The chemical class referred to as DPY19L1 Inhibitors primarily encompasses agents that can affect DPY19L1 indirectly through their modulation of various cellular pathways or processes. For instance, Wortmannin and LY294002 are phosphoinositide 3-kinase (PI3K) inhibitors. Their capability to inhibit PI3K allows them to modulate lipid signaling and membrane dynamics, which may interfere with the membrane localization and function of DPY19L1. Likewise, SB203580, a p38 MAPK inhibitor, can disrupt cellular stress signaling and thus, can alter DPY19L1's presumptive involvement in these pathways. Blebbistatin affects non-muscle myosin II, thereby altering cell migration and adhesion, processes where DPY19L1 could have regulatory input.
Chemicals like BAPTA, Ionomycin, and DAPT intervene in calcium and Notch signaling pathways, respectively, and could affect the expression or functional state of DPY19L1. Okadaic Acid, a serine/threonine phosphatase inhibitor, offers a more general approach to alter multiple cellular pathways that may involve DPY19L1. SU11274 and PD173074 are growth factor receptor inhibitors and have to modulate growth factor signaling that might implicate DPY19L1. Fenretinide serves to modulate retinoid signaling and can have an impact on the expression levels of proteins like DPY19L1. These chemicals provide a toolkit for affecting DPY19L1 through a variety of cellular mechanisms.
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