Synthesis and Biological Evaluation of Novel Dihydro [2,3D] Pyridine Substituted Enaminosulfonamide Compounds as Potent Human Erythrocyte Carbonic Anhydrase II (hCAII)

Yıl 2021, , 200 - 211, 01.02.2021

Tuna Demirci , Oğuzhan Özdemir , Mustafa Oğuzhan Kaya , Mustafa Arslan

https://doi.org/10.16984/saufenbilder.688414

Öz

Dihydro [2,3D] pyridine substituted enaminosulfonamide compounds have been synthesized and their effects on carbonic anhydrase II (hCAII) have been evaluated. Pyrido [2,3 d] pyrimidines were synthesized from barbituric acid derivatives, malonanitrile, aldehyde derivatives in basic condition and then hydrolyzed with hydrochloric acid. The targeted compounds were syn-thesized from amino sulfanilamide, dihydro [2,3D] pyridine compounds, and triethylorthoformate. 1H NMR, 13C NMR, FT-IR and elemental analysis were used for the structural analysis of the compounds. The half maximal inhibitory concentration (IC50) values of the compounds were determined to be between 27.03 and 104.39 μM for hCA II and 19.85-76.64 μM for Ki.

Anahtar Kelimeler

Barbituric acid, Carbonic anhydrase II, Dihydro 2 3 D pyridine, Enaminosulfonamide

Destekleyen Kurum

Sakarya University Scientific Research Projects Coordination Unit

Proje Numarası

2012-02-04-033/2016-50-02-002.

Teşekkür

Duzce University Scientific and Technological Research Laboratory

Kaynakça

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