ChemInform Abstract: Fischerindoline, a Pyrroloindole Sesquiterpenoid Isolated from Neosartorya pseudofischeri, with in vitro Growth Inhibitory Activity in Human Cancer Cell Lines.

ChemInform ◽  
2013 ◽  
Vol 44 (52) ◽  
pp. no-no
Author(s):  
Marco Masi ◽  
Anna Andolfi ◽  
Veronique Mathieu ◽  
Angela Boari ◽  
Alessio Cimmino ◽  
...  
Tetrahedron ◽  
2013 ◽  
Vol 69 (35) ◽  
pp. 7466-7470 ◽  
Author(s):  
Marco Masi ◽  
Anna Andolfi ◽  
Veronique Mathieu ◽  
Angela Boari ◽  
Alessio Cimmino ◽  
...  

2008 ◽  
Vol 18 (24) ◽  
pp. 6451-6453 ◽  
Author(s):  
Naoto Kojima ◽  
Hiromi Hayashi ◽  
Satoshi Suzuki ◽  
Hiroaki Tominaga ◽  
Naoyoshi Maezaki ◽  
...  

2016 ◽  
Vol 11 (10) ◽  
pp. 1934578X1601101
Author(s):  
Alessio Cimmino ◽  
Patrizia Scafato ◽  
Veronique Mathieu ◽  
Aude Ingels ◽  
Wanda D'Amico ◽  
...  

This paper describes the enantioselective synthesis of analogues of sapinofuranones A and B, namely 5-substitutes dihydro- and 5 H-furan-ones, and their in vitro growth inhibitory activity against six cancer cell lines in comparison with fungal furanones such as diplofuranone A, diplobifuranylones A and B, as well as ( S,S)-enantiomer of sapinofuranone B. The compounds under study displayed weak if any in vitro growth inhibitory activity against the analysed cancer cell lines. However, it seems that among dihydro- and 5 H-furan-ones bearing a 1-hydroxypentyl side chain, the stereochemistry of the furanone ring and that of hydroxylated methine could modify the in vitro growth activity of these compounds. The natural furanones that showed a different unsaturated chain at C-4 or rearranged into a dihydrofuran ring appeared to be inactive in terms of growth inhibitory activity, e.g. displaying growth inhibitory concentration at 50% (GI50) > 100 μM in all six cancer cell lines analysed.


2012 ◽  
Vol 66 ◽  
pp. 100-108 ◽  
Author(s):  
Kátia Roberta A. Belaz ◽  
Marina Denadai ◽  
Ana Paula Almeida ◽  
Raquel T. Lima ◽  
M. Helena Vasconcelos ◽  
...  

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