Volume 36, Issue 8 p. 780
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Back Cover: Bioactive Alkaloids from Indole-3-carbinol Exposed Culture of Daldiniaeschscholzii (Chin. J. Chem. 8/2018)

Li Ping Lin

Li Ping Lin

State Key Laboratory Cultivation Base for TCM Quality and Efficacy, Nanjing University of Chinese Medicine, Nanjing, Jiangsu, 210023 China

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Ren Xiang Tan

Corresponding Author

Ren Xiang Tan

State Key Laboratory Cultivation Base for TCM Quality and Efficacy, Nanjing University of Chinese Medicine, Nanjing, Jiangsu, 210023 China

Institute of Functional Biomolecules, State Key Laboratory of Pharmaceutical Biotechnology, Nanjing University, Nanjing, Jiangsu, 210023 China

E-mail: [email protected]Search for more papers by this author
First published: 13 July 2018

Abstract

The back cover picture shows Two new and rare bioactive indoles named dalesindoloids A (1) and B (3), along with 3-(1H-indole-3ylmethyl)-2-oxindole (2), were characterized from the indole-3-carbinol (I3C)-exposed culture of Daldinia eschscholzii. Dalesindoloids A and B were cytotoxic against the leukemia HL-60 cell line with the IC50 values of 1.0 and 7.4 mol/L, respectively, with the former being inhibitory on Staphylococcus aureus (MIC: 9.1 μmol/L). The simultaneous characterization of the alkaloids from the I3C-exposed fungal culture highlighted that the 2,3-epoxyindoline motif can be transformed into both lactam and indolin-3-one moieties. This is the first-time description of the 2,3-epoxyindoline chemical versatility and Wagner-Meerwein rearrangement (WMR) reaction in the microbial culture. More details are discussed in the article by Tan et al. on page 749–753.

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