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3,6-Dihydroxyflavone 是一种抗癌剂。它能够提高细胞内氧化应激和脂质过氧化。它是能够根据剂量和时间依赖性地降低细胞活力,并活化半胱天冬酶级联、切割聚 (ADP-核糖) 聚合酶 (PARP) 诱导细胞凋亡。
3,6-Dihydroxyflavone 是一种抗癌剂。它能够提高细胞内氧化应激和脂质过氧化。它是能够根据剂量和时间依赖性地降低细胞活力,并活化半胱天冬酶级联、切割聚 (ADP-核糖) 聚合酶 (PARP) 诱导细胞凋亡。
规格 | 价格 | 库存 | 数量 |
---|---|---|---|
10 mg | ¥ 460 | 现货 | |
100 mg | ¥ 1,900 | 现货 | |
1 mL x 10 mM (in DMSO) | ¥ 420 | 现货 |
产品描述 | 3,6-Dihydroxyflavone suppresses the epithelial-mesenchymal transition in breast cancer cells by inhibiting the Notch signaling pathway. |
体外活性 | 3,6-Dihydroxyflavone(3,6-DHF)能有效抑制体外和体内乳腺癌(BC)细胞的上皮间质转化(EMT)。研究表明,3,6-DHF有效抑制乳腺癌干细胞(BCSCs)的形成和增殖,从而降低了小鼠NOD/SCID中肿瘤细胞的肿瘤形成能力。体内光学成像显示,3,6-DHF治疗抑制了乳腺癌细胞在体内的肺转移。进一步研究指出,3,6-DHF通过下调Notch1、NICD、Hes-1和c-Myc,减少NICD-CSL-MAML功能性转录单元的形成,从而导致乳腺癌细胞中Notch信号通路的失活。Notch1的过度表达或miR-34a的抑制显著降低了3,6-DHF对EMT、CSCs以及乳腺癌细胞迁移和侵袭的抑制作用。 |
细胞实验 | Cells were cultured in six-well plates until they reached 100% confluence. A vertical or horizontal wound was gently created in monolayers using a 20 μl sterile pipette tip. The cells were then washed for 3 times with growth medium to remove the detached cells, and the medium was added with fresh medium treated with 3,6-DHF. Images were captured using an inverted microscope and camera at designed times to assess the inhibition of wound closure[1]. |
别名 | 3,6-二羟基黄酮,97% |
分子量 | 254.24 |
分子式 | C15H10O4 |
CAS No. | 108238-41-1 |
Smiles | Oc1ccc2oc(-c3ccccc3)c(O)c(=O)c2c1 |
密度 | 1.472g/cm3 |
存储 | Powder: -20°C for 3 years | In solvent: -80°C for 1 year | Shipping with blue ice. | |||||||||||||||||||||||||||||||||||
溶解度信息 | DMSO: 27.5 mg/mL (108.17 mM) | |||||||||||||||||||||||||||||||||||
溶液配制表 | ||||||||||||||||||||||||||||||||||||
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