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Mechanism of inhibition of connexin channels by the quinine derivative N-benzylquininium

The anti-malarial drug quinine and its quaternary derivative N-benzylquininium (BQ(+)) have been shown to inhibit gap junction (GJ) channels with specificity for Cx50 over its closely related homologue Cx46. Here, we examined the mechanism of BQ(+) action using undocked Cx46 and Cx50 hemichannels, w...

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Main Authors: Rubinos, Clio, Sánchez, Helmuth A., Verselis, Vytas K., Srinivas, Miduturu
Format: Artigo
Jezik:Inglês
Izdano: The Rockefeller University Press 2012
Teme:
Online dostop:https://ncbi.nlm.nih.gov/pmc/articles/PMC3250100/
https://ncbi.nlm.nih.gov/pubmed/22200948
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1085/jgp.201110678
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