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  4. Telomerase Inhibitors from Cyanobacteria: Isolation and Synthesis of Sulfoquinovosyl Diacylglycerols from
 
research article

Telomerase Inhibitors from Cyanobacteria: Isolation and Synthesis of Sulfoquinovosyl Diacylglycerols from

Makhlouf Brahmi, Malika
•
Portmann, Cyril
•
D'Ambrosio, Danilo
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2013
Chemistry - A European Journal

By using the Telospot assay, 27 different extracts of cyanobacteria were evaluated for telomerase inhibition. All extracts showed varying, but significant activity. We selected Microcystis aeruguinosa PCC 7806 to identify the active compound and a bioassay guided fractionation led us to isolate mixtures of sulfoquinovosyl diacylglycerols (SQDGs), which were identified by 2D NMR and MS/MS experiments. Pure SQDG derivatives were then synthesized. The IC50 values of pure synthetic sulfoquinovosyl dipalmitoylglycerol and the monopalmitoylated derivative against telomerase were determined to be 17 and 40M, respectively. A structureactivity relationship study allowed the identification of compounds with modified lipophilic acyl groups that display improved activity.

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Type
research article
DOI
10.1002/chem.201203296
Web of Science ID

WOS:000316625000027

Author(s)
Makhlouf Brahmi, Malika
Portmann, Cyril
D'Ambrosio, Danilo
Woods, Tom M.
Banfi, Damiano
Reichenbach, Patrick
Da Silva, Laeticia
Baudat, Emilie
Turcatti, Gerardo  

EPFL

Lingner, Joachim  
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Date Issued

2013

Publisher

Wiley-Blackwell

Published in
Chemistry - A European Journal
Volume

19

Issue

14

Start page

4596

End page

4601

Subjects

biological activity

•

enzymes

•

inhibitors

•

structureactivity relationships

•

structure elucidation

Editorial or Peer reviewed

REVIEWED

Written at

EPFL

EPFL units
UPLIN  
Available on Infoscience
April 12, 2013
Use this identifier to reference this record
https://infoscience.epfl.ch/handle/20.500.14299/91448
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