1-(2-(3-(4-methoxyphenyl)propoxy)-4-methoxyphenylethyl)-1h-imidazole has been researched along with 3'-o-(4-benzoyl)benzoyladenosine 5'-triphosphate in 3 studies
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 0 (0.00) | 18.7374 |
| 1990's | 1 (33.33) | 18.2507 |
| 2000's | 1 (33.33) | 29.6817 |
| 2010's | 1 (33.33) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
| Authors | Studies |
|---|---|
| Alzola, E; Chaïb, N; Dantinne, C; Dehaye, JP; Kabré, E; Marino, A; Métioui, M | 1 |
| Chin, TY; Chueh, SH | 1 |
| Jantaratnotai, N; McGeer, PL; McLarnon, JG | 1 |
3 other study(ies) available for 1-(2-(3-(4-methoxyphenyl)propoxy)-4-methoxyphenylethyl)-1h-imidazole and 3'-o-(4-benzoyl)benzoyladenosine 5'-triphosphate
| Article | Year |
|---|---|
Differential sensitivity to nickel and SK&F96365 of second messenger-operated and receptor-operated calcium channels in rat submandibular ductal cells.
Topics: Adenosine Triphosphate; Affinity Labels; Animals; Calcium; Calcium Channel Blockers; Calcium Channels; Calcium Chloride; Carbachol; Dose-Response Relationship, Drug; Imidazoles; Male; Manganese; Muscarinic Agonists; Nickel; Rats; Rats, Wistar; Receptors, Purinergic; Second Messenger Systems; Submandibular Gland; Thionucleotides; Time Factors | 1998 |
Distinct Ca(2+) signalling mechanisms induced by ATP and sphingosylphosphorylcholine in porcine aortic smooth muscle cells.
Topics: Adenosine; Adenosine Triphosphate; Animals; Aorta; Calcium; Calcium Channel Blockers; Calcium Signaling; Cells, Cultured; Cyclic AMP; Egtazic Acid; Estrenes; Imidazoles; Ionomycin; Manganese; Muscle, Smooth, Vascular; Phosphorylcholine; Pyrrolidinones; Sphingosine; Staurosporine; Swine; Thapsigargin; Thionucleosides; Thionucleotides; Virulence Factors, Bordetella | 2000 |
Mechanisms of Mg2+ inhibition of BzATP-dependent Ca2+ responses in THP-1 monocytes.
Topics: Adenosine Triphosphate; Calcium; Cell Line, Tumor; Humans; Imidazoles; Interferon-gamma; Lipopolysaccharides; Magnesium; Models, Biological; Monocytes; Purinergic P2X Receptor Agonists; Purinergic P2X Receptor Antagonists; Receptors, Purinergic P2X7; Receptors, Purinergic P2Y | 2012 |