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pubmed-article:11012032pubmed:abstractText2'-Deoxyguanosine residues of a 3',5'-end-modified hexadeoxyribonucleotide (R-95288) with anti-HIV-1 activity were substituted with N2-methyl-2'-deoxyguanosine (m2dG). These modified oligodeoxyribonucleotides (ODNs) showed a 2-fold higher activity than R-95288. Also, the CD spectra of these ODNs indicated that the m2dG modification stabilized the tertiary structure of the G-quadruplex.lld:pubmed
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pubmed-article:11012032pubmed:articleTitleBiologically active oligodeoxyribonucleotides. Part 12: N2-methylation of 2'-deoxyguanosines enhances stability of parallel G-quadruplex and anti-HIV-1 activity.lld:pubmed
pubmed-article:11012032pubmed:affiliationExploratory Chemistry Research Laboratories, Sankyo Co., Ltd, Tokyo, Japan. koizum@shina.sankyo.co.jplld:pubmed
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