Zobrazeno 1 - 10
of 15
pro vyhledávání: '"Hirohide Ishige"'
Autor:
Noriko Yamamoto, Yasuhisa Endo, Kazuyuki Furuya, Hirohide Ishige, Teruyuki Morikyu, Michael Albers, Yuki Ohyabu
Publikováno v:
Biological and Pharmaceutical Bulletin. 36:442-451
Selective androgen receptor modulators (SARMs) comprise a new class of molecules that induce anabolic effects with fewer side effects than those of other anabolic agents. We previously reported that the novel SARM S-101479 had a tissue-selective bone
Autor:
Nobuya Tamura, Yutaka Mizushima, Jingoro Shimada, Yoko Shoji, Miki Norimatsu, Wakao Iwatani, Hirohide Ishige
Publikováno v:
Journal of Drug Targeting. 5:261-273
We have previously shown that antisense phosphorothioate oligonucleotide (SON) targeted against immediate early (IE) pre-mRNA5 of the herpes simplex virus type I (HSV-I) possessed potent anti-herpetic activities in vitro system. However, anti-herpeti
Autor:
Akito Makino, Kazuyuki Furuya, Yuki Ohyabu, Noriko Yamamoto, Teruyuki Morikyu, Yasuhisa Endo, Kazuya Kuzutani, Hirohide Ishige
Publikováno v:
Biologicalpharmaceutical bulletin. 35(7)
We have studied non-steroidal selective androgen receptor modulators (SARMs) to develop anti-osteoporosis drugs for males and females. Many SARMs have been studied for their anabolic effects on bone or muscle with reduced virilizing effects in male a
Publikováno v:
ChemInform. 22
Publikováno v:
ChemInform. 23
(+)-Nonactic acid (1) has been synthesized by employing a condensation of the tetrahydro-2-furanthione (9) with dimethyl α-diazomalonate in the presence of rhodium acetate as a key reaction.
Publikováno v:
ChemInform. 24
Concise enantiospecific synthesis of the key intermediate for ajmalicine 1 and 19-epi-ajmalicine 2 has been achieved starting from a chiral cyclopentanone derivative, easily derived from (–)-carvone.
Publikováno v:
ChemInform. 26
An enantiospecific synthesis of clavukerin A, a novel trinorguaiane sesquiterpene, was accomplished starting from (–)-carvone.
Autor:
Toshio Honda, Hirohide Ishige
Publikováno v:
ChemInform. 26
An enantiospecific synthesis of curcumanolide A 1, a spirolactonic sesquiterpene, has been achieved starting from the chiral cyclopentane derivative 3, readily accessible from (-)-carvone. The absolute configuration of curcumanolide A 1 was unambiguo
Publikováno v:
Tetrahedron. 48:79-88
(+)-Nonactic acid (1) has been synthesized by employing a condensation of the tetrahydro-2-furanthione (9) with dimethyl α-diazomalonate in the presence of rhodium acetate as a key reaction.
Publikováno v:
Chemical and Pharmaceutical Bulletin. 39:1641-1643
(-)-Neonepetalactone (1) was synthesized using a rhodium acetate-catalyzad intramolecular cyclization of the γ, δ-unsaturated diazoketone (7), easily derived from (-)-carvone, as a key step.