1-benzylimidazole has been researched along with 4-(1H-imidazol-1-ylmethyl)benzonitrile in 3 studies
Timeframe | Studies, this research(%) | All Research% |
---|---|---|
pre-1990 | 0 (0.00) | 18.7374 |
1990's | 0 (0.00) | 18.2507 |
2000's | 1 (33.33) | 29.6817 |
2010's | 2 (66.67) | 24.3611 |
2020's | 0 (0.00) | 2.80 |
Authors | Studies |
---|---|
Ahmed, S; Dhanani, S; Owen, CP; Patel, CH; Shahid, I | 1 |
Beugels, IP; Custers, EM; de Gooyer, M; Emmen, JM; Hermans, JJ; Hilbers, PA; Janssen, HM; Leysen, D; Ottenheijm, HC; Peeters, JW; Pieterse, K; Plate, R; Roumen, L; Smits, JF; Vekemans, JA | 1 |
Cuperlović-Culf, M; Doiron, J; Picot, N; Richard, R; Robichaud, GA; Soultan, AH; Touaibia, M; Touré, MM | 1 |
3 other study(ies) available for 1-benzylimidazole and 4-(1H-imidazol-1-ylmethyl)benzonitrile
Article | Year |
---|---|
Synthesis and biochemical evaluation of a range of potent benzyl imidazole-based compounds as potential inhibitors of the enzyme complex 17alpha-hydroxylase/17,20-lyase (P450(17alpha)).
Topics: Enzyme Inhibitors; Imidazoles; Models, Molecular; Steroid 17-alpha-Hydroxylase | 2006 |
Synthesis, biological evaluation, and molecular modeling of 1-benzyl-1H-imidazoles as selective inhibitors of aldosterone synthase (CYP11B2).
Topics: 18-Hydroxycorticosterone; Animals; Benzyl Compounds; Catalytic Domain; Cell Line; Cricetinae; Cricetulus; Cytochrome P-450 CYP11B2; Fadrozole; Humans; Imidazoles; Models, Molecular; Molecular Dynamics Simulation; Protein Binding; Stereoisomerism; Structure-Activity Relationship | 2010 |
Synthesis and structure-activity relationship of 1- and 2-substituted-1,2,3-triazole letrozole-based analogues as aromatase inhibitors.
Topics: Aromatase Inhibitors; Cell Line, Tumor; Cell Proliferation; Computer Simulation; Humans; Inhibitory Concentration 50; Letrozole; Magnetic Resonance Spectroscopy; Mass Spectrometry; Nitriles; Structure-Activity Relationship; Triazoles | 2011 |