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Results for "

BRK

" in MedChemExpress (MCE) Product Catalog:

5

Inhibitors & Agonists

3

Recombinant Proteins

1

Antibodies

Targets Recommended:
Cat. No. Product Name Target Research Areas Chemical Structure
  • HY-108333
    SB-633825
    2 Publications Verification

    Tie BRK Cardiovascular Disease Cancer
    SB-633825 is a potent and ATP-competitive inhibitor of TIE2, LOK (STK10) and BRK with IC50s of 3.5 nM, 66 nM, 150 nM, respectively. SB-633825 can inhibit cancer cell growth and angiogenesis .
    SB-633825
  • HY-110244

    BRK Cancer
    Tilfrinib (compound 4f) is a potent and selective Brk/PTK6 inhibitor with an IC50 value of 3.15 nM for Brk. Tilfrinib shows good anti-proliferative activity and has potential of anti-tumour .
    Tilfrinib
  • HY-115514A

    BRK Cancer
    BRK inhibitor P21d hydrochloride is a potent breast tumor kinase (BRK/PTK6) inhibitor with an IC50 of 30 nM. BRK inhibitor P21d hydrochloride inhibits p-SAM68 with an IC50 of 52 nM. BRK inhibitor P21d hydrochloride can be used to evaluate the in vivo activity of BRK inhibitors in xenograft breast tumor models .
    <em>BRK</em> inhibitor P21d hydrochloride
  • HY-RS01625

    Small Interfering RNA (siRNA) Others

    BRK1 Human Pre-designed siRNA Set A contains three designed siRNAs for BRK1 gene (Human), as well as a negative control, a positive control, and a FAM-labeled negative control.

    BRK1 Human Pre-designed siRNA Set A
    BRK1 Human Pre-designed siRNA Set A
  • HY-122664

    BRK Cancer
    XMU-MP-2 is a BRK inhibitor with significant inhibitory activity on BRK-positive cells. XMU-MP-2 inhibits oncogenic BRK-driven tumor growth in a mouse xenograft model. XMU-MP-2 also synergizes with HER2 inhibitors or endoplasmic reticulum (ER) blockade to exert antiproliferative activity .
    XMU-MP-2

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