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Volumn 4, Issue 2, 2008, Pages 121-128
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Synthesis and pharmacological profile of a series of 1-substituted-2-carbonyl derivatives of diphenidol: Novel M4 muscarinic receptor antagonists
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Author keywords
Binding studies; cAMP; Diphenidol derivatives; Functional studies; Muscarinic antagonists; Subtype selectivity
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Indexed keywords
1 BENZYLOXY 1,1 DIPHENYL 4 PIPERIDIN 1 YLBUTAN 2 ONE;
1 BENZYLOXY 1,1 DIPHENYLPROPAN 2 ONE;
1 BENZYLSULFANYL 1,1 DIPHENYL 4 PIPERIDIN 1 YLBUTAN 2 ONE;
1 BENZYLSULFANYL 1,1 DIPHENYLPROPAN 2 ONE;
1 ISOBUTOXY 1,1 DIPHENYL 4 PIPERIDIN 1 YLBUTAN 2 ONE;
1 ISOBUTOXY 1,1 DIPHENYLPROPAN 2 ONE;
1 ISOPROPOXY 1,1 DIPHENYL 4 PIPERIDIN 1 YLBUTAN 2 ONE;
1 ISOPROPOXY 1,1 DIPHENYLPROPAN 2 ONE;
1 THIOPEN 3 YL 1,1 DIPHENYL 4 PIPERIDIN 1 YLBUTAN 2 ONE;
1,1 DIPHENYL 1 THIOPEN 3 YL PROPAN 2 ONE;
1,2 DIPHENYL 1 THIOPEN 3 YL PROPANE 1,2 DIOL;
2 HYDROXY 1,2 DIPHENYL 2 THIOPEN 3 YL ETHANONE;
CARBACHOL;
CHOLINERGIC RECEPTOR BLOCKING AGENT;
DIFENIDOL;
FORSKOLIN;
MUSCARINIC M4 RECEPTOR;
MUSCARINIC M4 RECEPTOR BLOCKING AGENT;
MUSCARINIC RECEPTOR BLOCKING AGENT;
PIPERIDINE DERIVATIVE;
ANIMAL EXPERIMENT;
ANIMAL TISSUE;
ARTICLE;
CENTRAL NERVOUS SYSTEM;
DRUG PROTEIN BINDING;
DRUG RECEPTOR BINDING;
DRUG STRUCTURE;
DRUG SYNTHESIS;
GEL CHROMATOGRAPHY;
HUMAN;
MALE;
NONHUMAN;
PERIPHERAL NERVOUS SYSTEM;
PRIORITY JOURNAL;
PROTEIN FOLDING;
PROTEIN FUNCTION;
RECEPTOR AFFINITY;
STRUCTURE ACTIVITY RELATION;
ANIMAL;
CHEMISTRY;
CHO CELL;
CRICETULUS;
DRUG ANTAGONISM;
GUINEA PIG;
HAMSTER;
RABBIT;
SYNTHESIS;
ANIMALS;
CHO CELLS;
CRICETINAE;
CRICETULUS;
GUINEA PIGS;
MUSCARINIC ANTAGONISTS;
PIPERIDINES;
RABBITS;
RECEPTOR, MUSCARINIC M4;
STRUCTURE-ACTIVITY RELATIONSHIP;
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EID: 42949136115
PISSN: 15734064
EISSN: None
Source Type: Journal
DOI: 10.2174/157340608783789211 Document Type: Article |
Times cited : (7)
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References (28)
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