LY294002 and PD98059 are compounds that can inhibit key signaling molecules PI3K and MEK1/2, respectively. Disruption of these enzymatic activities by these inhibitors can lead to alterations in the PI3K/Akt and MAPK/ERK pathways, which are fundamental to cell proliferation and survival. Rapamycin and Bortezomib represent inhibitors that can target mTOR and the ubiquitin-proteasome system, each a crucial node in the regulation of cell growth and protein turnover. SB203580 and SP600125 can inhibit p38 MAP kinase and JNK, modulating stress responses and apoptosis.
U0126, like PD98059, can inhibit MEK and thus impact the MAPK/ERK pathway. PP2, Dasatinib, and Gefitinib can alter signaling processes by targeting Src-family kinases, BCR-ABL, and EGFR, respectively. Such changes in tyrosine kinase activity can have broad implications for signal transduction networks. Sorafenib and Imatinib offer broader kinase inhibition, affecting multiple kinases and potentially leading to a wide array of alterations in cellular signaling.
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