Date published: 2025-10-13

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FAM178B Activators

Epigallocatechin gallate and Resveratrol engage in the subtle art of epigenetic modulation. By influencing the activity of enzymes that control the epigenetic landscape, these compounds can facilitate a chromatin context that is more permissive to the transcriptional activation of FAM178B. Similarly, Sodium butyrate and 5-Aza-2'-deoxycytidine disrupt epigenetic silencing, potentially leading to the derepression of FAM178B gene expression. SP600125, LY294002, PD98059, and SB203580, exert their influence by intercepting critical signaling pathways within the cell. By inhibiting the function of key kinases, these molecules introduce alterations in the cellular signaling milieu, which can culminate in the modulation of FAM178B's expression or its regulatory network. In this intricate dance of cellular signaling, Rapamycin emerges as a pivotal player, curtailing the mTOR pathway, hence affecting a plethora of cellular functions that can create an environment conducive to FAM178B's activation.

The diterpene Forskolin, alongside the cAMP analog Dibutyryl-cAMP, raises the levels of intracellular cAMP, subsequently activating PKA, a kinase with a broad spectrum of substrates. Through the phosphorylation of downstream targets, PKA orchestrates a cascade of intracellular events that can indirectly influence the activity of FAM178B. Adding to the complexity, Genistein, an isoflavone that acts as a tyrosine kinase inhibitor, modulates various signaling pathways, influencing the function and expression of proteins within the intricate web of cellular signaling in which FAM178B is entwined.

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