Literature DB >> 34142303

Hyperdioxanes, dibenzo-1,4-dioxane derivatives from the roots of Hypericum ascyron.

Kanji Niwa1, Naonobu Tanaka2, Yusei Shimomoto1, Daisuke Tsuji1, Sang-Yong Kim3, Mareshige Kojoma3, Kohji Itoh1, Chin-Ho Chen4, Kuo-Hsiung Lee5, Yoshiki Kashiwada6.   

Abstract

Six dibenzo-1,4-dioxane derivatives (1-6) were isolated from the roots of a Hypericaceous plant Hypericum ascyron. Spectroscopic analyses revealed 2 and 4-6 to be new compounds. The partial racemic natures of 1-3 were concluded by chiral HPLC analyses, while 5 was confirmed to be a racemate. The absolute configurations 1-4 were deduced on the basis of ECD calculations. Biological activity evaluation of the dibenzo-1,4-dioxane derivatives along with two related compounds: hyperdioxanes A (7) and B (8), previously isolated from the same plant material by our group demonstrated that 7 exhibit an anti-HIV activity (IC50 5.3 μM, TI 7.2) while 8 showed an inhibitory effect on IL-1β production (inhibition rate: 72.3% at 6.3 μM) from LPS-stimulated microglial cells.

Entities:  

Keywords:  Anti-HIV activity; Anti-neuroinflammatory activity; Dibenzo-1,4-dioxane derivatives; Hyperdioxanes; Hypericum ascyron

Year:  2021        PMID: 34142303     DOI: 10.1007/s11418-021-01540-y

Source DB:  PubMed          Journal:  J Nat Med        ISSN: 1340-3443            Impact factor:   2.343


  1 in total

1.  Glucosyl-hesperidin enhances the cyclic guanosine monophosphate-inducing effect of a green tea polyphenol EGCG.

Authors:  Motofumi Kumazoe; Yasutake Tanaka; Ren Yoshitomi; Yuki Marugame; Kwan-Woo Lee; Hiroaki Onda; Yoshinori Fujimura; Madoka Yonekura; Yasuyo Shimamoto; Hirofumi Tachibana
Journal:  J Nat Med       Date:  2021-06-07       Impact factor: 2.343

  1 in total
  1 in total

Review 1.  Hypericum Genus as a Natural Source for Biologically Active Compounds.

Authors:  Gonçalo Infante Caldeira; Luís Pleno Gouveia; Rita Serrano; Olga Duarte Silva
Journal:  Plants (Basel)       Date:  2022-09-26
  1 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.