2,3,7,8-tetrabromodibenzo-4-dioxin and imidazole

2,3,7,8-tetrabromodibenzo-4-dioxin has been researched along with imidazole in 2 studies

Research

Studies (2)

Timeframe	Studies, this research(%)	All Research%
pre-1990	0 (0.00)	18.7374
1990's	1 (50.00)	18.2507
2000's	1 (50.00)	29.6817
2010's	0 (0.00)	24.3611
2020's	0 (0.00)	2.80

Authors

Authors	Studies
Karplus, M; So, SS	1
Ahmed, S; Kikuchi, H; Shibazaki, M; Takeuchi, T	1

Other Studies

2 other study(ies) available for 2,3,7,8-tetrabromodibenzo-4-dioxin and imidazole

Article	Year
Three-dimensional quantitative structure-activity relationships from molecular similarity matrices and genetic neural networks. 2. Applications. Journal of medicinal chemistry, 1997, Dec-19, Volume: 40, Issue:26 Topics: Cholinesterase Inhibitors; Dopamine beta-Hydroxylase; Drug Design; Enzyme Inhibitors; GABA-A Receptor Agonists; GABA-A Receptor Antagonists; Molecular Conformation; Molecular Structure; Neural Networks, Computer; Phosphorylases; Receptors, Aryl Hydrocarbon; Static Electricity; Structure-Activity Relationship	1997
Suppression by p38 MAP kinase inhibitors (pyridinyl imidazole compounds) of Ah receptor target gene activation by 2,3,7,8-tetrachlorodibenzo-p-dioxin and the possible mechanism. The Journal of biological chemistry, 2004, Jan-30, Volume: 279, Issue:5 Topics: Animals; Blotting, Northern; Blotting, Western; Cell Line, Tumor; Chromatin; Cytochrome P-450 CYP1A1; Dioxins; Enzyme Inhibitors; Genes, Reporter; Histones; Humans; Imidazoles; Mice; Mitogen-Activated Protein Kinases; Models, Chemical; p38 Mitogen-Activated Protein Kinases; Plasmids; Precipitin Tests; Pyridines; Receptors, Aryl Hydrocarbon; RNA; RNA, Messenger; Time Factors; Transcription, Genetic; Transfection	2004

Article

Year

Three-dimensional quantitative structure-activity relationships from molecular similarity matrices and genetic neural networks. 2. Applications.

Journal of medicinal chemistry, 1997, Dec-19, Volume: 40, Issue:26

Topics: Cholinesterase Inhibitors; Dopamine beta-Hydroxylase; Drug Design; Enzyme Inhibitors; GABA-A Receptor Agonists; GABA-A Receptor Antagonists; Molecular Conformation; Molecular Structure; Neural Networks, Computer; Phosphorylases; Receptors, Aryl Hydrocarbon; Static Electricity; Structure-Activity Relationship

1997

Suppression by p38 MAP kinase inhibitors (pyridinyl imidazole compounds) of Ah receptor target gene activation by 2,3,7,8-tetrachlorodibenzo-p-dioxin and the possible mechanism.

The Journal of biological chemistry, 2004, Jan-30, Volume: 279, Issue:5

Topics: Animals; Blotting, Northern; Blotting, Western; Cell Line, Tumor; Chromatin; Cytochrome P-450 CYP1A1; Dioxins; Enzyme Inhibitors; Genes, Reporter; Histones; Humans; Imidazoles; Mice; Mitogen-Activated Protein Kinases; Models, Chemical; p38 Mitogen-Activated Protein Kinases; Plasmids; Precipitin Tests; Pyridines; Receptors, Aryl Hydrocarbon; RNA; RNA, Messenger; Time Factors; Transcription, Genetic; Transfection

2004