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filingDate 1993-02-22-04:00^^<http://www.w3.org/2001/XMLSchema#date>
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publicationDate 1993-09-01-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber EP-0558245-A1
titleOfInvention Heterobicyclic compounds as antagogists of alpha-1 adrenergic and SHT1A receptors
abstract There are disclosed compounds of the general formulan n The heteroatom X is preferably oxygen, but may have other values. The group W is preferably a carbonyl group, but may have other values. The preferred heterocyclic ring is thus a 4-oxo-4H-1-benzopyran ring. This may have a wide range of R₂, R₃, R₆ and R₇ substituents. Y is a linking group, chosen from a wide range, but including -COO- , -CONH- , -O- , -SO₂- and -SO₂NH-. Z is an alkylene chain, and B is a complex amine. These compounds and their prodrugs, enantiomers, diastereoisomers, N-oxides and pharmaceutically acceptable salts are useful for the treatment of hypertension and urinary tract troubles associated with benign prostatic hypertrophy, and for the treatment of other diseases.
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Total number of triples: 2331.