TY  - JOUR
AU  - Veljović, Elma
AU  - Spirtovic-Halilovic, S.
AU  - Muratovic, S.
AU  - Salihovic, M.
AU  - Novaković, Irena
AU  - Osmanovic, A.
AU  - Zavrsnik, D.
PY  - 2018
UR  - https://cer.ihtm.bg.ac.rs/handle/123456789/2383
AB  - Twelve previously synthesized biologically active 2,6,7-trihydroxy-9-aryl-3H-xanthen-3-one derivatives (1-12) were evaluated in vitro for their antimicrobial activity against four bacteria, S. aureus, B. subtilis P. aeruginosa and E. coli, and two fungi strains, C. albicans and S. cerevisiae. The most potent compound were derivatives 1 which possess hydroxyl group and bromine as substituent and 11 with bromine as substituent on phenyl ring. The results indicate that bromine increase antimicrobial activity of 2,6,7-trihydroxy-9-aryl-3-Hxanthen-3-one derivatives. Compound 7 with ethoxy substituent on phenyl ring showed the least activity against tested bacteria and fungi strains, which is in line with an earlier observation that ethoxy substitution decreases antimicrobial activity. The most and the least potent compounds were subjected to molecular docking simulations to preliminary find out the potential molecular target and at the same moment further support the experimental antimicrobial test of xanthen derivatives.
T2  - Research Journal of Pharmaceutical Biological and Chemical Sciences
T1  - Antimicrobial Activity and Docking Study of Synthesized Xanthen-3-on Derivatives
VL  - 9
IS  - 5
SP  - 777
EP  - 783
UR  - https://hdl.handle.net/21.15107/rcub_cer_2383
ER  - 

@article{
author = "Veljović, Elma and Spirtovic-Halilovic, S. and Muratovic, S. and Salihovic, M. and Novaković, Irena and Osmanovic, A. and Zavrsnik, D.",
year = "2018",
abstract = "Twelve previously synthesized biologically active 2,6,7-trihydroxy-9-aryl-3H-xanthen-3-one derivatives (1-12) were evaluated in vitro for their antimicrobial activity against four bacteria, S. aureus, B. subtilis P. aeruginosa and E. coli, and two fungi strains, C. albicans and S. cerevisiae. The most potent compound were derivatives 1 which possess hydroxyl group and bromine as substituent and 11 with bromine as substituent on phenyl ring. The results indicate that bromine increase antimicrobial activity of 2,6,7-trihydroxy-9-aryl-3-Hxanthen-3-one derivatives. Compound 7 with ethoxy substituent on phenyl ring showed the least activity against tested bacteria and fungi strains, which is in line with an earlier observation that ethoxy substitution decreases antimicrobial activity. The most and the least potent compounds were subjected to molecular docking simulations to preliminary find out the potential molecular target and at the same moment further support the experimental antimicrobial test of xanthen derivatives.",
journal = "Research Journal of Pharmaceutical Biological and Chemical Sciences",
title = "Antimicrobial Activity and Docking Study of Synthesized Xanthen-3-on Derivatives",
volume = "9",
number = "5",
pages = "777-783",
url = "https://hdl.handle.net/21.15107/rcub_cer_2383"
}

Veljović, E., Spirtovic-Halilovic, S., Muratovic, S., Salihovic, M., Novaković, I., Osmanovic, A.,& Zavrsnik, D.. (2018). Antimicrobial Activity and Docking Study of Synthesized Xanthen-3-on Derivatives. in Research Journal of Pharmaceutical Biological and Chemical Sciences, 9(5), 777-783.
https://hdl.handle.net/21.15107/rcub_cer_2383

Veljović E, Spirtovic-Halilovic S, Muratovic S, Salihovic M, Novaković I, Osmanovic A, Zavrsnik D. Antimicrobial Activity and Docking Study of Synthesized Xanthen-3-on Derivatives. in Research Journal of Pharmaceutical Biological and Chemical Sciences. 2018;9(5):777-783.
https://hdl.handle.net/21.15107/rcub_cer_2383 .

Veljović, Elma, Spirtovic-Halilovic, S., Muratovic, S., Salihovic, M., Novaković, Irena, Osmanovic, A., Zavrsnik, D., "Antimicrobial Activity and Docking Study of Synthesized Xanthen-3-on Derivatives" in Research Journal of Pharmaceutical Biological and Chemical Sciences, 9, no. 5 (2018):777-783,
https://hdl.handle.net/21.15107/rcub_cer_2383 .