DFT Study and Antiparasitic Activity of Some Azo Dyes Containing Uracil

In this study, for the first time, molecular modeling and antiparasitic activity studies were carried out on some azo dyes containing uracil, 6-amino-5-[(4-nitrophenyl) diazenyl] pyrimidine-2,4 (1H, 3H)-dione (dye I) and 6-amino-5-[(4-bromophenyl) diazenyl] pyrimidin-2,4 (1H, 3H)-dione (dye II), whi...

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Main Authors: Nevin Süleymanoğlu, Pınar Kubaşık, Şahin Direkel
Format: Article
Language:English
Published: Hindawi Limited 2021-01-01
Series:Journal of Chemistry
Online Access:http://dx.doi.org/10.1155/2021/6714151
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spelling doaj-aa8b0e38e088401ab1670956debe83bb2021-08-16T00:00:14ZengHindawi LimitedJournal of Chemistry2090-90712021-01-01202110.1155/2021/6714151DFT Study and Antiparasitic Activity of Some Azo Dyes Containing UracilNevin Süleymanoğlu0Pınar Kubaşık1Şahin Direkel2Vocational School of Technical SciencesGraduate School of Natural and Applied SciencesDepartment of Medical MicrobiologyIn this study, for the first time, molecular modeling and antiparasitic activity studies were carried out on some azo dyes containing uracil, 6-amino-5-[(4-nitrophenyl) diazenyl] pyrimidine-2,4 (1H, 3H)-dione (dye I) and 6-amino-5-[(4-bromophenyl) diazenyl] pyrimidin-2,4 (1H, 3H)-dione (dye II), which were resynthesized using the same method in the literature and whose molecular structures were confirmed using FTIR and 1H-NMR methods. In molecular modeling study, all calculations were performed using DFT/B3LYP/6-311++G(d,p) method. The molecular structures of the possible tautomeric forms of dyes I and II were optimized, and their molecular total energies were calculated in the gas phase and DMSO solvent. IR and 1H-NMR spectral data of the possible tautomeric forms of dyes were obtained, and theoretical spectral data were compared with experimental ones. The evaluations show that, for both dyes, the spectral data of the imine-diketo-hydrazone form, which has the lowest energy and is hence determined to be the most stable form, are in agreement with the experimental ones. In antiparasitic activity study, dyes I and II were tested for the first time against parasites Leishmania infantum, Leishmania major, Leishmania tropica promastigotes, and Trichomonas vaginalis trophozoites. In vitro antileishmanial activities against Leishmania promastigotes were tested by microdilution broth assay with Alamar Blue in RPMI 1640 medium, and in vitro trichomonacidal activities against Trichomonas vaginalis parasite were tested using TYM medium. In tests, antileishmanial and trichomonacidal effects were determined by comparing the obtained minimum inhibitory concentration (MIC) and minimum lethal concentration (MLC) values with those obtained for standard drugs (amphotericin B and metronidazole, respectively).http://dx.doi.org/10.1155/2021/6714151
collection DOAJ
language English
format Article
sources DOAJ
author Nevin Süleymanoğlu
Pınar Kubaşık
Şahin Direkel
spellingShingle Nevin Süleymanoğlu
Pınar Kubaşık
Şahin Direkel
DFT Study and Antiparasitic Activity of Some Azo Dyes Containing Uracil
Journal of Chemistry
author_facet Nevin Süleymanoğlu
Pınar Kubaşık
Şahin Direkel
author_sort Nevin Süleymanoğlu
title DFT Study and Antiparasitic Activity of Some Azo Dyes Containing Uracil
title_short DFT Study and Antiparasitic Activity of Some Azo Dyes Containing Uracil
title_full DFT Study and Antiparasitic Activity of Some Azo Dyes Containing Uracil
title_fullStr DFT Study and Antiparasitic Activity of Some Azo Dyes Containing Uracil
title_full_unstemmed DFT Study and Antiparasitic Activity of Some Azo Dyes Containing Uracil
title_sort dft study and antiparasitic activity of some azo dyes containing uracil
publisher Hindawi Limited
series Journal of Chemistry
issn 2090-9071
publishDate 2021-01-01
description In this study, for the first time, molecular modeling and antiparasitic activity studies were carried out on some azo dyes containing uracil, 6-amino-5-[(4-nitrophenyl) diazenyl] pyrimidine-2,4 (1H, 3H)-dione (dye I) and 6-amino-5-[(4-bromophenyl) diazenyl] pyrimidin-2,4 (1H, 3H)-dione (dye II), which were resynthesized using the same method in the literature and whose molecular structures were confirmed using FTIR and 1H-NMR methods. In molecular modeling study, all calculations were performed using DFT/B3LYP/6-311++G(d,p) method. The molecular structures of the possible tautomeric forms of dyes I and II were optimized, and their molecular total energies were calculated in the gas phase and DMSO solvent. IR and 1H-NMR spectral data of the possible tautomeric forms of dyes were obtained, and theoretical spectral data were compared with experimental ones. The evaluations show that, for both dyes, the spectral data of the imine-diketo-hydrazone form, which has the lowest energy and is hence determined to be the most stable form, are in agreement with the experimental ones. In antiparasitic activity study, dyes I and II were tested for the first time against parasites Leishmania infantum, Leishmania major, Leishmania tropica promastigotes, and Trichomonas vaginalis trophozoites. In vitro antileishmanial activities against Leishmania promastigotes were tested by microdilution broth assay with Alamar Blue in RPMI 1640 medium, and in vitro trichomonacidal activities against Trichomonas vaginalis parasite were tested using TYM medium. In tests, antileishmanial and trichomonacidal effects were determined by comparing the obtained minimum inhibitory concentration (MIC) and minimum lethal concentration (MLC) values with those obtained for standard drugs (amphotericin B and metronidazole, respectively).
url http://dx.doi.org/10.1155/2021/6714151
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