TY  - CONF
AU  - Avdović, Edina
AU  - Milenković, Dejan
AU  - Djorović, Jelena
AU  - Vuković, Nenad
AU  - Dolicanin, Zana
AU  - Trifunović, Srećko
AU  - Marković, Zoran
AU  - Jeremić, Svetlana
PY  - 2018
UR  - http://aspace.agrif.bg.ac.rs/handle/123456789/5654
AB  - The structure of the newly synthesized coumarin derivative, 3-(1-(3-hydroxypropylamino)-ethylidene)-chroman-2,4-dione, was investigated theoretically. The density functional theory calculations, with B3LYP functional (and with empirical dispersion corrections D3BJ) in combination with the 6–311+G(d,p) basis set, are performed in order to optimized the molecular structure of the investigated coumarin derivative. Molecular docking analysis was carried out in order to identify the potency of inhibition of the title molecule against human C-reactive protein. The inhibition activity was obtained for ten conformations of ligand inside protein.
AB  - Struktura novo sintetisanog derivata kumarina, 3- (1- (3-hidroksipropilamino) -etiliden) -hroman-2,4-diona, ispitana je primenom teorijskih metoda. Za optimizaciju strukture ispitivanog kumarinskog derivata korišćena je teorija funkcionalne gustine: B3LYP funkcional ( sa empirijskim ispravkama disperzije D3BJ) u kombinaciji sa 6-311+G(d, p) bazisnim setom. Urađen je molekulski doking, kao i analiza dobijenih rezultata kako bi se utvrdio potencijal inhibicije molekula ispitivanog jedinjenja prema humanom C-reaktivnom proteinu. Aktivnost inhibicije izračunata je za deset potencijalnih konformacija liganda unutar proteina.
C3  - 23. Savetovanje o biotehnologiji sa međunarodnim učešćem, Čačak, 09.-10. 03. 2018.
T1  - Ligand-Protein Interaction Of 3-(1-(3-Hydroxypropylamino)Etylidene)Chroman-2,4-Dione With Human C Reactive Protein
T1  - Ligand-protein interakcije 3-(1-(3-hidroksipropilamino)etiliden)hroman-2,4-diona sa humanim C reaktivnim proteinom
UR  - https://hdl.handle.net/21.15107/rcub_agrospace_5654
ER  - 

@conference{
author = "Avdović, Edina and Milenković, Dejan and Djorović, Jelena and Vuković, Nenad and Dolicanin, Zana and Trifunović, Srećko and Marković, Zoran and Jeremić, Svetlana",
year = "2018",
abstract = "The structure of the newly synthesized coumarin derivative, 3-(1-(3-hydroxypropylamino)-ethylidene)-chroman-2,4-dione, was investigated theoretically. The density functional theory calculations, with B3LYP functional (and with empirical dispersion corrections D3BJ) in combination with the 6–311+G(d,p) basis set, are performed in order to optimized the molecular structure of the investigated coumarin derivative. Molecular docking analysis was carried out in order to identify the potency of inhibition of the title molecule against human C-reactive protein. The inhibition activity was obtained for ten conformations of ligand inside protein., Struktura novo sintetisanog derivata kumarina, 3- (1- (3-hidroksipropilamino) -etiliden) -hroman-2,4-diona, ispitana je primenom teorijskih metoda. Za optimizaciju strukture ispitivanog kumarinskog derivata korišćena je teorija funkcionalne gustine: B3LYP funkcional ( sa empirijskim ispravkama disperzije D3BJ) u kombinaciji sa 6-311+G(d, p) bazisnim setom. Urađen je molekulski doking, kao i analiza dobijenih rezultata kako bi se utvrdio potencijal inhibicije molekula ispitivanog jedinjenja prema humanom C-reaktivnom proteinu. Aktivnost inhibicije izračunata je za deset potencijalnih konformacija liganda unutar proteina.",
journal = "23. Savetovanje o biotehnologiji sa međunarodnim učešćem, Čačak, 09.-10. 03. 2018.",
title = "Ligand-Protein Interaction Of 3-(1-(3-Hydroxypropylamino)Etylidene)Chroman-2,4-Dione With Human C Reactive Protein, Ligand-protein interakcije 3-(1-(3-hidroksipropilamino)etiliden)hroman-2,4-diona sa humanim C reaktivnim proteinom",
url = "https://hdl.handle.net/21.15107/rcub_agrospace_5654"
}

Avdović, E., Milenković, D., Djorović, J., Vuković, N., Dolicanin, Z., Trifunović, S., Marković, Z.,& Jeremić, S.. (2018). Ligand-Protein Interaction Of 3-(1-(3-Hydroxypropylamino)Etylidene)Chroman-2,4-Dione With Human C Reactive Protein. in 23. Savetovanje o biotehnologiji sa međunarodnim učešćem, Čačak, 09.-10. 03. 2018..
https://hdl.handle.net/21.15107/rcub_agrospace_5654

Avdović E, Milenković D, Djorović J, Vuković N, Dolicanin Z, Trifunović S, Marković Z, Jeremić S. Ligand-Protein Interaction Of 3-(1-(3-Hydroxypropylamino)Etylidene)Chroman-2,4-Dione With Human C Reactive Protein. in 23. Savetovanje o biotehnologiji sa međunarodnim učešćem, Čačak, 09.-10. 03. 2018.. 2018;.
https://hdl.handle.net/21.15107/rcub_agrospace_5654 .

Avdović, Edina, Milenković, Dejan, Djorović, Jelena, Vuković, Nenad, Dolicanin, Zana, Trifunović, Srećko, Marković, Zoran, Jeremić, Svetlana, "Ligand-Protein Interaction Of 3-(1-(3-Hydroxypropylamino)Etylidene)Chroman-2,4-Dione With Human C Reactive Protein" in 23. Savetovanje o biotehnologiji sa međunarodnim učešćem, Čačak, 09.-10. 03. 2018. (2018),
https://hdl.handle.net/21.15107/rcub_agrospace_5654 .

TY  - CONF
AU  - Avdović, Edina
AU  - Jeremić, Svetlana
AU  - Amić, Ana
AU  - Pirković, Marijana
AU  - Milenković, Dejan
AU  - Djorović, Jelena
AU  - Marković, Zoran
PY  - 2018
UR  - http://aspace.agrif.bg.ac.rs/handle/123456789/5655
AB  - In this paper was investigated the antioxidative activity of alizarin-2-glycoside. All results were obtained using the DFT method. For calculations, the M06-2X method was used in combination with the 6-311++G(d,p) base set. Water was used as a solvent. The values of enthalpy were used as thermodynamic parameters on the basis of which the antioxidative capacity of alizarin-2-glycoside was evaluated. The Molecular Docking method was used for assessing the ability of alizarin-2-glycoside to inhibit the negative effect of P-glycoprotein.
AB  - U ovom radu je ispitana antioksidativna aktivnost alizarin-2-glikozida. Svi rezultati dobijeni su primenom DFT metode. Za izračunavanja je korišćena M06-2X metoda u kombinaciji sa 6-311++G(d,p) bazisnim skupom. Kao rastvarač korišćena je voda. Vrednosti entalpija korišćene su kao termodinamički parametri na osnovu kojih je procenjen antioksidativni kapacitet alizarin-2-glikozida. Molecular Docking metodom procenjena je sposobnost alizarin-2-glikozida da inhibira negativan uticaj P-glikoproteina.
C3  - 23. Savetovanje o biotehnologiji sa međunarodnim učešćem, Čačak, 09.-10. 03. 2018.
T1  - Antioxidative and Inhibitor Activity of Alizarin-2-Glycoside
T1  - Antioksidativna i inhibitorska aktivnost Alizarin-2-glikozida
UR  - https://hdl.handle.net/21.15107/rcub_agrospace_5655
ER  - 

@conference{
author = "Avdović, Edina and Jeremić, Svetlana and Amić, Ana and Pirković, Marijana and Milenković, Dejan and Djorović, Jelena and Marković, Zoran",
year = "2018",
abstract = "In this paper was investigated the antioxidative activity of alizarin-2-glycoside. All results were obtained using the DFT method. For calculations, the M06-2X method was used in combination with the 6-311++G(d,p) base set. Water was used as a solvent. The values of enthalpy were used as thermodynamic parameters on the basis of which the antioxidative capacity of alizarin-2-glycoside was evaluated. The Molecular Docking method was used for assessing the ability of alizarin-2-glycoside to inhibit the negative effect of P-glycoprotein., U ovom radu je ispitana antioksidativna aktivnost alizarin-2-glikozida. Svi rezultati dobijeni su primenom DFT metode. Za izračunavanja je korišćena M06-2X metoda u kombinaciji sa 6-311++G(d,p) bazisnim skupom. Kao rastvarač korišćena je voda. Vrednosti entalpija korišćene su kao termodinamički parametri na osnovu kojih je procenjen antioksidativni kapacitet alizarin-2-glikozida. Molecular Docking metodom procenjena je sposobnost alizarin-2-glikozida da inhibira negativan uticaj P-glikoproteina.",
journal = "23. Savetovanje o biotehnologiji sa međunarodnim učešćem, Čačak, 09.-10. 03. 2018.",
title = "Antioxidative and Inhibitor Activity of Alizarin-2-Glycoside, Antioksidativna i inhibitorska aktivnost Alizarin-2-glikozida",
url = "https://hdl.handle.net/21.15107/rcub_agrospace_5655"
}

Avdović, E., Jeremić, S., Amić, A., Pirković, M., Milenković, D., Djorović, J.,& Marković, Z.. (2018). Antioxidative and Inhibitor Activity of Alizarin-2-Glycoside. in 23. Savetovanje o biotehnologiji sa međunarodnim učešćem, Čačak, 09.-10. 03. 2018..
https://hdl.handle.net/21.15107/rcub_agrospace_5655

Avdović E, Jeremić S, Amić A, Pirković M, Milenković D, Djorović J, Marković Z. Antioxidative and Inhibitor Activity of Alizarin-2-Glycoside. in 23. Savetovanje o biotehnologiji sa međunarodnim učešćem, Čačak, 09.-10. 03. 2018.. 2018;.
https://hdl.handle.net/21.15107/rcub_agrospace_5655 .

Avdović, Edina, Jeremić, Svetlana, Amić, Ana, Pirković, Marijana, Milenković, Dejan, Djorović, Jelena, Marković, Zoran, "Antioxidative and Inhibitor Activity of Alizarin-2-Glycoside" in 23. Savetovanje o biotehnologiji sa međunarodnim učešćem, Čačak, 09.-10. 03. 2018. (2018),
https://hdl.handle.net/21.15107/rcub_agrospace_5655 .

TY  - CONF
AU  - Petrović, Zorica
AU  - Simijonović, Dusica
AU  - Marković, Zoran
AU  - Petrović, Vladimir
AU  - Djorović, Jelena
PY  - 2016
UR  - http://aspace.agrif.bg.ac.rs/handle/123456789/5626
AB  - The UV-Vis properties of ten Schiff bases were systematically investigated. The time-dependent density functional theory (TDDFT) approach in combination with the B3LYP functional was used for simulation of UV-Vis spectra of examined compounds. The shapes of the Kohn-Sham molecular orbitals involved in electronic transitions were misleading. To provide better understanding of distribution of electron density natural bond orbital (NBO) analysis was used. NLMO clusters were constructed and they represent a part of a molecule characterized with eminent electron density. The TDDFT and NBO theories are complementary, and the results from these two approaches are combined to interpret the UV-Vis spectra.
C3  - 21. Savetovanje o biotehnologiji sa međunarodnim učešćem, Čačak, 11.- 12. 03. 2016.
T1  - Experimental and Theoretical Study Of UV-Vis Spectra of Schiff Bases
UR  - https://hdl.handle.net/21.15107/rcub_agrospace_5626
ER  - 

@conference{
author = "Petrović, Zorica and Simijonović, Dusica and Marković, Zoran and Petrović, Vladimir and Djorović, Jelena",
year = "2016",
abstract = "The UV-Vis properties of ten Schiff bases were systematically investigated. The time-dependent density functional theory (TDDFT) approach in combination with the B3LYP functional was used for simulation of UV-Vis spectra of examined compounds. The shapes of the Kohn-Sham molecular orbitals involved in electronic transitions were misleading. To provide better understanding of distribution of electron density natural bond orbital (NBO) analysis was used. NLMO clusters were constructed and they represent a part of a molecule characterized with eminent electron density. The TDDFT and NBO theories are complementary, and the results from these two approaches are combined to interpret the UV-Vis spectra.",
journal = "21. Savetovanje o biotehnologiji sa međunarodnim učešćem, Čačak, 11.- 12. 03. 2016.",
title = "Experimental and Theoretical Study Of UV-Vis Spectra of Schiff Bases",
url = "https://hdl.handle.net/21.15107/rcub_agrospace_5626"
}

Petrović, Z., Simijonović, D., Marković, Z., Petrović, V.,& Djorović, J.. (2016). Experimental and Theoretical Study Of UV-Vis Spectra of Schiff Bases. in 21. Savetovanje o biotehnologiji sa međunarodnim učešćem, Čačak, 11.- 12. 03. 2016..
https://hdl.handle.net/21.15107/rcub_agrospace_5626

Petrović Z, Simijonović D, Marković Z, Petrović V, Djorović J. Experimental and Theoretical Study Of UV-Vis Spectra of Schiff Bases. in 21. Savetovanje o biotehnologiji sa međunarodnim učešćem, Čačak, 11.- 12. 03. 2016.. 2016;.
https://hdl.handle.net/21.15107/rcub_agrospace_5626 .

Petrović, Zorica, Simijonović, Dusica, Marković, Zoran, Petrović, Vladimir, Djorović, Jelena, "Experimental and Theoretical Study Of UV-Vis Spectra of Schiff Bases" in 21. Savetovanje o biotehnologiji sa međunarodnim učešćem, Čačak, 11.- 12. 03. 2016. (2016),
https://hdl.handle.net/21.15107/rcub_agrospace_5626 .

TY  - CONF
AU  - Marković, Zoran
AU  - Jeremić, Svetlana
AU  - Filipović, Miloš
AU  - Milenković, Dejan
AU  - Djorović, Jelena
PY  - 2016
UR  - http://aspace.agrif.bg.ac.rs/handle/123456789/5623
AB  - Quantitative structure–activity relationship model (QSAR models) is useful method for predicting antioxidant capacity of a molecule based on some chemical-physics properties. In our development of QSAR model are included 21 structural similar antioxidants. It is shown that taking into account some thermodynamical and thermochemical parameters of antioxidant and chemical activity is possible to generate fair antiradical QSAR models.
C3  - 21. Savetovanje o biotehnologiji sa međunarodnim učešćem, Čačak, 11.- 12. 03. 2016.
T1  - QSAR Model for Predicting Antioxidan Capacity of Some Polyphenolic Antioxidants
UR  - https://hdl.handle.net/21.15107/rcub_agrospace_5623
ER  - 

@conference{
author = "Marković, Zoran and Jeremić, Svetlana and Filipović, Miloš and Milenković, Dejan and Djorović, Jelena",
year = "2016",
abstract = "Quantitative structure–activity relationship model (QSAR models) is useful method for predicting antioxidant capacity of a molecule based on some chemical-physics properties. In our development of QSAR model are included 21 structural similar antioxidants. It is shown that taking into account some thermodynamical and thermochemical parameters of antioxidant and chemical activity is possible to generate fair antiradical QSAR models.",
journal = "21. Savetovanje o biotehnologiji sa međunarodnim učešćem, Čačak, 11.- 12. 03. 2016.",
title = "QSAR Model for Predicting Antioxidan Capacity of Some Polyphenolic Antioxidants",
url = "https://hdl.handle.net/21.15107/rcub_agrospace_5623"
}

Marković, Z., Jeremić, S., Filipović, M., Milenković, D.,& Djorović, J.. (2016). QSAR Model for Predicting Antioxidan Capacity of Some Polyphenolic Antioxidants. in 21. Savetovanje o biotehnologiji sa međunarodnim učešćem, Čačak, 11.- 12. 03. 2016..
https://hdl.handle.net/21.15107/rcub_agrospace_5623

Marković Z, Jeremić S, Filipović M, Milenković D, Djorović J. QSAR Model for Predicting Antioxidan Capacity of Some Polyphenolic Antioxidants. in 21. Savetovanje o biotehnologiji sa međunarodnim učešćem, Čačak, 11.- 12. 03. 2016.. 2016;.
https://hdl.handle.net/21.15107/rcub_agrospace_5623 .

Marković, Zoran, Jeremić, Svetlana, Filipović, Miloš, Milenković, Dejan, Djorović, Jelena, "QSAR Model for Predicting Antioxidan Capacity of Some Polyphenolic Antioxidants" in 21. Savetovanje o biotehnologiji sa međunarodnim učešćem, Čačak, 11.- 12. 03. 2016. (2016),
https://hdl.handle.net/21.15107/rcub_agrospace_5623 .

TY  - CONF
AU  - Marković, Zoran
AU  - Milenković, Dejan
AU  - Jeremić, Svetlana
AU  - Djorović, Jelena
AU  - Dimitrić-Marković, Jasmina
PY  - 2016
UR  - http://aspace.agrif.bg.ac.rs/handle/123456789/5620
AB  - Cyanidin, as one important plant pigment, was theoretically (at M05-2X/6-311+G(d,p) level of theory) investigated for its ability to scavenge potentially, highly damaging hydroxyl radical. Free radical scavenging of cyanidin was studied through electron transfer mechanism – ET (the second step in SPLET mechanism) in water and ethanol, as solvents. Examination was performed using density functional theory (DFT) and Marcus theory. Based on the thermochemical and kinetic data, it is clear that O‒H group of cyanidin in position 3` is the most suitable for reaction with hydroxyl radical through mentioned antioxidant mechanism.
C3  - 21. Savetovanje o biotehnologiji sa međunarodnim učešćem, Čačak, 11.- 12. 03. 2016.
T1  - Examination of Electron Transfer Mechanism of Cyanidin
UR  - https://hdl.handle.net/21.15107/rcub_agrospace_5620
ER  - 

@conference{
author = "Marković, Zoran and Milenković, Dejan and Jeremić, Svetlana and Djorović, Jelena and Dimitrić-Marković, Jasmina",
year = "2016",
abstract = "Cyanidin, as one important plant pigment, was theoretically (at M05-2X/6-311+G(d,p) level of theory) investigated for its ability to scavenge potentially, highly damaging hydroxyl radical. Free radical scavenging of cyanidin was studied through electron transfer mechanism – ET (the second step in SPLET mechanism) in water and ethanol, as solvents. Examination was performed using density functional theory (DFT) and Marcus theory. Based on the thermochemical and kinetic data, it is clear that O‒H group of cyanidin in position 3` is the most suitable for reaction with hydroxyl radical through mentioned antioxidant mechanism.",
journal = "21. Savetovanje o biotehnologiji sa međunarodnim učešćem, Čačak, 11.- 12. 03. 2016.",
title = "Examination of Electron Transfer Mechanism of Cyanidin",
url = "https://hdl.handle.net/21.15107/rcub_agrospace_5620"
}

Marković, Z., Milenković, D., Jeremić, S., Djorović, J.,& Dimitrić-Marković, J.. (2016). Examination of Electron Transfer Mechanism of Cyanidin. in 21. Savetovanje o biotehnologiji sa međunarodnim učešćem, Čačak, 11.- 12. 03. 2016..
https://hdl.handle.net/21.15107/rcub_agrospace_5620

Marković Z, Milenković D, Jeremić S, Djorović J, Dimitrić-Marković J. Examination of Electron Transfer Mechanism of Cyanidin. in 21. Savetovanje o biotehnologiji sa međunarodnim učešćem, Čačak, 11.- 12. 03. 2016.. 2016;.
https://hdl.handle.net/21.15107/rcub_agrospace_5620 .

Marković, Zoran, Milenković, Dejan, Jeremić, Svetlana, Djorović, Jelena, Dimitrić-Marković, Jasmina, "Examination of Electron Transfer Mechanism of Cyanidin" in 21. Savetovanje o biotehnologiji sa međunarodnim učešćem, Čačak, 11.- 12. 03. 2016. (2016),
https://hdl.handle.net/21.15107/rcub_agrospace_5620 .

TY  - CONF
AU  - Marković, Zoran
AU  - Jeremić, Svetlana
AU  - Milenković, Dejan
AU  - Djorović, Jelena
PY  - 2015
UR  - http://aspace.agrif.bg.ac.rs/handle/123456789/5591
AB  - Different metabolic processes as nus products form variety free radicals. Those radicals have damaging influence to people health, when they are formed in human bodies, or react as active components in reactions of nutrients decay. In this article are investigated mechanisms of radical scavenging activity of alizarin in reactions with •OH, •OOH and CH3OO• radicals. All results are obtained using DFT method. For calculations is used M06-2X functional in combination with 6-311++G(d,p) basis set. Lipid and aqueous environment are imitated. All conclusions are based on ΔH values, as thermodynamically indicator for anticipation of reaction pathway.
AB  - Tokom različitih metaboličkih procesa kao nus-produkti nastaju mnoštvo slobodnih radikala . Ovi radikali imaju štetan uticaj na zdravlje ljudi, ukoliko nastaju u čovekovom organizmu, ili reaguju kao aktivne komponente u reakcijama kvarenja hrane. U ovom radu su ispitani mehanizmi antiradikalske aktivnosti alizarina u reakcijama sa •OH, •OOH i CH3OO• radikalom. Svi rezultati dobijeni su primenom DFT metode. Za izračunavanja je korišćen M06-2X funkcional u kombinaciji sa 6-311++G(d,p) bazisnim skupom. Simulirano je lipidno i vodeno okruženje. Svi zaključci bazirani su na ΔH vrednostima, kao termodinamičkom indikatoru za predviđanje reakcionog puta.
C3  - 20. Savetovanje o biotehnologiji sa međunarodnim učešćem, Čačak, 13.- 14. 03. 2015.
T1  - Mechanisms of Atioxidative Reactions of Alizarin with Free Radicals
T1  - Mehanizmi antioksidativnih reakcija alizarina sa slobodnim radikalima
UR  - https://hdl.handle.net/21.15107/rcub_agrospace_5591
ER  - 

@conference{
author = "Marković, Zoran and Jeremić, Svetlana and Milenković, Dejan and Djorović, Jelena",
year = "2015",
abstract = "Different metabolic processes as nus products form variety free radicals. Those radicals have damaging influence to people health, when they are formed in human bodies, or react as active components in reactions of nutrients decay. In this article are investigated mechanisms of radical scavenging activity of alizarin in reactions with •OH, •OOH and CH3OO• radicals. All results are obtained using DFT method. For calculations is used M06-2X functional in combination with 6-311++G(d,p) basis set. Lipid and aqueous environment are imitated. All conclusions are based on ΔH values, as thermodynamically indicator for anticipation of reaction pathway., Tokom različitih metaboličkih procesa kao nus-produkti nastaju mnoštvo slobodnih radikala . Ovi radikali imaju štetan uticaj na zdravlje ljudi, ukoliko nastaju u čovekovom organizmu, ili reaguju kao aktivne komponente u reakcijama kvarenja hrane. U ovom radu su ispitani mehanizmi antiradikalske aktivnosti alizarina u reakcijama sa •OH, •OOH i CH3OO• radikalom. Svi rezultati dobijeni su primenom DFT metode. Za izračunavanja je korišćen M06-2X funkcional u kombinaciji sa 6-311++G(d,p) bazisnim skupom. Simulirano je lipidno i vodeno okruženje. Svi zaključci bazirani su na ΔH vrednostima, kao termodinamičkom indikatoru za predviđanje reakcionog puta.",
journal = "20. Savetovanje o biotehnologiji sa međunarodnim učešćem, Čačak, 13.- 14. 03. 2015.",
title = "Mechanisms of Atioxidative Reactions of Alizarin with Free Radicals, Mehanizmi antioksidativnih reakcija alizarina sa slobodnim radikalima",
url = "https://hdl.handle.net/21.15107/rcub_agrospace_5591"
}

Marković, Z., Jeremić, S., Milenković, D.,& Djorović, J.. (2015). Mechanisms of Atioxidative Reactions of Alizarin with Free Radicals. in 20. Savetovanje o biotehnologiji sa međunarodnim učešćem, Čačak, 13.- 14. 03. 2015..
https://hdl.handle.net/21.15107/rcub_agrospace_5591

Marković Z, Jeremić S, Milenković D, Djorović J. Mechanisms of Atioxidative Reactions of Alizarin with Free Radicals. in 20. Savetovanje o biotehnologiji sa međunarodnim učešćem, Čačak, 13.- 14. 03. 2015.. 2015;.
https://hdl.handle.net/21.15107/rcub_agrospace_5591 .

Marković, Zoran, Jeremić, Svetlana, Milenković, Dejan, Djorović, Jelena, "Mechanisms of Atioxidative Reactions of Alizarin with Free Radicals" in 20. Savetovanje o biotehnologiji sa međunarodnim učešćem, Čačak, 13.- 14. 03. 2015. (2015),
https://hdl.handle.net/21.15107/rcub_agrospace_5591 .

TY  - CONF
AU  - Marković, Zoran
AU  - Petrović, Zorica
AU  - Simijonović, Dusica
AU  - Petrović, Vladimir
AU  - Djorović, Jelena
PY  - 2015
UR  - http://aspace.agrif.bg.ac.rs/handle/123456789/5582
AB  - Ten hydroxyl-substituted Schiff bases with the different number and position of hydroxyl group on the two aromatic rings (A and B rings) was synthesized and have been under experimental and theoretical investigation of antioxidant activity. DPPH method was used for experimental examination of antioxidant activity, and DFT method for theoretical investigation in polar and non polar solvents.
AB  - Sintetisano je deset različitih hidroksi-supstituisanih Šifovih baza, koje imaju različit broj i položaj hidroksilnih grupa koje se nalaze na dva aromatična prstena (prsten A i B). Ispitana je njihova antioksidativna aktivnost, eksperimentalnim i teorijskim metodama. Za eksperimentalna ispitivanja antioksidativne aktivnosti korišćena je DPPH metoda, dok su teorijska ispitivanja u polarnim i nepolarnim rastvaračima urađena DFT metodom.
C3  - 20. Savetovanje o biotehnologiji sa međunarodnim učešćem, Čačak, 13.- 14. 03. 2015.
T1  - Antioxidant Activity of Some Schiff Bases: Experimental and Theoretical Study
T1  - Antioksidativna aktivnost nekih šifovih: eksperimentalna i teorijaska ispitivanja
UR  - https://hdl.handle.net/21.15107/rcub_agrospace_5582
ER  - 

@conference{
author = "Marković, Zoran and Petrović, Zorica and Simijonović, Dusica and Petrović, Vladimir and Djorović, Jelena",
year = "2015",
abstract = "Ten hydroxyl-substituted Schiff bases with the different number and position of hydroxyl group on the two aromatic rings (A and B rings) was synthesized and have been under experimental and theoretical investigation of antioxidant activity. DPPH method was used for experimental examination of antioxidant activity, and DFT method for theoretical investigation in polar and non polar solvents., Sintetisano je deset različitih hidroksi-supstituisanih Šifovih baza, koje imaju različit broj i položaj hidroksilnih grupa koje se nalaze na dva aromatična prstena (prsten A i B). Ispitana je njihova antioksidativna aktivnost, eksperimentalnim i teorijskim metodama. Za eksperimentalna ispitivanja antioksidativne aktivnosti korišćena je DPPH metoda, dok su teorijska ispitivanja u polarnim i nepolarnim rastvaračima urađena DFT metodom.",
journal = "20. Savetovanje o biotehnologiji sa međunarodnim učešćem, Čačak, 13.- 14. 03. 2015.",
title = "Antioxidant Activity of Some Schiff Bases: Experimental and Theoretical Study, Antioksidativna aktivnost nekih šifovih: eksperimentalna i teorijaska ispitivanja",
url = "https://hdl.handle.net/21.15107/rcub_agrospace_5582"
}

Marković, Z., Petrović, Z., Simijonović, D., Petrović, V.,& Djorović, J.. (2015). Antioxidant Activity of Some Schiff Bases: Experimental and Theoretical Study. in 20. Savetovanje o biotehnologiji sa međunarodnim učešćem, Čačak, 13.- 14. 03. 2015..
https://hdl.handle.net/21.15107/rcub_agrospace_5582

Marković Z, Petrović Z, Simijonović D, Petrović V, Djorović J. Antioxidant Activity of Some Schiff Bases: Experimental and Theoretical Study. in 20. Savetovanje o biotehnologiji sa međunarodnim učešćem, Čačak, 13.- 14. 03. 2015.. 2015;.
https://hdl.handle.net/21.15107/rcub_agrospace_5582 .

Marković, Zoran, Petrović, Zorica, Simijonović, Dusica, Petrović, Vladimir, Djorović, Jelena, "Antioxidant Activity of Some Schiff Bases: Experimental and Theoretical Study" in 20. Savetovanje o biotehnologiji sa međunarodnim učešćem, Čačak, 13.- 14. 03. 2015. (2015),
https://hdl.handle.net/21.15107/rcub_agrospace_5582 .