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classificationCPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C12N9-1007
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C12Y201-01
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07H15-252
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C12P19-56
classificationIPCAdditional http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C12R1-465
classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07H15-252
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61P31-04
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C12P19-56
filingDate 2016-04-27-04:00^^<http://www.w3.org/2001/XMLSchema#date>
grantDate 2017-04-19-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationDate 2017-04-19-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber CN-105820198-B
titleOfInvention Puromycin derivative as well as preparation and application thereof
abstract The invention discloses a puromycin derivative as shown in the formula (I) as well as preparation and application thereof. A novel compound 12-demethylation-dutomycin which can inhibit gram positive bacteria is produced by using an engineering biological synthesis method for a first time, the bacteriostatic activity of b12-demethylation-dutomycin on gram positive bacteria is remarkably higher than that of a natural compound dutomycin as source of b12-demethylation-dutomycin, the yield of a method for producing the compound 12-demethylation-dutomycin for inhibiting gram positive bacteria by using the engineering biological synthesis method and an extraction process of the method can be 44mg/L at most, raw material sources are not limited, the operation process is easy to control, and the production cost is low.
priorityDate 2016-04-27-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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