Zobrazeno 1 - 10
of 24
pro vyhledávání: '"Shogo Nakatani"'
Publikováno v:
Electroorganic Synthesis ISBN: 9780203758571
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::0ff9b9ef70cfc2019ba19076e2b48ef6
https://doi.org/10.1201/9780203758571-23
https://doi.org/10.1201/9780203758571-23
Autor:
Tomoko Nakajima, Shogo Nakatani, Kentaro Takai, Setsuko Yamamoto, Naoki Chiyo, Tetsuro Nariai, Akihisa Ikeno, Chihiro Ishikawa, Toshihiko Sone
Publikováno v:
Bioorganic & Medicinal Chemistry Letters. 25:1705-1708
We have previously reported a series of cyclopropyl urea derivatives as potent orally available soluble epoxide hydrolase (sEH) inhibitors. Here, we designed and synthesized three substituted cyclopropane derivatives that occupy all available pockets
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::662e43d2c9d53c1a3a5ded18e0e78c16
https://doi.org/10.1016/j.bmcl.2015.02.076
https://doi.org/10.1016/j.bmcl.2015.02.076
Autor:
Naoki Chiyo, Tetsuro Nariai, Katsuya Fujita, Nobuyuki Yamaguchi, Chihiro Ishikawa, Kazuto Yamada, Toshihiko Sone, Kentaro Takai, Yosuke Takanashi, Shogo Nakatani, Tomoko Nakajima
Publikováno v:
Bioorganic & Medicinal Chemistry. 22:1548-1557
Epoxyeicosatrienoic acids (EETs) are known to have beneficial pharmacological effects on various cardiovascular events. However, EETs are biologically metabolized by soluble epoxide hydrolase (sEH) to less active metabolites. In our search for potent
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6fe9ccc936ea1db355259228e32e3364
https://doi.org/10.1016/j.bmc.2014.01.040
https://doi.org/10.1016/j.bmc.2014.01.040
Autor:
Gen Sunagawa, Hiroshi Tachibana, Haruo Inoue, Yasuyuki Tachikawa, Shinsuke Takagi, Dai Masui, Donald A. Tryk, Youki Kou, Shogo Nakatani, Tetsuya Shimada, Yu Nabetani
Publikováno v:
Journal of Catalysis. 310:57-66
Visible light-induced, two-electron reduction of carbon dioxide to carbon monoxide, catalyzed by a newly synthesized metal complex dyad composed of a zinc porphyrin as a light-harvesting sensitizer and a rhenium bipyridyl complex as a catalytic moiet
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::5a56f7dcb5f8af36b0cb00b66795e312
https://doi.org/10.1016/j.jcat.2013.03.025
https://doi.org/10.1016/j.jcat.2013.03.025
Autor:
Shogo Nakatani, Shigehiro Asano, Erina Koga, Yoshiaki Isobe, Nobuyuki Koike, Masafumi Komiya, Junetsu Igarashi
Publikováno v:
Chemical and Pharmaceutical Bulletin. 61:1094-1097
Based on the structure activity relationship of 2-(4-phenoxybenzoyl)-5-hydroxyindole (1), a novel structural class of Ca²⁺/calmodulin-dependent protein kinase II (CaMKII) inhibitors were synthesized. We show in this study that the acidic proton at
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::f8befc4d4bb879d1166cae57d59d762f
https://doi.org/10.1248/cpb.c13-00493
https://doi.org/10.1248/cpb.c13-00493
2H3-3 Usability of a Blackboard considering Physical Load and Sight Analysis based on Writing Height
Autor:
Shogo Nakatani, Noriyasu Hirokawa
Publikováno v:
The Japanese Journal of Ergonomics. 54:2H3-3
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::80e769208603dbf07f0d65e65a8a5f76
https://doi.org/10.5100/jje.54.2h3-3
https://doi.org/10.5100/jje.54.2h3-3
Publikováno v:
Bioorganic & Medicinal Chemistry Letters. 20:6696-6698
A novel series of 5,6,7,8-tetrahydropyrido[4,3-d]pyrimidines containing substituted phenyl sulfonamide are synthesized and evaluated for their inhibitory activity against CaMKII. Substituents on the phenyl group had significant impact on CaMKII inhib
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6feb9e974be39427e8197f2113475440
https://doi.org/10.1016/j.bmcl.2010.09.005
https://doi.org/10.1016/j.bmcl.2010.09.005
Publikováno v:
Tetrahedron. 53:10253-10270
The title synthesis was accomplished by a method which features (i) coupling of the aromatic segment 2 with the enantiomerically pure aliphatic segment 3 to install the requisite carbon unit ( 2+3→4 ); (ii) intramolecular aldol reaction of the high
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::0014d4724416d29a0e6376d43c9843c1
https://doi.org/10.1016/s0040-4020(97)00652-2
https://doi.org/10.1016/s0040-4020(97)00652-2
Autor:
Masafumi, Komiya, Shigehiro, Asano, Nobuyuki, Koike, Erina, Koga, Junetsu, Igarashi, Shogo, Nakatani, Yoshiaki, Isobe
Publikováno v:
Chemicalpharmaceutical bulletin. 61(10)
Based on the structure activity relationship of 2-(4-phenoxybenzoyl)-5-hydroxyindole (1), a novel structural class of Ca²⁺/calmodulin-dependent protein kinase II (CaMKII) inhibitors were synthesized. We show in this study that the acidic proton at
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::c65a0f27dd9821e3fc88736d5501e2a9
https://pubmed.ncbi.nlm.nih.gov/24088703
https://pubmed.ncbi.nlm.nih.gov/24088703
Publikováno v:
Tetrahedron Letters. 37:3479-3482
The title synthesis was accomplished by featuring (i) coupling of the aromatic fragment 2 with the optically active aliphatic fragment 3 to install the requisite carbon unit ( 2+3→4 ); (ii) intramolecular aldol reaction of the highly functionalized
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::1cd4ae2313373f47101bb39f40f60e75
https://doi.org/10.1016/0040-4039(96)00595-3
https://doi.org/10.1016/0040-4039(96)00595-3