thiazoles has been researched along with 1,4-dihydropyridine in 4 studies
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 0 (0.00) | 18.7374 |
| 1990's | 0 (0.00) | 18.2507 |
| 2000's | 2 (50.00) | 29.6817 |
| 2010's | 2 (50.00) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
| Authors | Studies |
|---|---|
| Bihel, F; Garino, C; Kraus, JL; Laras, Y; Pietrancosta, N; Quéléver, G; Sheha, M; Wolfe, MS | 1 |
| Andreani, A; Bedini, A; Budriesi, R; Chiarini, A; Cosconati, S; Di Toro, R; Ioan, P; Leoni, A; Locatelli, A; Marinelli, L; Novellino, E; Spampinato, S; Ugenti, MP | 1 |
| Al-Qasoumi, SI; Al-Said, MS; Bashandy, MS; Ghorab, MM | 1 |
| Fadda, AA; Refat, HM | 1 |
4 other study(ies) available for thiazoles and 1,4-dihydropyridine
| Article | Year |
|---|---|
Substituted thiazolamide coupled to a redox delivery system: a new gamma-secretase inhibitor with enhanced pharmacokinetic profile.
Topics: Alzheimer Disease; Amides; Amyloid Precursor Protein Secretases; Animals; Aspartic Acid Endopeptidases; Biological Availability; Blood-Brain Barrier; Dihydropyridines; Drug Delivery Systems; Endopeptidases; Enzyme Inhibitors; Humans; Male; Molecular Structure; Nicotinic Acids; Oxidation-Reduction; Rats; Rats, Sprague-Dawley; Thiazoles | 2005 |
Imidazo[2,1-b]thiazole system: a scaffold endowing dihydropyridines with selective cardiodepressant activity.
Topics: Animals; Binding Sites; Computer Simulation; Dihydropyridines; Drug Design; Drug Evaluation, Preclinical; Guinea Pigs; Heart; Heart Rate; Imidazoles; Ligands; Models, Molecular; Molecular Structure; Muscle, Smooth, Vascular; Myocardial Contraction; Myocytes, Cardiac; Small Molecule Libraries; Structure-Activity Relationship; Thiazoles | 2008 |
Anti-breast cancer activity of some novel 1,2-dihydropyridine, thiophene and thiazole derivatives.
Topics: Antineoplastic Agents; Breast Neoplasms; Cell Line, Tumor; Dihydropyridines; Humans; Inhibitory Concentration 50; Structure-Activity Relationship; Thiazoles; Thiophenes | 2011 |
Synthesis and antimicrobial activity of some novel hydrazide, benzochromenone, dihydropyridine, pyrrole, thiazole and thiophene derivatives.
Topics: Anti-Bacterial Agents; Antifungal Agents; Benzopyrans; Candida albicans; Dihydropyridines; Dose-Response Relationship, Drug; Escherichia coli; Hydrazones; Microbial Sensitivity Tests; Molecular Structure; Pyrroles; Staphylococcus aureus; Structure-Activity Relationship; Thiazoles; Thiophenes | 2013 |