Date published: 2025-9-15

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CRIK Activators

The CRIK activators represent a distinctive class of chemicals meticulously chosen to modulate the activity of the Cdc42/Rac interactive binding (CRIK) protein. These compounds exert their effects by precisely targeting key signaling pathways and cellular processes, orchestrating a sophisticated network that ultimately culminates in the activation of CRIK. One prominent member of this chemical class is Nordihydroguaiaretic acid (NDGA), which activates CRIK by inhibiting the c-Jun N-terminal kinase (JNK) signaling pathway. NDGA specifically targets the upstream kinases of JNK, preventing its activation and resulting in enhanced CRIK activity. This mechanism underscores the intricate connection between stress-activated signaling pathways and the regulation of CRIK, providing a nuanced understanding of the molecular events governing its activation.

Another noteworthy compound is Cerulenin, which activates CRIK by modulating the fatty acid synthesis pathway. By inhibiting fatty acid synthase (FAS), Cerulenin induces alterations in cellular lipid metabolism, leading to the subsequent activation of CRIK. This highlights the integration of metabolic pathways in the regulation of CRIK, showcasing the multifaceted nature of its activation. These CRIK activators collectively exemplify the targeted manipulation of cellular pathways to influence the activity of CRIK. Understanding the specific biochemical and cellular mechanisms impacted by each compound provides valuable insights into the molecular intricacies governing CRIK activation. This detailed knowledge opens avenues for targeted interventions in cellular processes and potential applications in research and biotechnology.

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