Zobrazeno 1 - 10
of 125
pro vyhledávání: '"Masayuki, Ninomiya"'
Publikováno v:
Arabian Journal of Chemistry, Vol 13, Iss 2, Pp 3856-3865 (2020)
Phthalide derivatives bearing indole or indoline moieties were successfully synthesized via eco-friendly method and were evaluated for their antiproliferative activity on HL-60 and HepG2 cell lines in vitro. At a final concentration of 100 μM, most
Externí odkaz:
https://doaj.org/article/76f65a3c84454e8e9500b4bccabfd846
Autor:
Atsuyoshi Nishina, Motohiko Ukiya, Kazuki Motegi, Risa Kiryu, Daisuke Sato, Mitsuru Sada, Yuki Hori, Hideo Satsu, Kazuhiro Uemura, Mamoru Koketsu, Masayuki Ninomiya, Lwin Mon Mon Myint, Hirokazu Kimura
Publikováno v:
Bioscience, Biotechnology & Biochemistry; Dec2023, Vol. 87 Issue 12, p1523-1531, 9p
Autor:
Thi-Kim-Dung Le, Ade Danova, Thammarat Aree, Thuc-Huy Duong, Mamoru Koketsu, Masayuki Ninomiya, Yoshiharu Sawada, Pharit Kamsri, Pornpun Pungpo, Warinthorn Chavasiri
Publikováno v:
Journal of Natural Products. 85:776-786
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::caa48f1aa04cd0844a59c748ae3d54da
https://doi.org/10.1021/acs.jnatprod.1c00765
https://doi.org/10.1021/acs.jnatprod.1c00765
Autor:
Haruna Nagao, Masayuki Ninomiya, Hodaka Sugiyama, Atsuya Itabashi, Kaho Uno, Kaori Tanaka, Mamoru Koketsu
Publikováno v:
Bioorganicmedicinal chemistry letters. 76
Quinones are widespread in plants, animals, insects, and microorganisms. Several anticancer agents contain quinone structures as critical parts to show remarkable potential and distinctive modes of actions. The purpose of this study was to investigat
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::df4a8e7b5f12d0d465e80f794e857392
https://pubmed.ncbi.nlm.nih.gov/36126897
https://pubmed.ncbi.nlm.nih.gov/36126897
Publikováno v:
Cureus. 14(6)
Background High blood pressure (HBP) has become a public health issue worldwide. The relationship between high BP and changes in the body mass index (BMI) category in Japanese pubertal children has not yet been examined. To resolve this issue, we exa
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d8b3082245bff13f0d6ba55f1dbb8704
https://pubmed.ncbi.nlm.nih.gov/35911320
https://pubmed.ncbi.nlm.nih.gov/35911320
Publikováno v:
Phytochemistry Letters. 40:135-138
Two new phenolic glycosides, 2-caffeoyl-3-hydroxy-3-methylbutyric 4′-β- d -glucopyranosyloxy-3′-hydroxybenzyl ester and 2-caffeoyl-3-hydroxy-3-methylbutyric 4′-β- d -glucopyranosyloxybenzyl ester (citrulluside H and citrulluside T) were isola
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::46cb84f6b0d5151d5838886504e02333
https://doi.org/10.1016/j.phytol.2020.09.014
https://doi.org/10.1016/j.phytol.2020.09.014
Publikováno v:
ChemistrySelect. 5:8609-8615
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::e856af9b230b5ddc3c078f9822d92ef4
https://doi.org/10.1002/slct.202002081
https://doi.org/10.1002/slct.202002081
Publikováno v:
Advanced Synthesis & Catalysis. 362:3485-3515
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::050d1b829d82970e74e99f04764eedff
https://doi.org/10.1002/adsc.202000490
https://doi.org/10.1002/adsc.202000490
Publikováno v:
Arabian Journal of Chemistry, Vol 13, Iss 2, Pp 3856-3865 (2020)
Phthalide derivatives bearing indole or indoline moieties were successfully synthesized via eco-friendly method and were evaluated for their antiproliferative activity on HL-60 and HepG2 cell lines in vitro. At a final concentration of 100 μM, most
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::bfb55d758e2c313c65ee703827ee8ef9
https://doi.org/10.1016/j.arabjc.2019.02.002
https://doi.org/10.1016/j.arabjc.2019.02.002
Publikováno v:
Organic & Biomolecular Chemistry. 18:4063-4070
In this paper, we report the novel synthesis of three different heterocycles, namely 2-arylselenopheno[2,3-b]quinoxaline, 3-(aryl/alkylselanyl)-2-arylselenopheno[2,3-b]quinoxaline and 6-phenyl-7-(arylselanyl)selenopheno[2,3-b]pyrazine derivatives, fr
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::095ca62ee0107631b12b6f56d1add5c6
https://doi.org/10.1039/d0ob00718h
https://doi.org/10.1039/d0ob00718h