Staurosporine is a potent kinase inhibitor with a broad spectrum of targets, making it capable of disrupting multiple signaling pathways that may be essential for the activity of LOC729464. U0126 specifically inhibits the MEK1/2, which are upstream of ERK, a pathway crucial for cell cycle progression and differentiation. Similarly, LY294002 targets PI3K and can therefore impede AKT signaling, influencing processes where LOC729464 might be implicated PP2's inhibition of Src family tyrosine kinases can lead to alterations in cell growth and differentiation, while Thapsigargin can elevate cytosolic calcium levels and affect calcium-dependent proteins. PD173074's blockade of FGFR can influence cell growth and angiogenesis, which are vital for tissue maintenance and repair. SP600125 disrupts JNK signaling, affecting cellular responses to stress and apoptosis.
The IκB kinase inhibitor blocks the activation of NF-κB, a transcription factor that regulates genes involved in inflammation and immune response. Bortezomib impedes the proteasome's ability to degrade proteins, affecting protein levels and turnover. 2-Deoxy-D-glucose hampers glycolysis, which is fundamental for energy production in cells. Sorafenib's inhibition of RAF kinase, as well as VEGFR and PDGFR, can interfere with cell proliferation and the development of new blood vessels. ZM-447439 targets Aurora kinases involved in cell division, potentially impacting proteins that are crucial for mitotic processes.
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Product Name | CAS # | Catalog # | QUANTITY | Price | Citations | RATING |
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Sorafenib | 284461-73-0 | sc-220125 sc-220125A sc-220125B | 5 mg 50 mg 500 mg | $56.00 $260.00 $416.00 | 129 | |
A RAF kinase inhibitor that can also inhibit VEGFR and PDGFR, affecting cell proliferation and angiogenesis. | ||||||
ZM-447439 | 331771-20-1 | sc-200696 sc-200696A | 1 mg 10 mg | $150.00 $349.00 | 15 | |
An Aurora kinase inhibitor that can disrupt cell division, potentially affecting proteins involved in mitosis. |