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Lipoxygenase inhibitors from the latex of Calotropis Procera

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Abstract

A radical-scavenging, guided phytochemical study of the latex of Calotropis Procera afforded five lignans (15), including a new one (4). The structural determination was accomplished using 1D- and 2D-NMR, high-resolution electrospray ionization mass spectrometry (HRESIMS), and correlation with known compounds. Among the isolated compounds, acylated lignans (35) showed stronger antioxidant activity than non-acylated derivatives (1,2). Anti-inflammatory activity was evaluated by determining the inhibitory potential against 5- and 15-lipoxygenase enzymes. The highest anti-inflammatory activity was observed in compound 4, with IC50s values of 7.6 µM and 2.7 µM against 5-LOX and 15-LOX, respectively.

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Acknowledgments

The authors would like to extend their sincere appreciation to the deanship of Scientific Research at King Saud University for its funding of this research through Research Group Project no. RGP-VPP-326.

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Correspondence to Xueting Liu, Lixin Zhang or Ahmed A. M. Shoreit.

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Abdel-Mageed, W.M., Mohamed, N.H., Liu, M. et al. Lipoxygenase inhibitors from the latex of Calotropis Procera . Arch. Pharm. Res. (2016). https://doi.org/10.1007/s12272-016-0725-9

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