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Epigenetics

Epigenetics research delves into the molecular mechanisms that control gene expression and cellular traits without altering the underlying DNA sequence. One crucial aspect of this field is the role of small molecules, which act as powerful regulators of epigenetic modifications. These small compounds, typically comprising a few dozen to a few hundred atoms, have emerged as essential tools in understanding and manipulating the epigenome.

  • DNA Methylation Inhibitors: Small molecules like 5-azacytidine and 5-aza-2'-deoxycytidine are DNA methyltransferase inhibitors. They block the addition of methyl groups to DNA, leading to DNA demethylation. This can reactivate silenced genes, potentially offering therapeutic avenues for conditions like cancer.
  • HDAC inhibitors: HDACs remove acetyl groups from histone proteins, contributing to gene repression. Small molecule HDAC inhibitors, such as Vorinostat and Romidepsin, can reverse this process by increasing histone acetylation, allowing genes to be more accessible for transcription. These inhibitors are being explored for cancer therapy and other conditions.
  • Histone Methyltransferase Inhibitors: Small molecules like GSK126 inhibit specific histone methyltransferases, affecting histone methylation patterns. This can alter gene expression, making them promising candidates for cancer and other diseases with epigenetic dysregulation.
  • RNA Modulators: Small molecules can also target non-coding RNAs involved in epigenetic regulation. For instance, small molecules called small interfering RNAs (siRNAs) can be designed to target and degrade specific long non-coding RNAs, influencing gene expression.
  • Epigenetic Reader Domain Inhibitors: These small molecules target proteins that recognize and bind to specific epigenetic marks. Examples include inhibitors of bromodomain-containing proteins (BET inhibitors), which can disrupt gene regulation by interfering with protein-DNA interactions.

Small molecules in epigenetics research not only provide insights into the fundamental biology of gene regulation but also hold immense promise for developing novel therapeutics. Their ability to selectively modulate specific epigenetic marks and pathways has led to ongoing clinical trials and drug development efforts for various diseases, including cancer, neurological disorders, and inflammatory conditions. Understanding and harnessing the power of these small molecules is at the forefront of modern epigenetics research, offering new hope for precision medicine and targeted therapies.


3 key components involved in the regulation of epigenetic modifications

Epigenetics Writer

Epigenetics writers are enzymes responsible for adding chemical marks or modifications to DNA or histone proteins. These marks include DNA methylation (addition of methyl groups to DNA) and histone modifications (such as acetylation, methylation, phosphorylation, etc.).

Epigenetics Reader

Function: Epigenetics readers are proteins that can recognize and bind to specific epigenetic marks on DNA or histones. These reader proteins interpret the epigenetic code and facilitate downstream cellular processes, such as gene activation or repression.

Epigenetics Eraser

Function: Epigenetics erasers are enzymes responsible for removing or reversing epigenetic marks on DNA or histones. This process allows for the dynamic regulation of gene expression and the resetting of epigenetic states during various stages of development and in response to environmental changes.

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  1. MDMX 抑制剂

    NSC207895 是一种细胞渗透性的苯并呋喃化合物,它通过抑制 MDMX 启动子的转录活性(在 HT1080 细胞中的 IC50 = 2.5 微摩尔),在 MCF-7、LNCaP 和 A549 细胞中(1 到 10 微摩尔,持续 16 到 24 小时)降低 p53 负调控因子 MDMX 蛋白的水平,从而增强 p53 的稳定性和激活。
  2. MDM2 抑制剂

    Nutlin 3a 是一种强效的 MDM2 (mouse double minute 2) 抑制剂,它能阻止 MDM2 与 p53 的结合,从而诱导 p53 调控基因的表达,并在表达功能性 p53 的细胞中显示出强大的抗增殖活性。
  3. MDM2 抑制剂

    Nutlin 3b 是一种 p53/MDM2 对抗剂或抑制剂,其 IC50 值为 13.6 uM,与相反的 (-)-对映体 Nutlin-3a 相比,其效力低 150 倍,是 Nutlin-3 的较弱的 (+)-对映体
  4. selective p53-MDM2 抑制剂

    RG7112 是首个临床级小分子 MDM2 抑制剂,设计用于占据 MDM2p53 结合口袋。
  5. MDM2 抑制剂

    APG-115 (AA-115) 是一种口服活性的 MDM2 蛋白抑制剂,与 MDM2 蛋白 结合,其 IC50Ki 值分别为 3.8 nM 和 1 nM。
  6. dual MDM2/NFAT1 抑制剂

    MA242 是一种用于胰腺癌治疗的双重抑制剂,它同时抑制小鼠双分子2号(MDM2)活化T细胞核因子1号(NFAT1)
  7. MDM2 抑制剂

    MDM2抑制剂是一种细胞渗透性硼基查尔酮,展示出对MDM2的强烈结合能力,并不可逆地破坏MDM2/p53蛋白复合体。
  8. Mdm2 抑制剂

    YH239-EE 是一种强效的 p53-MDM2 对抗剂和 凋亡 诱导剂。
  9. MDM2/p53 抑制剂

    Idasanutlin 是一种强效且选择性的 p53-MDM2 抑制剂
  10. MDM2 抑制剂

    AMG 232 是一种高效、选择性且口服生物利用度高的哆啦A梦抑制剂,专门针对 MDM2-p53 交互作用(SPR KD= 0.045 nMSJSA-1 EdU IC50=9.1 nM)。
  11. Mdm2 抑制剂

    MI-773 是一种新型小分子抑制剂,用于抑制 MDM2-p53 互作,它与 MDM2 高亲和力结合(Ki=0.88 nM),阻断 p53-MDM2 互作。
  12. p53-MDM2 interaction 抑制剂

    p53MDM2 蛋白相互作用抑制剂手性是一种抑制 p53MDM2 蛋白之间相互作用的抑制剂。
  13. p53-MDM2 interaction 抑制剂

    p53MDM2 蛋白相互作用抑制剂(外消旋体)是一种抑制 p53MDM2 蛋白之间相互作用的抑制剂。
  14. MDMX 抑制剂

    SJ 172550 是首个 MDMX 抑制剂,具有 0.84 uM 的 EC50;可逆性结合到 MDMX 上,并有效杀死 MDMX 表达增强的视网膜母细胞瘤细胞。
  15. MDM2 抑制剂

    MI-773是一种口服可用的MDM2拮抗剂,其Ki值为0.88 nM。
  16. MDM2 抑制剂

    NVP-CGM097 是一种强效且选择性的 MDM2 抑制剂;一种具有潜在抗肿瘤活性的口服可用 HDM2 拮抗剂
  17. MDM2/XIAP 抑制剂

    MX-69 是 MDM2/XIAP 抑制剂,用于癌症治疗。
  18. MDM2 抑制剂

    HDM201 是一种新型、高效且选择性的 p53-Mdm2 交互作用抑制剂,其对 Mdm2 的亲和常数在皮摩尔范围内,与 Mdm4 的选择性比率超过 10000 倍。
  19. MDM2 抑制剂

    MI-1061 是一种有效的、可口服生物利用度高、化学稳定性强的 MDM2 (MDM2-p53相互作用) 抑制剂(IC50=4.4 nM;Ki=0.16 nM)。MI-1061 强效激活 p53,诱导凋亡,并具有抗肿瘤活性。
  20. MDM2/MDMX 抑制剂

    RO-5963 是一种抑制剂,能够抑制 MDM2 和 MDMX 与 p53 的相互作用,其半抑制浓度(IC50)分别约为 17 nM24 nM
  21. MDM2 抑制剂

    PROTAC MDM2 Degrader-4 是基于 PROTAC 技术的 MDM2 降解剂。PROTAC MDM2 Degrader-4 包含一种强效的 MDM2 抑制剂、连接体和 E3 泛素连接酶 的 MDM2 配体。
  22. MDM2 抑制剂

    PROTAC MDM2 Degrader-2 是基于 PROTAC 技术的 MDM2 降解剂。PROTAC MDM2 Degrader-2 包含一个强效的 MDM2 抑制剂、连接体和 E3 泛素连接酶 的 MDM2 配体。
  23. MDM2 抑制剂

    Mliademetan 是一种特定的 MDM2 抑制剂,用于治疗急性髓性白血病(AML)的药物组合。
  24. Dual MDM2/TSPO 抑制剂

    PK 11195 是一种 2-苯基吲哚基乙酰二肽鼠双分钟(MDM)2/跨膜运输蛋白(TSPO)双重抑制剂,可能用于治疗胶质瘤
  25. MDM2-p53 抑制剂

    BI-0252 是一种口服活性的、选择性的 MDM2-p53 抑制剂,其 IC50 为 4 nM。
  26. MDM2 抑制剂

    RO8994 是一系列高效选择性的螺[3.4]环吲哚酮小分子 MDM2 抑制剂,在 HTRF 结合实验中的 IC50 为 5 nM,在 MTT 增殖实验中的 IC50 为 20 nM。

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