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classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D487-04
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61P31-04
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61K31-5025
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61P1-04
filingDate 2000-06-12-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_cfccb5d83826127aa602e04963ce1b21
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_67128404ec05a7656f1a3f988e1a5d49
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_b8c80b295c041cca1f922825ac4ee271
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publicationDate 2001-03-06-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber JP-2001058993-A
titleOfInvention Optically active pyrrolopyridazine compounds
abstract (57) [Summary]nPROBLEM TO BE SOLVED: To excellently suppress gastric acid secretion, protect gastric mucosa, etc. Medicines for warm-blooded animals (especially humans), especially ulcers Provide a drug useful as an agent for preventing or treating a disease.nSOLUTION: General formulanEmbedded imagen (Where R 1 : C 1 -C 6 Alkyl group, R Two , R Three : C 1 -C 6 Alkyl group, R Four C 1 -C 6 Alkyl, halogeno C 1 − C 6 Alkyl, C 1 -C 6 Alkoxy, halogeno C 1 -C 6 Substitution selected from the group consisting of alkoxy and halogen C optionally substituted with a group 6 -C Ten Aryl group, A; Optically active pyro-containing pyrrole having an amino group, an oxygen atom or a sulfur atom) A lopyridazine compound or a pharmacologically acceptable salt thereof.
isCitedBy http://rdf.ncbi.nlm.nih.gov/pubchem/patent/WO-2004058768-A1
http://rdf.ncbi.nlm.nih.gov/pubchem/patent/WO-2004084899-A1
priorityDate 1999-06-15-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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