bay-k-8644 has been researched along with h 89 in 7 studies
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 0 (0.00) | 18.7374 |
| 1990's | 3 (42.86) | 18.2507 |
| 2000's | 2 (28.57) | 29.6817 |
| 2010's | 2 (28.57) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
| Authors | Studies |
|---|---|
| Austin, CP; Fidock, DA; Hayton, K; Huang, R; Inglese, J; Jiang, H; Johnson, RL; Su, XZ; Wellems, TE; Wichterman, J; Yuan, J | 1 |
| Lambert, DG; Smart, D | 1 |
| Kobayashi, D; Miyamoto, K; Ohmae, S; Sanae, F; Takag, K | 1 |
| Giuliani, S; Maggi, CA; Santicioli, P | 1 |
| Iwata, S; Kon-ya, K; Ohizumi, Y; Saito, S; Shizuri, Y | 1 |
| Bryant, S; Chase, A; James, AF; Kimura, TE; Kong, CH; Orchard, CH; Suleiman, MS; Watson, JJ | 1 |
| Bova, S; Fusi, F; Sgaragli, G; Spiga, O; Trezza, A | 1 |
7 other study(ies) available for bay-k-8644 and h 89
| Article | Year |
|---|---|
Genetic mapping of targets mediating differential chemical phenotypes in Plasmodium falciparum.
Topics: Animals; Antimalarials; ATP Binding Cassette Transporter, Subfamily B, Member 1; Chromosome Mapping; Crosses, Genetic; Dihydroergotamine; Drug Design; Drug Resistance; Humans; Inhibitory Concentration 50; Mutation; Plasmodium falciparum; Quantitative Trait Loci; Transfection | 2009 |
Desensitization of the mu-opioid activation of phospholipase C in SH-SY5Y cells: the role of protein kinases C and A and Ca(2+)-activated K+ currents.
Topics: 3-Pyridinecarboxylic acid, 1,4-dihydro-2,6-dimethyl-5-nitro-4-(2-(trifluoromethyl)phenyl)-, Methyl ester; Analgesics, Opioid; Calcium; Calcium Channel Agonists; Calcium Channel Blockers; Cyclic AMP-Dependent Protein Kinases; Enzyme Activation; Enzyme Inhibitors; Fentanyl; Humans; Indoles; Inositol 1,4,5-Trisphosphate; Isoquinolines; Narcotics; Neuroblastoma; Nifedipine; Potassium Channels; Protein Kinase C; Receptors, Opioid, mu; Sensitivity and Specificity; Sulfonamides; Tumor Cells, Cultured; Type C Phospholipases | 1995 |
Negative inotropic action of denbufylline through interfering with the calcium channel independently of its PDE IV inhibitory activity in guinea pig ventricle papillary muscles.
Topics: 3-Pyridinecarboxylic acid, 1,4-dihydro-2,6-dimethyl-5-nitro-4-(2-(trifluoromethyl)phenyl)-, Methyl ester; Animals; Azides; Caffeine; Calcium Channels; Depression, Chemical; Dihydropyridines; Guinea Pigs; In Vitro Techniques; Isoquinolines; Male; Myocardial Contraction; Papillary Muscles; Phosphodiesterase Inhibitors; Ryanodine; Sulfonamides; Xanthines | 1996 |
CGRP inhibition of electromechanical coupling in the guinea-pig isolated renal pelvis.
Topics: 3-Pyridinecarboxylic acid, 1,4-dihydro-2,6-dimethyl-5-nitro-4-(2-(trifluoromethyl)phenyl)-, Methyl ester; Alkaloids; Animals; Arginine; Calcitonin Gene-Related Peptide; Calcium; Carbazoles; Enzyme Inhibitors; Glyburide; Guinea Pigs; In Vitro Techniques; Indoles; Isoquinolines; Kidney Pelvis; Male; Membrane Potentials; Nitroarginine; Potassium Channels; Ryanodine; Sucrose; Sulfonamides; Terpenes; Tetrodotoxin; Thapsigargin | 1995 |
Novel marine-derived halogen-containing gramine analogues induce vasorelaxation in isolated rat aorta.
Topics: 3-Pyridinecarboxylic acid, 1,4-dihydro-2,6-dimethyl-5-nitro-4-(2-(trifluoromethyl)phenyl)-, Methyl ester; Alkaloids; Animals; Aorta, Thoracic; Caffeine; Calcium; Calcium Channel Agonists; Dose-Response Relationship, Drug; In Vitro Techniques; Indole Alkaloids; Indoles; Isoquinolines; Male; Phenylephrine; Potassium; Rats; Rats, Wistar; Sulfonamides; Time Factors; Vasoconstriction; Vasoconstrictor Agents; Vasodilation | 2001 |
Stimulation of ICa by basal PKA activity is facilitated by caveolin-3 in cardiac ventricular myocytes.
Topics: 3-Pyridinecarboxylic acid, 1,4-dihydro-2,6-dimethyl-5-nitro-4-(2-(trifluoromethyl)phenyl)-, Methyl ester; Adrenergic beta-2 Receptor Agonists; Animals; Calcium Channels, L-Type; Calcium Signaling; Caveolin 3; Cyclic AMP-Dependent Protein Kinases; Ethanolamines; Heart Ventricles; Isoquinolines; Male; Myocytes, Cardiac; Patch-Clamp Techniques; Phosphorylation; Protein Binding; Protein Kinase Inhibitors; Protein Processing, Post-Translational; Rats; Rats, Wistar; Sarcolemma; Sulfonamides | 2014 |
Ca
Topics: 3-Pyridinecarboxylic acid, 1,4-dihydro-2,6-dimethyl-5-nitro-4-(2-(trifluoromethyl)phenyl)-, Methyl ester; Animals; Binding Sites; Calcium Channel Blockers; Calcium Channels, L-Type; Carbazoles; Cells, Cultured; Cyclic AMP-Dependent Protein Kinases; Electrophysiological Phenomena; In Vitro Techniques; Intracellular Signaling Peptides and Proteins; Isoquinolines; Male; Models, Molecular; Molecular Docking Simulation; Muscle, Smooth, Vascular; Myocytes, Smooth Muscle; Patch-Clamp Techniques; Peptide Fragments; Protein Kinase Inhibitors; Pyrroles; Rats, Wistar; Sulfonamides; Tail; Vasodilation | 2017 |