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 |
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Staurosporine | 62996-74-1 | sc-3510 sc-3510A sc-3510B | 100 µg 1 mg 5 mg | ¥925.00 ¥1692.00 ¥4377.00 | 113 | |
Staurosporine 是一种有效的蛋白激酶抑制剂。众所周知,EVI5 可调控细胞分裂,而且其定位对其功能非常重要,因此石硫合剂可通过改变 EVI5 在细胞周期中发挥作用所需的蛋白质的磷酸化状态来间接抑制 EVI5。 | ||||||
Mitoxantrone | 65271-80-9 | sc-207888 | 100 mg | ¥3148.00 | 8 | |
米托蒽醌是一种蒽二酮类抗肿瘤药物。它插入DNA并破坏DNA复制和RNA合成。EVI5在染色体分离中发挥作用;米托蒽醌可以破坏这一过程,导致EVI5的功能抑制。 | ||||||
Alsterpaullone | 237430-03-4 | sc-202453 sc-202453A | 1 mg 5 mg | ¥756.00 ¥3452.00 | 2 | |
紫檀烯酮是一种细胞周期蛋白依赖性激酶抑制剂。通过抑制 CDK,这种化合物可以改变细胞周期检查点,从而可能抑制 EVI5 在细胞周期调控中的作用。 | ||||||
Roscovitine | 186692-46-6 | sc-24002 sc-24002A | 1 mg 5 mg | ¥1038.00 ¥2933.00 | 42 | |
Roscovitine 是一种细胞周期蛋白依赖性激酶的选择性抑制剂。通过抑制这些激酶,细胞周期可以停止,从而抑制 EVI5 参与细胞周期控制。 | ||||||
Apigenin | 520-36-5 | sc-3529 sc-3529A sc-3529B sc-3529C sc-3529D sc-3529E sc-3529F | 5 mg 100 mg 1 g 5 g 25 g 100 g 1 kg | ¥361.00 ¥2369.00 ¥8123.00 ¥12726.00 ¥25971.00 ¥34591.00 ¥57606.00 | 22 | |
Apigenin是一种黄酮,具有抗增殖作用。它可以抑制激酶活性并影响细胞周期进程,从而间接抑制EVI5与细胞分裂相关的功能。 | ||||||
Sunitinib, Free Base | 557795-19-4 | sc-396319 sc-396319A | 500 mg 5 g | ¥1692.00 ¥10379.00 | 5 | |
舒尼替尼是一种受体酪氨酸激酶抑制剂。它可以抑制对细胞周期进展和有丝分裂事件至关重要的信号通路,而 EVI5 与细胞周期进展和有丝分裂事件有关。 | ||||||
Palbociclib | 571190-30-2 | sc-507366 | 50 mg | ¥3554.00 | ||
Palbociclib 是 CDK4/6 的选择性抑制剂,对细胞周期的进展至关重要。通过阻碍细胞周期,EVI5 在有丝分裂过程中的功能被间接抑制。 | ||||||
AZD7762 | 860352-01-8 | sc-364423 | 2 mg | ¥1207.00 | ||
AZD7762 是一种检查点激酶抑制剂。它可以破坏检查点激酶的正常功能,而检查点激酶对细胞周期控制至关重要,EVI5 在细胞周期控制中发挥着调节作用。 | ||||||
UCN-01 | 112953-11-4 | sc-202376 | 500 µg | ¥2775.00 | 10 | |
UCN-01(7-羟基司他夫定)是一种强效蛋白激酶C抑制剂。它会影响细胞周期和应激反应通路,从而抑制EVI5的相关功能。 | ||||||
SP600125 | 129-56-6 | sc-200635 sc-200635A | 10 mg 50 mg | ¥733.00 ¥3012.00 | 257 | |
SP600125 是一种 c-Jun N 终止子激酶(JNK)抑制剂。通过抑制 JNK,它可以调节细胞周期进程和应激反应,间接导致 EVI5 的功能抑制。 |