http://rdf.ncbi.nlm.nih.gov/pubchem/patent/WO-0062775-A1

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assignee http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_5961e579b3eeb92b8e6975825aa2d619
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classificationCPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A61K31-405
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classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61K31-55
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61K31-47
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61K31-405
filingDate 2000-04-14-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_34e2348416fdd3c4255fae9ab00b9af0
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_5d7690a5daeba5cdc1d664483a12736a
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publicationDate 2000-10-26-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber WO-0062775-A1
titleOfInvention Compositions and methods for increasing the bioavailability of lactone ring containing drugs
abstract Compositions and methods are described for increasing the bioavailability of drugs, and in particular, drugs and prodrugs containing lactone structures which are hydrolyzed to open forms (carboxylic acids and alcohols) by serum and tissue paraoxonase. Inhibitors of paraoxonase (e.g. lactams) are co-administered with such drugs, thereby preventing paraoxonase from acting on these lactone substrates. Such inhibitors are particularly suitable in conjunction with the administration of lovastatin, simvastatin or mevastatin.
isCitedBy http://rdf.ncbi.nlm.nih.gov/pubchem/patent/WO-03007993-A1
http://rdf.ncbi.nlm.nih.gov/pubchem/patent/WO-0190336-A3
http://rdf.ncbi.nlm.nih.gov/pubchem/patent/WO-0190336-A2
priorityDate 1999-04-19-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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