The chemical class of Centriolin activators consists of compounds that indirectly influence Centriolin function by modulating cell cycle pathways, microtubule dynamics, and signaling cascades relevant to centrosome function. These activators operate through different mechanisms, impacting cellular processes that are critical for the proper functioning of Centriolin. Compounds such as Paclitaxel, Vinblastine, and Nocodazole, known for their effects on microtubule dynamics, are significant contributors to this class. Paclitaxel stabilizes microtubules and can influence Centriolin activity by affecting spindle assembly and centrosome function. Vinblastine and Nocodazole, by disrupting microtubule dynamics, can indirectly affect Centriolin function in organizing centrosome structure. Cyclin-dependent kinase inhibitors like Roscovitine and Purvalanol A play a crucial role in cell cycle regulation. Their ability to modulate cell cycle progression can have downstream effects on Centriolin activity, given its involvement in cell division processes. Similarly, Colchicine, by disrupting microtubule polymerization, can impact Centriolin activity through alterations in centrosome dynamics.
Other compounds such as Forskolin, Rapamycin, and U0126 contribute to the regulation of Centriolin through their effects on cellular signaling pathways. Forskolin activates adenylate cyclase, influencing signaling pathways that can indirectly affect Centriolin function. Rapamycin, an mTOR inhibitor, and U0126, an MEK inhibitor, can impact cell cycle progression and MAPK signaling, respectively, potentially influencing Centriolin activity. Furthermore, Lithium Chloride, PD98059, and SP600125, through their modulation of Wnt signaling, MAPK/ERK pathway, and JNK inhibition, respectively, can influence Centriolin activity. Lithium Chloride's impact on Wnt signaling, PD98059's role as an MEK inhibitor, and SP600125's inhibition of JNK, all contribute to the regulation of cellular processes that are crucial for the function of Centriolin, especially in the context of cell cycle control and response to cellular stress.
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| Product Name | CAS # | Catalog # | QUANTITY | Price | Citations | RATING |
|---|---|---|---|---|---|---|
Taxol | 33069-62-4 | sc-201439D sc-201439 sc-201439A sc-201439E sc-201439B sc-201439C | 1 mg 5 mg 25 mg 100 mg 250 mg 1 g | $40.00 $73.00 $217.00 $242.00 $724.00 $1196.00 | 39 | |
Stabilizes microtubules, potentially influencing Centriolin activity by affecting centrosome function and spindle assembly. | ||||||
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 | |
Disrupts microtubule dynamics, which can indirectly influence Centriolin activity in centrosome organization. | ||||||
Purvalanol A | 212844-53-6 | sc-224244 sc-224244A | 1 mg 5 mg | $71.00 $291.00 | 4 | |
Another cyclin-dependent kinase inhibitor, may affect Centriolin function by modulating cell cycle regulation. | ||||||
Forskolin | 66575-29-9 | sc-3562 sc-3562A sc-3562B sc-3562C sc-3562D | 5 mg 50 mg 1 g 2 g 5 g | $76.00 $150.00 $725.00 $1385.00 $2050.00 | 73 | |
Activates adenylate cyclase, influencing cellular signaling pathways that can indirectly affect Centriolin function. | ||||||
Rapamycin | 53123-88-9 | sc-3504 sc-3504A sc-3504B | 1 mg 5 mg 25 mg | $62.00 $155.00 $320.00 | 233 | |
Inhibits mTOR signaling, which can influence cell cycle progression and potentially Centriolin activity. | ||||||
Lithium | 7439-93-2 | sc-252954 | 50 g | $214.00 | ||
Influences Wnt signaling pathway, potentially impacting Centriolin activity as part of cellular signaling regulation. | ||||||
PD 98059 | 167869-21-8 | sc-3532 sc-3532A | 1 mg 5 mg | $39.00 $90.00 | 212 | |
An MEK inhibitor, can indirectly influence Centriolin function by affecting MAPK/ERK pathway involved in cell cycle control. | ||||||
SP600125 | 129-56-6 | sc-200635 sc-200635A | 10 mg 50 mg | $40.00 $150.00 | 257 | |
An inhibitor of JNK, may modulate Centriolin activity through pathways related to cell stress and cycle regulation. | ||||||