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D H Jenkinson

Showing results (31-40 of 39) with videos related to

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Journal of Medicinal Chemistry|January 23, 1998
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+ channelJ C Rosa, D Galanakis, C R Ganellin, et al.
British Journal of Pharmacology|March 2, 1999
Differences in the actions of some blockers of the calcium-activated potassium permeability in mammalian red cellsD C Benton, C J Roxburgh, C R Ganellin, et al.
British Journal of Pharmacology|January 1, 1996
Discrimination between subtypes of apamin-sensitive Ca(2+)-activated K+ channels by gallamine and a novel bis-quaternary quinolinium cyclophane, UCL 1530P M Dunn, D C Benton, J Campos Rosa, et al.
Pharmacological Reviews|June 1, 1995
International Union of Pharmacology Committee on Receptor Nomenclature and Drug Classification. IX. Recommendations on terms and symbols in quantitative pharmacologyD H Jenkinson, E A Barnard, D Hoyer, et al.
Journal of Medicinal Chemistry|February 12, 2000
Synthesis, molecular modeling, and pharmacological testing of bis-quinolinium cyclophanes: potent, non-peptidic blockers of the apamin-sensitive Ca(2+)-activated K(+) channelJ Campos Rosa, D Galanakis, A Piergentili, et al.
Nature|November 22, 1979
Apamin blocks certain neurotransmitter-induced increases in potassium permeabilityB E Banks, C Brown, G M Burgess, et al.
Journal of Medicinal Chemistry|February 17, 1995
Synthesis and structure-activity relationships of dequalinium analogues as K+ channel blockers. Investigations on the role of the charged heterocycleD Galanakis, C A Davis, B Del Rey Herrero, et al.
The Journal of Pharmacy and Pharmacology|August 1, 1996
The synthesis and some pharmacological actions of the enantiomers of the K(+)-channel blocker cetiedilC J Roxburgh, C R Ganellin, M A Shiner, et al.
Journal of Medicinal Chemistry|September 21, 2001
Synthesis and structure-activity relationships of cetiedil analogues as blockers of the Ca(2+)-activated K+ permeability of erythrocytesC J Roxburgh, C R Ganellin, S Athmani, et al.
Pageof 4

Showing results (31-40 of 39) with videos related to

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Pageof 4
You have reached the last page of results.This site can display upto 39 results.
Journal of Medicinal Chemistry|January 23, 1998
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+ channelJ C Rosa, D Galanakis, C R Ganellin, et al.
British Journal of Pharmacology|March 2, 1999
Differences in the actions of some blockers of the calcium-activated potassium permeability in mammalian red cellsD C Benton, C J Roxburgh, C R Ganellin, et al.
British Journal of Pharmacology|January 1, 1996
Discrimination between subtypes of apamin-sensitive Ca(2+)-activated K+ channels by gallamine and a novel bis-quaternary quinolinium cyclophane, UCL 1530P M Dunn, D C Benton, J Campos Rosa, et al.
Pharmacological Reviews|June 1, 1995
International Union of Pharmacology Committee on Receptor Nomenclature and Drug Classification. IX. Recommendations on terms and symbols in quantitative pharmacologyD H Jenkinson, E A Barnard, D Hoyer, et al.
Journal of Medicinal Chemistry|February 12, 2000
Synthesis, molecular modeling, and pharmacological testing of bis-quinolinium cyclophanes: potent, non-peptidic blockers of the apamin-sensitive Ca(2+)-activated K(+) channelJ Campos Rosa, D Galanakis, A Piergentili, et al.
Nature|November 22, 1979
Apamin blocks certain neurotransmitter-induced increases in potassium permeabilityB E Banks, C Brown, G M Burgess, et al.
Journal of Medicinal Chemistry|February 17, 1995
Synthesis and structure-activity relationships of dequalinium analogues as K+ channel blockers. Investigations on the role of the charged heterocycleD Galanakis, C A Davis, B Del Rey Herrero, et al.
The Journal of Pharmacy and Pharmacology|August 1, 1996
The synthesis and some pharmacological actions of the enantiomers of the K(+)-channel blocker cetiedilC J Roxburgh, C R Ganellin, M A Shiner, et al.
Journal of Medicinal Chemistry|September 21, 2001
Synthesis and structure-activity relationships of cetiedil analogues as blockers of the Ca(2+)-activated K+ permeability of erythrocytesC J Roxburgh, C R Ganellin, S Athmani, et al.
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