o:1072 Sinteza, karakterizacija i ispitivanje biološke aktivnosti binuklearnih kompleksa bakra(II) sa S-alkenil derivatima tiosalicilne kiseline Synthesis, characterization and examination of the biological activity of binuclear complexes of copper(II) with S-alkenyl derivatives of thiosalicylic acid : doctoral dissertation sr Uvod: U ovoj Doktorskoj disertaciji ispitivane su kinetička, antimikrobna i antitumorska aktivnost novosintetisanih binuklearnih kompleksa bakra(II) sa S-alkenil derivatima tiosalicilne kiseline. Istraživanja u ovoj oblasti su fokusirana na pronalaženje biološki aktivnih kompleksnih jedinjenja. Tiosalicilna kiselina i njeni derivati su veoma interesantni kao ligandi, jer pokazuju veliku raznolikost u mogućnostima za koordinovanje. Materijal i metode: U okviru ovog istraživanja opisani su postupci sinteze Salkenil derivata tiosalicilne kiseline (alkenil = propenil- i izobutenil-) i odgovarajućih binuklearnih kompleksa bakra(II). Sastav nagrađenih jedinjenja potvrđen je na osnovu rezultata elementalne mikroanalize. Struktura sintetisanih bidentatnih liganada okarakterisana je na osnovu rezultata infracrvene (IR) i nuklearno-magnetno-rezonancione spektroskopije (1H i 13C NMR), dok je struktura odgovarajućih kompleksa pretpostavljena na osnovu rezultata infracrvene (IR) spektroskopije, magnetnih merenja i molarne provodljivosti. Stvarna struktura sintetisanog kompleksa bakra(II), predviđena je na osnovu rezultata rendgenske strukturne analize. Antimikrobna aktivnost je ispitivana mikrodilucionom metodom sa resazurinom. Supstitucione reakcije su praćene u prisustvu guanozin-5’- -monofosfata, kao i CT-DNK (DNK iz timusa govečeta). Citotoksična aktivnost novosintetisanih jedinjenja je ispitivana pomoću MTT kolorimetrijske tehnike. Rezultati: Potvrđena je stvarna struktura binuklearnog kompleksa bakra(II) sa S-izobutenil derivatom tiosalicilne kiseline. Među Gram-pozitivnim bakterijama, Staphylococcus aureus ATCC® 25923 je pokazao najveću otpornost, dok je najosetljiviji bio Bifidobacterium animalis subsp. lactis. Kompleksi bakra(II) pokazali su nisku antifungalnu aktivnost. Reakcije supstitucije ispitivanih kompleksa bile su veoma brze, a pokazano je da mogu interagovati sa ST-DNK. Bakar(II)-kompleksi su pokazali neznatno nižu citotoksičnost u poređenju sa cisplatinom. Njihov citotoksični efekat pri koncentracijama od 250 do 1000 μM na HCT-116 ćelije je kao efekat cisplatine. Zaključak: Otkriće kompleksa bakra(II) sa antimikrobnom i antitumorskom aktivnošću može bitno podstaći dalja istraživanja u oblasti koordinovanja bakar(II)-jona sa ligandima od farmakološkog značaja, koji će imati širi spektar dejstva u medicinskoj primeni sa prihvatljivim krajnjim ishodom lečenja. Introduction: This PhD thesis covers the examination of the kinetic, antimicrobial and anticancer activities of the newly synthesized binuclear complexes of copper(II) with S-alkenyl derivatives of thiosalicylic acid. Researches in this area are focused on finding biologically active complex compounds. Thiosalicylic acid and its derivatives are very interesting as ligands because they manifest a great diversity in coordination possibilities. Materials and methods: This study described the methods for the synthesis of the S-alkenyl derivatives of thiosalicylic acid (alkenyl = propenyl- and isobutenyl-) and the corresponding binuclear complexes of copper(II). The composition of the obtained compounds was confirmed by the results of the elemental microanalysis. The structure of synthesized bidentate ligands was characterized by the results of infrared (IR) and nuclear-magnetic-resonance spectroscopy (1H and 13C NMR), while the structure of the corresponding complexes was assumed by the results of infrared (IR) spectroscopy, magnetic measurements and molar conductivity. The real structure of the synthesized complex copper(II) was predicted by the results of the X-ray structural analysis. Тhe antimicrobial activity was examined by the microdilution method with resazurin. The substitution reactions were monitored in the presence of guanosine-5'-monophosphate, as well as CT-DNА (calf thymus DNA). The cytotoxic activity of the newly obtained compounds was examined by MTT colorimetric technique. Results: The real structure of the binuclear complex of copper(II) with S-isobutenyl derivative of thiosalicylic acid was confirmed. Among Gram-positive bacteria, Staphylococcus aureus ATCC® 25923 manifested the highest resistance, while Bifidobacterium animalis subsp. lactis was the most sensitive one. Copper(II)-complexes manifested a low antifungal activity. Substitution reactions of the tested complexes were very fast, and it was shown that they could interact with СT-DNA. Copper(II)-complexes displayed slightly lower cytotoxicity compared to cisplatin. Copper(II)-complexes with S-alkenyl derivatives of thiosalicylic acid (for concentrations from 250 to 1000 μM) had cytotoxic effect on HCT-116 cells as cisplatin. Conclusion: The discovery of the copper(II)-complexes with antimicrobial and anticancer activity can significantly stimulate further research in the field of copper(II) coordination with ligands of pharmacological significance, which will have a wider spectrum of effects in medical applications with the acceptable final outcome of a treatment. ID=524865429 ; D-3211 91552101 6558 91552100 524865429 2019-01-23T15:28:57.053Z 45 no 46 mentor Dušan Lj., 1988- Tomović 2018 63 mentor Gordana P. 1980- Radić 2018 63 predsednik komisije Nebojša N., 1958- Arsenijević 2018 63 član komisije Tibor J., 1958- Sabo 2018 63 član komisije Verica V., 1976- Jevtić 2018 63 član komisije Jovana V., 1980- Bogojeski 2018 63 član komisije Ivana D., 1973- Radojević 2018 III, 126 listova 5007236 http://phaidrabg.bg.ac.rs/o:1072 no yes 5 2019-01-23T15:28:57.320Z 70 S-alkenil derivati tiosalicilne kiseline, binuklearni kompleksibakra(II), kristalna struktura, biološka aktivnost S-alkenyl derivatives of thiosalicylic acid, binuclear copper(II)-complexes,crystal structure, biological activity 615.3:546.56(043.3) Bakar(II) - Binuklearni kompleksi - Doktorske disertacije 1738 34A05 2018