Ca v 1.2 channel current block by the PKA inhibitor H-89 in rat tail artery myocytes via a PKA-independent mechanism: Electrophysiological, functional, and molecular docking studies-Reference-Cited by-同舟云学术

Ca v 1.2 channel current block by the PKA inhibitor H-89 in rat tail artery myocytes via a PKA-independent mechanism: Electrophysiological, functional, and molecular docking studies

Published:2017-09 Issue: Volume:140 Page:53-63
ISSN:0006-2952
Container-title:Biochemical Pharmacology
language:en
Short-container-title:Biochemical Pharmacology

Author:

Fusi Fabio,Trezza Alfonso,Spiga Ottavia,Sgaragli Giampietro,Bova Sergio

Publisher

Elsevier BV

Subject

Pharmacology,Biochemistry

Reference45 articles.

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3. Inhibition of Kv1.3 channels by H-89 (N-[2-(p-bromocinnamylamino)ethyl]-5-isoquinolinesulfonamide) independent of protein kinase A;Choi;Biochem. Pharmacol.,2001

4. Metabotropic regulation of RhoA/Rho-associated kinase by L-type Ca2+ channels: new mechanism for depolarization-evoked mammalian arterial contraction;Fernández-Tenorio;Circ. Res.,2011

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