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Outgoing Links

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classificationCPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C08B37-0075
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C08B37-00
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classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C08B37-10
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C08B37-00
filingDate 1993-04-01-04:00^^<http://www.w3.org/2001/XMLSchema#date>
grantDate 1999-01-26-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_f32a8c9e8c9e753837863e1b140d747c
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_0be3f80ddc6795ae2a880ab26a48e762
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_11aa7caaf81d2a653aa1d462f25dc974
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_7d8bf66c2e55eb06ae770273f60dea48
publicationDate 1999-01-26-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber CA-2093147-C
titleOfInvention Semi-synthetic glycosaminoglycans with heparin or heparan structure of –-l-iduronic-2-sulfate acid modified in position 2
abstract The synthesis of new semi-synthetic glycosaminoglycans with heparin or heparan structure of .alpha.-L-iduronic-2-O-sulfate acid modified in position 2 is described in which the sulfate group is, entirely or in part, substituted with a nucleophilic radical. These new semi-synthetic glycosaminoglycans of general formula have good pharmaceutical properties in that they may also be absorbed orally and have good anti-thrombotic activity accompanied by low risk of haemorrhage and reduced anti-coagulating activity.
priorityDate 1992-04-17-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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