Date published: 2025-10-11

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LOC730205 Inhibitors

Wortmannin and Triciribine act on the PI3K/AKT pathway, a critical axis in the regulation of cell growth and survival, which LOC730205 may be part of. Rapamycin's inhibition of mTOR can have wide-ranging effects on cell growth and metabolism, which are likely to intersect with the functions of LOC730205. U0126's blockade of the MEK/ERK pathway and PD0332991's targeting of cyclin-dependent kinases can halt cell proliferation, a process where LOC730205 may be implicated.

Bortezomib disrupts protein degradation machinery, which can lead to an altered protein turnover rate, potentially affecting LOC730205's stability. Cyclopamine's interference with Hedgehog signaling and Ibrutinib's action on Bruton's tyrosine kinase can modify cell communication and immune responses, respectively, both of which may involve LOC730205. Thapsigargin's perturbation of calcium homeostasis can have implications for calcium-dependent signaling in which LOC730205 might play a part. Imatinib's broad-spectrum tyrosine kinase inhibition and Axitinib's vascular endothelial growth factor receptor (VEGFR) inhibition can alter growth factor signaling, affecting cellular processes that LOC730205 may be associated with. ABT-199, by inhibiting BCL-2, can trigger apoptotic pathways that are essential for cell fate decisions, which could be regulated by LOC730205.

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