dequalinium chloride has been researched along with ucl 1684 in 7 studies
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 0 (0.00) | 18.7374 |
| 1990's | 1 (14.29) | 18.2507 |
| 2000's | 6 (85.71) | 29.6817 |
| 2010's | 0 (0.00) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
| Authors | Studies |
|---|---|
| Dunn, PM; Galanakis, D; Ganellin, CR; Jenkinson, DH; Rosa, JC | 1 |
| Bhandari, K; Campos Rosa, J; Dunn, PM; Galanakis, D; Ganellin, CR; Jenkinson, DH; Piergentili, A | 1 |
| Chen, JQ; Dunn, PM; Galanakis, D; Ganellin, CR; Jenkinson, DH | 1 |
| Chen, JQ; Dunn, PM; Galanakis, D; Ganellin, CR; Gunasekera, D | 1 |
| Dunn, PM; Fletcher, DI; Ganellin, CR; Jenkinson, DH; Piergentili, A | 1 |
| Andres, C; Fiedler, T; Gentles, RG; Grant-Young, K; Harden, DG; Hu, S; Huang, Y; Knox, R; Lodge, N; Poss, MA; Weaver, CD | 1 |
| Christophersen, P; Hougaard, C; Jensen, ML; Nielsen, EØ; Peters, D; Strøbaek, D; Sørensen, US; Teuber, L | 1 |
7 other study(ies) available for dequalinium chloride and ucl 1684
| Article | Year |
|---|---|
Bis-quinolinium cyclophanes: 6,10-diaza-3(1,3),8(1,4)-dibenzena-1,5(1,4)- diquinolinacyclodecaphane (UCL 1684), the first nanomolar, non-peptidic blocker of the apamin-sensitive Ca(2+)-activated K+ channel.
Topics: Alkanes; Animals; Apamin; Brain; Humans; Molecular Structure; Oocytes; Potassium Channel Blockers; Potassium Channels; Potassium Channels, Calcium-Activated; Quinolinium Compounds; Rats; Small-Conductance Calcium-Activated Potassium Channels; Structure-Activity Relationship; Xenopus laevis | 1998 |
Synthesis, molecular modeling, and pharmacological testing of bis-quinolinium cyclophanes: potent, non-peptidic blockers of the apamin-sensitive Ca(2+)-activated K(+) channel.
Topics: Alkanes; Animals; Apamin; Cells, Cultured; Models, Molecular; Molecular Conformation; Potassium Channel Blockers; Potassium Channels; Potassium Channels, Calcium-Activated; Quinolinium Compounds; Rats; Small-Conductance Calcium-Activated Potassium Channels; Structure-Activity Relationship; Superior Cervical Ganglion | 2000 |
bis-Quinolinium cyclophanes: 8,14-diaza-1,7(1, 4)-diquinolinacyclotetradecaphane (UCL 1848), a highly potent and selective, nonpeptidic blocker of the apamin-sensitive Ca(2+)-activated K(+) channel.
Topics: Animals; Apamin; Calcium; Cells, Cultured; Neurons; Potassium Channel Blockers; Potassium Channels; Potassium Channels, Calcium-Activated; Quinolinium Compounds; Rats; Small-Conductance Calcium-Activated Potassium Channels; Structure-Activity Relationship | 2000 |
Bis-quinolinium cyclophanes: toward a pharmacophore model for the blockade of apamin-sensitive SKCa channels in sympathetic neurons.
Topics: Apamin; Calcium Channels; Models, Chemical; Molecular Structure; Neurons; Quinolines; Sympathetic Nervous System | 2004 |
Synthesis and pharmacological testing of polyaminoquinolines as blockers of the apamin-sensitive Ca2+-activated K+ channel (SK(Ca)).
Topics: Aminoquinolines; Animals; Apamin; Guanidine; Molecular Sequence Data; Molecular Structure; Neurons; Potassium Channel Blockers; Potassium Channels, Calcium-Activated; Rats; Structure-Activity Relationship; Tissue Culture Techniques | 2007 |
Initial SAR studies on apamin-displacing 2-aminothiazole blockers of calcium-activated small conductance potassium channels.
Topics: Apamin; Combinatorial Chemistry Techniques; Molecular Structure; Potassium Channel Blockers; Pyridines; Small-Conductance Calcium-Activated Potassium Channels; Structure-Activity Relationship; Thiazoles | 2008 |
Synthesis and structure-activity relationship studies of 2-(N-substituted)-aminobenzimidazoles as potent negative gating modulators ofsmall conductance Ca2+-activated K+ channels.
Topics: 1-Naphthylamine; Benzimidazoles; Dose-Response Relationship, Drug; Humans; Ion Channel Gating; Molecular Structure; Small-Conductance Calcium-Activated Potassium Channels; Stereoisomerism; Structure-Activity Relationship | 2008 |