| 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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Cancer Commun (Lond), 2024, 10.1002/cac2.12545
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Cancer Commun (Lond), 2024, 44(6):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 activates 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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Signal Transduct Target Ther, 2021, 6(1):77
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J Cell Physiol, 2021, 10.1002/jcp.30587
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PLoS One, 2017, 12(3):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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J Med Virol, 2023, 95(2):e28478
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Am J Cancer Res, 2021, 11(10):4994-5005
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J Med Virol, 2019, 91(8):1440-1447
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