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Volumn 53, Issue 4, 2001, Pages 369-376
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Substitution mode of the amide fragment in some new N-[ω-[4-(2-methoxyphenyl)piperazin-1-yl]alkyl pyrid-2(1H)-ones and their 5-HT1A/5-HT2A activity
a a a a a |
Author keywords
5 HT1A receptor antagonists; 5HT2A 5 HT1A selectivity; Pyrid 2(1H) one derivatives
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Indexed keywords
AROMATIC AMIDE;
LIGAND;
N [OMEGA [4 (2 METHOXYPHENYL)PIPERAZIN 1 YL]ALKYL]PYRID 2 (1H) ONE DERIVATIVE;
SEROTONIN 1A ANTAGONIST;
SEROTONIN 1A RECEPTOR;
SEROTONIN 2A RECEPTOR;
UNCLASSIFIED DRUG;
ANIMAL BEHAVIOR;
ANIMAL EXPERIMENT;
ANIMAL MODEL;
ANIMAL TISSUE;
ARTICLE;
BODY TEMPERATURE;
BRAIN CORTEX;
CONTROLLED STUDY;
DRUG ACTIVITY;
DRUG CONFORMATION;
DRUG SCREENING;
DRUG SELECTIVITY;
DRUG STRUCTURE;
DRUG SYNTHESIS;
HIPPOCAMPUS;
IN VITRO STUDY;
IN VIVO STUDY;
MALE;
NONHUMAN;
RAT;
RAT STRAIN;
RECEPTOR AFFINITY;
STRUCTURE ACTIVITY RELATION;
ADRENERGIC UPTAKE INHIBITORS;
ANIMALS;
BEHAVIOR, ANIMAL;
BODY TEMPERATURE;
CEREBRAL CORTEX;
CHROMATOGRAPHY, THIN LAYER;
HIPPOCAMPUS;
LIGANDS;
LIP;
MAGNETIC RESONANCE SPECTROSCOPY;
MALE;
MICE;
PYRIDONES;
RADIOLIGAND ASSAY;
RATS;
RATS, WISTAR;
RECEPTOR, SEROTONIN, 5-HT2A;
RECEPTORS, SEROTONIN;
RECEPTORS, SEROTONIN, 5-HT1;
RESERPINE;
SEROTONIN ANTAGONISTS;
STRUCTURE-ACTIVITY RELATIONSHIP;
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EID: 0034748186
PISSN: 12306002
EISSN: None
Source Type: Journal
DOI: None Document Type: Article |
Times cited : (7)
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References (21)
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