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  4. Automated approach for the evaluation of glutathione-S-transferase P1-1 inhibition by organometallic anticancer compounds
 
research article

Automated approach for the evaluation of glutathione-S-transferase P1-1 inhibition by organometallic anticancer compounds

Pereira, Sarah A. P.
•
Baptista, A. Catarina L.
•
Biancalana, Lorenzo
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December 31, 2022
Journal Of Enzyme Inhibition And Medicinal Chemistry

A novel automated method based on sequential injection analysis (SIA), a non-segmented flow injection technique, was developed to evaluate glutathione S-transferase P1-1 (GST P1-1) activity in the presence of organometallic complexes with putative anticancer activity. The assay is based on the reaction of L-glutathione (GSH) and 1-chloro-2,4-dinitrobenzene (CDNB) in the presence of GST P1-1 to afford the GS-DNB conjugate and the reaction may be monitored by an increase in absorbance at 340 nm. A series of ruthenium, iron, osmium and iridium complexes were evaluated as GST P1-1 inhibitors by evaluating their half-maximal inhibitory concentration (IC50). An iridium compound displays the lowest IC50 value of 6.7 +/- 0.7 mu M and an iron compound displays the highest IC50 value of 275 +/- 9 mu M. The SIA method is simple to use, robust, reliable, and efficient and uses fewer reagents than batch methods and each analysis takes only 5 minutes.

  • Details
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Type
research article
DOI
10.1080/14756366.2022.2073443
Web of Science ID

WOS:000802813800001

Author(s)
Pereira, Sarah A. P.
Baptista, A. Catarina L.
Biancalana, Lorenzo
Marchetti, Fabio
Dyson, Paul J.  
Saraiva, M. Lucia M. F. S.
Date Issued

2022-12-31

Publisher

TAYLOR & FRANCIS LTD

Published in
Journal Of Enzyme Inhibition And Medicinal Chemistry
Volume

37

Issue

1

Start page

1527

End page

1536

Subjects

Biochemistry & Molecular Biology

•

Chemistry, Medicinal

•

Pharmacology & Pharmacy

•

sequential injection analysis (sia)

•

glutathione s-transferase p1-1

•

enzyme inhibition assays

•

anticancer metal complexes

•

ruthenium arene complexes

•

in-vitro

•

enzyme

•

drug

•

mechanism

•

agents

Editorial or Peer reviewed

REVIEWED

Written at

EPFL

EPFL units
LCOM  
Available on Infoscience
June 20, 2022
Use this identifier to reference this record
https://infoscience.epfl.ch/handle/20.500.14299/188611
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