Date published: 2025-10-3

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BBS6 Inhibitors

BBS6 inhibitors are a class of chemical compounds that specifically target and inhibit the activity of the Bardet-Biedl Syndrome protein 6 (BBS6). BBS6 is one of the critical components of the BBSome, a protein complex that plays a significant role in the trafficking of cargo proteins to the primary cilia. Primary cilia are microtubule-based organelles that serve as cellular signaling hubs, coordinating a wide range of signaling pathways, including those involved in cellular development and homeostasis. BBS6, as part of the BBSome complex, assists in the assembly and stabilization of this protein structure, facilitating the proper functioning of cilia. By inhibiting BBS6, these inhibitors disrupt the normal functioning of the BBSome, leading to altered ciliary signaling and impairments in the associated cellular processes.

The chemical structure of BBS6 inhibitors varies but generally consists of a scaffold capable of interacting with the BBS6 protein at its key functional domains. These inhibitors are designed to bind to specific regions on the BBS6 protein that are involved in its interaction with other components of the BBSome. By blocking these interactions, BBS6 inhibitors effectively prevent the formation or functionality of the BBSome, resulting in defective intracellular transport processes, particularly those linked to the ciliary membrane. The development of BBS6 inhibitors involves understanding the structural biology of BBS6 and its role within the BBSome, providing a blueprint for designing molecules that can selectively hinder its function. This disruption has broader implications for studying the roles of cilia in cellular organization and signaling pathways, providing a window into understanding the underlying biochemical mechanisms that depend on ciliary function.

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