Date published: 2025-9-14

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POGZ Inhibitors

Chemical inhibitors of POGZ can modulate its function by targeting the cell cycle mechanisms in which it is involved. Alsterpaullone, Roscovitine, Olomoucine, Purvalanol A, Flavopiridol, Dinaciclib, and SNS-032 are known to inhibit cyclin-dependent kinases (CDKs), which are crucial in the regulation of the cell cycle. Alsterpaullone achieves this by acting as a potent antagonist to CDKs, thereby directly affecting the function of POGZ associated with cell cycle progression. Roscovitine, with its selective inhibition of CDKs, can interfere with the progression of the cell cycle, leading to a functional inhibition of POGZ. Similarly, Olomoucine's action on CDKs can suppress POGZ's activity by disrupting the cell cycle phases it regulates. Purvalanol A's targeting of CDKs disrupts the precise control of the cell cycle that POGZ might influence, while Flavopiridol, with its broader range of CDK inhibition, can affect multiple points of the cell cycle where POGZ is active.

Continuing with this theme, Dinaciclib's potent inhibition of CDKs can halt the cell cycle events regulated by POGZ, impacting its functional role. SNS-032 goes a step further by not only affecting cell cycle progression but also transcription regulation, which are processes where POGZ plays a regulatory role. Milciclib, although primarily a CDK inhibitor, also targets other kinases involved in cell cycle control, which can disrupt the kinase-dependent regulatory pathways of POGZ. PD0332991 (Palbociclib), Ribociclib, and Abemaciclib specifically inhibit CDK4/6, which leads to an arrest in the G1 phase of the cell cycle. This action can functionally inhibit POGZ by preventing the cell cycle from progressing past a phase where POGZ is functionally significant. LEE011, another name for Ribociclib, reinforces this inhibition of CDK4/6, further solidifying the functional impediment of POGZ at the G1 phase checkpoint. Through these mechanisms, the selected chemicals can modulate the activity of POGZ by directly disrupting the cellular processes it regulates.

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