Date published: 2025-9-11

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SPANX-N1 Inhibitors

SPANX-N1 inhibitors encompass a variety of chemical compounds that exert their inhibitory action through interference with cellular processes critical for mitotic function, where SPANX-N1 is known to play a role. Certain alkaloid agents target microtubule assembly, a key component of the mitotic spindle, which is essential for cell division and the proper function of SPANX-N1. By destabilizing the mitotic spindle, these compounds indirectly compromise the activity of SPANX-N1 during mitosis. Other inhibitors work by stabilizing microtubules and preventing their disassembly, which can adversely affect the mitotic spindle dynamics and, consequently, the activity of SPANX-N1. Furthermore, some compounds bind directly to tubulin, inhibiting microtubule polymerization, thereby disrupting the cytoskeletal organization and spindle formation that are essential for SPANX-N1's function in cell division.

Additional inhibitors operate by targeting specific proteins involved in mitotic spindle formation and function, such as kinesin Eg5 and various kinases. For instance, by inhibiting kinesin Eg5, certain inhibitors can prevent the proper assembly of the mitotic spindle, leading to a potential inhibition of SPANX-N1. Similarly, compounds that inhibit key kinases involved in chromosome alignment and segregation can indirectly affect the localization and function of SPANX-N1 during mitosis. Cyclin-dependent kinase inhibitors also play a role, potentially leading to the inhibition of SPANX-N1 by affecting cell cycle progression and thus the mitotic processes that SPANX-N1 is implicated in.

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