化合物 PTC-209【315704-66-6】产品图
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化合物 PTC-209【315704-66-6】

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  • ¥286 - 5272
  • TargetMol
  • T2345
  • 2026年07月07日
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    • 文献和实验
    • 技术资料
    • CAS号

      315704-66-6

    • 规格

      1mg/1mLx10mM(inDMSO)/5mg/10mg/25mg/50mg/100mg/200mg

    规格:1mg产品价格:¥286.0
    规格:1mLx10mM(inDMSO)产品价格:¥738.0
    规格:5mg产品价格:¥658.0
    规格:10mg产品价格:¥976.0
    规格:25mg产品价格:¥1912.0
    规格:50mg产品价格:¥2784.0
    规格:100mg产品价格:¥3784.0
    规格:200mg产品价格:¥5272.0

    Product Introduction

    Bioactivity

    名称 PTC-209
    描述 PTC-209 is a potent and selective BMI-1 inhibitor.
    细胞实验 To determine whether pretreatment with the inhibitor affects tumor cell growth, cells are plated with the inhibitor for 4 d in vitro and plated in limiting doses in vitro without adding further inhibitor. Trypan blue exclusion is used to count viable cells. The in vitro sphere-initiating cell frequency is calculated after inhibitor treatment by evaluating the number of wells containing spheres. For the experiments where LDAs are set up following recovery of PTC-209 treated cells, 6-well plates were seeded with 1E6 cells per well and incubated overnight. Cells are subsequently treated for 4 d in triplicate with either DMSO vehicle or PTC-209 (0.01, 0.1, 1 and 10 μM). Drug treatments are washed off and 4 mL fresh suspension medium added to all wells. To assess cell viability following the 4 d treatment window, cells are trypsinized and counted at 0, 24, 72 and 120 h after removal of the drug. Long-lasting effects of the drug treatment on sphere-forming ability are assessed by plating LDAs (50,000, 10,000, 1,000,100, 10 and 1 cell per well) using the cells obtained 120 h after the 4-d drug treatment.(Only for Reference)
    激酶实验 Untranslated region-mediated luciferase reporter expression: HEK293 cells are transfected with a GEMS reporter vector that contains the luciferase open-reading frame flanked by and under post-transcriptional control of the BMI-1 5′ and 3′ UTRs. The resulting stable cells (F8) are treated with PTC-209 or vehicle control overnight, and then luciferase reporter activity is determined using Bright-Glo assays. The assays are run in triplicate for each point, and the percentage of inhibition was calculated against vehicle control.
    体外活性 PTC-209能降低体内功能性的结直肠癌CICs的频率.PTC-209(60 mg/kg/day,s.c.)有效地抑制肿瘤组织中BMI-1的产生,并停止在具有原代人结肠癌异种移植物,人结肠癌细胞系LIM1215或HCT116异种移植物的小鼠中预先建立的肿瘤的生长.
    体内活性 PTC-209通过不可逆的生长抑制破坏结肠直肠癌起始细胞(CIC)。PTC-209抑制人结肠直肠HCT116和人纤维肉瘤HT1080肿瘤细胞中UTR介导的报道基因表达和内源性BMI-1表达。PTC-209以BMI-1依赖性减少直肠肿瘤细胞的生长。
    存储条件 Powder: -20°C for 3 years | In solvent: -80°C for 1 year Shipping with blue ice/Shipping at ambient temperature.
    溶解度 Ethanol : 9.9 mg/mL (19.99 mM), Sonication is recommended.
    DMSO : 50 mg/mL (100.97 mM), Sonication is recommended.
    关键字 tumor | PTC-209 | lung | Inhibitor | inhibit | HEK293T | colon | CICs | cells | cancer-initiating | breast | BMI-1 | BMI1 | Autophagy | anti-myeloma
    相关产品 Guanidine hydrochloride | Naringin | Enzalutamide | Aceglutamide | Alginic acid | Cysteamine hydrochloride | Hemin | Hydroxychloroquine | Sildenafil citrate | Stavudine | Tamoxifen | Paeonol
    相关库 Inhibitor Library | Anti-Cancer Active Compound Library | Bioactive Compound Library | Anti-Cancer Compound Library | Bioactive Compounds Library Max | Cell Cycle Compound Library | Autophagy Compound Library | Anti-Colorectal Cancer Compound Library | Anti-Aging Compound Library | NO PAINS Compound Library | DNA Damage & Repair Compound Library | Target-Focused Phenotypic Screening Library

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    图标文献和实验
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    相关实验
    •  杂环化合物和生物碱-- 杂环化合物

      网络 第十九章 杂环化合物和生物碱 杂环化合物在自然界分布很广,其数量几乎占已知有机化合物的三分之一,用途也很多。许多重要的物质如叶绿素、血红素、核酸以及临床应用的一些有显著疗效的天然药物和合成药物等,都含有杂环化合物的结构。生物碱多是中草药的有效成分,绝大多数是含氮的杂环化合物。本章内容与医学关系密切,具有重要意义。

    • 高能化合物 energy rich compound

          分子中具有高能键的化合物。在生物体内主要有上式(Ⅰ)和(Ⅱ)两种结构的高能化合物。其作用为贮藏能量(例如 ATP、肌酸磷酸)和作为产生 ATP源的中间代谢产物(例如磷酸烯醇丙酮酸)以及合成反应的中间物质(例如酰基辅酶 A),在蛋白质的结构( conformation)变化周期的第一阶段上(例如钠钾 ATP酶的羧基磷酸中间体)也具有重要作用。多数高等化合物具有磷酸基,但也有例外。  

    • 化合物

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    化合物 PTC-209【315704-66-6】
    ¥286 - 5272