Affiliations 

  • 1 Department of Chemistry, Faculty of Science, University Malaya, Kuala Lumpur 50603, Malaysia. libra_mine85@yahoo.co.uk
  • 2 Centre de Recherche de Gif, Institut de Chimie des Substances Naturelles (ICSN), CNRS, Labex LERMIT, Gif-sur-Yvette Cedex 91198, France. charlotte.geny@cnrs.fr
  • 3 Centre de Recherche de Gif, Institut de Chimie des Substances Naturelles (ICSN), CNRS, Labex LERMIT, Gif-sur-Yvette Cedex 91198, France. aurelie.leverrier@gmail.com
  • 4 Centre de Recherche de Gif, Institut de Chimie des Substances Naturelles (ICSN), CNRS, Labex LERMIT, Gif-sur-Yvette Cedex 91198, France. marc.litaudon@cnrs.fr
  • 5 Centre de Recherche de Gif, Institut de Chimie des Substances Naturelles (ICSN), CNRS, Labex LERMIT, Gif-sur-Yvette Cedex 91198, France. vincent.dumontet@cnrs.fr
  • 6 Centre de Recherche de Gif, Institut de Chimie des Substances Naturelles (ICSN), CNRS, Labex LERMIT, Gif-sur-Yvette Cedex 91198, France. nicolas.birlirakis@cnrs.fr
  • 7 Centre de Recherche de Gif, Institut de Chimie des Substances Naturelles (ICSN), CNRS, Labex LERMIT, Gif-sur-Yvette Cedex 91198, France. francoise.gueritte@wanadoo.fr
  • 8 Department of Pharmacy, Faculty of Medicine, University Malaya, Kuala Lumpur 50603, Malaysia. Leongkh@um.edu.my
  • 9 Department of Chemistry, Faculty of Science, University Malaya, Kuala Lumpur 50603, Malaysia. nadiahhalim@um.edu.my
  • 10 Department of Pharmacy, Faculty of Medicine, University Malaya, Kuala Lumpur 50603, Malaysia. khalitmohamad@um.edu.my
  • 11 Department of Chemistry, Faculty of Science, University Malaya, Kuala Lumpur 50603, Malaysia. khalijah@um.edu.my
Molecules, 2014;19(2):1732-47.
PMID: 24492595 DOI: 10.3390/molecules19021732

Abstract

A phytochemical investigation of the methanolic extract of the bark of Endiandra kingiana led to the isolation of seven new tetracyclic endiandric acid analogues, kingianic acids A-G (1-7), together with endiandric acid M (8), tsangibeilin B (9) and endiandric acid (10). Their structures were determined by 1D- and 2D-NMR analysis in combination with HRMS experiments. The structure of compounds 9 and 10 were confirmed by single-crystal X-ray diffraction analysis. These compounds were screened for Bcl-xL and Mcl-1 binding affinities and cytotoxic activity on various cancer cell lines. Compound 5 showed moderate cytotoxic activity against human colorectal adeno-carcinoma (HT-29) and lung adenocarcinoma epithelial (A549) cell lines, with IC50 values in the range 15-17 µM, and compounds 3, 6 and 9 exhibited weak binding affinity for the anti-apoptotic protein Mcl-1.

* Title and MeSH Headings from MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine.