Date published: 2025-9-19

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NCOAT Inhibitors

The identified chemicals, acting as indirect inhibitors of NCOAT, exert their effects through modulation of specific signaling pathways. Suramin, Resveratrol, Imatinib, Nifedipine, Wortmannin, AG-490, Rapamycin, PD98059, LY294002, SB203580, SP600125, and U0126 impact diverse cellular processes by influencing pathways such as purinergic signaling, sirtuin regulation, Bcr-Abl signaling, L-type calcium channels, PI3K-Akt, JAK-STAT, mTOR, MAPK/ERK, and JNK. The indirect modulation of NCOAT by these chemicals may involve alterations in phosphorylation status and enzymatic activity, contributing to the regulation of cellular functions influenced by NCOAT and the associated signaling cascades. NCOAT inhibitors encompass a range of compounds that, while not directly targeting NCOAT, exert their inhibitory effects through the modulation of specific signaling pathways. These pathways, including purinergic signaling, sirtuin regulation, Bcr-Abl signaling, L-type calcium channels, PI3K-Akt, JAK-STAT, mTOR, MAPK/ERK, and JNK, play crucial roles in cellular processes influenced by NCOAT. The identified chemicals, such as Suramin, Resveratrol, Imatinib, and others, can indirectly impact NCOAT activity, altering its phosphorylation status and enzymatic function. This class of inhibitors serves as valuable tools for exploring the intricate regulatory networks governing NCOAT and its involvement in various cellular functions. Understanding the specific pathways affected by these inhibitors contributes to advancing our knowledge of NCOAT-associated signaling and its implications in diverse biological contexts.

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