Date published: 2025-9-13

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SCAPER Inhibitors

SCAPER inhibitors are chemical compounds that impede the functional activity of SCAPER, a protein known to be involved in the regulation of the cell cycle, particularly in the transition from the G1 to S phase. Palbociclib, for example, is a selective inhibitor of CDK4/6, which are critical for the progression of the cell cycle. By preventing the cell from moving past the G1 phase, Palbociclib can indirectly hinder SCAPER's role in cell cycle regulation. Similarly, Roscovitine and Flavopiridol act as CDK inhibitors, with the former targeting multiple CDKs and the latter having a broad inhibitory effect on CDKs involved in transcription regulation. These inhibitors can impede the progression of the cell cycle, thereby reducing the functional relevance of SCAPER in this process. Sirolimus and Rapamycin, both mTOR inhibitors, disrupt essential signaling pathways for cell growth and proliferation, which in turn can decrease the activity of SCAPER by curbing the proliferative signals it may enhance.

Additional compounds such as Trichostatin A, a histone deacetylase inhibitor, and Nutlin-3, an MDM2 antagonist, indirectly modulate the expression and stability of SCAPER by altering the transcriptional landscape and stabilizing p53, respectively. U0126, a MEK inhibitor, blocks the MAPK/ERK pathway, reducing cell proliferation and thereby the activity of SCAPER. LY294002, a PI3K inhibitor, impedesAKT signaling, affecting cell growth and survival, which can also reduce SCAPER's role in the cell cycle. Thalidomide, by affecting cereblon binding and leading to the degradation of transcription factors, may indirectly alter the function of SCAPER by modifying the cell's transcriptional programs. Venetoclax, by inducing apoptosis, can decrease the levels of SCAPER indirectly through a reduction in cell proliferation. Alisertib, an inhibitor of Aurora kinase A, disrupts mitosis and subsequent cell cycle progression, thus affecting SCAPER's function in regulating the cell cycle. Collectively, these inhibitors demonstrate a range of mechanisms by which the functional activity of SCAPER can be indirectly diminished, elucidating the diverse cellular pathways and processes that SCAPER may be implicated in.

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