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Results for "

histone H3K9me3

" in MedChemExpress (MCE) Product Catalog:

3

Inhibitors & Agonists

2

Peptides

1

Antibodies

Cat. No. Product Name Target Research Areas Chemical Structure
  • HY-148807

    QC8222 free base; TACH 101 free base

    Histone Demethylase Apoptosis Cancer
    Zavondemstat (QC8222 free base; TACH 101 free base) is an orally active pan-KDM4 inhibitor, with a IC50 ≤ 0.08 μM against human KDM4A-D and a Kᵢ of 0.52 μM against human KDM4C. Zavondemstat induces cell apoptosis, causes S-phase cell cycle arrest, reduces the population of tumor-initiating cells and inhibits cancer cell proliferation. Zavondemstat suppresses tumor growth and induces tumor regression in mouse xenograft models. Zavondemstat can be used for the research of various cancers including colorectal cancer, esophageal squamous cell carcinoma and triple-negative breast cancer .
    Zavondemstat
  • HY-P10111A

    H3(1-15)K9me3 TFA

    Histone Methyltransferase Others
    Histone H3K9me3 (1-15) (H3(1-15)K9me3) TFA is used as substrate. Histone H3K9me3 is a histone posttranslational modification (PTM) that has emerged as hallmark of pericentromeric heterochromatin .
    Histone H3K9me3 (1-15) TFA
  • HY-126207

    Histone Demethylase Cancer
    CBN209350 is a selective KDM4 inhibitor with an IC50 of 4 μM. CBN209350 exerts antiproliferative effects on prostate cancer cells. CBN209350 can be used for the research of prostate cancer .
    CBN209350

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