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Original Articles

Synthesis and Biophysical Characterization of G-Rich Oligonucleotides Conjugated with Sugar-Phosphate Tails

, , , , , , , , & show all
Pages 1225-1229 | Published online: 05 Dec 2007

REFERENCES

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  • Hotoda , H. , Koizumi , M. , Koga , R. , Kaneko , M. , Momota , K. , Ohmine , T. , Furukawa , H. , Agatsuma , T. , Nishigaki , T. , Sone , J. , Tsutsumi , S. , Kosaka , T. , Abe , K. , Kimura , S. and Shimada , K. 1998 . Biologically active oligodeoxyribonucleotides. 5. 5′-End-substituted d(TGGGAG) possesses anti-human immunodeficiency virus type 1 activity by forming a G-quadruplex structure . J. Med. Chem. , 41 : 3655 – 3663 .
  • Koizumi , M. , Kaneko , M. , Ohmine , T. , Furukawa , H. and Nishigaki , T. Modified antisense oligodeoxyribonucleotides having TGGG sequence for treating AIDS . Patent JP98/04625; PCT/WO99/19474 . 1999 .
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  • Oligonucleotides c e g could have alternatively synthesized using commercially available universal solid supports and 2′-deoxyribonucleoside 5′-phosphoramidites, in connection with sugar phosphoramidite building block 5. This strategy was here not adopted on the basis of the overall higher costs and lower expected yields associated with the usage of nucleoside 5′-phosphoramidites

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