2'-HYDROXY-2,4,4',5,6'-PENTAMETHOXYCHALCONE structure
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Common Name | 2'-HYDROXY-2,4,4',5,6'-PENTAMETHOXYCHALCONE | ||
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CAS Number | 73694-15-2 | Molecular Weight | 374.38 | |
Density | N/A | Boiling Point | N/A | |
Molecular Formula | C20H22O7 | Melting Point | N/A | |
MSDS | Chinese USA | Flash Point | N/A |
Use of 2'-HYDROXY-2,4,4',5,6'-PENTAMETHOXYCHALCONERubone, a chalcone analog, is a modulator of miR-34a. Rubone upregulates miR-34a expression in a p53 dependent manner, downregulates the downstream target Bcl-2 and Cyclin D1 expression, and suppresses hepatocellular carcinoma (HCC) growth in vivo. Rubone enhances the anticancer effect of Paclitaxel (PTX; HY-B0015) in PTX-resistant prostate cancer cell lines by reversing the expression of miR-34a downstream targets[1][2][3]. |
Name | (E)-1-(2-hydroxy-4,6-dimethoxyphenyl)-3-(2,4,5-trimethoxyphenyl)prop-2-en-1-one |
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Synonym | More Synonyms |
Description | Rubone, a chalcone analog, is a modulator of miR-34a. Rubone upregulates miR-34a expression in a p53 dependent manner, downregulates the downstream target Bcl-2 and Cyclin D1 expression, and suppresses hepatocellular carcinoma (HCC) growth in vivo. Rubone enhances the anticancer effect of Paclitaxel (PTX; HY-B0015) in PTX-resistant prostate cancer cell lines by reversing the expression of miR-34a downstream targets[1][2][3]. |
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Related Catalog | |
In Vitro | Rubone (0-60 μM) 在 DU145-TXR 和 PC3-TXR 细胞中表现出显着的细胞毒性,表明 Rubone 在晚期前列腺癌细胞中具有更强的抗癌作用,这些细胞具有较低的 miR-34a 表达[3]。 Rubone (5, 10 uM; 48 小时) 显着逆转 DU145-TXR 和 PC3-TXR 细胞系的 miR-34a 下游基因靶标的表达。Rubone 以剂量依赖性方式上调 PTX 抗性 DU145-TXR 和 PC3-TXR 细胞系中的 miR-34a[3]。 Rubone (5 μM; 持续 2 周) 和 PTX (持续 2 周) 联合疗法抑制 3D 模型中的 PC3-TXR 细胞生长和球体形成,包括顶部 3D 和悬滴模型。Rubone 和 PTX 联合疗法抑制 p53 独立途径中的细胞侵袭、迁移和癌症干细胞样细胞 (CSC) 种群。Rubone 单一疗法或 Rubone 与 PTX 组合可显着增强 TAp73 和 Elk-1 的表达[3]。 Cell Cytotoxicity Assay[3] Cell Line: DU145, PC3, PTX resistant DU145-TXR, PC3-TXR, LNCaP, LNCaP developed C4-2 cells Concentration: 0-60 μM Incubation Time: Result: Exhibited significantly higher cytotoxicity in DU145-TXR and PC3-TXR cells. Western Blot Analysis[3] Cell Line: DU145-TXR and PC3-TXR cell lines Concentration: 5, 10 uM Incubation Time: 48 h Result: Significantly reversed the expression of miR-34a downstream gene targets of DU145-TXR and PC3-TXR cell lines, including E-cadherin, SIRT1, and Cyclin D1, whereas E-cadherin expression was not reversed in DU145-TXR cell line. Real Time qPCR[3] Cell Line: DU145-TXR and PC3-TXR cell lines Concentration: 5, 10 uM Incubation Time: 48 h Result: Upregulated miR-34a in PTX-resistant DU145-TXR and PC3-TXR cell lines in a dose dependent manner. |
In Vivo | Rubone 单一疗法 (装载 20 mg/kg 的 PEG-PCD 胶束; 每隔一天静脉注射; 共五剂) 或与 PTX 联合治疗 (PEG-PCD 胶束装载每种药物 10 mg/kg) 显着上调肿瘤中的 miR-34a 表达。联合疗法抑制肿瘤生长。Rubone 单一疗法未能抑制肿瘤细胞增殖[3]。 Animal Model: 8 weeks old male nude mice transfected prostate cancer cells[3] Dosage: 20 mg/kg or 10 mg/kg for each drug (PTX and Rubone) loaded PEG-PCD micelles Administration: Intravenously for five doses every other day Result: Had little effect on body weight loss and inhibited tumor growth. Monotherapy or combination therapy with PTX significantly upregulated miR-34a expression in tumor. Alone or with PTX significantly reversed E-cadherin, Cyclin D1, and SIRT1 expression. |
References |
Molecular Formula | C20H22O7 |
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Molecular Weight | 374.38 |
Exact Mass | 374.13700 |
PSA | 83.45000 |
LogP | 3.33130 |
Index of Refraction | 1.578 |
HS Code | 2914509090 |
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Summary | HS:2914509090 other ketones with other oxygen function VAT:17.0% Tax rebate rate:9.0% Supervision conditions:none MFN tariff:5.5% General tariff:30.0% |
Rubone |
2'-HYDROXY-2,4,4',5,6'-PENTAMETHOXYCHALCONE |