|
Volumn 24, Issue 5, 2014, Pages 1327-1333
|
Discovery of 2-(1H-indazol-1-yl)-thiazole derivatives as selective EP 1 receptor antagonists for treatment of overactive bladder by core structure replacement
|
Author keywords
Cystometry; Indazole; Overactive bladder; Thiazole
|
Indexed keywords
INDAZOLE DERIVATIVE;
PHENYL GROUP;
PROSTAGLANDIN E RECEPTOR 1;
PROSTAGLANDIN E RECEPTOR 1 ANTAGONIST;
PYRAZOLE DERIVATIVE;
THIAZOLE DERIVATIVE;
UNCLASSIFIED DRUG;
ARTICLE;
BLADDER CAPACITY;
CYSTOMETRY;
DRUG DESIGN;
DRUG POTENCY;
DRUG SELECTIVITY;
DRUG SYNTHESIS;
IC 50;
MICTURITION;
NONHUMAN;
OVERACTIVE BLADDER;
RAT;
STRUCTURE ACTIVITY RELATION;
URINE VOLUME;
RATTUS;
CYSTOMETRY;
EP(1) ANTAGONIST;
INDAZOLE;
OVERACTIVE BLADDER;
THIAZOLE;
ANIMALS;
DRUG EVALUATION, PRECLINICAL;
HALF-LIFE;
HUMANS;
INDAZOLES;
PROTEIN BINDING;
RATS;
RECEPTORS, PROSTAGLANDIN E, EP1 SUBTYPE;
STRUCTURE-ACTIVITY RELATIONSHIP;
THIAZOLES;
URINARY BLADDER;
URINARY BLADDER, OVERACTIVE;
|
EID: 84894574992
PISSN: 0960894X
EISSN: 14643405
Source Type: Journal
DOI: 10.1016/j.bmcl.2014.01.052 Document Type: Article |
Times cited : (19)
|
References (18)
|