C17orf82 inhibitors span a range of classes, including PI3K inhibitors like LY294002 and Wortmannin that modulate the phosphatidylinositol signaling system, which is a critical pathway for numerous cellular functions including growth and survival. Other chemicals listed, such as PD98059 and U0126, which are MEK inhibitors, along with SB203580 and SP600125, which inhibit different MAP kinases, are chosen based on the possible interaction with the MAPK/ERK pathway, a pivotal route for cell division, differentiation, and response to external stress signals.
Inhibitors such as Rapamycin affect the mTOR pathway, which is central to cell growth and proliferation, indicating a broad approach to downregulating complex pathways where C17orf82 might be implicated. Proteasome and kinase inhibitors like Bortezomib, ZM-447439, Dasatinib, Imatinib, and Sorafenib are selected on the premise that C17orf82 could be part of or influence protein degradation, cell cycle progression, integrin signaling, and oncogenic transformation. These inhibitors act on specific enzymes and proteins, potentially altering the protein stability, signaling, and functional state of pathways with which C17orf82 may interact.
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