Date published: 2025-11-2

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FAM60A Inhibitors

Chemical inhibitors of FAM60A can target and modulate the protein's activity by interfering with various signaling pathways and cellular mechanisms that are essential for its function in chromatin remodeling. For instance, PD173074, an inhibitor of the fibroblast growth factor receptor (FGFR), can suppress the downstream signaling required for the functions of FAM60A. Similarly, Y-27632 can disrupt the organization of the actin cytoskeleton, a structural component vital for the nuclear processes where FAM60A is operational. Inhibiting transforming growth factor-beta (TGF-β) receptors using SB431542 would impede the TGF-β signaling, potentially affecting chromatin dynamics and, consequently, the activity of FAM60A. LDN-193189, with its potent inhibition of the BMP pathway, can alter chromatin states and gene expression patterns, leading to the functional suppression of FAM60A. Additional chemical inhibitors work by targeting different aspects of the chromatin remodeling processes that involve FAM60A. For example, SP600125, which inhibits the c-Jun N-terminal kinase (JNK), can interfere with signaling pathways that overlap with those governing chromatin architecture and hence FAM60A's role. U0126, a MEK inhibitor, can indirectly affect FAM60A by inhibiting the MAPK/ERK pathway, which is integral to cell cycle control and gene expression. PI3K/AKT/mTOR signaling, critical for gene expression and chromatin remodeling, can be suppressed by LY294002, which would also impact FAM60A's function. Rapamycin, by inhibiting mTOR, affects cellular growth and gene expression processes that are essential for FAM60A's role in chromatin remodeling. Trichostatin A, as a histone deacetylase inhibitor, can alter the chromatin landscape and affect FAM60A's activity. SGC-CBP30 suppresses the acetylation of histones, potentially restricting FAM60A's regulatory role in chromatin remodeling. Lastly, ICG-001 and ZM447439 disrupt the Wnt/β-catenin signaling and Aurora kinase activity, respectively, both of which are critical to maintaining chromosomal architecture and gene expression patterns that FAM60A is known to influence.

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