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potent ahr antagonist  (MedChemExpress)


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    MedChemExpress potent ahr antagonist
    Potent Ahr Antagonist, supplied by MedChemExpress, used in various techniques. Bioz Stars score: 94/100, based on 14 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/result/potent ahr antagonist/product/MedChemExpress
    Average 94 stars, based on 14 article reviews
    potent ahr antagonist - by Bioz Stars, 2026-02
    94/100 stars

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    MedChemExpress potent ahr antagonist
    Potent Ahr Antagonist, supplied by MedChemExpress, used in various techniques. Bioz Stars score: 94/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    MedChemExpress ahr antagonist 5
    SARS-CoV-2-induced CD147 expression is regulated by transcription factor AHR. a The expressions of CD147 and ACE2 in BEAS-2B cells were determined by western blot. b The expressions of CD147, AHR, AHRR, and CYP1A1 in BEAS-2B cells were determined by western blot with SARS-CoV-2 pseudovirus infection or RBD incubation. c The expression of CD147 was determined in BEAS-2B cells by western blot with the addition of AHR agonist 2 or AHR antagonist 5. d The relative luciferase signals in pseudovirus-infected BEAS-2B cells were determined by dual-luciferase reporter assays with the addition of AHR agonist 2 or AHR antagonist 5, *** p < 0.001. e The expression of CD147 in BEAS-2B-shCD147 cells and its control was determined by western blot. f The transfection efficiency of plasmid AHR was evaluated by western blot in BEAS-2B-shCD147 cells. g The relative luciferase signals were determined by dual-luciferase reporter assays in pseudovirus-infected BEAS-2B cells and BEAS-2B-shCD147 cells with or without the transfection of plasmid AHR, ns, not significant, *** p < 0.001. h The expression of CD147 was determined in AHR knockdown BEAS-2B cells by western blot. i The expression of CD147 was determined in pseudovirus-infected BEAS-2B cells by western blot with the addition of AHR antagonist 5. j Dual-luciferase reporter assays were performed after co-transfecting of the pGL3-Basic-CD147 promoter (−2000– − 1), pRL-TK, and plasmid AHR into HEK293T cells. The relative luciferase signal was detected using a Dual-Luciferase® Reporter Assay System, *** p < 0.001. k Nuclear and cytoplasmic protein extraction assays were performed to determine the nuclear expression and cytoplasmic expression of AHR in BEAS-2B cells with pseudovirus infection or RBD incubation. Lamin B1 and GAPDH were selected as controls for nuclear protein and cytoplasmic protein, respectively
    Ahr Antagonist 5, supplied by MedChemExpress, used in various techniques. Bioz Stars score: 94/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    MedChemExpress ahr antagonist ch223191
    SARS-CoV-2-induced CD147 expression is regulated by transcription factor AHR. a The expressions of CD147 and ACE2 in BEAS-2B cells were determined by western blot. b The expressions of CD147, AHR, AHRR, and CYP1A1 in BEAS-2B cells were determined by western blot with SARS-CoV-2 pseudovirus infection or RBD incubation. c The expression of CD147 was determined in BEAS-2B cells by western blot with the addition of AHR agonist 2 or AHR antagonist 5. d The relative luciferase signals in pseudovirus-infected BEAS-2B cells were determined by dual-luciferase reporter assays with the addition of AHR agonist 2 or AHR antagonist 5, *** p < 0.001. e The expression of CD147 in BEAS-2B-shCD147 cells and its control was determined by western blot. f The transfection efficiency of plasmid AHR was evaluated by western blot in BEAS-2B-shCD147 cells. g The relative luciferase signals were determined by dual-luciferase reporter assays in pseudovirus-infected BEAS-2B cells and BEAS-2B-shCD147 cells with or without the transfection of plasmid AHR, ns, not significant, *** p < 0.001. h The expression of CD147 was determined in AHR knockdown BEAS-2B cells by western blot. i The expression of CD147 was determined in pseudovirus-infected BEAS-2B cells by western blot with the addition of AHR antagonist 5. j Dual-luciferase reporter assays were performed after co-transfecting of the pGL3-Basic-CD147 promoter (−2000– − 1), pRL-TK, and plasmid AHR into HEK293T cells. The relative luciferase signal was detected using a Dual-Luciferase® Reporter Assay System, *** p < 0.001. k Nuclear and cytoplasmic protein extraction assays were performed to determine the nuclear expression and cytoplasmic expression of AHR in BEAS-2B cells with pseudovirus infection or RBD incubation. Lamin B1 and GAPDH were selected as controls for nuclear protein and cytoplasmic protein, respectively
    Ahr Antagonist Ch223191, supplied by MedChemExpress, used in various techniques. Bioz Stars score: 95/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    TargetMol ahr antagonist
    SARS-CoV-2-induced CD147 expression is regulated by transcription factor AHR. a The expressions of CD147 and ACE2 in BEAS-2B cells were determined by western blot. b The expressions of CD147, AHR, AHRR, and CYP1A1 in BEAS-2B cells were determined by western blot with SARS-CoV-2 pseudovirus infection or RBD incubation. c The expression of CD147 was determined in BEAS-2B cells by western blot with the addition of AHR agonist 2 or AHR antagonist 5. d The relative luciferase signals in pseudovirus-infected BEAS-2B cells were determined by dual-luciferase reporter assays with the addition of AHR agonist 2 or AHR antagonist 5, *** p < 0.001. e The expression of CD147 in BEAS-2B-shCD147 cells and its control was determined by western blot. f The transfection efficiency of plasmid AHR was evaluated by western blot in BEAS-2B-shCD147 cells. g The relative luciferase signals were determined by dual-luciferase reporter assays in pseudovirus-infected BEAS-2B cells and BEAS-2B-shCD147 cells with or without the transfection of plasmid AHR, ns, not significant, *** p < 0.001. h The expression of CD147 was determined in AHR knockdown BEAS-2B cells by western blot. i The expression of CD147 was determined in pseudovirus-infected BEAS-2B cells by western blot with the addition of AHR antagonist 5. j Dual-luciferase reporter assays were performed after co-transfecting of the pGL3-Basic-CD147 promoter (−2000– − 1), pRL-TK, and plasmid AHR into HEK293T cells. The relative luciferase signal was detected using a Dual-Luciferase® Reporter Assay System, *** p < 0.001. k Nuclear and cytoplasmic protein extraction assays were performed to determine the nuclear expression and cytoplasmic expression of AHR in BEAS-2B cells with pseudovirus infection or RBD incubation. Lamin B1 and GAPDH were selected as controls for nuclear protein and cytoplasmic protein, respectively
    Ahr Antagonist, supplied by TargetMol, used in various techniques. Bioz Stars score: 94/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    MedChemExpress ahr antagonist
    SARS-CoV-2-induced CD147 expression is regulated by transcription factor AHR. a The expressions of CD147 and ACE2 in BEAS-2B cells were determined by western blot. b The expressions of CD147, AHR, AHRR, and CYP1A1 in BEAS-2B cells were determined by western blot with SARS-CoV-2 pseudovirus infection or RBD incubation. c The expression of CD147 was determined in BEAS-2B cells by western blot with the addition of AHR agonist 2 or AHR antagonist 5. d The relative luciferase signals in pseudovirus-infected BEAS-2B cells were determined by dual-luciferase reporter assays with the addition of AHR agonist 2 or AHR antagonist 5, *** p < 0.001. e The expression of CD147 in BEAS-2B-shCD147 cells and its control was determined by western blot. f The transfection efficiency of plasmid AHR was evaluated by western blot in BEAS-2B-shCD147 cells. g The relative luciferase signals were determined by dual-luciferase reporter assays in pseudovirus-infected BEAS-2B cells and BEAS-2B-shCD147 cells with or without the transfection of plasmid AHR, ns, not significant, *** p < 0.001. h The expression of CD147 was determined in AHR knockdown BEAS-2B cells by western blot. i The expression of CD147 was determined in pseudovirus-infected BEAS-2B cells by western blot with the addition of AHR antagonist 5. j Dual-luciferase reporter assays were performed after co-transfecting of the pGL3-Basic-CD147 promoter (−2000– − 1), pRL-TK, and plasmid AHR into HEK293T cells. The relative luciferase signal was detected using a Dual-Luciferase® Reporter Assay System, *** p < 0.001. k Nuclear and cytoplasmic protein extraction assays were performed to determine the nuclear expression and cytoplasmic expression of AHR in BEAS-2B cells with pseudovirus infection or RBD incubation. Lamin B1 and GAPDH were selected as controls for nuclear protein and cytoplasmic protein, respectively
    Ahr Antagonist, supplied by MedChemExpress, used in various techniques. Bioz Stars score: 94/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    MedChemExpress ahr specific antagonist ch 223191
    SARS-CoV-2-induced CD147 expression is regulated by transcription factor AHR. a The expressions of CD147 and ACE2 in BEAS-2B cells were determined by western blot. b The expressions of CD147, AHR, AHRR, and CYP1A1 in BEAS-2B cells were determined by western blot with SARS-CoV-2 pseudovirus infection or RBD incubation. c The expression of CD147 was determined in BEAS-2B cells by western blot with the addition of AHR agonist 2 or AHR antagonist 5. d The relative luciferase signals in pseudovirus-infected BEAS-2B cells were determined by dual-luciferase reporter assays with the addition of AHR agonist 2 or AHR antagonist 5, *** p < 0.001. e The expression of CD147 in BEAS-2B-shCD147 cells and its control was determined by western blot. f The transfection efficiency of plasmid AHR was evaluated by western blot in BEAS-2B-shCD147 cells. g The relative luciferase signals were determined by dual-luciferase reporter assays in pseudovirus-infected BEAS-2B cells and BEAS-2B-shCD147 cells with or without the transfection of plasmid AHR, ns, not significant, *** p < 0.001. h The expression of CD147 was determined in AHR knockdown BEAS-2B cells by western blot. i The expression of CD147 was determined in pseudovirus-infected BEAS-2B cells by western blot with the addition of AHR antagonist 5. j Dual-luciferase reporter assays were performed after co-transfecting of the pGL3-Basic-CD147 promoter (−2000– − 1), pRL-TK, and plasmid AHR into HEK293T cells. The relative luciferase signal was detected using a Dual-Luciferase® Reporter Assay System, *** p < 0.001. k Nuclear and cytoplasmic protein extraction assays were performed to determine the nuclear expression and cytoplasmic expression of AHR in BEAS-2B cells with pseudovirus infection or RBD incubation. Lamin B1 and GAPDH were selected as controls for nuclear protein and cytoplasmic protein, respectively
    Ahr Specific Antagonist Ch 223191, supplied by MedChemExpress, used in various techniques. Bioz Stars score: 95/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/result/ahr specific antagonist ch 223191/product/MedChemExpress
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    Selleck Chemicals ahr specific antagonist ch223191
    SARS-CoV-2-induced CD147 expression is regulated by transcription factor AHR. a The expressions of CD147 and ACE2 in BEAS-2B cells were determined by western blot. b The expressions of CD147, AHR, AHRR, and CYP1A1 in BEAS-2B cells were determined by western blot with SARS-CoV-2 pseudovirus infection or RBD incubation. c The expression of CD147 was determined in BEAS-2B cells by western blot with the addition of AHR agonist 2 or AHR antagonist 5. d The relative luciferase signals in pseudovirus-infected BEAS-2B cells were determined by dual-luciferase reporter assays with the addition of AHR agonist 2 or AHR antagonist 5, *** p < 0.001. e The expression of CD147 in BEAS-2B-shCD147 cells and its control was determined by western blot. f The transfection efficiency of plasmid AHR was evaluated by western blot in BEAS-2B-shCD147 cells. g The relative luciferase signals were determined by dual-luciferase reporter assays in pseudovirus-infected BEAS-2B cells and BEAS-2B-shCD147 cells with or without the transfection of plasmid AHR, ns, not significant, *** p < 0.001. h The expression of CD147 was determined in AHR knockdown BEAS-2B cells by western blot. i The expression of CD147 was determined in pseudovirus-infected BEAS-2B cells by western blot with the addition of AHR antagonist 5. j Dual-luciferase reporter assays were performed after co-transfecting of the pGL3-Basic-CD147 promoter (−2000– − 1), pRL-TK, and plasmid AHR into HEK293T cells. The relative luciferase signal was detected using a Dual-Luciferase® Reporter Assay System, *** p < 0.001. k Nuclear and cytoplasmic protein extraction assays were performed to determine the nuclear expression and cytoplasmic expression of AHR in BEAS-2B cells with pseudovirus infection or RBD incubation. Lamin B1 and GAPDH were selected as controls for nuclear protein and cytoplasmic protein, respectively
    Ahr Specific Antagonist Ch223191, supplied by Selleck Chemicals, used in various techniques. Bioz Stars score: 95/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/result/ahr specific antagonist ch223191/product/Selleck Chemicals
    Average 95 stars, based on 1 article reviews
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    SARS-CoV-2-induced CD147 expression is regulated by transcription factor AHR. a The expressions of CD147 and ACE2 in BEAS-2B cells were determined by western blot. b The expressions of CD147, AHR, AHRR, and CYP1A1 in BEAS-2B cells were determined by western blot with SARS-CoV-2 pseudovirus infection or RBD incubation. c The expression of CD147 was determined in BEAS-2B cells by western blot with the addition of AHR agonist 2 or AHR antagonist 5. d The relative luciferase signals in pseudovirus-infected BEAS-2B cells were determined by dual-luciferase reporter assays with the addition of AHR agonist 2 or AHR antagonist 5, *** p < 0.001. e The expression of CD147 in BEAS-2B-shCD147 cells and its control was determined by western blot. f The transfection efficiency of plasmid AHR was evaluated by western blot in BEAS-2B-shCD147 cells. g The relative luciferase signals were determined by dual-luciferase reporter assays in pseudovirus-infected BEAS-2B cells and BEAS-2B-shCD147 cells with or without the transfection of plasmid AHR, ns, not significant, *** p < 0.001. h The expression of CD147 was determined in AHR knockdown BEAS-2B cells by western blot. i The expression of CD147 was determined in pseudovirus-infected BEAS-2B cells by western blot with the addition of AHR antagonist 5. j Dual-luciferase reporter assays were performed after co-transfecting of the pGL3-Basic-CD147 promoter (−2000– − 1), pRL-TK, and plasmid AHR into HEK293T cells. The relative luciferase signal was detected using a Dual-Luciferase® Reporter Assay System, *** p < 0.001. k Nuclear and cytoplasmic protein extraction assays were performed to determine the nuclear expression and cytoplasmic expression of AHR in BEAS-2B cells with pseudovirus infection or RBD incubation. Lamin B1 and GAPDH were selected as controls for nuclear protein and cytoplasmic protein, respectively

    Journal: Signal Transduction and Targeted Therapy

    Article Title: Inducible CD147 up-regulation boosts extended SARS-CoV-2 infection triggering severe COVID-19 independent of ACE2

    doi: 10.1038/s41392-025-02551-x

    Figure Lengend Snippet: SARS-CoV-2-induced CD147 expression is regulated by transcription factor AHR. a The expressions of CD147 and ACE2 in BEAS-2B cells were determined by western blot. b The expressions of CD147, AHR, AHRR, and CYP1A1 in BEAS-2B cells were determined by western blot with SARS-CoV-2 pseudovirus infection or RBD incubation. c The expression of CD147 was determined in BEAS-2B cells by western blot with the addition of AHR agonist 2 or AHR antagonist 5. d The relative luciferase signals in pseudovirus-infected BEAS-2B cells were determined by dual-luciferase reporter assays with the addition of AHR agonist 2 or AHR antagonist 5, *** p < 0.001. e The expression of CD147 in BEAS-2B-shCD147 cells and its control was determined by western blot. f The transfection efficiency of plasmid AHR was evaluated by western blot in BEAS-2B-shCD147 cells. g The relative luciferase signals were determined by dual-luciferase reporter assays in pseudovirus-infected BEAS-2B cells and BEAS-2B-shCD147 cells with or without the transfection of plasmid AHR, ns, not significant, *** p < 0.001. h The expression of CD147 was determined in AHR knockdown BEAS-2B cells by western blot. i The expression of CD147 was determined in pseudovirus-infected BEAS-2B cells by western blot with the addition of AHR antagonist 5. j Dual-luciferase reporter assays were performed after co-transfecting of the pGL3-Basic-CD147 promoter (−2000– − 1), pRL-TK, and plasmid AHR into HEK293T cells. The relative luciferase signal was detected using a Dual-Luciferase® Reporter Assay System, *** p < 0.001. k Nuclear and cytoplasmic protein extraction assays were performed to determine the nuclear expression and cytoplasmic expression of AHR in BEAS-2B cells with pseudovirus infection or RBD incubation. Lamin B1 and GAPDH were selected as controls for nuclear protein and cytoplasmic protein, respectively

    Article Snippet: AHR agonist 2 (HY-144339, MCE) and AHR antagonist 5 (HY-141609, MCE) are potent agonist and inhibitor of AHR, respectively, which can regulate the transcription of AHR’s downstream genes by affecting its nuclear localization.

    Techniques: Expressing, Western Blot, Infection, Incubation, Luciferase, Control, Transfection, Plasmid Preparation, Knockdown, Reporter Assay, Protein Extraction