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Volumn 64, Issue , 2013, Pages 252-259
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Synthesis and evaluation of 4-substituted coumarins as novel acetylcholinesterase inhibitors
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Author keywords
Acetylcholinesterase; Alzheimer's disease; Coumarins; Docking study
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Indexed keywords
2 (2 OXO 2H CHROMEN 4 YLOXY)ACETIC ACID;
4 (2 OXO 2H CHROMEN 4 YLOXY)BUTANOIC ACID;
4 [2 (4 BENZYLPIPERIDIN 1 YL) 2 OXOETHOXY) 2H CHROMEN 2 ONE;
4 [2 [4 (2 FLUOROPHENYL)PIPERAZIN 1 YL] 2 OXOETHOXY) 2H CHROMEN 2 ONE;
4 [2 [4 (2 HYDROXYPHENYL)PIPERAZIN 1 YL] 2 OXOETHOXY] 2H CHROMEN 2 ONE;
4 [2 [4 (3,4 DICHLOROPHENYL)PIPERAZIN 1 YL] 2 OXOETHOXY 2H CHROMEN 2 ONE;
4 [2 [4 (4 BROMOPHENYL) 4 HYDROXYPIPERIDIN 1 YL] 2 OXOETHOXY] 2H CHROMEN 2 ONE;
4 [2 [4 (4 CHLOROPHENYL) 4 HYDROXYPIPERIDIN 1 YL] 2 OXOETHOXY] 2H CHROMEN 2 ONE;
4 [2 [4 (4 FLUOROPHENYL)PIPERAZIN 1 YL] 2 OXOETHOXY] 2H CHROMEN 2 ONE;
4 [2 OXO 2 (4 PHENYLPIPERAZIN 1 YL)ETHOXY)] 2H CHROMEN 2 ONE;
4 [4 (4 BENZYLPIPERIDIN 1 YL) 4 OXOBUTOXY] 2H CHROMEN 2 ONE;
4 [4 [4 (2 FLUOROPHENYL)PIPERAZIN 1 YL] 4 OXOBUTOXY] 2H CHROMEN 2 ONE;
4 [4 [4 (2 HYDROXYPHENYL)PIPERAZIN 1 YL] 4 OXOBUTOXY] 2H CHROMEN 2 ONE;
4 [4 [4 (3,4 DICHLOROPHENYL)PIPERAZIN 1 YL] 4 OXOBUTOXY] 2H CHROMEN 2 ONE;
4 [4 [4 (4 BROMOPHENYL) 4 HYDROXYPIPERIDIN 1 YL] 4 OXOBUTOXY] 2H CHROMEN 2 ONE;
4 [4 [4 (4 CHLOROPHENYL) 4 HYDROXYPIPERIDIN 1 YL] 4 OXOBUTOXY] 2H CHROMEN 2 ONE;
4 [4 [4 (4 FLUOROPHENYL)PIPERAZIN 1 YL] 4 OXOBUTOXY] 2H CHROMEN 2 ONE;
4 [4 OXO 4 (4 PHENYLPIPERAZIN 1 YL)BUTOXY] 2H CHROMEN 2 ONE;
ACETYLCHOLINESTERASE;
AP 2238;
CHOLINESTERASE;
CHOLINESTERASE INHIBITOR;
COUMARIN DERIVATIVE;
ENSACULINE;
ENZYME INHIBITOR;
N(1 BENZYLPIPERIDIN 4 YL) 2 (2 OXO 2H CHROMEN 4 YLOXY)ACETAMIDE;
N(1 BENZYLPIPERIDIN 4 YL) 4 (2 OXO 2H CHROMEN 4 YLOXY)BUTANAMIDE;
N(3,4 DIMETHOXYPHENETHYL) 4 (2 OXO 2H CHROMEN 4 YLOXY)BUTANAMIDE;
UNCLASSIFIED DRUG;
ANTIOXIDANT ACTIVITY;
ARTICLE;
DRUG DESIGN;
DRUG SELECTIVITY;
DRUG SYNTHESIS;
ELECTROPHORUS;
ENZYME INHIBITION;
EVALUATION;
HORSE;
IC 50;
MOLECULAR DOCKING;
MOLECULAR RECOGNITION;
NONHUMAN;
SUBSTITUTION REACTION;
ACETYLCHOLINESTERASE;
ANIMALS;
BUTYRYLCHOLINESTERASE;
CHOLINESTERASE INHIBITORS;
COUMARINS;
DOSE-RESPONSE RELATIONSHIP, DRUG;
ELECTROPHORUS;
HORSES;
MODELS, MOLECULAR;
MOLECULAR STRUCTURE;
STRUCTURE-ACTIVITY RELATIONSHIP;
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EID: 84877026618
PISSN: 02235234
EISSN: 17683254
Source Type: Journal
DOI: 10.1016/j.ejmech.2013.03.021 Document Type: Article |
Times cited : (112)
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References (24)
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