Zobrazeno 1 - 10
of 127
pro vyhledávání: '"Nakamura, Asao"'
Autor:
Nakamura, Asao, Jardetzky, Oleg
Publikováno v:
Proceedings of the National Academy of Sciences of the United States of America, 1967 Dec . 58(6), 2212-2219.
Externí odkaz:
https://www.jstor.org/stable/58704
Autor:
Yang, Cheng, Fukuhara, Gaku, Nakamura, Asao, Origane, Yumi, Fujita, Kahee, Yuan, De-Qi, Mori, Tadashi, Wada, Takehiko, Inoue, Yoshihisa *
Publikováno v:
In Journal of Photochemistry & Photobiology, A: Chemistry 2005 173(3):375-383
Autor:
Nishino, Hideo, Nakamura, Asao, Terada, Mariko, Kosaka, Atsuko, Fukui, Mieko, Aoki, Noriko, Inoue, Yoshihisa
Publikováno v:
In Journal of Photochemistry & Photobiology, A: Chemistry 2002 147(1):1-14
Autor:
Imai, Kohei, Nakanishi, Ikuo, Ohno, Akiko, Kurihara, Masaaki, Miyata, Naoki, Matsumoto, Ken-Ichiro, Nakamura, Asao, Fukuhara, Kiyoshi
Publikováno v:
Bioorganic & Medicinal Chemistry Letters. 24(11):2582-2584
Catechin analogue 1 with methyl substituents ortho to the catechol hydroxyl groups was synthesized to improve the antioxidant ability of (+)-catechin. The synthetic scheme involved a solid acid catalyzed Friedel-Crafts coupling of a cinnamyl alcohol
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=jairo_______::e72a391bd8f0ee137f81da34a098290f
https://repo.qst.go.jp/records/48529
https://repo.qst.go.jp/records/48529
Autor:
Fukuhara, Kiyoshi, Ohno, Akiko, Nakanishi, Ikuo, Imai, Kohei, Nakamura, Asao, Anzai, Kazunori, Miyata, Naoki, Okuda, Haruhiro
Publikováno v:
Tetrahedron Letters. 50(50):6989-6992
The reaction of ninhydrin with (+)-catechin in the presence of TMSOTf resulted in condensation product, which consists of a 2:1 mixture of epimers at the C-2 position. The antioxidative radical-scavenging activity of this catechin derivative against
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=jairo_______::067812b86dae1244a7e3250e5591cd44
https://repo.qst.go.jp/records/45671
https://repo.qst.go.jp/records/45671
Autor:
Imai, Kohei, Nakanishi, Ikuo, Ohno, Akiko, Kurihara, Masaaki, Miyata, Naoki, Matsumoto, Ken-ichiro, Nakamura, Asao, Fukuhara, Kiyoshi
Publikováno v:
In Bioorganic & Medicinal Chemistry Letters 1 June 2014 24(11):2582-2584
Autor:
Fukuhara, Kiyoshi, Nakanishi, Ikuo, Ohkubo, Kei, Obara, Yoshinori, Tada, Ayako, Imai, Kohei, Ohno, Akiko, Nakamura, Asao, Ozawa, Toshihiko, Urano, Shiro, Saito, Shinichi, Fukuzumi, Shunichi, Anzai, Kazunori, Miyata, Naoki, Okuda, Haruhiro
Publikováno v:
Chemical Communications. 2009(41):6180-6182
A planar catechin derivatives incorporating a lysine moiety was synthesized and showed ~400-fold increased radical-scavenging activity relative to naturally-occurring (+)-catechin.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=jairo_______::d93878aa1da715abb3a70048eaae9986
https://repo.qst.go.jp/records/45666
https://repo.qst.go.jp/records/45666
Akademický článek
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Autor:
Imai, Kohei, Nakanishi, Ikuo, Nakanishi, Satomi, Takagaki, Ryohei, Ozawa, Toshihiko, Okuda, Haruhiro, Miyata, Naoki, Matsumoto, Kenichiro, Nakamura, Asao, Fukuhara, Kiyoshi
Radical-scavenging reactivities of newly synthesized 7 planar catechin derivatives substituted by an amino acid, which is lysine, arginine, histidine, asparagine acid, glutamic acid, serine, or cysteine, have been examined by the quenching kinetics o
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=jairo_______::e28688cebbabbc773aee9e820e292eeb
https://repo.qst.go.jp/records/70656
https://repo.qst.go.jp/records/70656
Publikováno v:
e-Archivo. Repositorio Institucional de la Universidad Carlos III de Madrid
instname
instname
Molecular Mechanics calculations with the Tripos Force Field were employed to study the complexation of 4-(dimethylamino)benzonitrile (DMABN) and/or benzonitrile (BN) with β-cyclodextrin (βCD). The systems studied have 1 : 1 (DMABN : βCD and BN :
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=dedup_wf_001::9df777a23748b4052dc0810a703c27ca
https://hdl.handle.net/10016/24502
https://hdl.handle.net/10016/24502