Date published: 2025-10-13

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CIN85 Inhibitors

The class of CIN85 inhibitors represents a diverse array of chemical compounds strategically designed to interfere with the intricate cellular processes and signaling pathways associated with CIN85. These inhibitors operate with precision, targeting specific biochemical and cellular pathways to disrupt the elaborate network that governs CIN85 expression and functionality. BMS-536924, for instance, functions as a dual inhibitor targeting the IGF-1R and IR receptors, disrupting downstream signaling pathways linked to CIN85. Another notable inhibitor, NSC 697923, targets the SH3 domains crucial for protein-protein interactions, interfering with the assembly of protein complexes involving CIN85. Dacinostat, a histone deacetylase inhibitor, indirectly influences CIN85 by modulating epigenetic modifications and gene expression patterns. Tyrphostin AG 1478, a selective EGFR inhibitor, disrupts EGFR-mediated signaling cascades involving CIN85, highlighting a regulatory link between EGFR and CIN85 in cellular processes. PD 98059 inhibits MEK1, indirectly modulating the MAPK pathway and impacting CIN85 downstream effects. NSC 23766 targets the Rho GTPase Rac1, disrupting the RhoA/ROCK signaling pathway and modulating cellular processes governed by CIN85. Wortmannin inhibits PI3K, impacting the PI3K/Akt pathway, while C646 selectively inhibits the histone acetyltransferase p300, influencing epigenetic regulation. Sorafenib, a multi-kinase inhibitor, disrupts the Raf/MEK/ERK signaling cascade, indirectly affecting CIN85 downstream events. Triciribine inhibits Akt, revealing the interconnectedness of the PI3K/Akt pathway with CIN85 functions. PP2, a selective Src family kinase inhibitor, influences cellular processes governed by CIN85 by disrupting the role of Src family kinases. AG-490 inhibits JAK2, providing insights into the regulatory crosstalk between JAK/STAT signaling and CIN85-mediated cellular functions. These inhibitors collectively exemplify the precision and specificity achieved in targeting CIN85, illustrating the complex regulatory landscape governing its cellular functions.

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