http://rdf.ncbi.nlm.nih.gov/pubchem/patent/US-5158942-A

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classificationCPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07F9-10
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classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07F9-09
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http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61P31-12
filingDate 1990-08-23^^<http://www.w3.org/2001/XMLSchema#date>
grantDate 1992-10-27^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_99e25c52b2d1828eadcb1ab1065c53cc
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_95544e2ed0162393e3834540e345a866
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publicationDate 1992-10-27^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber US-5158942-A
titleOfInvention Process of using phospholipid derivatives to inhibit multiplication of the human immunodeficiency virus
abstract The present invention is concerned with the use of compounds of the general formula: <IMAGE> (I) and of the pharmacologically acceptable salts thereof, as well as of the optical isomers thereof for the preparation of pharmaceutical compositions with antiviral action. The present invention also provides new phospholipid derivatives.
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priorityDate 1989-09-02^^<http://www.w3.org/2001/XMLSchema#date>
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