http://rdf.ncbi.nlm.nih.gov/pubchem/patent/WO-9719916-A2

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http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C09B33-048
filingDate 1996-11-26-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_ba4fdc05f9e647bb2dc259ac26613c90
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_a6ca6d7721dae6c76f9aa163ea21029b
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_606458ec7fb3d5880a7d9cfe46ae400d
publicationDate 1997-06-05-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber WO-9719916-A2
titleOfInvention Bisazo compounds, intermediates thereof, process for synthesizing the same and therapeutic agent for viral infection containing the same
abstract The present invention provides a bisazo compound of formula (A) useful as a therapeutic agent for viral infection such as AIDS, an amidonaphtholsulfonic acid compound useful as an intermediate thereof, a process for synthesizing such a compound and a therapeutic agent for viral infection comprising the bisazo compound. Formula (A): Ar?1-N=N-(Y1¿)-NH-CO-(X1)-CO-NH-(Y1')-N=N-Ar1', wherein Ar?1 and Ar1¿' represent an aryl group having 15 or less carbon atoms or a 5- or 6-membered ring heteroaryl group, (X1) represents a naphthylene or biphenylene group having 20 or less carbon atoms, (Y1) and (Y1') represent a naphthylene group having 15 or less carbon atoms with the proviso that at least 2 sulfo groups or salts thereof are contained in the molecule.
isCitedBy http://rdf.ncbi.nlm.nih.gov/pubchem/patent/CN-100377003-C
priorityDate 1995-11-29-04:00^^<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: 429.