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Potassium channels – multiplicity and challenges

British journal of pharmacology, 2006-01, Vol.147 (S1), p.S63-S71

Jenkinson, Donald H

2006

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SK3 is an important component of K+ channels mediating the afterhyperpolarization in cultured rat SCG neurones

The Journal of physiology, 2001-09, Vol.535 (2), p.323-334

2001

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Synthesis, Molecular Modeling, and Pharmacological Testing of Bis-Quinolinium Cyclophanes: Potent, Non-Peptidic Blockers of the Apamin-Sensitive Ca2+-Activated K+ Channel

Journal of medicinal chemistry, 2000-02, Vol.43 (3), p.420-431

2000

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Further studies on bis-charged tetraazacyclophanes as potent inhibitors of small conductance Ca(2+)-activated K+ channels

European journal of medicinal chemistry, 2013-05, Vol.63, p.907-923

2013

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Synthesis and pharmacological testing of polyaminoquinolines as blockers of the apamin-sensitive Ca2+ activated K+ channel (SKCa)

Bioorganic & medicinal chemistry, 2007-08, Vol.15 (16), p.5457-5479

2007

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Further studies on bis-charged tetraazacyclophanes as potent inhibitors of small conductance Ca2+-activated K+ channels

European journal of medicinal chemistry, 2013-05, Vol.63, p.907-923

2013

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Synthesis and Structure−Activity Relationships of Cetiedil Analogues as Blockers of the Ca2+-Activated K+ Permeability of Erythrocytes

Journal of medicinal chemistry, 2001-09, Vol.44 (20), p.3244-3253

2001

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Synthesis and Structure-Activity Relationships of Dequalinium Analogs as K+ Channel Blockers. Investigations on the Role of the Charged Heterocycle

Journal of medicinal chemistry, 1995-02, Vol.38 (4), p.595-606

1995

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Bis-Quinolinium Cyclophanes: 8,14-Diaza-1,7(1,4)-diquinolinacyclotetradecaphane (UCL 1848), a Highly Potent and Selective, Nonpeptidic Blocker of the Apamin-Sensitive Ca2+-Activated K+ Channel

Journal of medicinal chemistry, 2000-09, Vol.43 (19), p.3478-3481

2000

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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 Ca2+-Activated K+ Channel

Journal of medicinal chemistry, 1998-01, Vol.41 (1), p.2-5

1998

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Synthesis, molecular modeling, and pharmacological testing of bis-quinolinium cyclophanes: potent, non-peptidic blockers of the apamin-sensitive Ca(2+)-activated K(+) channel

Journal of medicinal chemistry, 2000-02, Vol.43 (3), p.420-431

2000

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The Synthesis and Some Pharmacological Actions of the Enantiomers of the K+-Channel Blocker Cetiedil

Journal of pharmacy and pharmacology, 1996-08, Vol.48 (8), p.851-859

1996

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International Union of Pharmacology Committee on Receptor Nomenclature and Drug Classification. IX. Recommendations on terms and symbols in quantitative pharmacology

Pharmacological reviews, 1995-06, Vol.47 (2), p.255

1995

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Synthesis and pharmacological testing of polyaminoquinolines as blockers of the apamin-sensitive Ca 2+-activated K + channel (SK Ca)

Bioorganic & medicinal chemistry, 2007, Vol.15 (16), p.5457-5479

2007

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Bis-quinolinium cyclophanes: 8,14-diaza-1,7(1,4)-diquinolinacyclo-tetradecaphane (UCL 1848), a highly potent and selective, nonpeptidic blocker of the apamin-sensitive Ca2+-activated K+ channel

Journal of medicinal chemistry, 2000-09, Vol.43 (19), p.3478-3481

2000

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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

Journal of medicinal chemistry, 1998-01, Vol.41 (1), p.2-5

1998

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How we describe competitive antagonists: three questions of usage

Trends in pharmacological sciences (Regular ed.), 1991, Vol.12 (2), p.53-54

Jenkinson, Donald H.

1991

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Dequalinium: a potent inhibitor of apamin-sensitive K + channels in hepatocytes and of nicotinic responses in skeletal muscle

European journal of pharmacology, 1993-05, Vol.236 (2), p.201-207

1993

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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

Journal of medicinal chemistry, 2000-09, Vol.43 (19), p.3478-3481

2000

Volltextzugriff (PDF)

Synthesis, Molecular Modeling, and Pharmacological Testing of Bis-Quinolinium Cyclophanes: Potent, Non-Peptidic Blockers of the Apamin-Sensitive Ca 2+ -Activated K + Channel

Journal of medicinal chemistry, 2000-02, Vol.43 (3), p.420-431

2000

Volltextzugriff (PDF)

Synthesis and Structure−Activity Relationships of Cetiedil Analogues as Blockers of the Ca 2+ -Activated K + Permeability of Erythrocytes

Journal of medicinal chemistry, 2001-09, Vol.44 (20), p.3244-3253

2001

Volltextzugriff (PDF)

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

Journal of medicinal chemistry, 1998-01, Vol.41 (1), p.2-5

1998

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Synthesis and qsar of dequalinium analogues AS K + channel blockers. investigations on the role of the 4-amino group

Bioorganic & medicinal chemistry letters, 1995-03, Vol.5 (6), p.559-562

1995

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On the Concept of a Bivalent Pharmacophore for SKCa Channel Blockers: Synthesis, Pharmacological Testing, and Radioligand Binding Studies on Mono-, Bis-, and Tris-quinolinium Compounds

Archiv der Pharmazie (Weinheim), 1996-12, Vol.329 (12), p.524-528

1996

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Bis-quinolinium cyclophanes: A novel class of potent blockers of the apamin-sensitive Ca 2+-activated K + channel

Bioorganic & medicinal chemistry letters, 1997, Vol.7 (1), p.7-10

1997

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Potassium channels – multiplicity and challenges

SK3 is an important component of K+ channels mediating the afterhyperpolarization in cultured rat SCG neurones

Synthesis, Molecular Modeling, and Pharmacological Testing of Bis-Quinolinium Cyclophanes: Potent, Non-Peptidic Blockers of the Apamin-Sensitive Ca2+-Activated K+ Channel

Further studies on bis-charged tetraazacyclophanes as potent inhibitors of small conductance Ca(2+)-activated K+ channels

Synthesis and pharmacological testing of polyaminoquinolines as blockers of the apamin-sensitive Ca2+ activated K+ channel (SKCa)

Further studies on bis-charged tetraazacyclophanes as potent inhibitors of small conductance Ca2+-activated K+ channels

Synthesis and Structure−Activity Relationships of Cetiedil Analogues as Blockers of the Ca2+-Activated K+ Permeability of Erythrocytes

Synthesis and Structure-Activity Relationships of Dequalinium Analogs as K+ Channel Blockers. Investigations on the Role of the Charged Heterocycle

Bis-Quinolinium Cyclophanes: 8,14-Diaza-1,7(1,4)-diquinolinacyclotetradecaphane (UCL 1848), a Highly Potent and Selective, Nonpeptidic Blocker of the Apamin-Sensitive Ca2+-Activated K+ Channel

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 Ca2+-Activated K+ Channel

Synthesis, molecular modeling, and pharmacological testing of bis-quinolinium cyclophanes: potent, non-peptidic blockers of the apamin-sensitive Ca(2+)-activated K(+) channel

The Synthesis and Some Pharmacological Actions of the Enantiomers of the K+-Channel Blocker Cetiedil

International Union of Pharmacology Committee on Receptor Nomenclature and Drug Classification. IX. Recommendations on terms and symbols in quantitative pharmacology

Synthesis and pharmacological testing of polyaminoquinolines as blockers of the apamin-sensitive Ca 2+-activated K + channel (SK Ca)

Bis-quinolinium cyclophanes: 8,14-diaza-1,7(1,4)-diquinolinacyclo-tetradecaphane (UCL 1848), a highly potent and selective, nonpeptidic blocker of the apamin-sensitive Ca2+-activated K+ channel

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

How we describe competitive antagonists: three questions of usage

Dequalinium: a potent inhibitor of apamin-sensitive K + channels in hepatocytes and of nicotinic responses in skeletal muscle

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

Synthesis, Molecular Modeling, and Pharmacological Testing of Bis-Quinolinium Cyclophanes: Potent, Non-Peptidic Blockers of the Apamin-Sensitive Ca 2+ -Activated K + Channel

Synthesis and Structure−Activity Relationships of Cetiedil Analogues as Blockers of the Ca 2+ -Activated K + Permeability of Erythrocytes

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

Synthesis and qsar of dequalinium analogues AS K + channel blockers. investigations on the role of the 4-amino group

On the Concept of a Bivalent Pharmacophore for SKCa Channel Blockers: Synthesis, Pharmacological Testing, and Radioligand Binding Studies on Mono-, Bis-, and Tris-quinolinium Compounds

Bis-quinolinium cyclophanes: A novel class of potent blockers of the apamin-sensitive Ca 2+-activated K + channel

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