Date published: 2025-10-11

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AP-4 Inhibitors

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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Items 11 to 12 of 12 total

Display:

Product NameCAS #Catalog #QUANTITYPriceCitationsRATING

Vinblastine

865-21-4sc-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
(0)

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

31430-18-9sc-3518B
sc-3518
sc-3518C
sc-3518A
5 mg
10 mg
25 mg
50 mg
$58.00
$83.00
$140.00
$242.00
38
(2)

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.