1. Academic Validation
  2. Bioactive compounds from Peperomia pellucida

Bioactive compounds from Peperomia pellucida

  • J Nat Prod. 2006 Feb;69(2):247-50. doi: 10.1021/np050457s.
Su Xu 1 Na Li Meng-Meng Ning Cai-Hong Zhou Qiao-Rong Yang Ming-Wei Wang
Affiliations

Affiliation

  • 1 The National Center for Drug Screening, Chinese Academy of Sciences, Shanghai 201203, People's Republic of China.
Abstract

Five new compounds (1-5), including two secolignans, two tetrahydrofuran Lignans, and one highly methoxylated dihydronaphthalenone, were isolated from the whole plant of Peperomia pellucida. These compounds were accompanied by the known peperomins A, B, C, and E, 7,8-trans-8,8'-trans-7',8'-cis-7,7'-bis(5-methoxy-3,4-methylenedioxyphenyl)-8-acetoxymethyl-8'-hydroxymethyltetrahydrofuran, 7,8-trans-8,8'-trans-7',8'-cis-7-(5-methoxy-3,4-methylenedioxyphenyl)-7'-(4-hydroxy-3,5-dimethoxyphenyl)-8,8'-diacetoxymethyltetrahydrofuran, sesamin, and isoswertisin. New structures were elucidated mainly by NMR and MS techniques, and Anticancer activities evaluated in HL-60, MCF-7, and HeLa cell lines. Compound 1 and peperomin E show growth inhibitory effects on the three Cancer cell lines with IC(50) values ranging between 1.4 and 9.1 and between 1.8 and 11.1 microM, respectively. Compound 2 has a weak suppressive activity on HL-60 cells (IC(50) = 10.8 microM), while 7,8-trans-8,8'-trans-7',8'-cis-7,7'-bis(5-methoxy-3,4-methylenedioxyphenyl)-8-acetoxymethyl-8'-hydroxymethyltetrahydrofuran exhibits estrogen-like properties (EC(50) = 3.1 microM) in CV-1 cells transfected with human Estrogen Receptor (ERalpha).

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