Eurycomalactone
CAS No. 23062-24-0
Eurycomalactone ( —— )
产品货号. M22811 CAS No. 23062-24-0
东革阿里内酯是从东革阿里中分离出来的天然产物,是一种有效的 NF-κB 抑制剂(IC50 为 0.5 μM)。 Eurycomalactone 抑制蛋白质合成,消耗细胞周期蛋白 D1,但不影响 TNFα 诱导的 IκBα 降解或 IKKα/β 和 IκBα 磷酸化。
纯度: >98% (HPLC)
COA
Datasheet
HNMR
HPLC
MSDS
Handing Instructions
| 规格 | 价格/人民币 | 库存 | 数量 |
| 5MG | ¥3382 | 有现货 |
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| 10MG | ¥4722 | 有现货 |
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| 25MG | ¥7152 | 有现货 |
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| 50MG | ¥9179 | 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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| 1 mL x 10 mM in DMSO | ¥3496 | 有现货 |
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生物学信息
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产品名称Eurycomalactone
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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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产品简述东革阿里内酯是从东革阿里中分离出来的天然产物,是一种有效的 NF-κB 抑制剂(IC50 为 0.5 μM)。 Eurycomalactone 抑制蛋白质合成,消耗细胞周期蛋白 D1,但不影响 TNFα 诱导的 IκBα 降解或 IKKα/β 和 IκBα 磷酸化。
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产品描述Eurycomalactone is a natural product isolated from Eurycoma longifolia Jack., acts as a potent NF-κB inhibitor( IC50 of 0.5 μM).?Eurycomalactone inhibits protein synthesis, depletes cyclin D1, but does not affect TNFα-induced degradation of IκBα or the phosphorylation of IKKα/β and IκBα.Eurycomalactone (ECL), an active quassinoid isolated from Eurycoma longifolia Jack, has been demonstrated to possess anticancer activity.?ECL exhibited selective cytotoxicity against the NSCLC cells A549 and COR-L23 compared to the normal lung fibroblast.?Clonogenic survival results indicated that ECL treatment prior to irradiation synergistically decreased the A549 and COR-L23 colony number.?ECL treatment reduced the expression of cyclin B1 and CDK1/2 leading to induce cell cycle arrest at the radiosensitive G /M phase.?Moreover, ECL markedly delayed the repair of radiation-induced DNA double-strand breaks (DSBs).?In A549 cells, pretreatment with ECL not only delayed the resolving of radiation-induced γ-H2AX foci but also blocked the formation of 53BP1 foci at the DSB sites.?In addition, ECL pretreatment attenuated the expression of DNA repair proteins Ku-80 and KDM4D in both NSCLC cells.?Consequently, these effects led to an increase in apoptosis in irradiated cells.?Thus, ECL radiosensitized the NSCLC cells to X-ray via G /M arrest induction and delayed the repair of X-ray-induced DSBs. It has?a great potential for ECL as an alternative safer radiosensitizer for increasing the RT efficiency against NSCLC.
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体外实验Eurycomalactone (24, 48 and 72 h) selectively inhibits the viability of A549 and COR-L23 cells Eurycomalactone inhibits the viability of A549 cells with IC50 values of 20.17, 3.77, and 1.90 μM for 24, 48 and 72 hours, respectively. Eurycomalactone inhibits the viability of COR-L23 cells with IC50 values of 25.02, 2.74, and 1.80 μM for 24, 48 and 72 hours, respectively.Eurycomalactone (2.29-156.3 μM; 24 h; A549 and Calu-1 cells) promotes Non-small cell lung cancer (NSCLC) cells apoptosis.Eurycomalactone (0-25.05 μM; 24 h; A549 and COR-L23 cells) induces cell cycle arrest at the radiosensitive G2/M phase and induces apoptosis in irradiated Non-small cell lung cancer (NSCLC) cells. Eurycomalactone downregulated the key G2/M regulatory proteins in irradiated Non-small cell lung cancer (NSCLC) cells.Eurycomalactone (2.5-25 μM; 24 h; A549 cells) suppressed the repair of radiation-Induced DNA double-strand breaks.Eurycomalactone (2.29-156.3 μM; 24 h; A549 and Calu-1 cells) suppresses AKT/NF-κB activation in Non-small cell lung cancer (NSCLC) cells. Apoptosis Analysis Cell Line:A549 and Calu-1 cells Concentration:2.29, 10.14, 12.02, 20.81, 80.77, and 156.3 μM Incubation Time:24 hours Result:Increased the apoptotic rates in a dose-dependent manner.Cell Cycle Analysis Cell Line:A549 and COR-L23 cells Concentration:1.57, 2.57, 20.17 and 25.05 μM Incubation Time:24 hours Result:Induced cell cycle arrest at G2/M phase in irradiated cells and increased the sub-G1 population.A549 and COR-L23 cells Western Blot Analysis Cell Line:A549 and Calu-1 cells Concentration:2.29, 10.14, 12.02, 20.81, 80.77, and 156.3 μM Incubation Time:24 hours Result:Induced the expression levels of active caspase-3 and active PARP (cleaved form), while decreased Bcl-xL and surviving.Western Blot Analysis Cell Line:A549 and COR-L23 cellsConcentration:1.57, 2.57, 20.17 and 25.05 μM Incubation Time:24 hours Result:Downregulated the expression of both G2/M regulatory proteins in a dose-dependent manner.Western Blot Analysis Cell Line:A549 and COR-L23 cells Concentration:2.29, 10.14, 12.02, 20.81, 80.77, and 156.3 μM Incubation Time:24 hours Result:inhibited the expression levels of p(S473)-AKT, total AKT, p(S536)-NF-κB p65 and total NF-κB p65.
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体内实验——
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同义词——
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通路Apoptosis
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靶点NF-κB
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受体NF-κB|Antifection
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研究领域——
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适应症——
化学信息
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CAS Number23062-24-0
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分子量348.4
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分子式C19H24O6
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纯度>98% (HPLC)
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溶解度In Vitro:?DMSO : 100 mg/mL (287.03 mM)
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SMILESC[C@]12[C@@]([C@H]([C@@](O3)([H])[C@@](C)([H])[C@]2([H])C3=O)O)([H])[C@]([C@@](C(C)=CC4=O)([H])CC1=O)([C@@H]4O)C
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化学全称——
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. Cytotoxic activity of quassinoids from Eurycoma longifolia.Nat Prod Commun. 2010 Jul;5(7):1009-12.
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