Date published: 2025-11-24

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MATH-5 Inhibitors

MATH-5 (atonal bHLH transcription factor 7) inhibitors encompass a variety of chemical compounds that interact with different cellular signaling pathways, ultimately leading to the decreased functional activity of MATH-5. Specifically, some of these compounds inhibit kinase activity, which is crucial for the phosphorylation that regulates transcription factor functions, including those of MATH-5. Kinase inhibitors, by modulating phosphorylation states, have the ability to alter the activity of MATH-5 indirectly. Similarly, inhibition of the PI3K/Akt pathway affects cellular signaling contexts, which may impact the functional state of MATH-5 by preventing the activation of downstream targets that could be necessary for MATH-5's activity. Inhibition of the mTOR signaling pathway also results in reduced protein synthesis and may affect transcription factor activity, potentially leading to an indirect inhibition of MATH-5 due to decreased protein availability or altered regulatory mechanisms.

Furthermore, compounds that interfere with specific signaling pathways such as Hedgehog, TGF-beta, or Wnt/β-catenin can modulate the transcriptional profile of cells, thereby influencing the activity of transcription factors like MATH-5. For instance, the disruption of Smoothened within the Hedgehog pathway can alter downstream transcriptional events that affect MATH-5 activity. Inhibitors of proteasome function may lead to an accumulation of regulatory proteins that compete with or destabilize MATH-5, while compounds that affect the hypoxic response in cells can shift transcriptional dynamics, indirectly affecting MATH-5 activity. Moreover, cell cycle inhibitors that target CDKs can impact MATH-5 by altering cell cycle-dependent signaling pathways, potentially leading to reduced MATH-5 activity.

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Product NameCAS #Catalog #QUANTITYPriceCitationsRATING

(±)-JQ1

1268524-69-1sc-472932
sc-472932A
5 mg
25 mg
$226.00
$846.00
1
(0)

Inhibits BET bromodomain proteins, which can result in altered chromatin states and transcription factor accessibility, potentially decreasing MATH-5 mediated transcriptional activity.