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Chemical Papers

, Volume 70, Issue 11, pp 1439–1444 | Cite as

3′-O-(3-Chloropivaloyl)quercetin, α-glucosidase inhibitor with multi-targeted therapeutic potential in relation to diabetic complications

  • Marta Soltesova-Prnova
  • Ivana Milackova
  • Milan Stefek
Original Paper
  • 27 Downloads

Abstract

The novel derivative of quercetin 3′-O-(3-chloropivaloyl)quercetin (CPQ) inhibited a-glucosidase in a non-competitive manner with an efficacy exceeding that of the parent quercetin. In addition, it inhibited aldose reductase isolated from rat lenses with an IC50 in the low micromolar range and attenuated sorbitol accumulation in isolated rat eye lenses with an activity comparable with that of quercetin. Moreover, it scavenged stable free-radicals of DPPH more efficiently than did quercetin. By inhibiting α-glucosidase and affecting both the polyol pathway and oxidative stress, CPQ represents a promising agent for the multi-targeted pharmacology of diabetic complications.

Keywords

3′-O-(3-chloropivaloyl)quercetin α-glucosidase inhibitor aldose reductase inhibitor antioxidant diabetic complications 

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Copyright information

© Institute of Chemistry, Slovak Academy of Sciences 2016

Authors and Affiliations

  • Marta Soltesova-Prnova
    • 1
  • Ivana Milackova
    • 2
  • Milan Stefek
    • 1
  1. 1.Institute of Experimental Pharmacology and ToxicologySlovak Academy of SciencesBratislavaSlovakia
  2. 2.Faculty of PharmacyComenius University in BratislavaBratislavaSlovakia

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