http://rdf.ncbi.nlm.nih.gov/pubchem/patent/AU-2017364806-A1

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classificationCPCAdditional http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C12N2310-14
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classificationCPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C12N15-113
classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C12N15-113
filingDate 2017-11-27-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_38bbe7be887b91632a88d80acaca741d
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_d83bc47832cf352bb914ee5b6f1a00ab
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_554e59043bcf9496da580232cc18d427
publicationDate 2019-06-13-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber AU-2017364806-A1
titleOfInvention Chemically-modified siRNA
abstract The purpose of the present invention is to provide a chemically-modified siRNA in which polydeoxyadenylic acid is added to the 5' end of the sense strand thereof, wherein when the chemically-modified siRNA is complexed with sizofiran, the chemically-modified siRNA becomes highly resistant to RNase, and effectively exhibits RNAi activity. The problem can be solved by, in a modified siRNA in which polydeoxyadenylic acid is added to the 5' end of the sense strand thereof, applying a specific chemical modification to dinucleotide sequences CA, UA, and UG in the base sequence of the sense strand, and to dinucleotide sequences CA, UA, and UG located at or beyond the eighth base from the 5' end in the base sequence of the antisense strand.
priorityDate 2016-11-28-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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