Zobrazeno 1 - 10
of 83
pro vyhledávání: '"Hirotaka Uzawa"'
Autor:
Hirotaka Uzawa, Satoshi Kondo, Takehiro Nagatsuka, Hajime Miyaguchi, Yasuo Seto, Aguri Oshita, Hirofumi Dohi, Yoshihiro Nishida, Masato Saito, Eiichi Tamiya
Publikováno v:
ACS Omega, Vol 6, Iss 48, Pp 32597-32606 (2021)
Externí odkaz:
https://doaj.org/article/3b0f040fd9424999b8ce5712302973b9
Publikováno v:
ACS Omega, Vol 4, Iss 3, Pp 5776-5783 (2019)
Externí odkaz:
https://doaj.org/article/31d6e2a80cf54756a75126515fc5a38b
Publikováno v:
Beilstein Journal of Organic Chemistry, Vol 13, Iss 1, Pp 1999-2009 (2017)
Cell-membrane glycerolipids exhibit a common structural backbone of asymmetric 1,2-diacyl-sn-glycerol bearing polar head groups in the sn-3 position. In this study, the possible effects of sn-3 head groups on the helical conformational property aroun
Externí odkaz:
https://doaj.org/article/7ed7b608fb234a77a3167507ccf5f359
Autor:
Hisanori Iwasa, Atsunori Hiratsuka, Kenji Yokoyama, Hirotaka Uzawa, Kouhei Orihara, Hitoshi Muguruma
Publikováno v:
ACS Omega, Vol 2, Iss 4, Pp 1660-1665 (2017)
Externí odkaz:
https://doaj.org/article/4f24a64b74ce4023a80b224ddc7cb23b
Autor:
Hirofumi Dohi, Takeru Kanazawa, Akihiro Saito, Keita Sato, Hirotaka Uzawa, Yasuo Seto, Yoshihiro Nishida
Publikováno v:
Beilstein Journal of Organic Chemistry, Vol 10, Iss 1, Pp 1504-1512 (2014)
Glycosyl-[60]fullerenes were first used as decontaminants against ricin, a lactose recognition proteotoxin in the Ricinus communis family. A fullerene glycoconjugate carrying two lactose units was synthesized by a [3 + 2] cycloaddition reaction betwe
Externí odkaz:
https://doaj.org/article/45e8d68cbd134dbb82dd4ede280d35c8
Autor:
Hirotaka Uzawa, Takehiro Nagatsuka, Yasuo Seto, Yoshihiro Nishida, Masato Saito, Eiichi Tamiya
Publikováno v:
ACS Omega. 8:13754-13762
Publikováno v:
Chemistry of Materials. 34:9425-9436
Publikováno v:
International Journal of Molecular Sciences
Volume 24
Issue 3
Pages: 2766
Volume 24
Issue 3
Pages: 2766
Glycerol is a symmetrical, small biomolecule with high flexibility in molecular conformations. Using a 1H-NMR spectroscopic Karplus analysis in our way, we analyzed a rotational isomerism in the glycero backbone which generates three kinds of stagger
Autor:
Yuan Mengfei, Sakura Kitagawa, Hirofumi Dohi, Yoshihiro Nishida, Kaito Fujisawa, Hirotaka Uzawa
Publikováno v:
Tetrahedron: Asymmetry. 28:1435-1443
Cell-membrane glycerophospholipids and glycolipids have a common asymmetric skeleton of 1,2-diacyl-sn-glycerols. The 1,2-diacyl moiety in solutions permits a rapid equilibrium among three helical conformers, namely gt(+), gg(−), and tg, to display
Publikováno v:
Beilstein Journal of Organic Chemistry
Beilstein Journal of Organic Chemistry, Vol 13, Iss 1, Pp 1999-2009 (2017)
Beilstein Journal of Organic Chemistry, Vol 13, Iss 1, Pp 1999-2009 (2017)
Cell-membrane glycerolipids exhibit a common structural backbone of asymmetric 1,2-diacyl-sn-glycerol bearing polar head groups in the sn-3 position. In this study, the possible effects of sn-3 head groups on the helical conformational property aroun