Zobrazeno 1 - 10
of 52
pro vyhledávání: '"Shoko, Taniguchi"'
Publikováno v:
Molecules, Vol 20, Iss 7, Pp 12500-12511 (2015)
Two new flavonoids, bakuisoflavone (1) and bakuflavanone (2), together with 15 known compounds, were isolated from the fruits of Psoralea corylifolia, and their structures were characterized by spectroscopic data. The effects of the isolated compound
Externí odkaz:
https://doaj.org/article/75dad50edb2146249d6f114e15a7f888
Autor:
Tsutomu Hatano, Shoko Taniguchi, Yoshiaki Amakura, Lih Geeng Chen, Morio Yoshimura, Shinji Yoshikawa
Publikováno v:
Bioscience, Biotechnology, and Biochemistry. 85:1609-1620
Our examination of high molecular weight polyphenolic constituents in the leaves of Barringtonia racemosa of the family Lecythidaceae uncovered 5 previously undescribed ellagitannins. One, barringtin M1 (1), among them was a hydrolysable tannin monom
Autor:
Atsumi Miyazaki, Tsugumi Shiokawa, Eerdunbayaer, Hiroko Tada, Shoko Taniguchi, Tsutomu Hatano, Yunhe Lian
Publikováno v:
Bioscience, Biotechnology, and Biochemistry. 84:2128-2138
Various pharmacological properties of Xinjiang licorice flavonoids have been reported recently. We have investigated constituents corresponding to distinct peaks on the high-performance liquid chromatography (HPLC) profile of a flavonoid-rich extract
Autor:
Tsutomu Hatano, Esam A. Orabi, Mohamed A.A. Orabi, Hiroshi Sakagami, Yoshiaki Amakura, Morio Yoshimura, Shoko Taniguchi
Publikováno v:
Journal of Natural Products. 82:2682-2695
Ellagitannin oligomers are large molecules habitually showing complex NMR spectra that are sometimes misinterpreted and lead to incorrect structures. Understanding the NMR spectroscopic features of a group of ellagitannins would overcome these inadeq
Publikováno v:
Bioscience, Biotechnology, and Biochemistry. 83:892-900
We used quantitative nuclear magnetic resonance analyses to measure the contents of major constituents of Acorus rhizome materials used as herbal drugs. The inhibitory effects of crude n-hexane extracts and their individual constituents on in vitro a
Autor:
Mohamed A A, Orabi, Esam A, Orabi, Shoko, Taniguchi, Hiroshi, Sakagami, Morio, Yoshimura, Yoshiaki, Amakura, Tsutomu, Hatano
Publikováno v:
Journal of natural products. 82(10)
Ellagitannin oligomers are large molecules habitually showing complex NMR spectra that are sometimes misinterpreted and lead to incorrect structures. Understanding the NMR spectroscopic features of a group of ellagitannins would overcome these inadeq
Autor:
Hiroshi Sakagami, Mohamed A.A. Orabi, Yoshiaki Amakura, Morio Yoshimura, Tsutomu Hatano, Shoko Taniguchi
Publikováno v:
Journal of Natural Products. 79:984-995
Partially unacylated new oligomeric hydrolyzable tannins, nilotinin T2 (1, trimer) and nilotinin Q1 (2, tetramer), together with four known trimers, nilotinin T1 (3) and hirtellins T1-T3 (4-6), and a dimer, tamarixinin B (7), were isolated from the a
Publikováno v:
Molecules, Vol 20, Iss 7, Pp 12500-12511 (2015)
Molecules
Volume 20
Issue 7
Pages 12500-12511
Molecules
Volume 20
Issue 7
Pages 12500-12511
Two new flavonoids, bakuisoflavone (1) and bakuflavanone (2), together with 15 known compounds, were isolated from the fruits of Psoralea corylifolia, and their structures were characterized by spectroscopic data. The effects of the isolated compound
Autor:
Wakano Ogawa, Eri Nishiyama, Teruo Kuroda, Shinya Okamura, Tsutomu Hatano, Tomohiro Yamazaki, Nao Otsuka, Tomofusa Tsuchiya, Shoko Taniguchi
Publikováno v:
Biochimica et Biophysica Acta (BBA) - General Subjects. 1850:1245-1252
Background Multidrug-resistant bacteria, such as methicillin-resistant Staphylococcus aureus (MRSA) and vancomycin resistant enterococci (VRE), cause serious infections at clinical sites, for which the development of new drugs is necessary. We screen
Publikováno v:
HETEROCYCLES. 98:895