Zobrazeno 1 - 10
of 13
pro vyhledávání: '"Kaori, RYU"'
Publikováno v:
Frontiers in Chemistry, Vol 9 (2021)
Natural products are an excellent source of skeletons for medicinal seeds. Triterpenes and saponins are representative natural products that exhibit anti-herpes simplex virus type 1 (HSV-1) activity. However, there has been a lack of comprehensive in
Externí odkaz:
https://doaj.org/article/fbf9900e0ccb444abe066560a4233cc6
Publikováno v:
Phytochemistry Letters. 49:120-124
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::bb8c4c36ccfeedab9a4b3f2b0d50f72a
https://doi.org/10.1016/j.phytol.2022.03.013
https://doi.org/10.1016/j.phytol.2022.03.013
Publikováno v:
Frontiers in Chemistry, Vol 9 (2021)
Frontiers in Chemistry
Frontiers in Chemistry
Natural products are an excellent source of skeletons for medicinal seeds. Triterpenes and saponins are representative natural products that exhibit anti-herpes simplex virus type 1 (HSV-1) activity. However, there has been a lack of comprehensive in
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ec98dc22b854887f3696383459d4a1fa
https://www.frontiersin.org/articles/10.3389/fchem.2021.763794/full
https://www.frontiersin.org/articles/10.3389/fchem.2021.763794/full
Publikováno v:
Journal of natural medicines. 75(2)
The enantioselective synthesis of (S)-(-)-spirobrassinin, which features a unique sulfur-containing spirooxindole skeleton, was achieved by focusing on the phytoalexin generation in Brassicaceae plants. Specifically, (S)-(-)-spirobrassinin was obtain
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::98ea39be8b72d23079d55a3a88105c88
https://pubmed.ncbi.nlm.nih.gov/33389552
https://pubmed.ncbi.nlm.nih.gov/33389552
Autor:
Seikou, Nakamura, Jiang, Liu, Souichi, Nakashima, Keiko, Ogawa, Takashi, Ueda, Eri, Onishi, Kiwako, Kurooka, Yuko, Moriwaki, Kaori, Ryu, Bin, Xu, Takahiro, Matsumoto, Tomoe, Ohta, Masashi, Fukaya, Masayuki, Yoshikawa, Hisashi, Matsuda
Publikováno v:
Natural product communications. 11(8)
A coumaric acid analogue with a monoterpene moiety named floraosmanol A (1) was isolated from the flowers of Osmanthisfragrans var. aurantiacus. The chemical structure was elucidated on the basis of chemical and physicochemical evidence. Floraosmanol
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::d51a5814b5aeeb0c39390742fca75de3
https://pubmed.ncbi.nlm.nih.gov/30725574
https://pubmed.ncbi.nlm.nih.gov/30725574
Publikováno v:
HETEROCYCLES. 103:416
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::6b3993477be03d889e44aac9b5ec7720
https://doi.org/10.3987/com-20-s(k)28
https://doi.org/10.3987/com-20-s(k)28
Autor:
Masahiro Fujimuro, Souichi Nakashima, Keiko Ogawa, Seikou Nakamura, Hanako Ishimaru, Kaori Ryu, Hisashi Matsuda, Natsuki Saito, Kohei Hosokawa
Publikováno v:
Journal of natural medicines. 72(2)
Nigella species are rich source of dolabellane diterpenes. During our study of Nigella species, new dolabellane diterpenes, damasterpenes V–VIII were isolated. The structural determination of new compounds damasterpenes V–VIII is described with c
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d0cfc0e2d2c6415b8b00b0d2af8a5268
https://pubmed.ncbi.nlm.nih.gov/29288328
https://pubmed.ncbi.nlm.nih.gov/29288328
Autor:
Masayuki Yoshikawa, Kaori Ryu, Masaaki Aihara, Hisashi Matsuda, Junko Iwami, Yasunobu Asao, Souichi Nakashima, Masashi Fukaya, Seikou Nakamura
Publikováno v:
Scopus-Elsevier
The methanolic extract [inhibition (%): 61.2±3.8 ( p
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4b45b67576ec8f7a837aa909b351084a
https://doi.org/10.1177/1934578x1701200221
https://doi.org/10.1177/1934578x1701200221
Autor:
Tomoe Ohta, Masayuki Yoshikawa, Kaori Ryu, Takahiro Matsumoto, Bin Xu, Yuko Moriwaki, Takashi Ueda, Keiko Ogawa, Hisashi Matsuda, Seikou Nakamura, Masashi Fukaya, Kiwako Kurooka, Eri Onishi, Souichi Nakashima, Jiang Liu
Publikováno v:
Natural Product Communications. 11:1934578X1601100
A coumaric acid analogue with a monoterpene moiety named floraosmanol A (1) was isolated from the flowers of Osmanthus fragrans var. aurantiacus. The chemical structure was elucidated on the basis of chemical and physicochemical evidence. Floraosmano
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::c8fb57e640412f9b2714aaf86f644fdd
https://doi.org/10.1177/1934578x1601100824
https://doi.org/10.1177/1934578x1601100824
