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Anti-inflammation compounds from the seedpods of Pongamia pinnata (L.) Pierre guided by the bioactivity and UPLC-HRESIMS

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Abstract

Pongamia pinnata (Linn.) Pierre has anti-inflammatory activity and could significantly decrease serum tumor necrosis factor-α and IL-10 in arthritic rats. Previous research indicated the typical chemical constituent in P. pinnata is furanoflavone. Guided by anti-inflammatory active assay and UPLC-HRESIMS chromatography, 22 compounds were isolated from the ethanol extract of P. pinnata seedpods. One novel furanoflavone, 4′-hydroxypinnatin, was elucidated by HRESIMS, 1D- and 2D-NMR spectra. The 21 known compounds, including 9 furanoflavone, were identified by comparing their NMR data with the previous data in reference. In the known compounds, 5 were isolated for the first time from the species. The anti-inflammatory activities were assayed by assessing LPS-induced NO production in BV-2 cells. 12 compounds can inhibit the production of NO without cytotoxicity at concentration of 50 μM. Among them, compounds 4 can significantly inhibit the production of NO, with the IC50 value of 31.36 μM.

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Acknowledgements

This work was supported partially by National Natural Science Foundation of China (Nos. 81303183, 81303182 and U1403102) and by the Project of Science and Technology Correspondent of Tian** (No. 15JCTPJC60000).

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Correspondence to Peng Zhang.

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All authors have declared no conflict of interest.

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Hong Guo and Zisong Bai have equally contributed to this work.

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Guo, H., Bai, Z., Xu, Y. et al. Anti-inflammation compounds from the seedpods of Pongamia pinnata (L.) Pierre guided by the bioactivity and UPLC-HRESIMS. Arch. Pharm. Res. 40, 818–824 (2017). https://doi.org/10.1007/s12272-017-0913-2

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