Design of antagonists for NMDA and AMPA receptors

Neuropharmacology

Volumn 49, Issue 2, 2005, Pages 144-155

  Bolshakov, K V ^a   Kim, K H ^a   Potapjeva, N N ^a   Gmiro, V E ^b   Tikhonov, D B ^a   Usherwood, P N R ^c   Mellor, I R ^c   Magazanik, L G ^a  

^a SECHENOV INSTITUTE OF EVOLUTIONARY PHYSIOLOGY AND BIOCHEMISTRY   (Russian Federation)

^b INSTITUTE OF BIOMEDICAL CHEMISTRY   (Russian Federation)

^c UNIVERSITY OF NOTTINGHAM   (United Kingdom)

Author keywords

AMPA; Channel block; Ion channel; NMDA; Structure activity relationships

Indexed keywords

1 (1 ADAMANTYLMETHYLAMMONIO) 5 TRIMETHYLAMMONIOPENTANE DIBROMIDE; 1 ADAMANTYLMETHYLAMMONIO 5 AMMONIOPENTANE DIBROMIDE; ADAMANTANE DERIVATIVE; AMMONIUM DERIVATIVE; AMPA RECEPTOR; AMPA RECEPTOR ANTAGONIST; GLUCOCORTICOID RECEPTOR; IEM 1288; IEM 1617; IEM 1618; IEM 1921; IEM 1923; IEM 1957; IEM 1995; IEM 1997; IEM 2008; IEM 2009; IEM 2010; IEM 2011; IEM 2014; IEM 2015; IEM 2018; IEM 2041; IEM 2044; IEM 2046; IEM 2057; IEM 2059; IEM 2062; IEM 2063; IEM 2069; IEM 2085; N (5 AMMONIOPENTYL) 1 PHENYLCYCLOHEXYLAMMONIUM DIBROMIDE; N METHYL DEXTRO ASPARTIC ACID RECEPTOR; N METHYL DEXTRO ASPARTIC ACID RECEPTOR BLOCKING AGENT; TRIMETHYLAMMONIUM SALT DERIVATIVE; TRIPHENYLMETHANE DERIVATIVE; UNCLASSIFIED DRUG; UNINDEXED DRUG;

AMINO TERMINAL SEQUENCE; ANIMAL CELL; ARTICLE; CONTROLLED STUDY; DRUG DESIGN; DRUG MECHANISM; DRUG POTENCY; DRUG RECEPTOR BINDING; DRUG SELECTIVITY; DRUG STRUCTURE; HYDROPHOBICITY; NERVE CELL; NONHUMAN; OOCYTE; PRIORITY JOURNAL; RAT; STRUCTURE ACTIVITY RELATION; XENOPUS;

ADAMANTANE; ANIMALS; ANIMALS, NEWBORN; BRAIN; CALCIUM CHANNEL BLOCKERS; CALCIUM CHANNELS; DOSE-RESPONSE RELATIONSHIP, DRUG; DRUG DESIGN; EXCITATORY AMINO ACID ANTAGONISTS; INHIBITORY CONCENTRATION 50; MEMBRANE POTENTIALS; MICROINJECTIONS; MODELS, MOLECULAR; NEURONS; OOCYTES; PATCH-CLAMP TECHNIQUES; QUATERNARY AMMONIUM COMPOUNDS; RATS; RATS, WISTAR; RECEPTORS, AMPA; RECEPTORS, N-METHYL-D-ASPARTATE; XENOPUS;

EID: 21644481069     PISSN: 00283908     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.neuropharm.2005.02.007     Document Type: Article

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