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. HAT Inhibitor

    SYY-B085-1 is a histone acetyltransferase (HAT) inhibitor with specific activity against various HAT enzymes. This compound plays a critical role in the regulation of gene expression and cellular processes by modulating acetylation levels on histones. SYY-B085-1 is utilized in research to explore the effects of HAT inhibition in cancer biology and epigenetic regulation. Its unique mechanism offers valuable insights for studies focused on transcriptional modulation and potential therapeutic interventions.
  2. p300/CBP HAT Inhibitor

    CBP/p300-IN-19 is a potent inhibitor of the histone acetyltransferase (HAT) activity of p300 and CBP, exhibiting IC50 values of 1.4 µM and 2.2 µM, respectively, while showing limited inhibition of PCAF and Myst3 (>100 µM). This compound demonstrates significant anti-tumor activity, making it valuable for research into cancer biology and epigenetic regulation. Its ability to selectively target p300/CBP HAT provides a useful tool for investigating the role of acetylation in various cellular processes and disease states.
  3. EP300/CBP Inhibitor

    EP300/CBP-IN-1 is a highly selective inhibitor targeting the EP300 and CBP bromodomain proteins, exhibiting IC50 values of 2.3 nM and 2.1 nM for CBP and EP300, respectively. This compound demonstrates significant anti-proliferative effects on CWR22RV1 prostate cancer cells, making it a valuable tool for research in cancer biology and epigenetic regulation. Its application extends towards elucidating the roles of EP300 and CBP in various cellular processes and disease states.
  4. HAT Inhibitor

    DS-9300 is a selective inhibitor of the EP300/CBP histone acetyltransferases (HATs) with a potent IC50 value of 28 nM. This compound demonstrates significant anticancer activity and is applicable in prostate cancer research, providing valuable insights into the mechanisms of acetylation in tumorigenesis. DS-9300 serves as a critical tool for studying the role of HATs in cancer progression and therapeutic resistance.
  5. CBP/p300 Inhibitor

    CBP/p300 Ligand 3 is a selective inhibitor targeting the CBP/p300 proteins, which function as histone acetyltransferases (HATs). By binding to specific domains within CBP/p300, this compound effectively inhibits their enzymatic activity and modulates interactions with transcription factors. This inhibition alters chromatin structure and gene expression, making CBP/p300 Ligand 3 a valuable tool for studying the role of CBP/p300 in various biological processes, including cancer progression and neurodegenerative diseases, where dysregulation of CBP/p300 is implicated.
  6. HAT Inhibitor

    NSC 694623 is a potent inhibitor of histone acetyltransferases (HATs), with an IC50 value of 15.9 μM for recombinant p300/CBP-associated factor (PCAF). This compound exhibits antiproliferative effects on various cancer cell lines, making it a valuable tool for cancer research. Its capacity to modulate histone acetylation offers potential insights into epigenetic regulation and therapeutic strategies in oncology.
  7. CBP/p300 Inhibitor

    PU141 is a selective inhibitor of the histone acetyltransferases CBP and p300. This compound induces cellular histone hypoacetylation, leading to significant inhibition of cell growth in various neoplastic cell lines derived from multiple tissue types. PU141 is primarily utilized in cancer research to explore mechanisms of transcriptional regulation and therapeutic interventions.
  8. p300/CBP HAT Inhibitor

    CBP/p300-IN-19 hydrochloride is a selective inhibitor of the histone acetyltransferases (HAT) p300 and CBP, exhibiting IC50 values of 1.4 µM and 2.2 µM, respectively. It demonstrates significant antitumor activity, making it a valuable tool for cancer research. This compound can be applied in studies investigating the roles of acetylation in gene regulation and cell proliferation, as well as in the development of targeted therapies.
  9. CBP HAT Inhibitor

    NiCur is a potent and selective inhibitor of CBP histone acetyltransferase (HAT) with an IC50 value of 0.35 μM. By targeting CBP HAT activity, NiCur effectively downregulates p53 activation in response to genotoxic stress. This compound is suitable for mechanistic studies, allowing researchers to investigate pathways involving histone acetylation without altering the expression of target proteins.
  10. HAT Inhibitor

    SYY-B029-2 is a potent inhibitor of histone acetyltransferases (HATs), exhibiting an IC50 of 1.4 nM. This compound demonstrates significant anti-proliferative effects on human mantle cell lymphoma (MCL) cell line MAVER-1 and human castration-resistant prostate cancer cell line LNCaP clone FGC, with IC50 values of 15 nM and 13 nM, respectively. SYY-B029-2 serves as a valuable tool for research into epigenetic regulation and cancer therapy.
  11. P300/CBP Inhibitor

    Pocenbrodib is a potent inhibitor of the P300/CBP transcriptional coactivators. By blocking the function of these coactivators, Pocenbrodib effectively inhibits the acetylation of both histone and non-histone proteins, impacting gene expression regulation. This compound is particularly valuable for research into castration-resistant prostate cancer and other cancer types that are associated with dysregulated acetylation processes.
  12. p300/CBP Inhibitor

    CBP/p300-IN-5 is a potent inhibitor of p300/CBP histone acetyltransferase, demonstrating an IC50 value of 18.8 nM. This compound serves as a valuable tool for studying the role of histone acetylation in gene regulation and various biological processes. Its application is significant in cancer research and therapeutic development, where modulation of acetylation pathways is of interest.
  13. p300/CBP HAT Inhibitor

    B026 is a selective and potent inhibitor of the p300/CBP histone acetyltransferase (HAT) with IC50 values of 1.8 nM for p300 and 9.5 nM for CBP. This compound exhibits significant anticancer activity against androgen receptor-positive (AR+) prostate cancer cell lines, making it a valuable tool for research in cancer biology and epigenetic regulation. Its oral bioavailability enables easy administration for in vivo studies targeting p300/CBP-mediated pathways.
  14. CBP/p300 Inhibitor

    CBP/p300-IN-20 is a selective inhibitor of the p300/CBP transcriptional coactivators, displaying a high potency with a pIC50 of 10.1 for p300. This compound is useful in cancer research, providing insights into the role of p300/CBP in oncogenic transcriptional regulation and potential therapeutic interventions. Its specificity towards p300 allows for targeted studies in related signaling pathways and tumor biology.
  15. CBP/EP300 Inhibitor

    CBP/p300-IN-14 is a highly potent inhibitor of CBP/EP300, a lysine acetyltransferase, with an IC50 of 3.3 nM. This compound is utilized to study the role of CBP/EP300 in various biological processes, including transcriptional regulation and cellular signaling pathways. Its application is critical in research focused on cancer, metabolic disorders, and other diseases where histone acetylation plays a significant role.
  16. EP300/CBP HAT Inhibitor

    CBP/p300-IN-18 is a potent inhibitor of the EP300 and CBP histone acetyltransferases (HATs), exhibiting IC50 values of 0.056 µM and 0.46 µM for EP300 and LK2 H3K27, respectively. This compound serves as a valuable tool for investigating the role of histone acetylation in various biological processes and disease states. It is particularly useful in studies focused on chromatin remodeling, gene expression, and potential therapeutic applications in cancer and other disorders associated with dysregulated acetylation.
  17. CBP/p300 Inhibitor

    CBP/p300-IN-21 is a selective inhibitor of the CBP/p300 transcriptional co-activators, exhibiting IC50 values of 0.07 μM for p300 and 1.755 μM for CBP. This compound effectively reduces the acetylation level of histone H3 at lysine 18 (H3K18Ac), implicating a potential role in modulating gene expression. Furthermore, CBP/p300-IN-21 has demonstrated efficacy in inhibiting the growth of 4T1 tumors in murine models, highlighting its relevance in cancer research and therapeutic applications.
  18. CBP/p300 Inhibitor

    CBP/p300-IN-15 is a potent inhibitor of the CBP/p300 coactivators, exhibiting IC50 values of 2.50 nM for p300 and 28.0 nM for CBP. This compound demonstrates significant biological activity in ovarian cancer cell lines, with EC50 values of 0.865 μM for OVCAR-3 and 2.71 μM for A2780. CBP/p300-IN-15 is a valuable tool for investigating the role of CBP/p300 in ovarian cancer research and could provide insights into therapeutic strategies targeting these coactivators.
  19. Ep300/CREBBP Inhibitor

    Ep300/CREBBP-IN-3 is a potent inhibitor of the Ep300 and CREBBP enzymes, demonstrating IC50 values of 0.056 μM and 0.095 μM, respectively. This compound is primarily utilized in cancer research, facilitating investigations into the role of histone acetylation in tumor progression and therapy resistance. Its ability to selectively inhibit these acetyltransferases makes it a valuable tool for understanding the epigenetic regulation of gene expression in oncology.
  20. HAT Inhibitor

    PU139 is a potent pan-histone acetyltransferase (HAT) inhibitor that specifically targets Gcn5, p300/CBP-associated factor (PCAF), CREB-binding protein (CBP), and p300. This compound demonstrates inhibitory activity with IC50 values of 8.39 μM, 9.74 μM, 2.49 μM, and 5.35 μM for each respective HAT. PU139 is valuable for research applications exploring histone acetylation and its roles in gene regulation, cellular signaling, and cancer biology.
  21. EP300/CBP Inhibitor

    CPI-1612 is a potent, orally active inhibitor of EP300/CREB-binding protein (CBP) histone acetyltransferase, exhibiting an IC50 of 8.1 nM for EP300 HAT. This compound demonstrates significant anticancer activity, making it a valuable tool for cancer research. Its ability to modulate acetylation pathways enables investigations into epigenetic regulation and therapeutic strategies targeting malignancies.
  22. KDM2B Inhibitor

    KDM2B-IN-3 is a selective inhibitor of the histone demethylase KDM2B, designed to modulate epigenetic regulation. By inhibiting KDM2B, this compound can alter histone methylation patterns, making it a valuable tool for cancer research and investigations into epigenetic modifications. Its potential applications include studying the role of KDM2B in tumorigenesis and evaluating therapeutic strategies targeting epigenetic regulators.
  23. LSD1 Inhibitor

    Pulrodemstat (hydrochloride) is a potent and selective reversible inhibitor of lysine-specific demethylase-1 (LSD1), exhibiting an IC50 value of 0.25 nM. This compound demonstrates minimal enzymatic inhibition of LSD2, MAO-A, and MAO-B, making it a highly specific agent. Pulrodemstat (hydrochloride) promotes differentiation in acute myeloid leukemia (AML) and small cell lung cancer (SCLC) cells, showcasing significant anticancer activity. It serves as a valuable tool for research in cancer biology and therapeutic development.
  24. JMJD3/KDM6B Inhibitor

    GSK-J1 sodium is a selective inhibitor of the histone demethylases JMJD3 (KDM6B) and UTX (KDM6A), exhibiting an IC50 value of 60 nM for KDM6B. This compound modulates H3K27me3/me2 levels, thereby influencing gene expression and cellular differentiation. GSK-J1 sodium is useful in research applications focused on epigenetic regulation, cancer biology, and developmental processes.
  25. AW4

    LSD1 Inhibitor

    AW4 is a selective inhibitor of lysine-specific demethylase 1 (LSD1), effectively targeting the ΔTTAS activity during H3K4me2 demethylation assays. This compound demonstrates significant potential in studying the biological implications of LSD1 modulation and can be utilized in research related to drug resistance mechanisms. AW4's ability to interfere with LSD1 activity positions it as a valuable tool in epigenetic research and therapeutic development.
  26. KDM5A Inhibitor

    JQKD82 is a selective inhibitor of the lysine demethylase KDM5A. It effectively increases levels of trimethylated histone H3 at lysine 4 (H3K4me3), facilitating research into epigenetic regulation and its implications in various cancers, including multiple myeloma. This compound is suitable for studies investigating KDM5A's role in oncogenic processes and potential therapeutic strategies.
  27. KDM5A Inhibitor

    JQKD82 dihydrochloride is a selective inhibitor of the lysine demethylase KDM5A. This compound enhances levels of trimethylation at histone H3 lysine 4 (H3K4me3), making it a valuable tool for studying epigenetic regulation in various cellular contexts. Its application in research includes investigations into the mechanisms underlying multiple myeloma and other hematological malignancies.
  28. LSD1 Inhibitor

    LSD1-IN-29 is a potent inhibitor of Lysine-specific demethylase 1 (LSD1), demonstrating an IC50 value of 19 nM. This compound effectively modulates LSD1 activity, making it a valuable tool for investigating epigenetic regulation and gene expression mechanisms. It is applicable in research focusing on cancer biology, neurodegenerative diseases, and other conditions influenced by methylation status.
  29. LSD1 Inhibitor

    NCD-25 is a selective inhibitor of lysine-specific demethylase 1 (LSD1), exhibiting an IC50 of 0.48 μM. This compound is effective in modulating epigenetic regulation through its inhibition of LSD1, which plays a key role in the demethylation of histone proteins. NCD-25 is valuable for research applications focused on cancer biology, developmental processes, and drug discovery involving epigenetic mechanisms.
  30. LSD1 Inhibitor

    rel-OG-L002 (hydrochloride) is a selective inhibitor of lysine-specific demethylase 1 (LSD1). It demonstrates potent inhibition of LSD1 activity, leading to increased levels of methylated histones, which can influence gene expression regulation. This compound is valuable for research in cancer biology, epigenetics, and the study of histone methylation pathways.
  31. LSD1 Inhibitor

    OG-L002 hydrochloride is a selective inhibitor of lysine-specific demethylase 1 (LSD1) with an IC50 value of 0.02 μM, demonstrating robust inhibition of this target. Additionally, it acts as a potent monoamine oxidase (MAO) inhibitor, with IC50 values of 1.38 μM and 0.72 μM for MAO-A and MAO-B, respectively. This compound has potential applications in research related to gene expression regulation and the modulation of herpes simplex virus immediate early genes.
  32. LSD1 Inhibitor

    LSD1-IN-46 is a potent and orally bioavailable inhibitor of Lysine-specific demethylase 1 (LSD1), exhibiting an IC50 of 0.082 μM. By disrupting the β-catenin-mediated transcriptional program, LSD1-IN-46 effectively diminishes the stemness characteristics of gastric cancer cells. This compound demonstrates significant anti-tumor activity, making it a valuable reagent for research into gastric cancer therapeutics.
  33. LSD1 Inhibitor

    LSD1-IN-22 is a potent inhibitor of Lysine-specific demethylase 1 (LSD1) with an inhibitory constant (Ki) of 98 nM. This compound exhibits anti-proliferative activity in various cancer cell lines, making it a valuable tool for studying the role of LSD1 in cancer biology. Its inhibition of LSD1 can aid in exploring therapeutic strategies targeting epigenetic modifications in cancer treatment.
  34. LSD1 Inhibitor

    LSD1-IN-39 is a reversible inhibitor of lysine-specific demethylase 1 (LSD1) with an IC50 of 0.18 μM. This compound demonstrates significant anti-proliferative effects across various cancer cell lines, effectively inhibits HepG2 cell migration, and prevents epithelial-mesenchymal transition. Furthermore, LSD1-IN-39 exhibits notable antitumor activity in murine models, making it a valuable tool for cancer research.
  35. KDM5B Inhibitor

    KDM5B-IN-3 is a selective inhibitor of histone lysine-specific demethylase 5B (KDM5B/JARID1B), displaying an IC50 of 9.32 μM. This compound is instrumental in studying the epigenetic regulation associated with gastric cancer. It provides a valuable tool for researchers investigating KDM5B's role in tumorigenesis and therapeutic strategies targeting histone modifications.
  36. LSD1 Inhibitor

    LSD1-IN-19 is a potent and selective inhibitor of the lysine-specific demethylase 1 (LSD1), exhibiting a Ki value of 0.108 μM and a KD of 0.068 μM. This compound demonstrates significant antiproliferative activity in THP-1 leukemia cells and MDA-MB-231 breast cancer cells, with IC50 values of 0.17 μM and 0.40 μM, respectively, over a 72-hour treatment period. LSD1-IN-19 is valuable for investigating the role of LSD1 in cancer biology and may serve as a potential therapeutic candidate in the treatment of cancers driven by epigenetic regulation.
  37. LSD1 Inhibitor

    LSD1-IN-12 is a potent inhibitor of lysine-specific demethylase 1 (LSD1), exhibiting a Ki value of 1.1 μM for LSD1. Additionally, it demonstrates moderate inhibition of LSD2, MAO-A, and MAO-B with Ki values of 61 μM, 2.3 μM, and 3.5 μM, respectively. This compound is valuable for studying the role of LSD1 in epigenetic regulation and its implications in various diseases, including cancer and neurodegenerative disorders.
  38. LSD1 Inhibitor

    LSD1-IN-13 is a potent inhibitor of lysine-specific demethylase 1 (LSD1), exhibiting an IC50 of 24.43 nM. This orally active compound has been shown to enhance CD86 expression with an EC50 of 470 nM. Additionally, LSD1-IN-13 promotes differentiation in acute myeloid leukemia (AML) cell lines, making it a valuable tool for investigating epigenetic regulation in cancer research.
  39. LSD1 Inhibitor

    LSD1/2-IN-3 is a selective inhibitor of lysine-specific demethylase 1 (LSD1) with a Ki value of 11 nM, demonstrating significantly lower affinity for LSD2 (7 μM). This compound effectively inhibits LSD1-mediated cell proliferation, particularly in cancer stem cells, highlighting its potential for oncological research. It is valuable for investigations into epigenetic regulation and therapeutic strategies targeting LSD1 in cancer.
  40. JMJD7 Inhibitor

    JMJD7-IN-1 is a selective inhibitor of the JMJD7 enzyme, exhibiting an IC50 value of 6.62 μM. This compound effectively inhibits JMJD7 activity in cells with elevated JMJD7 expression levels. It serves as a valuable tool for investigating the biological functions of JMJD7 and its role in various cellular processes. This compound is suitable for research applications in epigenetics and cancer biology.
  41. LSD1 Inhibitor

    LSD1-IN-24 is a selective inhibitor of lysine-specific demethylase 1 (LSD1) with an IC50 of 0.247 μM. This compound has been shown to modulate the expression of PD-L1, thereby enhancing T cell-mediated cytotoxicity. It is primarily utilized in cancer research to explore the effects of LSD1 inhibition on immune response and tumor progression.
  42. LSD1 Inhibitor

    Pulrodemstat is a potent and reversible inhibitor of lysine specific demethylase-1 (LSD1), exhibiting an IC50 of 0.25 nM, while demonstrating minimal inhibition of LSD2, MAO-A, and MAO-B. This compound effectively promotes differentiation in acute myeloid leukemia (AML) and small cell lung cancer (SCLC) cells, showcasing its significant anticancer properties. Due to its selective action, Pulrodemstat serves as a valuable tool for exploring the therapeutic potential of LSD1 inhibition in cancer research.
  43. LSD1 Inhibitor

    INCB059872 dihydrochloride is a selective and irreversible inhibitor of Lysine-Specific Demethylase 1 (LSD1). This compound demonstrates potent biological activity and is primarily utilized in research focused on myeloid leukemia. Its ability to modulate LSD1 activity makes it a valuable tool for exploring demethylation processes in cancer biology.
  44. LSD1 Inhibitor

    CBB1007 trihydrochloride is a reversible and selective inhibitor of lysine-specific demethylase 1 (LSD1), exhibiting an IC50 of 5.27 µM for human LSD1. It effectively inhibits LSD1's demethylase activity on H3K4Me2 and H3K4Me, demonstrating notable selectivity for LSD1 over LSD2 and JARID1A. This compound has significant implications in cancer research, particularly in non-pluripotent models, as it promotes the expression of differentiation-related genes in pluripotent cells and is being explored in the context of teratocarcinoma, embryonic carcinoma, and seminoma.
  45. LSD1 Inhibitor

    Bizine is a selective inhibitor of lysine-specific demethylase 1 (LSD1), exhibiting a Ki value of 59 nM. This compound effectively modulates bulk histone methylation in cancer cells, contributing to alterations in gene expression. Additionally, Bizine demonstrates neuroprotective properties, making it a valuable tool for research into mechanisms of neurodegeneration and cancer biology.
  46. LSD1 Inhibitor

    LSD1-IN-30 is a potent inhibitor of lysine-specific demethylase 1 (LSD1), exhibiting an IC50 value of 0.291 μM. This compound effectively inhibits LSD1 activity, making it a valuable tool for studies investigating epigenetic regulation and its implications in various biological processes. Additionally, LSD1-IN-30 can be utilized in research related to cancer, neurobiology, and other disorders associated with dysregulated histone methylation.
  47. KDM4D Inhibitor

    Zavondemstat L-lysine is a selective inhibitor of histone lysine demethylase 4D (KDM4D), a crucial enzyme involved in histone modification and epigenetic regulation. This compound exhibits notable antineoplastic activity, making it valuable in cancer research and investigations into epigenetic therapies. Its ability to modulate histone methylation contributes to the understanding of tumor biology and the development of novel therapeutic strategies targeting KDM4D-related pathways.
  48. KDM5 Inhibitor

    KDOAM-25 is a selective inhibitor of histone lysine demethylases 5 (KDM5) with reported IC50 values of 71 nM, 19 nM, 69 nM, and 69 nM for KDM5A, KDM5B, KDM5C, and KDM5D, respectively. This compound enhances global H3K4 methylation at transcriptional start sites, thereby modulating gene expression. KDOAM-25 demonstrates potential in addressing proliferative disorders, particularly in multiple myeloma cell lines such as MM1S, making it a valuable tool for investigating epigenetic regulation and its implications in cancer research.
  49. KDM4 inhibitor

    NCDM-32B is a selective inhibitor of KDM4, demonstrating IC50 values of 3.0 μM for KDM4A and 1.0 μM for KDM4C in in vitro enzyme assays. This compound significantly enhances global levels of H3K9me3/me2 in basal breast cancer cells, contributing to impaired cell viability in KDM4C-amplified breast cancer cell lines such as HCC1954 and Colo824. NCDM-32B serves as a valuable tool for investigating the role of KDM4 in breast cancer research and therapeutic development.
  50. LSD1 Inhibitor

    CBB1007 hydrochloride is a reversible and selective inhibitor of lysine-specific demethylase 1 (LSD1), exhibiting an IC50 of 5.27 µM for human LSD1. It effectively inhibits the demethylase activity of LSD1 on histone substrates H3K4Me2 and H3K4Me, demonstrating selectivity over LSD2 and JARID1A. This compound is involved in promoting the expression of differentiation-related genes in pluripotent cells and finds applications in cancer research, particularly in the study of teratocarcinoma, embryonic carcinoma, and seminoma.

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