Zobrazeno 1 - 10
of 23
pro vyhledávání: '"Minoru Tamiya"'
Publikováno v:
PLoS ONE, Vol 10, Iss 5, p e0126921 (2015)
Among proteins utilized as sweeteners, neoculin and miraculin are taste-modifying proteins that exhibit pH-dependent sweetness. Several experiments on neoculin have shown that His11 of neoculin is responsible for pH dependence. We investigated the mo
Externí odkaz:
https://doaj.org/article/a843986fab8d45c3a18de7c27df87407
Autor:
Kenichi Nomura, Satoshi Hashimoto, Ryuuichi Takeyama, Minoru Tamiya, Tatsuya Kato, Terushige Muraoka, Mirai Kage, Keiji Nii, Kenichiro Kotake, Satomi Iida, Takashi Emura, Mikimasa Tanada, Hitoshi Iikura
Publikováno v:
Journal of Medicinal Chemistry. 65:13401-13412
Autor:
Kazuya Ishizawa, Nobuhisa Isaka, Minoru Tamiya, Atsushi Hasegawa, Takaaki Kitazawa, Mayu Ikeda, Masaji Ishiguro, Saki Kawada
Publikováno v:
Bulletin of the Chemical Society of Japan. 92:1474-1494
We describe here the syntheses of velutinol A (1) and the structurally similar compounds 2–4 sharing a highly oxygenated seco-pregnane cage-like structure. The synthesis of velutinol A (1, 15,16-se...
Autor:
Minoru Tamiya, Masaji Ishiguro, Kana Saida–Tamiya, Takaaki Kitazawa, Nobuhisa Isaka, Ayako Matsukawa, Genki Sekiya, Kohichi Kawahara, Kazunori Isobe, Akihiko Komuro
Publikováno v:
Bioorganicmedicinal chemistry letters. 29(11)
A study of the structural requirements of cholic acid derivatives as liver X receptor (LXR) ligands was performed. A model of cholenamide derivative 1 complexed with LXR showed that the C24 carbonyl oxygen forms a hydrogen bond with His435 located cl
Publikováno v:
European Journal of Organic Chemistry. 2012:665-668
A concise route to the bradykinin B1 receptor antagonist velutinol A, a natural product isolated from the rhizomatous of mandevilla velutina (Apocynaceae), has been developed. This synthesis features the highly regioselective construction of Δ 14 si
Publikováno v:
Chemistry Letters. 43:1704-1706
2,6-Dideoxy-3-O-methylpyranosylillustrol (3) was stereoselectively synthesized through the oxidative construction of a cage-like DEF ring moiety and stereoselective glycosylation of a 2,6-dideoxysa...
Autor:
Louis Morency, Vilnis Liepins, Daniel Laurich, Jaques-Alexis Funel, Laure C. Bouchez, Minoru Tamiya, Florent Beaufils, Ryan Gilmour, François-Hugues Porée, Alois Fürstner
Publikováno v:
Chemistry - A European Journal. 15:3983-4010
Nature is a pretty unselective "chemist" when it comes to making the highly cytotoxic amphidinolide macrolides of the B/G/H series. To date, 16 different such compounds have been isolated, all of which could now be approached by a highly convergent a
Publikováno v:
Synlett. 2007:0780-0784
Stereoselective access to 9-alkyl-10-hydroxy-9,10-dihydrophenanthrenes has been developed via the samarium(II) iodide mediated reductive cyclization of an ene-aldehyde appended to a biphenyl scaffold.
Publikováno v:
PLoS ONE, Vol 10, Iss 5, p e0126921 (2015)
PLoS ONE
PLoS ONE
Among proteins utilized as sweeteners, neoculin and miraculin are taste-modifying proteins that exhibit pH-dependent sweetness. Several experiments on neoculin have shown that His11 of neoculin is responsible for pH dependence. We investigated the mo
Publikováno v:
ChemInform. 42
Title reaction of cyclic silylenol ethers derived from dehydroepiandrosterone, e.g. (I), affords α,β-unsaturated lactones like (III).