| S8842 |
BAY-218
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BAY-218 is a potent and selective small-molecule AhR inhibitor, inhibiting AhR nuclear translocation, dioxin response element (DRE)-luciferase reporter expression and AhR-regulated target gene expression induced by both exogenous and endogenous AhR ligands.
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Sci Rep, 2025, 15(1):8826
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Scientific Reports, 2025, 8826
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Cancer Communications, 2024, 670-694
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| S3205 |
Perillaldehyde
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Perillaldehyde (Perilladehyde, Perillal, PAE, PA), the main component of Perilla frutescens (a traditional medicinal antioxidant herb), inhibits BaP-induced AHR activation and ROS production, inhibits BaP/AHR-mediated release of the CCL2 chemokine, and activats the NRF2/HO1 antioxidant pathway.
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Front Cell Dev Biol, 2025, 13:1598520
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| S1891 |
Carbidopa
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Carbidopa is an aromatic-L-amino-acid decarboxylase inhibitor with an IC50 of 29 ± 2 μM.
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Communications Medicine, October 9, 2025, 420
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PLoS One, March 2, 2017, e0173240
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PLOS One, March 02, 2017, e0173240
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| S2313 |
Indole-3-carbinol
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Indole-3-carbinol suppresses NF-κB and IκBα kinase activation, and it is also an inhibitor of WWP1 (E3 ubiquitin ligase with WW domain).
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American Journal of Cancer Research, October 15, 2021, 4994-5005
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Therapeutic Advances in Medical Oncology, July 29, 2020, 1758835920937891
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J Med Virol, 2023, 95(2):e28478
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