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filingDate 1999-07-15-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_feb120ac9cddb7f87f5c2cb671462be5
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_e8def5dca72ff10849c1bdee77487966
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_806a157df34f5b6e9e5cc15579b8b7dc
publicationDate 2007-10-31-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber PL-195736-B1
titleOfInvention (1S, 2R) -3 - [[(4-aminophenyl) sulfonyl] (isobutyl) amino] -1-benzyl-2- (phosphonooxy) propylcarbamate (3S) tetrahydro-3-furanyl calcium salt, method of preparation and use, and composition pharmaceutical
abstract The invention relates to calcium (3S) tetrahydro-3-furanyl(1S,2R)-3-ÄÄ(4-aminophenyl)sulfonylÜ(isobutyl)amin oÜ-1-benzyl-2-(phosphonooxy) propylcarbamate combined with the HIV protease inhibitor 10-hydroxy-2-methyl-5-(1-methylethyl)-1-Ä2-(1-methylethyl)4-thiazolylÜ -3,6-dioxo-8,1 1-bis(phenylmethyl)-2,4,7,12-tetraazatridecan-13-oic acid, 5-thiazolylmethyl ester (ritonavir), and to the use thereof in the treatment of diseases caused by retroviruses. <CHEM>
priorityDate 1998-07-18-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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