http://rdf.ncbi.nlm.nih.gov/pubchem/patent/WO-9849180-A1

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classificationCPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07H21-00
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classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07H21-00
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C12Q1-68
filingDate 1998-04-29-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_b6c6af7dc8ce3547ad76123fd82fdf2d
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_a56571f86684e2f3a3321cfde384e40e
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_7fdb22f60d65e47903226159379de28a
publicationDate 1998-11-05-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber WO-9849180-A1
titleOfInvention Triplex forming oligonucleotides including pyrazolo(3,4-d)pyrimidine bases
abstract A triplex forming oligonucleotide is complementary pursuant to the G/T or A/G recognition motif to a homopurine, or substantially homopurine target sequence in double stranded nucleic acids, and at least one and preferably all of the guanine bases are replaced by their pyrazolo[3,4-d]pyrimidine analog, namely by 6-amino-1H-pyrazolo[3,4-d]pyrimidin-4(5H)-one. The oliginucleotides containing the pyrazolo[3,4-d]pyrimidine analog of guanine exhibit a lesser degree of self-association, and lack the nucleophilic nitrogen atom in the 7 position of guanine. The latter feature results in a diminished extent of self-cross-linking in ODNs which also have a covalently attached cross-linking agent.
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