Direct and practical synthesis of 2′-O,4′-C-aminomethylene-bridged nucleic acid purine derivatives by transglycosylation
Umemoto, Tadashi, Masada, Shinichi, Miyata, Kenichi, Ogasawara-Shimizu, Mari, Murata, Shumpei, Nishi, Kazunori, Ogi, Kazuhiro, Hayase, Yoji, Cho, Nobuo
Published in Tetrahedron (02.03.2017)
Published in Tetrahedron (02.03.2017)
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Synthesis and hybridization studies on two complementary nona(2'-O-methyl)ribonucleotides
INOUE, H, HAYASE, Y, IMURA, A, IWAI, S, MIURA, K, OHTSUKA, E
Published in Nucleic acids research (11.08.1987)
Published in Nucleic acids research (11.08.1987)
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Design, synthesis and structure–activity relationships of 1,3,4-oxadiazole derivatives as novel inhibitors of glycogen synthase kinase-3β
Saitoh, Morihisa, Kunitomo, Jun, Kimura, Eiji, Hayase, Yoji, Kobayashi, Hiromi, Uchiyama, Noriko, Kawamoto, Tomohiro, Tanaka, Toshimasa, Mol, Clifford D., Dougan, Douglas R., Textor, Garret S., Snell, Gyorgy P., Itoh, Fumio
Published in Bioorganic & medicinal chemistry (01.03.2009)
Published in Bioorganic & medicinal chemistry (01.03.2009)
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Design of RNA enzymes distinguishing a single base mutation in RNA
KOIZUMI, M, HAYASE, Y, IWAI, S, KAMIYA, H, IMOUE, H, OHTSUKA, E
Published in Nucleic acids research (1989)
Published in Nucleic acids research (1989)
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Design, Synthesis, and Structure−Activity Relationships of Thieno[2,3-b]pyridin-4-one Derivatives as a Novel Class of Potent, Orally Active, Non-Peptide Luteinizing Hormone-Releasing Hormone Receptor Antagonists
Imada, Takashi, Cho, Nobuo, Imaeda, Toshihiro, Hayase, Yoji, Sasaki, Satoshi, Kasai, Shizuo, Harada, Masataka, Matsumoto, Hirokazu, Endo, Satoshi, Suzuki, Nobuhiro, Furuya, Shuichi
Published in Journal of medicinal chemistry (29.06.2006)
Published in Journal of medicinal chemistry (29.06.2006)
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A new solid-phase synthesis of oligoribonudeotides by the pbosphoro- p -anisidate method using tetrahydrofuranyl protection of 2'-hydroxyl groups
Jwai, Shigenori, Yamada, Emi, Asaka, Miyuki, Hayase, Yoji, Inoue, Hideo, Ohtsuka, Eiko
Published in Nucleic acids research (1987)
Published in Nucleic acids research (1987)
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Discovery of a Novel, Potent, and Orally Active Nonpeptide Antagonist of the Human Luteinizing Hormone-Releasing Hormone (LHRH) Receptor
Cho, Nobuo, Harada, Masataka, Imaeda, Toshihiro, Imada, Takashi, Matsumoto, Hirokazu, Hayase, Yoji, Sasaki, Satoshi, Furuya, Shuichi, Suzuki, Nobuhiro, Okubo, Shoichi, Ogi, Kazuhiro, Endo, Satoshi, Onda, Haruo, Fujino, Masahiko
Published in Journal of medicinal chemistry (22.10.1998)
Published in Journal of medicinal chemistry (22.10.1998)
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A new class of potent nonpeptide luteinizing hormone-releasing hormone (LHRH) antagonists: design and synthesis of 2-phenylimidazo[1,2- a]pyrimidin-5-ones
Sasaki, Satoshi, Imaeda, Toshihiro, Hayase, Yoji, Shimizu, Yoshiaki, Kasai, Shizuo, Cho, Nobuo, Harada, Masataka, Suzuki, Nobuhiro, Furuya, Shuichi, Fujino, Masahiko
Published in Bioorganic & medicinal chemistry letters (19.08.2002)
Published in Bioorganic & medicinal chemistry letters (19.08.2002)
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AGENT FOR CONTROLLING FUNCTION OF GPR34 RECEPTOR
KOHARA, YASUHISA, SUGO, TSUKASA, IMAI, TOMOMI, ITO, FUMIO, KOBAYASHI, HIROMI, ARAMAKI, YOSHIO, HAYASE, YOJI, MORI, MASAAKI, OGI, KAZUHIRO, KIMURA, EIJI
Year of Publication 24.08.2006
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Year of Publication 24.08.2006
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