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Volumn 58, Issue 12, 1996, Pages 991-1000
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S-(-)-ET 126 : A potent and selective M1 antagonist in vitro and in vivo
a,c
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Author keywords
Analgesia; M1 selective muscarinic antagonist; M1, M2 and M3 subtype; S ( ) ET 126
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Indexed keywords
[4 [(3 CHLOROPHENYL)CARBAMOYLOXY] 2 BUTYNYL]TRIMETHYLAMMONIUM;
ACETYLCHOLINE;
ALPHA (HYDROXYMETHYL)BENZENEACETIC ACID 1 METHYL 4 PIPERIDYL ESTER;
ATROPINE;
CARBACHOL;
CEVIMELINE;
MUSCARINIC AGENT;
MUSCARINIC M1 RECEPTOR;
MUSCARINIC M1 RECEPTOR AGONIST;
MUSCARINIC M1 RECEPTOR ANTAGONIST;
MUSCARINIC M2 RECEPTOR;
MUSCARINIC M3 RECEPTOR;
MUSCARINIC RECEPTOR;
MUSCARINIC RECEPTOR BLOCKING AGENT;
PIRENZEPINE;
RECEPTOR SUBTYPE;
UNCLASSIFIED DRUG;
ANIMAL EXPERIMENT;
ANIMAL TISSUE;
ANTINOCICEPTION;
ARTICLE;
BLOOD BRAIN BARRIER;
CONCENTRATION RESPONSE;
CONTROLLED STUDY;
DRUG ANTAGONISM;
DRUG POTENCY;
DRUG SELECTIVITY;
HEART LEFT ATRIUM;
ILEUM;
INTRACEREBROVENTRICULAR DRUG ADMINISTRATION;
INTRAPERITONEAL DRUG ADMINISTRATION;
MALE;
MOUSE;
NONHUMAN;
RABBIT;
RAT;
SMOOTH MUSCLE CONTRACTILITY;
VAS DEFERENS;
ACETYLCHOLINE;
ANIMALS;
ATRIAL FUNCTION, LEFT;
CARBACHOL;
DOSE-RESPONSE RELATIONSHIP, DRUG;
ILEUM;
MALE;
MICE;
MUSCARINIC ANTAGONISTS;
PHENYLACETATES;
PIPERIDINES;
PIRENZEPINE;
RABBITS;
RATS;
VAS DEFERENS;
ANIMALIA;
ORYCTOLAGUS CUNICULUS;
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EID: 0029874664
PISSN: 00243205
EISSN: None
Source Type: Journal
DOI: 10.1016/0024-3205(96)00047-1 Document Type: Article |
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Times cited : (16)
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References (29)
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