http://rdf.ncbi.nlm.nih.gov/pubchem/patent/DE-60019619-T2

Outgoing Links

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filingDate 2000-08-18-04:00^^<http://www.w3.org/2001/XMLSchema#date>
grantDate 2006-03-02-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_af1c75c0671904d02c75514c2d168aae
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_3a145d205878bd08820d1d70f46c848d
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_c007cff22ea7c63a77a66d6b633ef7b7
publicationDate 2006-03-02-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber DE-60019619-T2
titleOfInvention DIHYDROBENZOFURANDERIVATE, PROCESS FOR THEIR MANUFACTURE AND MEDIUM
abstract A compound represented by the formula (I): <CHEM> or a salt thereof exhibits excellent inhibitory activity of lipid peroxidation and is useful as an agent for inhibiting lipoperoxide production, wherein A ring denotes a non-aromatic 5- to 7-membered nitrogen-containing heterocyclic ring which may be further substituted, B ring denotes a benzene ring which may be further substituted, C ring denotes a dihydrofuran ring which may be further substituted, and R denotes hydrogen atom or an acyl group, provided that: (1) when A ring is a non-aromatic 5-membered nitrogen-containing heterocyclic ring substituted with a group represented by the general formula: -(CH2)m-N(R")-C(=C)-R' (wherein R' denotes an optionally substituted hydrocarbon group, an optionally substituted amino group, or an optionally substituted heterocyclic group, R" denotes hydrogen atom or an optionally substituted hydrocarbon group, and m is an integer of 1 to 4), B ring denotes an further substituted benzene ring, and (2) when A ring denotes a non-aromatic 6-membered nitrogen-containing oxo-substituted heterocyclic ring, B ring denotes a wholly substituted benzene ring.
priorityDate 1999-08-20-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

Incoming Links

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Total number of triples: 39.