analysis Cell Line:TC32, HEK, HEC and HFK cell lines Concentration:50 μM Incubation Time:6 h Result:Induced apoptosis of ESFT cells and increased caspase-3 activity.Cell Viability Assay Cell Line:TC32, TC71, RDES, SKES, MMH-ES-1, STA-ET 7.2, A4573, PC3, MCF7, MDA-MB-231, PANC1 and ASPC1 cell lines Concentration:0.1-30 μM Incubation Time:72 h Result:Inhibited cell growth with IC50s of 0.94, 1.83, 1.03, 0.33, 0.94, 0.60, 1.46, 4.95, 22.82, 0.82, 1.514 and 14.28 μM for TC32, TC71, RDES, SKES, MMH-ES-1, STA-ET 7.2, A4573, PC3, MCF7, MDA-MB-231, PANC1 and ASPC1 cells, respectively.
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体内实验Animal Model:Beige mice with orthotopic ESFT and ESFT xenografts Dosage:1.5 mg Administration:Intraperitoneal injection; 1.5 mg once Result:Effectively redeced tumor volume of CHP100 and ESFT xenografts (TC71 and CHP100).
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同义词YK-4-279 | YK4-279 | YK 4-279 | YK 4279
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通路Others
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靶点Other Targets
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受体RNA helicase A
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研究领域Cancer
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适应症——
化学信息
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CAS Number1037184-44-3
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分子量366.2
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分子式C17H13Cl2NO4
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纯度>98% (HPLC)
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溶解度DMSO : 25 mg/mL. 68.27 mM;
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SMILESCOC1=CC=C(C=C1)C(=O)CC1(O)C(=O)NC2=C(Cl)C=CC(Cl)=C12
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化学全称4,7-dichloro-1,3-dihydro-3-hydroxy-3-[2-(4-methoxyphenyl)-2-oxoethyl]-2H-indole-2-one
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. Erkizan HV, et al. Nat Med. 2009, 15(7), 750-756.2. Rahim S, et al. PLoS One. 2011, 6(4), e19343.
产品手册
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