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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. BRD4 protein degrader

    dBET1 是一种基于 PROTAC 技术的强效 BRD4 蛋白降解剂,其 EC50 为 430 nM。
  2. BRD4 protein degrader

    MZ1 是一种强效诱导剂,能够可逆地、持久地选择性地去除 BRD4,而对 BRD2 和 BRD3 的影响较小。
  3. PROTAC BRD4 degrader

    ZXH-3-26 是一种选择性的 PROTAC BRD4 降解剂,其 DC50/5h(DC50/5h 指治疗 5 小时后的半最大降解)约为 5 nM。
  4. dual BRD7/9 PROTAC degrader

    VZ185 是一种强效、快速且选择性的双重 BRD7/9 PROTAC 降解剂,其 DC50 分别为 4.5 和 1.8 nM。
  5. BRD4BD1degrader

    dBET57 是一种基于 PROTAC 技术的 BRD4BD1 的强效和选择性降解剂。
  6. BRD3/4 degrader

    MZP-55 是一种基于 PROTAC 技术的 BRD3/4 选择性降解剂,对 Brd4BD2 的 Kd 为 8 nM。
  7. BRD3/4 degrader

    MZP-54 是一种基于 PROTAC 技术的 BRD3/4 选择性降解剂,对 Brd4BD2 的 Kd 为 4 nM。
  8. Brd4 degrader

    AT6 是 PROTAC AT1 类似物,是一种高度选择性的溴结构域(Brd4)降解剂。
  9. Brd4 degrader

    BRD4降解剂AT1是基于PROTAC技术的高度选择性Brd4降解剂,在细胞中对Brd4BD2的Kd为44 nM。
  10. Sirt2 degrader

    PROTAC Sirt2 Degrader-1 是基于 SirReal 的 PROTAC,作为 Sirt2 降解剂,由高效且同型选择性的 Sirt2 抑制剂、连接体和真正的 cereblon 配体组成,用于 E3 泛素连接酶。
  11. BET degrader

    PROTAC BET Degrader-1 是一种基于 PROTAC 的强效 BET 降解剂,能在低浓度下降低 BRD2BRD3BRD4 蛋白水平。
  12. PROTAC BRD9 degrader

    PROTAC BRD9 Degrader-1 是一种领先的 PROTAC BRD9 化学降解剂(IC50=13.5 nM),可作为选择性探针用于研究 BAF 复合体 生物学。
  13. BET degrader

    dBET6 是一种基于 PROTAC 的 BET 降解剂,具有高效、选择性和细胞渗透性,IC50 为 14 nM,并具有抗肿瘤活性。

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