The discovery of novel openers of Ca2+-dependent large-conductance potassium channels: Pharmacophore search and physiological evaluation of flavonoids
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V. Gribkoff | N. Meanwell | S. Dworetzky | W. Harte | C. Boissard | J. Starrett | G. Johnson | Yi Li
[1] V. Gribkoff,et al. N-Benzylated benzimidazol-2-one derivatives: activators of large-conductance Ca2+-dependent K+ channels , 1996 .
[2] V. Gribkoff,et al. Effects of channel modulators on cloned large-conductance calcium-activated potassium channels. , 1996, Molecular pharmacology.
[3] V. Gribkoff,et al. Cloning and expression of a human large-conductance calcium-activated potassium channel. , 1994, Brain research. Molecular brain research.
[4] I. Kubo,et al. Tyrosinase inhibitory flavonoids fromheterotheca inuloides and their structural functions , 1994 .
[5] V. Gribkoff,et al. Opening of large-conductance calcium-activated potassium channels by the substituted benzimidazolone NS004. , 1994, Journal of neurophysiology.
[6] S. Olesen,et al. Selective activation of Ca(2+)-dependent K+ channels by novel benzimidazolone. , 1994, European journal of pharmacology.
[7] D. Koh,et al. Effect of the flavoid phloretin on Ca2+-activated K+ channels in myelinated nerve fibres of Xenopus laevis , 1994, Neuroscience Letters.
[8] L. Salkoff,et al. mSlo, a complex mouse gene encoding "maxi" calcium-activated potassium channels. , 1993, Science.
[9] O. McManus,et al. An activator of calcium-dependent potassium channels isolated from a medicinal herb. , 1993, Biochemistry.
[10] P. Bonnet,et al. Evaluation of the relaxant effects of SCA40, a novel charybdotoxin‐sensitive potassium channel opener, in guinea‐pig isolated trachealis , 1993, British journal of pharmacology.
[11] P. Erhardt,et al. A topographical model for the c-AMP phosphodiesterase III active site. , 1991, Life sciences.
[12] R Latorre,et al. Varieties of calcium-activated potassium channels. , 1989, Annual review of physiology.
[13] M. Sabio,et al. Cardiotonic agents. 3. A topographical model of the cardiac cAMP phosphodiesterase receptor. , 1988, Molecular pharmacology.
[14] C. Humblet,et al. Cardiotonic agents. 8. Selective inhibitors of adenosine 3',5'-cyclic phosphate phosphodiesterase III. Elaboration of a five-point model for positive inotropic activity. , 1987, Journal of medicinal chemistry.