硫蒽酮 T4569
品牌 | 厂商性质 | 产地 | 货期 |
---|---|---|---|
TargetMol | 生产商 | 美国 | 现货 |
性能特点
生化试剂,可用于动物细胞实验
规格 | CAS号 | 价格 | 操作 |
---|---|---|---|
25 mg | 479-50-5 | ¥2,960.00 | 询底价 |
1 mg | 479-50-5 | ¥428.00 | 询底价 |
100 mg | 479-50-5 | ¥6,170.00 | 询底价 |
10 mg | 479-50-5 | ¥1,690.00 | 询底价 |
50 mg | 479-50-5 | ¥4,370.00 | 询底价 |
1 mL | 479-50-5 | ¥1,170.00 | 询底价 |
5 mg | 479-50-5 | ¥1,060.00 | 询底价 |
2 mg | 479-50-5 | ¥623.00 | 询底价 |
Product Introduction
Bioactivity
英文名: Lucanthone
描述: Lucanthone (Lucanthonum) 是一种 Apurinic 核酸内切酶-1 的抑制剂。
细胞实验: Cell viability is assessed by MTT assay. Cells are seeded into 96-well microculture plates at 10,000 cells per well and allowed to attach for 24 h. Cells are then treated with Lucanthone (0, 0.5, 1, 5, 10, 20 and 40 μM), Chloroquine, Vorinostat, or combinations for 72 h. Following drug treatment, MTT is added and cell viability is quantified using a BioTek microplate reader. Effects on cell viability are also determined by measuring ATP levels using the ATPlite assay system and by trypan blue exclusion. Pro-apoptotic effects following in vitro drug exposure are quantified by propidium iodide (PI) staining and fluorescence-activated cell sorting (FACS) analysis of sub-G0/G1 DNA content[2]
体外活性: Lucanthone is a novel inhibitor of autophagy that induces cathepsin D-mediated apoptosis. Cell viability is measured by MTT assay to investigate the anticancer activity of Lucanthone. Lucanthone reduces cell viability to a similar extent in a panel of seven breast cancer cell lines. In addition, a direct comparison reveals that Lucanthone is significantly more potent than Chloroquine (CQ) at reducing breast cancer cell viability with a mean IC50 of 7.2 μM versus 66 μM for CQ. Measurement of cell viability in two representative cell lines (MDA-MB-231 and BT-20) by ATPlite assay and trypan blue exclusion reveals comparable results[2].
存储条件: Powder: -20°C for 3 years | In solvent: -80°C for 1 year
溶解度: DMSO : 60 mg/mL (176.22 mM)
关键字: Autophagy | inhibit | Inhibitor | Lucanthone
相关产品: Gemcitabine hydrochloride | Azelaic acid | 3'-Demethylnobiletin | YK-4-279 | CID 5951923 | Streptozocin | Taq DNA polymerase | AP-1/NF-κB activation inhibitor 1 | Farudodstat | Osalmid
相关库: Drug Repurposing Compound Library | Anti-Breast Cancer Compound Library | ReFRAME Related Library | Anti-Cancer Drug Library | Bioactive Compounds Library Max | Inhibitor Library | Anti-Cancer Clinical Compound Library | Anti-Cancer Active Compound Library | NO PAINS Compound Library | Bioactive Compound Library
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注:该产品未在中华人民共和国食品药品监督管理部门申请医疗器械注册和备案,不可用于临床诊断或治疗等相关用途