Date published: 2025-10-7

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C1orf151-NBL1 Activators

The functional activity of the C1orf151-NBL1 fusion protein can be influenced by various chemical compounds that target the distinct functionalities of the C1orf151 and NBL1 gene products. Retinoic acid and Genistein, known for their roles in gene expression and cell differentiation, might enhance the NBL1 component's involvement in developmental processes. Retinoic acid's influence on gene expression and Genistein's tyrosine kinase inhibitory action could modulate pathways relevant to cell differentiation and development, aligning with NBL1's biological role. Forskolin, through its effect on increasing cAMP levels, and Dibutyryl-cAMP, a cAMP analog, could potentially modulate the C1orf151 component's function in cellular signaling processes influenced by cAMP. Curcumin, with its wide-ranging effects on cell signaling, including pathways involved in proliferation and apoptosis, could impact both C1orf151 and NBL1 components, influencing various cellular processes.

Compounds like LY294002, a PI3K inhibitor, and Rapamycin, an mTOR inhibitor, could play a role in modulating cell survival and proliferation pathways, potentially affecting the functionality of both components of the fusion protein. Trichostatin A, an HDAC inhibitor, may influence gene expression and protein acetylation, thus affecting both C1orf151 and NBL1 functions within the fusion protein. Additionally, Spermidine and Resveratrol, known for promoting autophagy and influencing cellular aging and differentiation, might support the NBL1 component's involvement in development within the fusion protein. Epigallocatechin gallate (EGCG), by modulating cell proliferation and apoptosis pathways, and 17-AAG (Tanespimycin), an HSP90 inhibitor affecting protein folding, could also influence the functional activity of both components of the fusion protein. Together, these compounds illustrate the complexity in modulating the activity of the C1orf151-NBL1 fusion protein, reflecting the diverse functional aspects and regulatory mechanisms of its constituent parts.

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