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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. p53 activator

    Tenovin-6 是 tenovin-1 的类似物。Tenovin-6 在体外抑制纯化的人类 SIRT1SIRT2SIRT3 的蛋白去乙酰化酶活性,其 IC50 值分别为 21、10 和 67 微摩尔。
  2. p53 activator

    JNJ-26854165 是一种 p53激活剂,并且与AraC或多柔比星协同作用,以诱导 p53介导的凋亡,可能为急性白血病的治疗提供一种新的治疗方法。
  3. p53 activator

    RITA,也被称为 NSC 652287,是一种三环噻吩衍生物,它能够结合到 MDM2,打断 MDM2-p53 复合体,随后激活 p53 并诱导凋亡。
  4. p53 activator

    Tenovin-1 是一种小分子激活剂,能够激活 p53 的转录活性,保护 p53 免受 MDM2 介导的降解。
  5. p53R175 activator

    NSC 319726 是一种强效且选择性的突变型 p53R175激活剂。
  6. P53 Activator

    NSC59984 通过 MDM2 和泛素-蛋白酶体途径诱导突变型 p53 蛋白的降解。在大多数癌细胞中,NSC59984 的 EC50 显著低于正常细胞,p53 缺失的 HCT116 细胞的 EC50 为 8.38 uM。
  7. p53 reactivator

    PRIMA-1是一种小分子,因其对p53的重新激活效果而被识别。
  8. p53 activator

    Tenovin-3 是一种sirtuin 抑制剂
  9. p53 activator

    NSC 146109 盐酸盐是一种细胞渗透性、基因型选择性的抗肿瘤剂,能够激活p53依赖的转录
  10. mutant p53 Reactivator

    RETRA 盐酸盐是一种抗肿瘤药物,它能够在体外和体内通过依赖突变的 p53p73 来抑制肿瘤细胞的生长。
  11. P53/p21waf-1/MDM2 activator

    WR 1065,一种去磷酸化的阿米福斯汀(Ethyol)代谢物,可以保护机体免受辐射暴露的即刻和延迟效应
  12. p53 activator

    PK11007 是一种针对 p53 的抗癌药物,它通过选择性烷基化两个表面暴露的半胱氨酸来稳定野生型和突变型 p53,而不影响其 DNA 结合活性。它不仅通过重新激活 p53 来发挥抗肿瘤功能,还通过其他细胞机制发挥作用,例如增加细胞 ROS 至毒性水平和激活 UPR。
  13. 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)。

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