gnf351 Search Results


gnf 351 calbiochem  (MedChemExpress)
93
MedChemExpress gnf 351 calbiochem
Gnf 351 Calbiochem, supplied by MedChemExpress, used in various techniques. Bioz Stars score: 93/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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gnf 351 calbiochem - by Bioz Stars, 2026-02
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gnf 351  (Selleck Chemicals)
92
Selleck Chemicals gnf 351
Gnf 351, supplied by Selleck Chemicals, used in various techniques. Bioz Stars score: 92/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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Average 92 stars, based on 1 article reviews
gnf 351 - by Bioz Stars, 2026-02
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gnf  (Santa Cruz Biotechnology)
93
Santa Cruz Biotechnology gnf
Antagonism of CYP1A1 catalytic activity induced by halogenated indoles. HepG2 cells were treated with 10 µM of the halogenated indoles for 24 h both alone and in combination with the AhR antagonist, <t>GNF-351</t> (0.25 µM). CYP1A1 activity was determined via the EROD assay and is expressed as a percentage of the vehicle control (0.5% DMSO). Bars represent the mean ± SEM of three independent experiments performed in duplicate. Data were analyzed using a one-tailed t-test. *significantly decreased compared to the respective indole-only response, p < 0.05.
Gnf, supplied by Santa Cruz Biotechnology, used in various techniques. Bioz Stars score: 93/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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Average 93 stars, based on 1 article reviews
gnf - by Bioz Stars, 2026-02
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aryl hydrocarbon receptor (ahr) antagonist iii (gnf351)  (Merck KGaA)
90
Merck KGaA aryl hydrocarbon receptor (ahr) antagonist iii (gnf351)
Antagonism of CYP1A1 catalytic activity induced by halogenated indoles. HepG2 cells were treated with 10 µM of the halogenated indoles for 24 h both alone and in combination with the AhR antagonist, <t>GNF-351</t> (0.25 µM). CYP1A1 activity was determined via the EROD assay and is expressed as a percentage of the vehicle control (0.5% DMSO). Bars represent the mean ± SEM of three independent experiments performed in duplicate. Data were analyzed using a one-tailed t-test. *significantly decreased compared to the respective indole-only response, p < 0.05.
Aryl Hydrocarbon Receptor (Ahr) Antagonist Iii (Gnf351), supplied by Merck KGaA, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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Average 90 stars, based on 1 article reviews
aryl hydrocarbon receptor (ahr) antagonist iii (gnf351) - by Bioz Stars, 2026-02
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gnf351  (Merck & Co)
90
Merck & Co gnf351
Antagonism of CYP1A1 catalytic activity induced by halogenated indoles. HepG2 cells were treated with 10 µM of the halogenated indoles for 24 h both alone and in combination with the AhR antagonist, <t>GNF-351</t> (0.25 µM). CYP1A1 activity was determined via the EROD assay and is expressed as a percentage of the vehicle control (0.5% DMSO). Bars represent the mean ± SEM of three independent experiments performed in duplicate. Data were analyzed using a one-tailed t-test. *significantly decreased compared to the respective indole-only response, p < 0.05.
Gnf351, supplied by Merck & Co, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/result/gnf351/product/Merck & Co
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gnf351 - by Bioz Stars, 2026-02
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gnf351  (Novartis)
90
Novartis gnf351
Antagonism of CYP1A1 catalytic activity induced by halogenated indoles. HepG2 cells were treated with 10 µM of the halogenated indoles for 24 h both alone and in combination with the AhR antagonist, <t>GNF-351</t> (0.25 µM). CYP1A1 activity was determined via the EROD assay and is expressed as a percentage of the vehicle control (0.5% DMSO). Bars represent the mean ± SEM of three independent experiments performed in duplicate. Data were analyzed using a one-tailed t-test. *significantly decreased compared to the respective indole-only response, p < 0.05.
Gnf351, supplied by Novartis, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/result/gnf351/product/Novartis
Average 90 stars, based on 1 article reviews
gnf351 - by Bioz Stars, 2026-02
90/100 stars
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gnf351  (GlpBio Technology Inc)
90
GlpBio Technology Inc gnf351
Antagonism of CYP1A1 catalytic activity induced by halogenated indoles. HepG2 cells were treated with 10 µM of the halogenated indoles for 24 h both alone and in combination with the AhR antagonist, <t>GNF-351</t> (0.25 µM). CYP1A1 activity was determined via the EROD assay and is expressed as a percentage of the vehicle control (0.5% DMSO). Bars represent the mean ± SEM of three independent experiments performed in duplicate. Data were analyzed using a one-tailed t-test. *significantly decreased compared to the respective indole-only response, p < 0.05.
Gnf351, supplied by GlpBio Technology Inc, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/result/gnf351/product/GlpBio Technology Inc
Average 90 stars, based on 1 article reviews
gnf351 - by Bioz Stars, 2026-02
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gnf351  (Cosmo Bio USA)
90
Cosmo Bio USA gnf351
Antagonism of CYP1A1 catalytic activity induced by halogenated indoles. HepG2 cells were treated with 10 µM of the halogenated indoles for 24 h both alone and in combination with the AhR antagonist, <t>GNF-351</t> (0.25 µM). CYP1A1 activity was determined via the EROD assay and is expressed as a percentage of the vehicle control (0.5% DMSO). Bars represent the mean ± SEM of three independent experiments performed in duplicate. Data were analyzed using a one-tailed t-test. *significantly decreased compared to the respective indole-only response, p < 0.05.
Gnf351, supplied by Cosmo Bio USA, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/result/gnf351/product/Cosmo Bio USA
Average 90 stars, based on 1 article reviews
gnf351 - by Bioz Stars, 2026-02
90/100 stars
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Image Search Results


Antagonism of CYP1A1 catalytic activity induced by halogenated indoles. HepG2 cells were treated with 10 µM of the halogenated indoles for 24 h both alone and in combination with the AhR antagonist, GNF-351 (0.25 µM). CYP1A1 activity was determined via the EROD assay and is expressed as a percentage of the vehicle control (0.5% DMSO). Bars represent the mean ± SEM of three independent experiments performed in duplicate. Data were analyzed using a one-tailed t-test. *significantly decreased compared to the respective indole-only response, p < 0.05.

Journal: Toxicology Reports

Article Title: Characterization of marine-derived halogenated indoles as ligands of the aryl hydrocarbon receptor

doi: 10.1016/j.toxrep.2022.05.016

Figure Lengend Snippet: Antagonism of CYP1A1 catalytic activity induced by halogenated indoles. HepG2 cells were treated with 10 µM of the halogenated indoles for 24 h both alone and in combination with the AhR antagonist, GNF-351 (0.25 µM). CYP1A1 activity was determined via the EROD assay and is expressed as a percentage of the vehicle control (0.5% DMSO). Bars represent the mean ± SEM of three independent experiments performed in duplicate. Data were analyzed using a one-tailed t-test. *significantly decreased compared to the respective indole-only response, p < 0.05.

Article Snippet: 2,3,7,8-Tetrachlorodibenzo- p -dioxin (TCDD, 50 μg/mL in DMSO, >99.9%) was purchased from Cambridge Isotope Laboratories (Tewksbury, MA) and GNF-351 was purchased from Santa Cruz Biotechnology (Dallas, TX).

Techniques: Activity Assay, One-tailed Test