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(+)- and (−)-Ecarlottones, Uncommon Chalconoids from Fissistigma latifolium with Pro-Apoptotic Activity

Authors :
Alma Abou Samra
Fanny Roussi
Khalijah Awang
Pascal Retailleau
Hristo Nedev
Vincent Dumontet
Charlotte Gény
Marc Litaudon
Bogdan I. Iorga
Institut de Chimie des Substances Naturelles (ICSN)
Institut de Chimie du CNRS (INC)-Université Paris-Saclay-Centre National de la Recherche Scientifique (CNRS)
University of Malaya [Kuala Lumpur, Malaisie]
Source :
Journal of Natural Products, Journal of Natural Products, American Chemical Society, 2017, 80 (12), pp.3179-3185. ⟨10.1021/acs.jnatprod.7b00494⟩
Publication Year :
2017
Publisher :
HAL CCSD, 2017.

Abstract

Four new compounds, (+)- and (−)-ecarlottone (1), (±)-fislatifolione (5), (±)-isofislatifolione (6), and (±)-fislatifolic acid (7), and the known desmethoxyyangonin (2), didymocarpin-A (3), and dehydrodidymocarpin-A (4) were isolated from the stem bark of Fissistigma latifolium, by means of bioassay-guided purification using an in vitro affinity displacement assay based on the modulation of Bcl-xL/Bak and Mcl-1/Bid interactions. The structures of the new compounds were elucidated by NMR spectroscopic data analysis, and the absolute configurations of compounds (+)-1 and (−)-1 were assigned by comparison of experimental and computed ECD spectra. (−)-Ecarlottone 1 exhibited a potent antagonistic activity on both protein–protein associations with Ki values of 4.8 μM for Bcl-xL/Bak and 2.4 μM for Mcl-1/Bid.

Details

Language :
English
ISSN :
01633864 and 15206025
Database :
OpenAIRE
Journal :
Journal of Natural Products, Journal of Natural Products, American Chemical Society, 2017, 80 (12), pp.3179-3185. ⟨10.1021/acs.jnatprod.7b00494⟩
Accession number :
edsair.doi.dedup.....91484d90637405acf28438e86811ffe2
Full Text :
https://doi.org/10.1021/acs.jnatprod.7b00494⟩