http://rdf.ncbi.nlm.nih.gov/pubchem/patent/US-7427672-B2

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classificationCPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07H21-00
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07H19-04
classificationIPCAdditional http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A01N43-04
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classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C12N15-00
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http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07H21-00
filingDate 2004-08-25-04:00^^<http://www.w3.org/2001/XMLSchema#date>
grantDate 2008-09-23-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_541ae5fe8ab9b84e41ce427189cdfbf3
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_0ef27c7ee81aac2d364ed88f5f0bf0ab
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_5a780034b5e553742430262e31cdf26d
publicationDate 2008-09-23-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber US-7427672-B2
titleOfInvention Artificial nucleic acids of n-o bond crosslinkage type
abstract An oligonucleotide analogue useful for the antisense method, etc., having excellent enzyme resistance, having potent selective binding affinity for single-stranded RNA, and further having an excellent triplex-forming capacity with double-stranded DNA, and a nucleoside analogue useful for its production are provided. n Nucleoside analogues, which are compounds of the general formula (I) and salts thereof, and oligonucleotide analogues containing one or more of the nucleoside analogues: n nwhere Base is an aromatic heterocyclic group or the like optionally having a substituent; R 1 , R 2 and R 3 are each a hydrogen atom, a protective group for an amino group, a protective group for a hydroxyl group, a phosphate group, or —P(R 4 )R 5 [where R 4 and R 5 are each a hydroxyl group, a protected hydroxyl group, a mercapto group, a protected mercapto group, etc.]; m=0 to 2; and n=1 to 3].
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Total number of triples: 1603.