http://rdf.ncbi.nlm.nih.gov/pubchem/patent/EP-0809504-A4

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assignee http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_ff81a650b70e913d3b2524b45e4c7320
classificationCPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A61P31-18
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classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61K31-18
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D255-02
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61P31-12
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61K31-395
filingDate 1996-02-16-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_3cb9a8e6e68f3b88a98bdd2c8e3fee9e
publicationDate 1998-11-04-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber EP-0809504-A4
titleOfInvention ANTIVIRAL TRIAZA CONNECTIONS
abstract A method of inhibiting viruses in which a virus is contacted with an antiviral amount of a compound of formula I. Activity is shown against HIV and other viruses. formula I: <IMAGE> wherein W is a bridge carbon which has a polar or non-polar side group; X and Y independently are an aromatic group or an alkyl group, said aromatic group is selected from the group consisting of Ar, Ar sulfonyl, Ar carboxy and Ar alkyl, where Ar is an aromatic cyclic or aromatic heterocyclic ring having from five to seven members; said alkyl groups having from one to ten carbons; at least one of X and Y is an aromatic group; Z is a group listed for X and Y, a fused aryl moiety having from seven to ten carbons or hydrogen; a, d and e independently are a number from zero to 10; c and b independently are a number from one to 10; and the formula includes sufficient hydrogens for a stable molecule.
priorityDate 1995-02-17-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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