Date published: 2025-9-20

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EG236749 Inhibitors

Tesl1, predicted to enable zinc ion binding activity and play a role in the negative regulation of cell population proliferation, emerges as a key regulator in cellular processes. The direct and indirect inhibitors presented in the table highlight diverse strategies for modulating Tesl1. Direct inhibitors like TPEN specifically target Tesl1's predicted zinc ion binding activity, potentially disrupting its functional role and leading to inhibition of cell proliferation.

Indirect inhibitors, such as PD 0332991 and Wortmannin, modulate pathways related to Tesl1, impacting its negative regulation of cell population proliferation. Sorafenib and Rapamycin influence pathways like Raf/MEK/ERK and mTORC1, respectively, showcasing the intricate regulatory network that Tesl1 is a part of. Inhibition of Tesl1 involves interference at multiple levels, including cellular energy balance, cytoskeletal dynamics, and growth factor signaling. These inhibitors provide a comprehensive approach to understanding Tesl1's function and present potential avenues for further investigation into its precise role in cellular processes.

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