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Volumn 53, Issue 7, 2005, Pages 764-769
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Preparation of highly potent and selective non-peptide antagonists of the arginine vasopressin V1A receptor by introduction of a 2-ethyl-1H-1-imidazolyl group
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Author keywords
2 Ethyl 1H 1 imidazole; Arginine vasopressin; V1A receptor selective antagonist
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Indexed keywords
2 (1H 1,2,4 TRIAZOL 1 YL) 4' [(2,3,4,5 TETRAHYDRO 1H 1 BENZAZEPIN 1 YL)CARBONYL]BENZANILIDE;
2 (1H IMIDAZOL 1 YL) 4' [(2,3,4,5 TETRAHYDRO 1H 1 BENZAZEPIN 1 YL)CARBONYL]BENZANILIDE;
2 (2 ETHYL 1H IMIDAZOL 1 YL) 4' [(2,3,4,5 TETRAHYDRO 1H 1 BENZAZEPIN 1 YL)CARBONYL]BENZANILIDE;
2 (2 METHYL 1H IMIDAZOL 1 YL) 4' [(2,3,4,5 TETRAHYDRO 1H 1 BENZAZEPIN 1 YL)CARBONYL]BENZANILIDE;
2 (2 PHENYL 1H IMIDAZOL 1 YL) 4' [(2,3,4,5 TETRAHYDRO 1H 1 BENZAZEPIN 1 YL)CARBONYL]BENZANILIDE;
2 (2 PROPYL 1H IMIDAZOL 1 YL) 4' [(2,3,4,5 TETRAHYDRO 1H 1 BENZAZEPIN 1 YL)CARBONYL]BENZANILIDE;
2 PHENYL 4' [(2,3,4,5 TETRAHYDRO 1H 1 BENZAZEPIN 1 YL)CARBONYL]BENZANILIDE;
4' [(2,3,4,5 TETRAHYDRO 1H 1 BENZAZEPIN 1 YL)CARBONYL] 2 (1H TETRAZOL 5 YL)BENZANILIDE;
4' [(5 CARBAMOYLMETHYLENE 4,4 DIFLUORO 2,3,4,5 TETRAHYDRO 1H 1 BENZAZEPIN 1 YL)CARBONYL] 2 (2 ETHYL 1H IMIDAZOL 1 YL)BENZANILIDE;
4' [[4,4 DIFLUORO 5 (2 MORPHOLINO 2 OXOETHYLIDENE) 2,3,4,5 TETRAHYDRO 1H 1 YL]CARBONYL] 2 (2 ETHYL 1H 1 IMIDAZOL 1 YL)BENZANILIDE;
4' [[4,4 DIFLUORO 5 [(N (2 METHOXYETHYL)CARBAMOYL]METHYLENE] 2,3,4,5 TETRAHYDRO 1H 1 YL]CARBONYL] 2 (2 ETHYL 1H 1 IMIDAZOL 1 YL)BENZANILIDE;
4' [[4,4 DIFLUORO 5 [(N 1 PROPYLCARBAMOYL)METHYLENE] 2,3,4,5 TETRAHYDRO 1H 1 YL]CARBONYL] 2 (2 ETHYL 1H 1 IMIDAZOL 1 YL)BENZANILIDE;
4' [[4,4 DIFLUORO 5 [(N 2 PROPYLCARBAMOYL)METHYLENE] 2,3,4,5 TETRAHYDRO 1H 1 YL]CARBONYL] 2 (2 ETHYL 1H 1 IMIDAZOL 1 YL)BENZANILIDE;
4' [[4,4 DIFLUORO 5 [(N CYCLOPROPYLCARBAMOYL)METHYLENE] 2,3,4,5 TETRAHYDRO 1H 1 YL]CARBONYL] 2 (2 ETHYL 1H 1 IMIDAZOL 1 YL)BENZANILIDE;
4' [[4,4 DIFLUORO 5 [(N ETHYLCARBAMOYL)METHYLENE] 2,3,4,5 TETRAHYDRO 1H 1 YL]CARBONYL] 2 (2 ETHYL 1H 1 IMIDAZOL 1 YL)BENZANILIDE;
4' [[4,4 DIFLUORO 5 [(N METHYLCARBAMOYL)METHYLENE] 2,3,4,5 TETRAHYDRO 1H 1 YL]CARBONYL] 2 (2 ETHYL 1H 1 IMIDAZOL 1 YL)BENZANILIDE;
4' [[4,4 DIFLUORO 5 [(N,N DIETHYLCARBAMOYL)METHYLENE] 2,3,4,5 TETRAHYDRO 1H 1 YL]CARBONYL] 2 (2 ETHYL 1H 1 IMIDAZOL 1 YL)BENZANILIDE;
4' [[4,4 DIFLUORO 5 [(N,N DIMETHYLCARBAMOYL)METHYLENE] 2,3,4,5 TETRAHYDRO 1H 1 YL]CARBONYL] 2 (2 ETHYL 1H 1 IMIDAZOL 1 YL)BENZANILIDE;
4' [[4,4 DIFLUORO 5 [2 OXO 2 (1 PIPERIDINYL)ETHYLIDENE] 2,3,4,5 TETRAHYDRO 1H 1 YL]CARBONYL] 2 (2 ETHYL 1H 1 IMIDAZOL 1 YL)BENZANILIDE;
4' [[5 [(4 DIMETHYLAMINOPIPERIDINO)CARBONYLMETHYLENE] 4,4 DIFLUORO 2,3,4,5 TETRAHYDRO 1H 1 BENZAZEPIN 1 YL]CARBONYL] 2 PHENYLBENZANILIDE;
ANILIDE;
ARGININE VASOPRESSIN V1A RECEPTOR ANTAGONIST;
ARGIPRESSIN RECEPTOR;
IMIDAZOLE DERIVATIVE;
RECEPTOR BLOCKING AGENT;
UNCLASSIFIED DRUG;
ANIMAL EXPERIMENT;
ARTICLE;
BINDING AFFINITY;
CONTROLLED STUDY;
DRUG POTENCY;
DRUG RECEPTOR BINDING;
DRUG SELECTIVITY;
DRUG SYNTHESIS;
NONHUMAN;
RAT;
ARGININE VASOPRESSIN;
IMIDAZOLES;
MAGNETIC RESONANCE SPECTROSCOPY;
RECEPTORS, VASOPRESSIN;
SPECTROMETRY, MASS, FAST ATOM BOMBARDMENT;
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EID: 24944527847
PISSN: 00092363
EISSN: None
Source Type: Journal
DOI: 10.1248/cpb.53.764 Document Type: Article |
Times cited : (10)
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References (16)
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