Date published: 2025-9-12

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NO145 Inhibitors

Chemical inhibitors of NO145 act by disrupting the dynamics of the cellular cytoskeleton, which is essential for its function in meiotic processes. Phalloidin and Jasplakinolide target actin filaments, a key component of the cytoskeleton. Phalloidin binds to F-actin, stabilizing the filaments and thereby preventing their depolymerization. This stabilization can inhibit NO145 by disrupting the delicate balance of actin filament turnover required for its localization and function. Jasplakinolide also affects actin dynamics but does so by promoting polymerization and filament stability, which similarly can alter the actin dynamics necessary for NO145's role. In contrast, Latrunculin A, Cytochalasin D, Swinholide A, and Chondramide disrupt actin filaments through different mechanisms. Latrunculin A sequesters actin monomers, while Cytochalasin D caps the growing ends of filaments, both preventing the addition of new monomers. Swinholide A severs actin filaments and Chondramide binds to actin, inhibiting its polymerization, all of which can inhibit NO145 by altering the actin framework it relies on.

The inhibitors that target microtubules, another cytoskeletal element, also affect NO145's function. Colchicine, Nocodazole, and Vinblastine disrupt microtubule polymerization, while Paclitaxel and Epothilone B stabilize microtubules beyond their normal dynamics. Colchicine binds to tubulin, preventing microtubule assembly, and Nocodazole blocks polymerization, altering the dynamics and possibly the chromosome movements NO145 is associated with. Vinblastine binds to tubulin to prevent microtubule assembly, potentially affecting NO145's role in chromosome pairing. Conversely, Paclitaxel and Epothilone B prevent microtubule disassembly, which can also inhibit NO145 by preventing the normal dynamics of microtubules required for its function. Lastly, Griseofulvin disrupts microtubule function by binding to tubulin, which can inhibit NO145 by impairing the microtubule-dependent processes critical for the assembly or function of the synaptonemal complex during meiosis. Each of these chemicals, by affecting either actin or microtubule structures, can inhibit the normal function of NO145 in meiotic chromosome organization.

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