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CB7993113

CB7993113
CB7993113 is a potent AHR antagonist with an IC50 of 0.33 μM, directly binding the AHR protein and blocking its nuclear translocation. It inhibits polycyclic aromatic hydrocarbon (PAH)- and TCDD-induced reporter activity by 75% and 90%, respectively [1].
Catalog No. T86013Cas No. 819827-50-4

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CB7993113

Catalog No. T86013Cas No. 819827-50-4

CB7993113 is a potent AHR antagonist with an IC50 of 0.33 μM, directly binding the AHR protein and blocking its nuclear translocation. It inhibits polycyclic aromatic hydrocarbon (PAH)- and TCDD-induced reporter activity by 75% and 90%, respectively [1].
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10 mgInquiry10-14 weeks
50 mgInquiry10-14 weeks
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Product Introduction

Bioactivity
Description
CB7993113 is a potent AHR antagonist with an IC50 of 0.33 μM, directly binding the AHR protein and blocking its nuclear translocation. It inhibits polycyclic aromatic hydrocarbon (PAH)- and TCDD-induced reporter activity by 75% and 90%, respectively [1].
In vitro
CB7993113 exhibits no toxicity when added at concentrations of at least 20 μM to various human cells, including HepG2 liver cancer cells, BP1, D3, Hs578T, or MDA-MB-231 breast cancer cells, as well as primary human induced pluripotent stem cells [1]. Additionally, CB7993113 significantly reduces the in vitro invasive phenotype of ER-/PR-/HER2- breast cancer cells [1].
In vivo
CB7993113 is effective in blocking the acute hepatic CYP1A1 induction and in vivo bone marrow toxicity induced by 50 mg/kg DMBA [1].
Chemical Properties
Molecular Weight364.15
FormulaC15H10BrNO5
Cas No.819827-50-4
Storage & Solubility Information
StoragePowder: -20°C for 3 years | In solvent: -80°C for 1 year | Shipping with blue ice.

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