84765-89-9Relevant academic research and scientific papers
Biologically active oligodeoxyribonucleotides, 5. 5'-end-substituted d(TGGGAG) possesses anti-human immunodeficiency virus type 1 activity by forming a G-quadruplex structure
Hotoda, Hitoshi,Koizumi, Makoto,Koga, Rika,Kaneko, Masakatsu,Momota, Kenji,Ohmine, Toshinori,Furukawa, Hidehiko,Agatsuma, Toshinori,Nishigaki, Takashi,Sone, Junko,Tsutsumi, Shinya,Kosaka, Toshiyuki,Abe, Koji,Kimura, Satoshi,Shimada, Kaoru
, p. 3655 - 3663 (2007/10/03)
A series of hexadeoxyribonucleotides (6-mers), d(TGGGAG), substituted with a variety of aromatic groups at the 5'-end were synthesized and tested for anti-human immunodeficiency virus type 1 (HIV-1) activity. While unmodified d(TGGGAG) (31) had no anti-HI
OLIGODEOXYRIBONUCLEOTIDE SYNTHESIS BY USE OF S,S-DIPHENYL DEOXYRIBONUCLEOSIDE 3'-PHOSPHORODITHIOATES AND BIFUNCTIONAL CONDENSING REAGENTS IN THE PHOSPHOTRIESTER APPROACH
Sekine, Mitsuo,Matsuzaki, Jun-Ichi,Hata, Tsujiaki
, p. 5279 - 5288 (2007/10/02)
Four kinds of arenedisulphonyl chlorides as condensing reagents for oligodeoxyribonucleotide synthesis have been synthesised and their condensing abilities were examined in the synthesis of thymidylyl(3'-5')thymidine.Among them, mesitylenedisulphonyl chlo
