Planta Med 2015; 81(14): 1285-1289
DOI: 10.1055/s-0035-1546257
Natural Product Chemistry
Original Papers
Georg Thieme Verlag KG Stuttgart · New York

Pestalpolyols A–D, Cytotoxic Polyketides from Pestalotiopsis sp. cr013

Authors

  • Jing Li

    1   State Key Laboratory of Phytochemistry and Plant Resources in West China, Kunming Institute of Botany, Chinese Academy of Sciences, Kunming, China
    2   Life Science College, Southwest Forestry University, Kunming, China
    3   University of Chinese Academy of Sciences, Beijing, China
  • Jin Xie

    1   State Key Laboratory of Phytochemistry and Plant Resources in West China, Kunming Institute of Botany, Chinese Academy of Sciences, Kunming, China
    2   Life Science College, Southwest Forestry University, Kunming, China
  • Yin-He Yang

    1   State Key Laboratory of Phytochemistry and Plant Resources in West China, Kunming Institute of Botany, Chinese Academy of Sciences, Kunming, China
  • Xiao-Lian Li

    1   State Key Laboratory of Phytochemistry and Plant Resources in West China, Kunming Institute of Botany, Chinese Academy of Sciences, Kunming, China
  • Ying Zeng

    1   State Key Laboratory of Phytochemistry and Plant Resources in West China, Kunming Institute of Botany, Chinese Academy of Sciences, Kunming, China
  • Pei-Ji Zhao

    1   State Key Laboratory of Phytochemistry and Plant Resources in West China, Kunming Institute of Botany, Chinese Academy of Sciences, Kunming, China
Further Information

Publication History

received 04 January 2015
revised 17 April 2015

accepted 07 June 2015

Publication Date:
30 July 2015 (online)

Abstract

Four novel polyketides, named pestalpolyols A (1), B (2), C (3), and D (4), were isolated from solid fermentation products of Pestalotiopsis sp. cr013. Their structures were elucidated by extensive spectroscopic methods, including 1D and 2D nuclear magnetic resonance and high-resolution electrospray ionization mass spectrometry experiments, and the absolute configuration was confirmed by single-crystal X-ray diffraction analysis using the anomalous scattering of Cu Kα radiation. The inhibitory activities of compounds 1, 2, and 4 against five human tumor lines were tested in vitro, and showed IC50 values 2.3–31.2 µM.