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filingDate 1996-03-07-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_6aa678214f7481ad9936bb0619d67ba7
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_f21c1420e24b4616e7cddccd9e88949a
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_14665d23fc5ca98dfab2c7c8385bcca2
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_7c4f39c30410fd65bec8a6898c375e68
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_e98c68285915894eb9a72a6d1a93c9de
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_56ff211ef821322f182c67025b3ba492
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_670dbce8a3ca1ec385bf244ef54dc1b0
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_f78c8afc8c81098bff4d3b911636707a
publicationDate 1998-02-04-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber SK-122397-A3
titleOfInvention Sulfonylalkanoylamino hydroxyethylamino sulfonamide retroviral protease inhibitors
abstract Selected sulfonylalkanoylamino hydroxyethylamine sulphonamide compounds of general formula (I) or pharmaceutical acceptable salts thereof, medicament precursors or esters thereof, wherein in the formula (I) the substituents R1, R2, R3, R4 and R5 have their meaning specified in description and patent claims, whilst n and t are individually 0, 1 or 2. These compounds are effective as retroviral protease inhibitors, and in particular as inhibitors of HIV protease. The present invention relates to such retroviral protease inhibitors and, more particularly, relates to selected novel compounds, composition and method for inhibiting retroviral proteases, such as human immunodeficiency virus (HIV) protease, prophylactically preventing retroviral infection or the spread of a retrovirus, and treatment of a retroviral infection.
priorityDate 1995-03-10-04:00^^<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: 577.