4-anisaldehyde has been researched along with 2-Methoxybenzaldehyde in 6 studies
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 0 (0.00) | 18.7374 |
| 1990's | 0 (0.00) | 18.2507 |
| 2000's | 1 (16.67) | 29.6817 |
| 2010's | 5 (83.33) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
| Authors | Studies |
|---|---|
| Jiang, L; Luo, WC; Xiao, T; Xie, XY; Xue, CB; Zhang, L | 1 |
| Alam, MA; Alam, MI; Alam, O; Koul, S; Nargotra, A; Taneja, SC | 1 |
| Boufadi, MY; Dufrasne, F; Furtmüller, PG; Gelbcke, M; Meyer, F; Nève, J; Obinger, C; Soubhye, J; Van Antwerpen, P; Zouaoui Boudjeltia, K | 1 |
| Hauke, TJ; Höfner, G; Wanner, KT; Wein, T | 1 |
| Kern, F; Wanner, KT | 1 |
| Höfner, G; Huber, SK; Wanner, KT | 1 |
6 other study(ies) available for 4-anisaldehyde and 2-Methoxybenzaldehyde
| Article | Year |
|---|---|
3D-QSAR and molecular docking studies of benzaldehyde thiosemicarbazone, benzaldehyde, benzoic acid, and their derivatives as phenoloxidase inhibitors.
Topics: Benzaldehydes; Benzoic Acid; Enzyme Inhibitors; Hydrogen Bonding; Models, Molecular; Monophenol Monooxygenase; Quantitative Structure-Activity Relationship; Thiosemicarbazones | 2007 |
Molecular modeling and snake venom phospholipase A2 inhibition by phenolic compounds: Structure-activity relationship.
Topics: Antivenins; Biological Products; Dose-Response Relationship, Drug; Models, Molecular; Molecular Structure; Phenols; Phospholipase A2 Inhibitors; Phospholipases A2; Plant Extracts; Plant Roots; Snake Venoms; Structure-Activity Relationship | 2016 |
From Dynamic Combinatorial Chemistry to
Topics: | 2017 |
Novel Allosteric Ligands of γ-Aminobutyric Acid Transporter 1 (GAT1) by MS Based Screening of Pseudostatic Hydrazone Libraries.
Topics: Aldehydes; Allosteric Regulation; Drug Evaluation, Preclinical; GABA Plasma Membrane Transport Proteins; Humans; Hydrazones; Ligands; Mass Spectrometry; Models, Molecular; Protein Conformation | 2018 |
Screening oxime libraries by means of mass spectrometry (MS) binding assays: Identification of new highly potent inhibitors to optimized inhibitors γ-aminobutyric acid transporter 1.
Topics: Binding Sites; Dose-Response Relationship, Drug; Drug Evaluation, Preclinical; Enzyme Inhibitors; HEK293 Cells; Humans; Mass Spectrometry; Molecular Structure; N-Acetylglucosaminyltransferases; Oximes; Small Molecule Libraries; Structure-Activity Relationship | 2019 |
Application of the concept of oxime library screening by mass spectrometry (MS) binding assays to pyrrolidine-3-carboxylic acid derivatives as potential inhibitors of γ-aminobutyric acid transporter 1 (GAT1).
Topics: GABA Plasma Membrane Transport Proteins; GABA Uptake Inhibitors; Oximes; Pyrrolidines; Spectrometry, Mass, Electrospray Ionization; Structure-Activity Relationship | 2019 |