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

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
› Author Affiliations
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.

Supporting Information

 
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