Authors:
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
SHIMADA K
Citation: H. Hotoda et al., BIOLOGICALLY-ACTIVE OLIGODEOXYRIBONUCLEOTIDES - 5.(1)5'-END-SUBSTITUTED D(TGGGAG) POSSESSES ANTI-HUMAN-IMMUNODEFICIENCY-VIRUS TYPE-1 ACTIVITY BY FORMING A G-QUADRUPLEX STRUCTURE, Journal of medicinal chemistry, 41(19), 1998, pp. 3655-3663
Authors:
KOIZUMI M
KOGA R
HOTODA H
MOMOTA K
OHMINE T
FURUKAWA H
AGATSUMA T
NISHIGAKI T
ABE K
KOSAKA T
TSUTSUMI S
SONE J
KANEKO M
KIMURA S
SHIMADA K
Citation: M. Koizumi et al., BIOLOGICALLY-ACTIVE OLIGODEOXYRIBONUCLEOTIDES - IX - SYNTHESIS AND ANTI-HIV-1 ACTIVITY OF HEXADEOXYRIBONUCLEOTIDES, TGGGAG, BEARING 3'-END-MODIFICATION AND 5'-END-MODIFICATION, Bioorganic & medicinal chemistry, 5(12), 1997, pp. 2235-2243
Authors:
HOTODA H
KOIZUMI M
KOGA R
MOMOTA K
OHMINE T
FURUKAWA H
NISHIGAKI T
KINOSHITA T
KANEKO M
KIMURA S
SHIMADA K
Citation: H. Hotoda et al., BIOLOGICALLY-ACTIVE OLIGODEOXYRIBONUCLEOTIDES .4. ANTI-HIV-1 ACTIVITYOF TGGGAG HAVING HYDROPHOBIC SUBSTITUENT AT ITS 5'-END VIA PHOSPHODIESTER LINKAGE, Nucleosides & nucleotides, 15(1-3), 1996, pp. 531-538