DESIGN, SYNTHESIS, AND ALDOSE REDUCTASE ACTIVITY OF SOME ARYL CARBOXYLIC ACID DERIVATIVES BEARING 2-SUBSTITUTED-6-OXO-PYRIDAZİNONE MOIETY

Akdağ M., Özçelik A. B., Demir Y., Beydemir Ş.

EFMC-ISMC 2021, Basel, İsviçre, 29 Ağustos - 02 Eylül 2021, ss.441

  • Yayın Türü: Bildiri / Özet Bildiri
  • Basıldığı Şehir: Basel
  • Basıldığı Ülke: İsviçre
  • Sayfa Sayıları: ss.441
  • Gazi Üniversitesi Adresli: Evet

Özet

Aldose reductase is an enzyme that is responsible for the convertion of glucose to sorbitol. Increased activity of this pathway has been associated with diabetic complications thus making aldose reductase enzyme a pharmacological target(1).There are some compounds which were evaulated in clinical trials bearing pyridazinone moiety like ponalrestat. So,  pyridazinone is a heterocyclic core having a potential for inhibiton of aldose reductase and chalcones are priviliged structures having antioxidant activity(2,,3).Moreover, after tetramethyleneglutaric acid had been shown as a aldose reductase inhibitor, various acid derivatives were synthesized and evaluated for aldose reductase inhibition(4). Given these data,combination of these structures can give rise to potent inhibitors of aldose reductase and also antioxidant compounds. In this study, we synthesized a representing compound of 2-(6-Chalconoxy-Pyridazin-3(2H)-One) Acetic Acid serie and performed molecular modelling studies of this compound. The success of sythesis was comfirmed evaluating 1H-NMR and LC-MS spectra.