Zobrazeno 1 - 6
of 6
pro vyhledávání: '"Ryosuke Namie"'
Autor:
Shohei Takase, Takashi Hiroyama, Fumiyuki Shirai, Yuki Maemoto, Akiko Nakata, Mayumi Arata, Seiji Matsuoka, Takeshi Sonoda, Hideaki Niwa, Shin Sato, Takashi Umehara, Mikako Shirouzu, Yosuke Nishigaya, Tatsunobu Sumiya, Noriaki Hashimoto, Ryosuke Namie, Masaya Usui, Tomokazu Ohishi, Shun-ichi Ohba, Manabu Kawada, Yoshihiro Hayashi, Hironori Harada, Tokio Yamaguchi, Yoichi Shinkai, Yukio Nakamura, Minoru Yoshida, Akihiro Ito
Publikováno v:
Nature Communications, Vol 14, Iss 1, Pp 1-18 (2023)
This study describes RK-701, an inhibitor of histone methyltransferases G9a/GLP, as a promising therapeutic candidate for sickle cell disease and a universal role of BGLT3 lncRNA in fetal hemoglobin reactivation by chemical inducers including RK-701.
Externí odkaz:
https://doaj.org/article/854cca959e544001b639a7418e25c89f
Autor:
Yosuke Nishigaya, Shohei Takase, Tatsunobu Sumiya, Ko Kikuzato, Tomohiro Sato, Hideaki Niwa, Shin Sato, Akiko Nakata, Takeshi Sonoda, Noriaki Hashimoto, Ryosuke Namie, Teruki Honma, Takashi Umehara, Mikako Shirouzu, Hiroo Koyama, Minoru Yoshida, Akihiro Ito, Fumiyuki Shirai
Publikováno v:
Journal of Medicinal Chemistry. 66:4059-4085
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::b9a221523e9478c8605cd7012c963963
https://doi.org/10.1021/acs.jmedchem.2c02059
https://doi.org/10.1021/acs.jmedchem.2c02059
Autor:
Shunichi Hashimoto, Masahiro Anada, Motoki Ito, Yuji Kondo, Ryosuke Namie, Yoshihiro Natori, Koji Takeda, Hisanori Nambu, Yasunori Yamamoto
Publikováno v:
HETEROCYCLES. 103:1078
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::f9bae0c1aadcc5326c24e24acb2700c7
https://doi.org/10.3987/com-20-s(k)61
https://doi.org/10.3987/com-20-s(k)61
Autor:
Hisanori Nambu, Shunichi Hashimoto, Ryosuke Namie, Hitomi Miyamae, Motoki Ito, Janagiraman Krishnamurthi, Koji Takeda
Publikováno v:
Synlett. 25:288-292
An asymmetric total synthesis of (–)-trans-blechnic acid, a dihydrobenzofuran neolignan, has been achieved. The key steps involve an elaboration of the cis-2,3-dihydrobenzofuran core structure by enantio- and diastereoselective intramolecular C–H
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::22317410a4df08a4c9c974619cc12f97
https://doi.org/10.1055/s-0033-1340291
https://doi.org/10.1055/s-0033-1340291
Autor:
Motoki Ito, Hisanori Nambu, Shunichi Hashimoto, Ryosuke Namie, Hitomi Miyamae, Janagiraman Krishnamurthi, Koji Takeda
Publikováno v:
ChemInform. 45
(-)-trans-blechnic acid (I) has an uncommon 2,3-cis-stereochemistry and belongs to the dihydrobenzofuran neolignans, which exhibit several biological activities.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::272c4dabbd825d2f3e94288ceb08d66a
https://doi.org/10.1002/chin.201428227
https://doi.org/10.1002/chin.201428227
Autor:
Motoki Ito, Ryosuke Namie, Krishnamurthi, Janagiraman, Hitomi Miyamae, Koji Takeda, Hisanori Nambu, Shunichi Hashimoto
Publikováno v:
Synlett; 2014, Vol. 25 Issue 2, p288-292, 5p