Date published: 2025-9-14

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DEPDC1 Activators

DEPDC1 Activators encompass a diverse range of chemicals associated with the modulation or influence on the DEPDC1 protein function. DEPDC1, or DEP domain-containing protein 1, holds significance in cell cycle progression and other cellular processes. While the identification of direct chemical activators for DEPDC1 remains elusive, a multitude of chemicals have been identified which can indirectly influence its activity.

Among these, Forskolin, known for activating adenylate cyclase, elevates cAMP levels, which can intersect with DEPDC1-related pathways. Retinoic acid, a Vitamin A metabolite, plays a role in modulating cell growth and differentiation, thereby potentially having an indirect effect on DEPDC1. Rapamycin, an mTOR inhibitor, by affecting cell growth and metabolism pathways, provides an avenue for DEPDC1 interaction. The EGFR inhibitor Erlotinib, by modulating cell growth signaling pathways, also presents a context for affecting DEPDC1. Similarly, Wortmannin and LY294002, both PI3K inhibitors, play roles in cell survival and growth pathways, offering another potential connection to DEPDC1. Trichostatin A, as a histone deacetylase inhibitor, and 5-Azacytidine, a DNA methyltransferase inhibitor, can alter gene expression landscapes, creating a backdrop for DEPDC1 modulation. Staurosporine, recognized as a potent protein kinase inhibitor, and Genistein, a tyrosine kinase inhibitor, both govern cell signaling, forging yet another link to DEPDC1. 2-Deoxyglucose, by affecting cellular energy metabolism, can indirectly influence DEPDC1-associated processes. Lastly, U0126, as an inhibitor of MEK1/2, steers the MAPK signaling pathway, a potential influencer of DEPDC1.

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