1. Academic Validation
  2. Potent cytotoxic arylnaphthalene lignan lactones from Phyllanthus poilanei

Potent cytotoxic arylnaphthalene lignan lactones from Phyllanthus poilanei

  • J Nat Prod. 2014 Jun 27;77(6):1494-504. doi: 10.1021/np5002785.
Yulin Ren 1 Daniel D Lantvit Youcai Deng Ragu Kanagasabai Judith C Gallucci Tran Ngoc Ninh Hee-Byung Chai Djaja D Soejarto James R Fuchs Jack C Yalowich Jianhua Yu Steven M Swanson A Douglas Kinghorn
Affiliations

Affiliation

  • 1 Division of Medicinal Chemistry and Pharmacognosy, College of Pharmacy, The Ohio State University , Columbus, Ohio 43210, United States.
Abstract

Two new (1 and 2) and four known arylnaphthalene lignan lactones (3-6) were isolated from different plant parts of Phyllanthus poilanei collected in Vietnam, with two further known analogues (7 and 8) being prepared from phyllanthusmin C (4). The structures of the new compounds were determined by interpretation of their spectroscopic data and by chemical methods, and the structure of phyllanthusmin D (1) was confirmed by single-crystal X-ray diffraction analysis. Several of these arylnaphthalene lignan lactones were cytotoxic toward HT-29 human colon Cancer cells, with compounds 1 and 7-O-[(2,3,4-tri-O-acetyl)-α-L-arabinopyranosyl)]diphyllin (7) found to be the most potent, exhibiting IC50 values of 170 and 110 nM, respectively. Compound 1 showed activity when tested in an in vivo hollow fiber assay using HT-29 cells implanted in immunodeficient NCr nu/nu mice. Mechanistic studies showed that this compound mediated its cytotoxic effects by inducing tumor cell Apoptosis through activation of Caspase-3, but it did not inhibit DNA Topoisomerase IIα activity.

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