Modification of the philanthotoxin-343 polyamine moiety results in different structure-activity profiles at muscle nicotinic ACh, NMDA and AMPA receptors

Author:

Mellor I.R,Brier T.J,Pluteanu F,Strømgaard K,Saghyan A,Eldursi N,Brierley M.J,Andersen K,Jaroszewski J.W,Krogsgaard-Larsen P,Usherwood P.N.R

Publisher

Elsevier BV

Subject

Cellular and Molecular Neuroscience,Pharmacology

Reference33 articles.

1. Phencyclidine selectively blocks a spinal action of N-methyl-d-aspartate in mice;Aanonsen;Neuroscience Letters,1986

2. Structure-activity relationships of philanthotoxin analogues and polyamines on N-methyl-d-aspartate and nicotinic acetylcholine receptors;Anis;Journal of Pharmacology and Experimental Therapeutics,1990

3. Permeation and block of rat GluR6 glutamate receptor channels by internal and external polyamines;Bähring;Journal of Physiology (London),1997

4. An analysis of philanthotoxin block for recombinant rat GluR6(Q) glutamate receptor channels;Bähring;Journal of Physiology (London),1998

5. The physiological action of analogues of philanthotoxin-4.3.3 at insect nicotinic acetylcholine receptors;Benson;Comparative Biochemistry and Physiology C,1993

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