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Volumn 54, Issue 6, 2002, Pages 827-834
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Synthesis and evaluation of N1-substituted-3-propyl-1,4-benzodiazepine-2-ones as cholecystokinin (CCK2) receptor ligands
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Author keywords
[No Author keywords available]
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Indexed keywords
1 (2,3 DIHYDRO 1 METHYL 2 OXO 5 PHENYL 1H 1,4 BENZODIAZEPIN 3 YL) 3 (3 METHYLPHENYL)UREA;
1 ALLYL 7 CHLORO 5 PHENYL 3 PROPYL 1,3 DIHYDRO 2H 1,4 BENZODIAZEPIN 2 ONE;
1 SEC BUTYL 7 CHLORO 5 PHENYL 3 PROPYL 1,3 DIHYDRO 2H 1,4 BENZODIAZEPIN 2 ONE;
2 (7 CHLORO 2 OXO 5 PHENYL 3 PROPYL 2,3 DIHYDRO 1H 1,4 BENZODIAZEPIN 1 YL)ACETAMIDE;
2 (7 CHLORO 2 OXO 5 PHENYL 3 PROPYL 2,3 DIHYDRO 1H 1,4 BENZODIAZEPIN 1 YL)ACETONITRILE;
2 BROMO N [4 CHLORO 2 [(HYDROXYIMINO) (PHENYL)METHYL]PHENYL]PENTAMIDE;
3 PROPYL 1,4 BENZODIAZEPINE;
4 AMINOBUTYRIC ACID A RECEPTOR;
7 CHLORO 1 (2 HYDROXOETHYL) 5 PHENYL 3 PROPYL 1,3 DIHYDRO 2H 1,4 BENZODIAZEPIN 2 ONE;
7 CHLORO 1 (2 MORPHOLIN 4 YLETHYL) 5 PHENYL 3 PROPYL 1,3 DIHYDRO 2H 1,4 BENZODIAZEPIN 2 ONE;
7 CHLORO 1 (3,3 DIMETHYL 2 OXOBUTYL) 5 PHENYL 3 PROPYL 1,3 DIHYDRO 2H 1,4 BENZODIAZEPIN 2 ONE;
7 CHLORO 1 METHYL 5 PHENYL 3 PROPYL 1,3 DIHYDRO 2H 1,4 BENZODIAZEPIN 2 ONE;
7 CHLORO 1 PHENETHYL 5 PHENYL 3 PROPYL 1,3 DIHYDRO 2H 1,4 BENZODIAZEPIN 2 ONE;
7 CHLORO 2 OXO 5 PHENYL 3 PROPYL 2,3 DIHYDRO 1H 1,4 BENZODIAZEPIN 4 IUM 4 OLATE;
7 CHLORO 5 PHENYL 3 PROPYL 1 PROP 2 YNYL 1,3 DIHYDRO 2H 1,4 BENZODIAZEPIN 2 ONE;
7 CHLORO 5 PHENYL 3 PROPYL 1,3 DIHYDRO 2H 1,4 BENZODIAZEPIN 2 ONE;
BENZODIAZEPIN 2 ONE DERIVATIVE;
BENZODIAZEPINE DERIVATIVE;
BENZOPHENONE DERIVATIVE;
CHOLECYSTOKININ B RECEPTOR;
CHOLECYSTOKININ OCTAPEPTIDE;
CHOLECYSTOKININ RECEPTOR BLOCKING AGENT;
DEVAZEPIDE;
DIAZEPAM;
DIHYDROHONOKIOL;
LIGAND;
N ALLYL 3 PROPYLBENZODIAZEPINE;
UNCLASSIFIED DRUG;
CHOLECYSTOKININ RECEPTOR;
NEUROLEPTIC AGENT;
ALKYLATION;
ANIMAL EXPERIMENT;
ANIMAL TISSUE;
ARTICLE;
BINDING AFFINITY;
BINDING ASSAY;
COMPARATIVE STUDY;
CONTROLLED STUDY;
DRUG DETERMINATION;
DRUG RECEPTOR BINDING;
DRUG SCREENING;
DRUG SYNTHESIS;
EXPERIMENTAL TEST;
GUINEA PIG;
IC 50;
IN VIVO STUDY;
ISOTOPE LABELING;
MALE;
MAZE TEST;
MOTOR ACTIVITY;
MOUSE;
MUSCLE RELAXATION;
NONHUMAN;
SEDATION;
STRUCTURE ACTIVITY RELATION;
TRANQUILIZING ACTIVITY;
ANIMAL;
ATMOSPHERIC PRESSURE;
BINDING COMPETITION;
CHEMICAL STRUCTURE;
CHEMISTRY;
MASS SPECTROMETRY;
METABOLISM;
METHODOLOGY;
RADIOASSAY;
SYNTHESIS;
ANIMALS;
ANTIPSYCHOTIC AGENTS;
ATMOSPHERIC PRESSURE;
BENZODIAZEPINES;
BINDING, COMPETITIVE;
LIGANDS;
MALE;
MASS SPECTROMETRY;
MICE;
MOLECULAR STRUCTURE;
RADIOLIGAND ASSAY;
RECEPTOR, CHOLECYSTOKININ B;
RECEPTORS, CHOLECYSTOKININ;
STRUCTURE-ACTIVITY RELATIONSHIP;
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EID: 0035997897
PISSN: 00223573
EISSN: None
Source Type: Journal
DOI: 10.1211/0022357021779005 Document Type: Article |
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Times cited : (14)
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References (21)
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