http://rdf.ncbi.nlm.nih.gov/pubchem/patent/US-2002133018-A1

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filingDate 2001-05-02-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_07a79529fd0c6a5457489e8669634273
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_c8a5448e8a56801a2bf4edd46a5be439
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_c899f19d6ca9f54f8f87b32ce3d1a03c
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_9d5fdf5357b65babdf32f29bac4b793a
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_a5de4e7bb250dd301254623db4d2e7a4
publicationDate 2002-09-19-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber US-2002133018-A1
titleOfInvention Dihydropyridine soft drugs, and related compositions and methods
abstract This invention relates to novel dihydropyridine soft drugs of the formula ΦOOR 1 , where Φ is a dihydropyridine moiety. These compounds are useful as calcium channel antagonists with cardiovascular, antiasthmatic and antibroncho-constriction activity. Use of such soft drug analogs permits the administration of greater doses of the claimed dihydropyridine compounds without intolerable systemic effects. Thus, this invention also provides pharmaceutical compositions, as well as methods, for preventing and treating disorders such as hypersensitivity, allergy, asthma, bronchospasim, dysmenorrhea, esophageal spasm, glaucoma, premature labor, urinary tract disorders, gastrointestinal motility disorders and cardiovascular disorders, while avoiding unwanted systemic effects.
priorityDate 2000-05-30-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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Total number of triples: 842.