http://rdf.ncbi.nlm.nih.gov/pubchem/patent/US-2002010200-A1

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assignee http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_ebb6a553affdc364c91cffe3baf12564
classificationCPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A61K31-44
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classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61K31-44
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filingDate 2001-07-27-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_5ca36d47a11e747fc370dd1e4126f914
publicationDate 2002-01-24-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber US-2002010200-A1
titleOfInvention Optically pure (-) amlodipine compositions
abstract Methods and compositions are disclosed utilizing the optically pure (−) isomer of amlodipine. This compound is a potent drug for the treatment of hypertension while avoiding the concomitant liability of adverse effects associated with the racemic mixture of amlodipine. The (−) isomer of amlodipine is also useful for the treatment of angina and such other conditions as may be related to the activity of (−) amlodipine as a calcium channel antagonist such as cerebral ischemia, cerebral disorders, arrhythmias, cardiac hypertrophy, coronary vasospasm, myocardial infarction, renal impairment and acute renal failure, without the concomitant liability of adverse effects associated with the racemic mixture of amlodipine.
isCitedBy http://rdf.ncbi.nlm.nih.gov/pubchem/patent/WO-2005089353-A3
http://rdf.ncbi.nlm.nih.gov/pubchem/patent/US-2007004783-A1
http://rdf.ncbi.nlm.nih.gov/pubchem/patent/US-2006035940-A1
priorityDate 1991-11-26-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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