Polysubstituted Phenyl Glucosides Produced by the Fungus Metarrhizium anisopliae

MetarhizosidesA-G(1-7),seven new polysubstituted phenyl glucosides,were isolated from the extracts of solid rice medium of a marine-derived fungus Metarrhizium anisopliae.Compounds 1-7 all contain a polysubstituted phenyl group and the sugar unit is identified as 4'-O-methyl-β-D-glucopyranose.Their structures were elucidated by NMR spectroscopy and chemical method.These compounds were evaluated for anti-inflammatory activity by using LPS-stimulated murine macrophage RAW 264.7 cells and the cytotoxicities against four human cancer cell lines.

Erratum to:Polysubstituted Phenyl Glucosides Produced by the Fungus Metarrhizium anisopliae

The article“Polysubstituted Phenyl Glucosides Produced by the Fungus Metarrhizium anisopliae”,written by Wen-jing WANG,Chong DAI,Jian-ping WANG,Hu-cheng ZHU,Chun-mei CHEN,Yong-hui ZHANG,was originally published electronically on the publisher’s internet portal on May 2020 without open access.With the author(s)’decision to opt for Open Choice,the copyright of the article is changed to©The Author(s)2020 and the article is forthwith distributed under a Creative Commons Attribution 4.0 International License(https://creativecommons.org/licenses/by/4.0/),which permits use,sharing,adaptation,distribution and reproduction in any medium or format,as long as you give appropriate credit to the original author(s)and the source,provide a link to the Creative Commons license,and indicate if changes were made.

Hyperisampsins N and O,two new benzoylated phloroglucinol derivatives from Hypericum sampsonii

Twenty-one benzoylated phloroglucinol derivatives bearing homoadamantyl frameworks were isolated from the aerial parts of Hypericum sampsonii,including two new ones named hyperisampsins N and O（1 and 2）.The structures of 1 and 2 were elucidated by extensive NMR and mass spectrometric analyses.Their absolute configurations were further determined by using TDDFT ECD calculations.Compounds 2,7,and 8 were evaluated for their cytotoxic activities against five human cancer cell lines,of which,2 and 8 exhibited significant cytotoxic activities toward HL-60 cell and moderate activities against others cell lines.

Two pairs of chlorine-containing phenylpropanoid enantiomers from Acorus tatarinowii

Two pairs of chlorine-containing phenylpropanoid enantiomers（1a/1b and 2a/2b） were isolated from the rhizomes of Acorus tatarinowii. Interestingly, these optical isomers（1a/1b and 2a/2b） were co-existed in the same plant, which were characterized as the first halogen-containing natural products from the genus Acorus. Their structures and absolute configurations were elucidated by a combination of spectroscopic analysis and a single-crystal X-ray diffraction, assisted by a modified Mosher＇s method. The phenylpropanoid isomers（1a/1b and 2a/2b） were evaluated for their antioxidant activities using DPPH assay and cytotoxic activities against five human cancer cell lines.