## Abstract Three new arylnaphthalide lignans named 6′‐hydroxy justicidin A (1), 6′‐hydroxy justicidin B (2) and 6′‐hydroxy justicidin C (3) have been isolated from the whole plant of __Justicia procumbens__, together with four known ones, neojusticin A (4), chinensinaphthol methyl ester (5), isodi
1H and 13 C NMR assignments for two lignans from the heartwood of Streblus asper
✍ Scribed by Jun Li; Yan-Jun Zhang; Bai-Feng Jin; Xiao-Jian Su; Yi-Wen Tao; Zhi-Gang She; Yong-Cheng Lin
- Publisher
- John Wiley and Sons
- Year
- 2008
- Tongue
- English
- Weight
- 103 KB
- Volume
- 46
- Category
- Article
- ISSN
- 0749-1581
- DOI
- 10.1002/mrc.2186
No coin nor oath required. For personal study only.
✦ Synopsis
Abstract
In our ongoing investigation of the bioactive constituents from plants, two new lignans, magnolignan A‐2‐O‐β‐D‐glucopyranoside and strebluslignanol were isolated from heartwood of Streblus asper, along with three known lignans, magnolignan A, magnolol, and magnaldehyde D. 1D and 2D NMR experiments, including COSY, HMQC, and HMBC, and other spectroscopic methods, including UV, IR, and MS were used for the determination of the structures and NMR assignments. Primary bioassays showed that magnolignan A‐2‐O‐β‐D‐glucopyranoside and strebluslignanol have medium cytotoxic activity against HEp‐2 and HepG2 cells, with IC~50~ of 13.3 µM, 46.4 µM and 10.1 µM, 21.7 µM, respectively. Copyright © 2008 John Wiley & Sons, Ltd.
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