http://rdf.ncbi.nlm.nih.gov/pubchem/patent/CA-2158534-A1

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classificationCPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07H15-04
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07H3-04
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07H3-06
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A61P31-18
classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07H15-04
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07H3-06
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07H3-04
filingDate 1995-09-18-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_9257b38ed7da54e1623aeb3d15407565
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_981b7d71685adfffe1771d6e9f24f03c
publicationDate 1996-12-08-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber CA-2158534-A1
titleOfInvention Modified .alpha.-d-glcp-(1,2)-.alpha.-d-glcp-(1-3)-.alpha.-d-glcp-analogues
abstract Human immunodeficiency viruses (HIV-I and HIV-2) are known to be the etiological agents of acquired immunodeficiency syndrome (AIDS). The carbohydrate structures on the virus coat proteins, gp120, are necessary for cell-cell fusion. the oligosaccharides on gp120 are processed by the enzyme glycosidase. The trisaccharide, .alpha.-D-Glcp-(1-2)-.alpha.-D-Glcp-(1-3)-.alpha.-D-GlcpO(CH2)8COOMe and its analogues modified at its terminal glucose residues are recognized by the enzyme and can inhibit glycosylation.
priorityDate 1995-06-07-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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