Document Detail


Recognition of T.A interruption by 2',4'-BNAs bearing heteroaromatic nucleobases through parallel motif triplex formation.
MedLine Citation:
PMID:  18255299     Owner:  NLM     Status:  MEDLINE    
Abstract/OtherAbstract:
2'-O,4'-C-methylene bridged nucleic acid (2',4'-BNA) monomers bearing novel unnatural nucleobases, 4-(3-benzamidophenyl)-2-pyridone and 2-(N-methylbenzamido)thiazole, were synthesized and successfully incorporated into oligonucleotides. UV melting experiments showed that the corresponding oligonucleotide derivatives formed stable triplexes with dsDNA targets even in the presence of a T.A interruption.
Authors:
Satoshi Obika; Hiroyasu Inohara; Yoshiyuki Hari; Takeshi Imanishi
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Publication Detail:
Type:  Journal Article; Research Support, Non-U.S. Gov't     Date:  2007-12-25
Journal Detail:
Title:  Bioorganic & medicinal chemistry     Volume:  16     ISSN:  1464-3391     ISO Abbreviation:  Bioorg. Med. Chem.     Publication Date:  2008 Mar 
Date Detail:
Created Date:  2008-03-31     Completed Date:  2008-06-13     Revised Date:  -    
Medline Journal Info:
Nlm Unique ID:  9413298     Medline TA:  Bioorg Med Chem     Country:  England    
Other Details:
Languages:  eng     Pagination:  2945-54     Citation Subset:  IM    
Affiliation:
Graduate School of Pharmaceutical Sciences, Osaka University, 1-6 Yamadaoka, Suita, Osaka 565-0871, Japan.
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MeSH Terms
Descriptor/Qualifier:
Base Pairing*
Benzamides / chemistry*
Bridged Compounds
Nucleic Acid Conformation
Nucleic Acid Denaturation
Nucleic Acid Hybridization
Nucleic Acids / chemistry*
Oligonucleotides / chemistry*
Chemical
Reg. No./Substance:
0/Benzamides; 0/Bridged Compounds; 0/Nucleic Acids; 0/Oligonucleotides

From MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine


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