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filingDate 2000-06-23-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_1f3ce78a3d94c11e87a68b5b4aaa0118
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_32bdc052d03614617c3ff7c0dc4f0b2b
publicationDate 2001-03-13-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber JP-2001064297-A
titleOfInvention New bicyclonucleoside derivatives
abstract (57) Abstract: An intermediate for producing a non-natural oligonucleotide analog having excellent antisense or antigene activity and being stable in vivo, and 2-5A. An object is to provide an intermediate for producing an analog. A compound represented by the following structural formula (1) or a pharmacologically acceptable salt thereof. Embedded image R 1 and R 3 are the same or different and each represent a hydrogen atom, a hydroxyl group-protecting group for nucleic acid synthesis, and R 2 is a hydrogen atom, a C 1 to C 6 alkyl group or amino group for protecting nucleic acid synthesis And B represents purin-9-yl or 2-oxo-1,2 which may have a substituent selected from the following α group. -Dihydropyrimidin-1-yl group. (Α group) halogen atom, alkyl group having 1 to 6 carbon atoms, hydroxyl group, mercapto group, amino group and the like.
isCitedBy http://rdf.ncbi.nlm.nih.gov/pubchem/patent/JP-2005534629-A
http://rdf.ncbi.nlm.nih.gov/pubchem/patent/JP-4657609-B2
priorityDate 1999-06-25-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID415793908
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID6380

Total number of triples: 305.