CAS NO: | 1070773-09-9 |
包装 | 价格(元) |
10mM (in 1mL DMSO) | 电议 |
2mg | 电议 |
5mg | 电议 |
25mg | 电议 |
Physical Appearance | A solid |
Storage | Store at -20°C |
M.Wt | 428.44 |
Cas No. | 1070773-09-9 |
Formula | C23H20N6O3 |
Solubility | ≥21.4 mg/mL in DMSO; insoluble in H2O; insoluble in EtOH |
Chemical Name | 3,7-bis(4-methoxybenzyl)-3,7-dihydro-2H-diimidazo[4,5-d:4',5'-f][1,3]diazepin-2-one |
Canonical SMILES | COC1=CC=C(CN2C=NC3=C2N=CN=C(N4CC5=CC=C(OC)C=C5)C3=NC4=O)C=C1 |
运输条件 | 蓝冰运输或根据您的需求运输。 |
一般建议 | 为了使其更好的溶解,请用37℃加热试管并在超声波水浴中震动片刻。不同厂家不同批次产品溶解度各有差异,仅做参考。若实验所需浓度过大至产品溶解极限,请添加助溶剂助溶或自行调整浓度。溶液形式一般不宜长期储存,请尽快用完。 |
作用于具有高水平DDX3表达的癌细胞系(A549、H1299、H23和H460),IC50为4.4-8.4 μM。
RK-33是一种DDX3抑制剂。
已鉴定DDX3为一种RNA解旋酶,在多种癌症类型(例如肺癌)中过表达,并且与肺癌患者较低的存活相关。
体外:据报道,RK-33结合DDX3并消除其活性。在DDX3过表达细胞中,RK-33对 DDX3的抑制导致G1细胞周期停滞、诱导凋亡,并促进放射敏化。此外,由RK-33引起的DDX3功能丧失通过破坏DDX3-β-连环蛋白轴来削弱Wnt信号传导[1]。
体内:在Twist1 / KrasG12D肺癌模型中使用分次给药方案研究RK-33的作用。结果表明,在3周治疗期间,放射治疗引起肿瘤生长适度减少,并且RK-33和放射联合治疗肿瘤生长减少更多。因此,这些数据表明RK-33与低分光放射联合能够在临床前肺癌模型中有效地减少肺肿瘤负荷,并且比常用的放射增敏剂卡铂效果更好[1]。
临床试验:到目前为止,RK-33仍处于临床前研究阶段。
参考文献:
[1] Bol GM et al. Targeting DDX3 with a small molecule inhibitor for lung cancer therapy. EMBO Mol Med.2015 Mar 27;7(5):648-69.
Cell experiment:[1] | |
Cell lines | Various lung cancer cell lines |
Reaction Conditions | 72 h incubation |
Applications | Cancer cell lines with high levels of DDX3 expression (A549, H1299, H23, and H460) were more sensitive to RK-33 (IC50 = 4.4 ~ 8.4 μM) as compared to H3255, a cell line with low DDX3 expression (IC50 >25 μM). In addition, RK-33 also sensitized A549 cells to γ-radiation whilst it had no effect on the sensitivity of H3255 cells to γ-radiation. Therefore, RK-33 was able to inhibit cancer growth and radiosensitize lung cancer cells in a DDX3-dependent manner. |
Animal experiment:[1] | |
Animal models | Athymic NCr-nu/nu mice injected with A549 cells |
Dosage form | 20 mg/kg Injected intraperitoneally |
Applications | RK-33 significantly enhanced radiation-induced tumor regression in the orthotopic human lung cancer model. Hence, inhibition of DDX3 by RK-33 could be potentially utilized for lung cancer therapy. |
Note | The technical data provided above is for reference only. |
References: 1. Bol GM, Vesuna F, Xie M, et al. Targeting DDX3 with a small molecule inhibitor for lung cancer therapy. EMBO Molecular Medicine, 2015, 7(5): 648-669. |