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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. FACT 抑制剂

    CBL0137 是一种 FACT 抑制剂,它能够功能性地失活 促进染色质转录复合体(FACT),从而影响 p53 和 NF-κB,并促进癌细胞死亡。
  2. 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。
  3. p53 抑制剂

    抑制 p53 与线粒体的结合,通过降低其对抗凋亡蛋白 Bcl-2Bcl-XL 的亲和力。
  4. p53 抑制剂

    Pifithrin-beta 是一种小分子p53抑制剂
  5. p53 抑制剂

    Pifithrin-α hydrobromide 是一种可逆的 p53 介导的凋亡和 p53 依赖的基因转录抑制剂,如 cyclin G、p21/waf1 和 mdm2 的表达。
  6. nucleophosmin 抑制剂

    NSC348884 是一种核仁磷酸蛋白,具有多种生物活性,包括核糖体生物生成细胞增殖细胞质/核穿梭运输核酸结合核糖核酸切割中心体复制。NSC 348884 是一种假定的核磷蛋白(NPM)抑制剂。NSC 348884 抑制 NMP 寡聚体形成,上调 p53 并诱导凋亡。
  7. MDM2/p53 抑制剂

    Idasanutlin 是一种强效且选择性的 p53-MDM2 抑制剂
  8. 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。
  9. 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。
  10. 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。
  11. p53 activator / NF-κB 抑制剂

    CBL0137(CBL-0137)在基于细胞的p53和NF-kB报告检测中,分别以EC50为0.37 μM和0.47 μM激活p53并抑制NF-kB。它还抑制组腺体伴侣FACT(促进染色质转录复合体)。
  12. 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。
  13. p53 抑制剂

    Pifithrin-β (PFT β) 是一种强效的 p53 抑制剂,其 IC50 为 23 μM。

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