The chemical class of AP-4 inhibitors is a theoretical grouping of compounds that would affect the Adaptor Protein complex 4 (AP-4) indirectly. Since direct inhibitors of AP-4 are not well-defined, this class includes a variety of chemical compounds that influence cellular processes or signaling pathways related to AP-4's function. These chemicals span multiple classes, including kinase inhibitors, vesicular transport disruptors, and microtubule affecting agents.
Each chemical listed operates within a unique mechanism, affecting various aspects of cellular function that would, in turn, affect AP-4 activity. The listed compounds are capable of altering vesicular trafficking, affecting vesicle formation, stabilizing or destabilizing cytoskeletal elements, or disrupting intracellular signaling that would indirectly influence AP-4 functions. The mode of action for each compound interacts with cellular components that are known to either directly or indirectly associate with the functions of the AP-4 complex. The disruption of these components can result in the impairment of AP-4's role in sorting and trafficking proteins to specific destinations within the cell. These chemicals represent a broad spectrum of potential indirect modulators of AP-4, reflecting the complexity of targeting a protein involved in such a fundamental and intricate cellular process as vesicular transport.
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Product Name | CAS # | Catalog # | QUANTITY | Price | Citations | RATING |
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Vinblastine | 865-21-4 | sc-491749 sc-491749A sc-491749B sc-491749C sc-491749D | 10 mg 50 mg 100 mg 500 mg 1 g | $100.00 $230.00 $450.00 $1715.00 $2900.00 | 4 | |
Vinblastine binds to tubulin and inhibits microtubule formation. Since AP-4-mediated sorting and trafficking of vesicles is microtubule-dependent, vinblastine can impede AP-4’s function in these pathways. | ||||||
Nocodazole | 31430-18-9 | sc-3518B sc-3518 sc-3518C sc-3518A | 5 mg 10 mg 25 mg 50 mg | $58.00 $83.00 $140.00 $242.00 | 38 | |
Nocodazole is a microtubule-depolymerizing agent. It can disrupt microtubule networks and thereby impede processes, including those involving AP-4, that are dependent on intact microtubule transport systems. |