GNE-272

≥98%

  • Product Code: 100684
  CAS:    1936428-93-1
Molecular Weight: 424.47 g./mol Molecular Formula: C₂₂H₂₅FN₆O₂
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Density: Storage Condition: 2-8℃
Product Description: GNE-272 is primarily utilized in the field of oncology research due to its role as a potent and selective inhibitor of the BRD4 protein, which is implicated in the regulation of gene expression. This compound is particularly significant in studies focusing on cancers driven by aberrant gene transcription, such as certain types of leukemia and solid tumors. By inhibiting BRD4, GNE-272 helps in disrupting the transcription of oncogenes, thereby potentially halting the proliferation of cancer cells. Its application extends to preclinical research where it is used to understand the mechanisms of BRD4 in cancer biology and to evaluate the therapeutic potential of BRD4 inhibition in various cancer models. Additionally, GNE-272 serves as a valuable tool in the development of novel cancer therapies, aiding in the identification of biomarkers and the optimization of drug candidates targeting epigenetic regulators.
Sizes / Availability / Pricing:
Size (g) Availability Price Quantity
0.002 10-20 days $530.04
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0.005 10-20 days $915.52
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GNE-272
GNE-272 is primarily utilized in the field of oncology research due to its role as a potent and selective inhibitor of the BRD4 protein, which is implicated in the regulation of gene expression. This compound is particularly significant in studies focusing on cancers driven by aberrant gene transcription, such as certain types of leukemia and solid tumors. By inhibiting BRD4, GNE-272 helps in disrupting the transcription of oncogenes, thereby potentially halting the proliferation of cancer cells. Its application extends to preclinical research where it is used to understand the mechanisms of BRD4 in cancer biology and to evaluate the therapeutic potential of BRD4 inhibition in various cancer models. Additionally, GNE-272 serves as a valuable tool in the development of novel cancer therapies, aiding in the identification of biomarkers and the optimization of drug candidates targeting epigenetic regulators.
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