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Publikationer som ChEBI hänvisar till för UCL 1684. Visa hela publikationsregistret

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Publications in the selection

39 hits

Bibliografisk träff 2005-02-01

Role of SK(Ca) and IK(Ca) in endothelium-dependent hyperpolarizations of the guinea-pig isolated carotid artery.

Gluais P, Edwards G, Weston AH, Falck JR, Vanhoutte PM, Félétou M.

Br J Pharmacol · research-article; journal article · DOI 10.1038/sj.bjp.0706003

Bibliografisk träff 2004-06-01

Small conductance Ca2+-activated K+ channels as targets of CNS drug development.

Blank T, Nijholt I, Kye MJ, Spiess J.

Curr Drug Targets CNS Neurol Disord · review; journal article · DOI 10.2174/1568007043337472

Bibliografisk träff 2003-04-01

Modulation of small conductance calcium-activated potassium (SK) channels: a new challenge in medicinal chemistry.

Liégeois JF, Mercier F, Graulich A, Graulich-Lorge F, Scuvée-Moreau J, Seutin V.

Curr Med Chem · research support, non-u.s. gov't; review; journal article · DOI 10.2174/0929867033457908

Bibliografisk träff 2000-04-01

Compounds that block both intermediate-conductance (IK(Ca)) and small-conductance (SK(Ca)) calcium-activated potassium channels.

Malik-Hall M, Ganellin CR, Galanakis D, Jenkinson DH.

Br J Pharmacol · research support, non-u.s. gov't; research-article; journal article · DOI 10.1038/sj.bjp.0703233

Bibliografisk träff 2000-04-01

Effects of inhibitors of small- and intermediate-conductance calcium-activated potassium channels, inwardly-rectifying potassium channels and Na(+)/K(+) ATPase on EDHF relaxations in the rat hepatic artery.

Andersson DA, Zygmunt PM, Movahed P, Andersson TL, Högestätt ED.

Br J Pharmacol · research support, non-u.s. gov't; research-article; journal article · DOI 10.1038/sj.bjp.0703226

Bibliografisk träff 2000-03-01

Pharmacological characterization of small-conductance Ca(2+)-activated K(+) channels stably expressed in HEK 293 cells.

Strøbaek D, Jørgensen TD, Christophersen P, Ahring PK, Olesen SP.

Br J Pharmacol · research support, non-u.s. gov't; research-article; journal article · DOI 10.1038/sj.bjp.0703120

Bibliografisk träff 2000-02-01

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

Campos Rosa J, Galanakis D, Piergentili A, Bhandari K, Ganellin CR, Dunn PM, Jenkinson DH.

J Med Chem · research support, non-u.s. gov't; journal article · DOI 10.1021/jm9902537

Bibliografisk träff 1999-02-01

UCL 1684: a potent blocker of Ca2+ -activated K+ channels in rat adrenal chromaffin cells in culture.

Dunn PM.

Eur J Pharmacol · research support, non-u.s. gov't; journal article · DOI 10.1016/s0014-2999(99)00029-1

Bibliografisk träff 1998-01-01

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.

Rosa JC, Galanakis D, Ganellin CR, Dunn PM, Jenkinson DH.

J Med Chem · research support, non-u.s. gov't; journal article · DOI 10.1021/jm970571a