Literature DB >> 18071272

First stereoselective synthesis of meso-secoisolariciresinol and comparison of its biological activity with (+) and (-)-secoisolariciresinol.

Takuya Sugahara1, Satoshi Yamauchi, Ai Kondo, Fumi Ohno, Siori Tominaga, Yuki Nakashima, Taro Kishida, Koichi Akiyama, Masafumi Maruyama.   

Abstract

The first stereoselective synthesis of meso-secoisolariciresinol is reported. A comparison of the cytotoxic and immunosuppressive activity between meso-secoisolariciresinol and optically active secoisolariciresinols was similarly performed for the first time. Both enantiomers of secoisolariciresinol accelerated IgM production, although meso-secoisolariciresinol did not affect IgM production. Only meso-secoisolariciresinol showed cytotoxic activity.

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Year:  2007        PMID: 18071272     DOI: 10.1271/bbb.70358

Source DB:  PubMed          Journal:  Biosci Biotechnol Biochem        ISSN: 0916-8451            Impact factor:   2.043


  2 in total

Review 1.  Bioinspired syntheses of dimeric hydroxycinnamic acids (lignans) and hybrids, using phenol oxidative coupling as key reaction, and medicinal significance thereof.

Authors:  George E Magoulas; Dionissios Papaioannou
Journal:  Molecules       Date:  2014-11-28       Impact factor: 4.411

2.  Lignan Glycosides and Flavonoid Glycosides from the Aerial Portion of Lespedeza cuneata and Their Biological Evaluations.

Authors:  Jiwon Baek; Tae Kyoung Lee; Jae-Hyoung Song; Eunyong Choi; Hyun-Jeong Ko; Sanghyun Lee; Sang Un Choi; Seong Lee; Sang-Woo Yoo; Seon-Hee Kim; Ki Hyun Kim
Journal:  Molecules       Date:  2018-08-01       Impact factor: 4.411

  2 in total

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