Zobrazeno 1 - 4
of 4
pro vyhledávání: '"Yudai Satake"'
Autor:
Yoshihiko Noguchi, Shogo Sekikawa, Yutaka Nogaki, Yudai Satake, Norifumi Murashima, Takashi Kirisawa, Guido Schiffer, Johannes Köebberling, Tomoyasu Hirose, Toshiaki Sunazuka
Publikováno v:
Tetrahedron. 128:133100
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::0c29ef99dbb8074be892d6919077a2f9
https://doi.org/10.1016/j.tet.2022.133100
https://doi.org/10.1016/j.tet.2022.133100
Autor:
Tomoyasu Hirose, Souichi Monma, Kazuro Shiomi, Norifumi Murashima, Satoshi Ōmura, Yoshihiko Noguchi, Kei Masuda, Yudai Satake, Toshiaki Sunazuka, Takahiro Arai, Akito Watanabe
Publikováno v:
Tetrahedron Letters. 61:151699
Intracellular Ca+ release channel ryanodine receptors play a critical role in excitable tissue. They represent a highly attractive drug target to promote the possible development of selective insecticides and useful agriculture chemicals. The symmetr
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::f2ac2be4c7481a3847b4011a6ad17e1f
https://doi.org/10.1016/j.tetlet.2020.151699
https://doi.org/10.1016/j.tetlet.2020.151699
Autor:
Takeshi Matsuzaki, Shusuke Hashimoto, Yudai Satake, Tsutomu Shiina, Teruo Kurihara, Koichi Takeya, Haruhiko Fukaya, Yutaka Aoyagi, Ritsuo Aiyama, Yoshinao Takahashi
Publikováno v:
Tetrahedron Letters. 46:7885-7887
Grandione, a unique isetexane diterpene dimer, was synthesized from demethylsalvicanol via the solid state hetero-Diels–Alder type dimerization reaction. By X-ray crystallography, grandione was determined to have the structure, in which the two iso
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::9d23c3ef62349f381852d2587a79cca7
https://doi.org/10.1016/j.tetlet.2005.09.104
https://doi.org/10.1016/j.tetlet.2005.09.104
Autor:
Ritsuo Aiyama, Yudai Satake, Yoshinao Takahashi, Takeshi Matsuzaki, Koichi Takeya, Teruo Kurihara, Yutaka Aoyagi, Shusuke Hashimoto
Publikováno v:
Bioorganicmedicinal chemistry. 14(15)
Seven known abietane diterpenoids and 11-O- and 12-O-acetylcarnosic acids were isolated from a methanol extract of Perovskia abrotanoides (Labiatae). Structure and cytotoxic activity relationships (SAR) of the natural and semisynthetic analogues of t
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::78dc518d938a67b716ebd212d3bc1181
https://pubmed.ncbi.nlm.nih.gov/16626958
https://pubmed.ncbi.nlm.nih.gov/16626958