EVI5L inhibitors encompass a range of compounds that can indirectly influence the function of EVI5L as a GTPase-activating protein. These modulators primarily target various aspects of GTPase signaling pathways, either by inhibiting specific GTPases or by affecting upstream or downstream components of these pathways. Inhibitors like NSC 23766 Trihydrochloride and ML 141 target specific GTPases such as Rac1 and Cdc42. By modulating these GTPases, these compounds can indirectly influence the broader signaling pathways in which EVI5L operates. Brefeldin A and SecinH3 affect the ARF GTPase family, either by disrupting GEF activity or inhibiting cytohesins. These alterations in GTPase signaling pathways can have downstream effects on the functions regulated by GTPase-activating proteins like EVI5L.
Statins, including Lovastatin and Simvastatin, and specific inhibitors like Farnesyltransferase Inhibitors (Tipifarnib) and Geranylgeranyltransferase Inhibitors (GGTI 298), impact the prenylation and localization of GTPases. Such modifications can indirectly affect the signaling pathways involving EVI5L. In summary, while direct inhibitors of EVI5L are not well-documented, the compounds listed provide avenues to modulate the GTPase pathways and related signaling mechanisms where EVI5L is involved. These inhibitors are valuable tools for investigating EVI5L's role in cellular signaling, providing insights into its biological functions.
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产品名称 | CAS # | 产品编号 | 数量 | 价格 | 应用 | 排名 |
---|---|---|---|---|---|---|
ZM-447439 | 331771-20-1 | sc-200696 sc-200696A | 1 mg 10 mg | ¥1692.00 ¥3937.00 | 15 | |
ZM447439 是一种极光激酶抑制剂。极光激酶对有丝分裂的进行至关重要;通过抑制极光激酶,ZM447439 可以间接抑制 EVI5 在有丝分裂中的功能。 |