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classificationCPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A61P31-04
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D471-04
classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61K31-435
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61P31-04
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D471-04
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D405-06
filingDate 1980-02-08-04:00^^<http://www.w3.org/2001/XMLSchema#date>
grantDate 1981-04-07-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_43b04fa81975662aaa00c8c190b2274d
publicationDate 1981-04-07-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber US-4260614-A
titleOfInvention 4-(2-(1H-Imidazol-1-ylmethyl)-1,3-dioxolan-4-yl)methoxypyrazolo(3,4-b)pyridines
abstract Compounds are provided having the formula <IMAGE> wherein R1 is hydrogen, lower alkyl; substituted or unsubstituted phenyl-lower alkyl; substituted or unsubstituted phenyl; substituted or unsubstituted 5- or 6-membered monocyclic aromatic heterocyclic containing one O, S or N atom; in the above substituted groups, the phenyl groups bear one or two substituents and the heterocyclic bears one substituent which may be a halogen, hydroxy, lower alkyl, lower alkoxy, lower alkylthio, cyano or nitro group; R2 is hydrogen, lower alkyl, or substituted or unsubstituted phenyl; and R3 is substituted 1H-pyrazolo[3,4-b]pyridine or substituted 2H-pyrazolo[3,4-b]pyridine The above compound as well as their physiologically acceptable acid-addition salts are useful as antimicrobial agents, especially, antifungal agents.
isCitedBy http://rdf.ncbi.nlm.nih.gov/pubchem/patent/WO-0198301-A1
priorityDate 1980-02-08-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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