http://rdf.ncbi.nlm.nih.gov/pubchem/patent/EP-0400978-A2

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assignee http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_d202e9e866984fe229f6facc38f1d740
classificationCPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A61P33-10
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07H19-01
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A01N43-90
classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07H17-08
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07H19-01
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http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61P33-10
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http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A01N43-22
filingDate 1990-05-30-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_c141df783d057e13ece7514999acd10b
publicationDate 1990-12-05-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber EP-0400978-A2
titleOfInvention Avermectin -3,4-oxide derivatives useful as antiparasitic agents and insecticides
abstract There are disclosed avermectin derivatives of formula (I) in which the 3,4-double bond of the avermectins has been epoxidized. The compounds are prepared by oxidation of 7-O-trimethylsilyl-avermectins followed by deprotection. The compounds are active antiparasitic agents and insecticides and compositions for these uses are disclosed. wherein: nR 4˝ = OH, NH₂, NH-lower alkyl, NH-lower alkanoyl; nR₂₃ = H or OH and R₂₃ is present only when the broken line indicates a single bond; nR₂₅ = lower alkyl; nand the broken line indicates a single or double bond.
priorityDate 1989-06-02-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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