Compounds > 1-phenylimidazole

Page last updated: 2024-08-25

1-phenylimidazole and 4(5)-phenylimidazole

1-phenylimidazole has been researched along with 4(5)-phenylimidazole in 6 studies

Research

Studies (6)

Timeframe	Studies, this research(%)	All Research%
pre-1990	1 (16.67)	18.7374
1990's	2 (33.33)	18.2507
2000's	0 (0.00)	29.6817
2010's	2 (33.33)	24.3611
2020's	1 (16.67)	2.80

Authors

Authors	Studies
James, MO; Sloan, KB	1
Fesik, SW; Hajduk, PJ; Martin, YC; Muegge, I	1
Halpert, JR	1
Abell, C; Bender, A; Chenge, J; Coyne, AG; Kavanagh, ME; McLean, KJ; Munro, AW; Zoufir, A	1
Ascencao, K; Coukos, G; Dilek, N; Irving, M; Majjigapu, SR; Michielin, O; Pojer, F; Reichenbach, P; Reynaud, A; Röhrig, UF; Vogel, P; Zoete, V	1
Datto, GA; Samatovicz, RA; Tempsick, RA; Wolff, DJ	1

Other Studies

6 other study(ies) available for 1-phenylimidazole and 4(5)-phenylimidazole

Article	Year
Structural features of imidazole derivatives that enhance styrene oxide hydrolase activity in rat hepatic microsomes. Journal of medicinal chemistry, 1985, Volume: 28, Issue:8 Topics: Animals; Antifungal Agents; Enzyme Activation; Epoxide Hydrolases; Imidazoles; In Vitro Techniques; Male; Methylcholanthrene; Microsomes, Liver; Phenobarbital; Rats; Rats, Inbred Strains; Structure-Activity Relationship	1985
Evaluation of PMF scoring in docking weak ligands to the FK506 binding protein. Journal of medicinal chemistry, 1999, Jul-15, Volume: 42, Issue:14 Topics: Binding Sites; Immunophilins; Immunosuppressive Agents; Ligands; Magnetic Resonance Spectroscopy; Models, Molecular; Molecular Weight; Structure-Activity Relationship; Tacrolimus; Tacrolimus Binding Proteins	1999
Structure and function of cytochromes P450 2B: from mechanism-based inactivators to X-ray crystal structures and back. Drug metabolism and disposition: the biological fate of chemicals, 2011, Volume: 39, Issue:7 Topics: Catalytic Domain; Cloning, Molecular; Crystallography, X-Ray; Cytochrome P-450 Enzyme System; DNA, Complementary; Ligands; Models, Molecular; Protein Conformation; Structure-Activity Relationship	2011
Fragment Profiling Approach to Inhibitors of the Orphan M. tuberculosis P450 CYP144A1. Biochemistry, 2017, 03-21, Volume: 56, Issue:11 Topics: Bacterial Proteins; Binding Sites; Cloning, Molecular; Computational Biology; Cytochrome P-450 Enzyme Inhibitors; Cytochrome P-450 Enzyme System; Escherichia coli; Gene Expression; Ligands; Models, Molecular; Mycobacterium tuberculosis; Peptide Fragments; Phylogeny; Protein Binding; Recombinant Proteins; Structural Homology, Protein	2017
Azole-Based Indoleamine 2,3-Dioxygenase 1 (IDO1) Inhibitors. Journal of medicinal chemistry, 2021, 02-25, Volume: 64, Issue:4 Topics: Azoles; Enzyme Inhibitors; HEK293 Cells; Humans; Indoleamine-Pyrrole 2,3,-Dioxygenase; Molecular Dynamics Simulation; Molecular Structure; Protein Binding; Quantitative Structure-Activity Relationship	2021
Calmodulin-dependent nitric-oxide synthase. Mechanism of inhibition by imidazole and phenylimidazoles. The Journal of biological chemistry, 1993, May-05, Volume: 268, Issue:13 Topics: Amino Acid Oxidoreductases; Animals; Brain; Calmodulin; Cattle; Imidazoles; Kinetics; NADP; Nitric Oxide Synthase; Pituitary Neoplasms; Rats; Tumor Cells, Cultured	1993