Abstract
This study reported a new cyclopeptide alkaloid, justicianene A (1), and a new lignan glycoside, procumbenoside H (2), isolated from Justicia procumbens. The structures of the new compounds were elucidated by means of spectroscopic analysis, including extensive 2D NMR studies and mass spectrometry. Cyclopeptide alkaloids were first observed from the genus Justicia. Compound 2 was cytotoxic against human LoVo colon carcinoma cells with an IC50 value of 17.908 ± 1.949 μM.
Acknowledgments
The authors thank Mrs Yan Xue, Mrs Mei-feng Xu, and Mrs Yu-mei Zhao of the National Center of Biomedical Analysis for the measurements of the HR-ESI-MS and NMR spectra.