TY  - JOUR
AU  - Radosavljevic, Jasna Simonovic
AU  - Pristov, Jelena Bogdanovic
AU  - Mitrović, Aleksandra Lj.
AU  - Steinbach, Gabor
AU  - Mouille, Gregory
AU  - Tufegdžić, Srđan
AU  - Maksimović, Vuk
AU  - Mutavdzic, Dragosav
AU  - Janosevic, Dusica
AU  - Vuković, Marina
AU  - Garab, Gyozo
AU  - Radotić, Ksenija
PY  - 2018
UR  - https://cer.ihtm.bg.ac.rs/handle/123456789/2480
AB  - In the original publication of the article, one of the project numbers was omitted in the Acknowledgments. The correct version is provided below.
PB  - Springer, Dordrecht
T2  - Cellulose
T1  - Correction to: Parenchyma cell wall structure in twining stem of Dioscorea balcanica (vol 24, pg 4653, 2017)
VL  - 25
IS  - 4
SP  - 2767
EP  - 2767
DO  - 10.1007/s10570-018-1706-6
ER  - 

@article{
author = "Radosavljevic, Jasna Simonovic and Pristov, Jelena Bogdanovic and Mitrović, Aleksandra Lj. and Steinbach, Gabor and Mouille, Gregory and Tufegdžić, Srđan and Maksimović, Vuk and Mutavdzic, Dragosav and Janosevic, Dusica and Vuković, Marina and Garab, Gyozo and Radotić, Ksenija",
year = "2018",
abstract = "In the original publication of the article, one of the project numbers was omitted in the Acknowledgments. The correct version is provided below.",
publisher = "Springer, Dordrecht",
journal = "Cellulose",
title = "Correction to: Parenchyma cell wall structure in twining stem of Dioscorea balcanica (vol 24, pg 4653, 2017)",
volume = "25",
number = "4",
pages = "2767-2767",
doi = "10.1007/s10570-018-1706-6"
}

Radosavljevic, J. S., Pristov, J. B., Mitrović, A. Lj., Steinbach, G., Mouille, G., Tufegdžić, S., Maksimović, V., Mutavdzic, D., Janosevic, D., Vuković, M., Garab, G.,& Radotić, K.. (2018). Correction to: Parenchyma cell wall structure in twining stem of Dioscorea balcanica (vol 24, pg 4653, 2017). in Cellulose
Springer, Dordrecht., 25(4), 2767-2767.
https://doi.org/10.1007/s10570-018-1706-6

Radosavljevic JS, Pristov JB, Mitrović AL, Steinbach G, Mouille G, Tufegdžić S, Maksimović V, Mutavdzic D, Janosevic D, Vuković M, Garab G, Radotić K. Correction to: Parenchyma cell wall structure in twining stem of Dioscorea balcanica (vol 24, pg 4653, 2017). in Cellulose. 2018;25(4):2767-2767.
doi:10.1007/s10570-018-1706-6 .

Radosavljevic, Jasna Simonovic, Pristov, Jelena Bogdanovic, Mitrović, Aleksandra Lj., Steinbach, Gabor, Mouille, Gregory, Tufegdžić, Srđan, Maksimović, Vuk, Mutavdzic, Dragosav, Janosevic, Dusica, Vuković, Marina, Garab, Gyozo, Radotić, Ksenija, "Correction to: Parenchyma cell wall structure in twining stem of Dioscorea balcanica (vol 24, pg 4653, 2017)" in Cellulose, 25, no. 4 (2018):2767-2767,
https://doi.org/10.1007/s10570-018-1706-6 . .

TY  - JOUR
AU  - Anđelković, Uroš
AU  - Tufegdžić, Srđan
AU  - Popović, Milica
PY  - 2017
UR  - https://cer.ihtm.bg.ac.rs/handle/123456789/2122
AB  - The exclusive properties of monolithic supports enable fast mass transfer, high porosity, low back pressure, easy preparation process and miniaturisation, and the availability of different chemistries make them particularly suitable materials for high-throughput (HTP) protein and peptide separation. In this review recent advances in monolith-based chromatographic supports for HTP screening of protein and peptide samples are presented and their application in HTP sample preparation (separation, enrichment, depletion, proteolytic digestion) for HTP proteomics is discussed. Development and applications of different monolithic capillary columns in HTP MS-based bottom-up and top-down proteomics are overviewed. By discussing the chromatographic conditions and the mass spectrometric data acquisition conditions an attempt is made to present currently demonstrated capacities of monolithic capillary columns for HTP identification and quantification of proteins and peptides from complex biological samples by MS-based proteomics. Some recent advances in basic monolith technology of importance for proteomics are also discussed.
PB  - Wiley, Hoboken
T2  - Electrophoresis
T1  - Use of monolithic supports for high-throughput protein and peptide separation in proteomics
VL  - 38
IS  - 22-23
SP  - 2851
EP  - 2869
DO  - 10.1002/elps.201700260
ER  - 

@article{
author = "Anđelković, Uroš and Tufegdžić, Srđan and Popović, Milica",
year = "2017",
abstract = "The exclusive properties of monolithic supports enable fast mass transfer, high porosity, low back pressure, easy preparation process and miniaturisation, and the availability of different chemistries make them particularly suitable materials for high-throughput (HTP) protein and peptide separation. In this review recent advances in monolith-based chromatographic supports for HTP screening of protein and peptide samples are presented and their application in HTP sample preparation (separation, enrichment, depletion, proteolytic digestion) for HTP proteomics is discussed. Development and applications of different monolithic capillary columns in HTP MS-based bottom-up and top-down proteomics are overviewed. By discussing the chromatographic conditions and the mass spectrometric data acquisition conditions an attempt is made to present currently demonstrated capacities of monolithic capillary columns for HTP identification and quantification of proteins and peptides from complex biological samples by MS-based proteomics. Some recent advances in basic monolith technology of importance for proteomics are also discussed.",
publisher = "Wiley, Hoboken",
journal = "Electrophoresis",
title = "Use of monolithic supports for high-throughput protein and peptide separation in proteomics",
volume = "38",
number = "22-23",
pages = "2851-2869",
doi = "10.1002/elps.201700260"
}

Anđelković, U., Tufegdžić, S.,& Popović, M.. (2017). Use of monolithic supports for high-throughput protein and peptide separation in proteomics. in Electrophoresis
Wiley, Hoboken., 38(22-23), 2851-2869.
https://doi.org/10.1002/elps.201700260

Anđelković U, Tufegdžić S, Popović M. Use of monolithic supports for high-throughput protein and peptide separation in proteomics. in Electrophoresis. 2017;38(22-23):2851-2869.
doi:10.1002/elps.201700260 .

Anđelković, Uroš, Tufegdžić, Srđan, Popović, Milica, "Use of monolithic supports for high-throughput protein and peptide separation in proteomics" in Electrophoresis, 38, no. 22-23 (2017):2851-2869,
https://doi.org/10.1002/elps.201700260 . .

TY  - JOUR
AU  - Anđelković, Uroš
AU  - Tufegdžić, Srđan
AU  - Popović, Milica
PY  - 2017
UR  - https://cer.ihtm.bg.ac.rs/handle/123456789/2985
AB  - The exclusive properties of monolithic supports enable fast mass transfer, high porosity, low back pressure, easy preparation process and miniaturisation, and the availability of different chemistries make them particularly suitable materials for high-throughput (HTP) protein and peptide separation. In this review recent advances in monolith-based chromatographic supports for HTP screening of protein and peptide samples are presented and their application in HTP sample preparation (separation, enrichment, depletion, proteolytic digestion) for HTP proteomics is discussed. Development and applications of different monolithic capillary columns in HTP MS-based bottom-up and top-down proteomics are overviewed. By discussing the chromatographic conditions and the mass spectrometric data acquisition conditions an attempt is made to present currently demonstrated capacities of monolithic capillary columns for HTP identification and quantification of proteins and peptides from complex biological samples by MS-based proteomics. Some recent advances in basic monolith technology of importance for proteomics are also discussed.
PB  - Wiley, Hoboken
T2  - Electrophoresis
T1  - Use of monolithic supports for high-throughput protein and peptide separation in proteomics
VL  - 38
IS  - 22-23
SP  - 2851
EP  - 2869
DO  - 10.1002/elps.201700260
ER  - 

@article{
author = "Anđelković, Uroš and Tufegdžić, Srđan and Popović, Milica",
year = "2017",
abstract = "The exclusive properties of monolithic supports enable fast mass transfer, high porosity, low back pressure, easy preparation process and miniaturisation, and the availability of different chemistries make them particularly suitable materials for high-throughput (HTP) protein and peptide separation. In this review recent advances in monolith-based chromatographic supports for HTP screening of protein and peptide samples are presented and their application in HTP sample preparation (separation, enrichment, depletion, proteolytic digestion) for HTP proteomics is discussed. Development and applications of different monolithic capillary columns in HTP MS-based bottom-up and top-down proteomics are overviewed. By discussing the chromatographic conditions and the mass spectrometric data acquisition conditions an attempt is made to present currently demonstrated capacities of monolithic capillary columns for HTP identification and quantification of proteins and peptides from complex biological samples by MS-based proteomics. Some recent advances in basic monolith technology of importance for proteomics are also discussed.",
publisher = "Wiley, Hoboken",
journal = "Electrophoresis",
title = "Use of monolithic supports for high-throughput protein and peptide separation in proteomics",
volume = "38",
number = "22-23",
pages = "2851-2869",
doi = "10.1002/elps.201700260"
}

Anđelković, U., Tufegdžić, S.,& Popović, M.. (2017). Use of monolithic supports for high-throughput protein and peptide separation in proteomics. in Electrophoresis
Wiley, Hoboken., 38(22-23), 2851-2869.
https://doi.org/10.1002/elps.201700260

Anđelković U, Tufegdžić S, Popović M. Use of monolithic supports for high-throughput protein and peptide separation in proteomics. in Electrophoresis. 2017;38(22-23):2851-2869.
doi:10.1002/elps.201700260 .

Anđelković, Uroš, Tufegdžić, Srđan, Popović, Milica, "Use of monolithic supports for high-throughput protein and peptide separation in proteomics" in Electrophoresis, 38, no. 22-23 (2017):2851-2869,
https://doi.org/10.1002/elps.201700260 . .

TY  - JOUR
AU  - Radosavljevic, Jasna Simonovic
AU  - Pristov, Jelena Bogdanovic
AU  - Mitrović, Aleksandra Lj.
AU  - Steinbach, Gabor
AU  - Mouille, Gregory
AU  - Tufegdžić, Srđan
AU  - Maksimović, Vuk
AU  - Mutavdzic, Dragosav
AU  - Janosevic, Dusica
AU  - Vuković, Marina
AU  - Garab, Gyozo
AU  - Radotić, Ksenija
PY  - 2017
UR  - https://cer.ihtm.bg.ac.rs/handle/123456789/2090
AB  - Anatomical adaptation of liana plants includes structural changes in cell walls of different tissues: fibers, vessel elements and tracheids. However, the contribution of parenchyma cells to stem twining in liana plants is mostly unknown. The aim of this investigation is to determine changes in stem parenchyma cell walls that are correlated with the twinning process in liana plants. Parenchyma cell wall structure was studied on the stem cross sections of straight and twisted internodes of monocotyledonous liana Dioscorea balcanica, by different microscopy techniques: light microscopy, scanning electron microscopy, fluorescence detected linear dichroism microscopy and Fourier transform infrared microspectrometry. In addition, chemical analysis of the entire stem internodes was performed using photometric and chromatographic methods. Parenchyma cell walls of twisted D. balcanica internodes are characterized by: lower amounts of cellulose (obtained by FTIR microspectrometry) with different cellulose microfibril orientation (shown by Scanning electron microscopy), but no changes in "cellulose fibril order" (obtained by Differential polarization laser scanning microscopy); lower amounts of xyloglucan, higher amounts of xylan, higher amounts of lignin with modified organization-less condensed lignin (obtained by FTIR microspectrometry). At the same time, chemical analysis of the entire internodes did not show significant differences in lignin content and cell wall bound phenols related to stem twining, except for the presence of diferulate cross-links exclusively in twisted internodes. Our results indicate that adaptations to mechanical strain in D. balcanica stems involve modifications in parenchyma cell wall structure and chemistry, which provide decreased stiffness, higher strength and increased elasticity of twisted internodes.
PB  - Springer, Dordrecht
T2  - Cellulose
T1  - Parenchyma cell wall structure in twining stem of Dioscorea balcanica
VL  - 24
IS  - 11
SP  - 4653
EP  - 4669
DO  - 10.1007/s10570-017-1460-1
ER  - 

@article{
author = "Radosavljevic, Jasna Simonovic and Pristov, Jelena Bogdanovic and Mitrović, Aleksandra Lj. and Steinbach, Gabor and Mouille, Gregory and Tufegdžić, Srđan and Maksimović, Vuk and Mutavdzic, Dragosav and Janosevic, Dusica and Vuković, Marina and Garab, Gyozo and Radotić, Ksenija",
year = "2017",
abstract = "Anatomical adaptation of liana plants includes structural changes in cell walls of different tissues: fibers, vessel elements and tracheids. However, the contribution of parenchyma cells to stem twining in liana plants is mostly unknown. The aim of this investigation is to determine changes in stem parenchyma cell walls that are correlated with the twinning process in liana plants. Parenchyma cell wall structure was studied on the stem cross sections of straight and twisted internodes of monocotyledonous liana Dioscorea balcanica, by different microscopy techniques: light microscopy, scanning electron microscopy, fluorescence detected linear dichroism microscopy and Fourier transform infrared microspectrometry. In addition, chemical analysis of the entire stem internodes was performed using photometric and chromatographic methods. Parenchyma cell walls of twisted D. balcanica internodes are characterized by: lower amounts of cellulose (obtained by FTIR microspectrometry) with different cellulose microfibril orientation (shown by Scanning electron microscopy), but no changes in "cellulose fibril order" (obtained by Differential polarization laser scanning microscopy); lower amounts of xyloglucan, higher amounts of xylan, higher amounts of lignin with modified organization-less condensed lignin (obtained by FTIR microspectrometry). At the same time, chemical analysis of the entire internodes did not show significant differences in lignin content and cell wall bound phenols related to stem twining, except for the presence of diferulate cross-links exclusively in twisted internodes. Our results indicate that adaptations to mechanical strain in D. balcanica stems involve modifications in parenchyma cell wall structure and chemistry, which provide decreased stiffness, higher strength and increased elasticity of twisted internodes.",
publisher = "Springer, Dordrecht",
journal = "Cellulose",
title = "Parenchyma cell wall structure in twining stem of Dioscorea balcanica",
volume = "24",
number = "11",
pages = "4653-4669",
doi = "10.1007/s10570-017-1460-1"
}

Radosavljevic, J. S., Pristov, J. B., Mitrović, A. Lj., Steinbach, G., Mouille, G., Tufegdžić, S., Maksimović, V., Mutavdzic, D., Janosevic, D., Vuković, M., Garab, G.,& Radotić, K.. (2017). Parenchyma cell wall structure in twining stem of Dioscorea balcanica. in Cellulose
Springer, Dordrecht., 24(11), 4653-4669.
https://doi.org/10.1007/s10570-017-1460-1

Radosavljevic JS, Pristov JB, Mitrović AL, Steinbach G, Mouille G, Tufegdžić S, Maksimović V, Mutavdzic D, Janosevic D, Vuković M, Garab G, Radotić K. Parenchyma cell wall structure in twining stem of Dioscorea balcanica. in Cellulose. 2017;24(11):4653-4669.
doi:10.1007/s10570-017-1460-1 .

Radosavljevic, Jasna Simonovic, Pristov, Jelena Bogdanovic, Mitrović, Aleksandra Lj., Steinbach, Gabor, Mouille, Gregory, Tufegdžić, Srđan, Maksimović, Vuk, Mutavdzic, Dragosav, Janosevic, Dusica, Vuković, Marina, Garab, Gyozo, Radotić, Ksenija, "Parenchyma cell wall structure in twining stem of Dioscorea balcanica" in Cellulose, 24, no. 11 (2017):4653-4669,
https://doi.org/10.1007/s10570-017-1460-1 . .

TY  - JOUR
AU  - Vilipić, Jovana P.
AU  - Novaković, Irena
AU  - Zlatović, Mario
AU  - Vujčić, Miroslava
AU  - Tufegdžić, Srđan
AU  - Sladić, Dušan
PY  - 2016
UR  - https://cer.ihtm.bg.ac.rs/handle/123456789/2049
AB  - The interactions of nine amino acid derivatives of tert-butylquinone with biomacromolecules were studied. Sodium dodecyl sulphate (SDS) gel electrophoresis and mass spectrometry confirmed the absence of modifications of lysozyme by any of the synthesized compounds. Spectrophotometric studies demonstrated hyperchromism, i.e., the existence of interactions between the quinones and calf thymus DNA (CT-DNA). Determination of the binding constants by absorption titration indicated weak interactions between the quinone derivatives and CT-DNA. The quenching of fluorescence of the intercalator ethidium bromide (EB) from the EB-CT-DNA system and of the minor groove binder Hoechst 33258 (H) from the H-CT-DNA system by the synthesized derivatives indicated interactions of the compounds and CT-DNA. Circular dichroism (CD) spectra demonstrated a non-intercalative binding mode of the quinone derivatives to CT-DNA. Molecular docking results confirmed binding to the minor groove. The electrophoretic pattern showed no cleavage of the pUC19 plasmid in the presence of any of the synthesized compounds. The ability of the derivatives to scavenge radicals was confirmed by the 2,2-diphenyl-1-picrylhydrazyl (DPPH) test. All the presented results suggest that the DNA minor groove binding is the principal mechanism of action of the examined amino acid derivatives.
PB  - Serbian Chemical Soc, Belgrade
T2  - Journal of the Serbian Chemical Society
T1  - Interactions of cytotoxic amino acid derivatives of tert-butylquinone with DNA and lysozyme
VL  - 81
IS  - 12
SP  - 1345
EP  - 1358
DO  - 10.2298/JSC160725101V
ER  - 

@article{
author = "Vilipić, Jovana P. and Novaković, Irena and Zlatović, Mario and Vujčić, Miroslava and Tufegdžić, Srđan and Sladić, Dušan",
year = "2016",
abstract = "The interactions of nine amino acid derivatives of tert-butylquinone with biomacromolecules were studied. Sodium dodecyl sulphate (SDS) gel electrophoresis and mass spectrometry confirmed the absence of modifications of lysozyme by any of the synthesized compounds. Spectrophotometric studies demonstrated hyperchromism, i.e., the existence of interactions between the quinones and calf thymus DNA (CT-DNA). Determination of the binding constants by absorption titration indicated weak interactions between the quinone derivatives and CT-DNA. The quenching of fluorescence of the intercalator ethidium bromide (EB) from the EB-CT-DNA system and of the minor groove binder Hoechst 33258 (H) from the H-CT-DNA system by the synthesized derivatives indicated interactions of the compounds and CT-DNA. Circular dichroism (CD) spectra demonstrated a non-intercalative binding mode of the quinone derivatives to CT-DNA. Molecular docking results confirmed binding to the minor groove. The electrophoretic pattern showed no cleavage of the pUC19 plasmid in the presence of any of the synthesized compounds. The ability of the derivatives to scavenge radicals was confirmed by the 2,2-diphenyl-1-picrylhydrazyl (DPPH) test. All the presented results suggest that the DNA minor groove binding is the principal mechanism of action of the examined amino acid derivatives.",
publisher = "Serbian Chemical Soc, Belgrade",
journal = "Journal of the Serbian Chemical Society",
title = "Interactions of cytotoxic amino acid derivatives of tert-butylquinone with DNA and lysozyme",
volume = "81",
number = "12",
pages = "1345-1358",
doi = "10.2298/JSC160725101V"
}

Vilipić, J. P., Novaković, I., Zlatović, M., Vujčić, M., Tufegdžić, S.,& Sladić, D.. (2016). Interactions of cytotoxic amino acid derivatives of tert-butylquinone with DNA and lysozyme. in Journal of the Serbian Chemical Society
Serbian Chemical Soc, Belgrade., 81(12), 1345-1358.
https://doi.org/10.2298/JSC160725101V

Vilipić JP, Novaković I, Zlatović M, Vujčić M, Tufegdžić S, Sladić D. Interactions of cytotoxic amino acid derivatives of tert-butylquinone with DNA and lysozyme. in Journal of the Serbian Chemical Society. 2016;81(12):1345-1358.
doi:10.2298/JSC160725101V .

Vilipić, Jovana P., Novaković, Irena, Zlatović, Mario, Vujčić, Miroslava, Tufegdžić, Srđan, Sladić, Dušan, "Interactions of cytotoxic amino acid derivatives of tert-butylquinone with DNA and lysozyme" in Journal of the Serbian Chemical Society, 81, no. 12 (2016):1345-1358,
https://doi.org/10.2298/JSC160725101V . .

TY  - CONF
AU  - Anđelković, Uroš
AU  - Pajic, I.
AU  - Vizovisek, M.
AU  - Vidmar, R.
AU  - Prislan, I.
AU  - Tufegdžić, Srđan
AU  - Fonovic, M.
AU  - Lah, Jurij
AU  - Turk, B.
AU  - Sladić, Dušan
PY  - 2013
UR  - https://cer.ihtm.bg.ac.rs/handle/123456789/1302
PB  - Wiley-Blackwell, Hoboken
C3  - FEBS Journal
T1  - A new lectin from coral Gerardia savaglia: purification, physico-chemical characterization and thermodynamics of saccharide binding
VL  - 280 (Supp. 1)
SP  - 531
EP  - 531
UR  - https://hdl.handle.net/21.15107/rcub_cherry_1419
ER  - 

@conference{
author = "Anđelković, Uroš and Pajic, I. and Vizovisek, M. and Vidmar, R. and Prislan, I. and Tufegdžić, Srđan and Fonovic, M. and Lah, Jurij and Turk, B. and Sladić, Dušan",
year = "2013",
publisher = "Wiley-Blackwell, Hoboken",
journal = "FEBS Journal",
title = "A new lectin from coral Gerardia savaglia: purification, physico-chemical characterization and thermodynamics of saccharide binding",
volume = "280 (Supp. 1)",
pages = "531-531",
url = "https://hdl.handle.net/21.15107/rcub_cherry_1419"
}

Anđelković, U., Pajic, I., Vizovisek, M., Vidmar, R., Prislan, I., Tufegdžić, S., Fonovic, M., Lah, J., Turk, B.,& Sladić, D.. (2013). A new lectin from coral Gerardia savaglia: purification, physico-chemical characterization and thermodynamics of saccharide binding. in FEBS Journal
Wiley-Blackwell, Hoboken., 280 (Supp. 1), 531-531.
https://hdl.handle.net/21.15107/rcub_cherry_1419

Anđelković U, Pajic I, Vizovisek M, Vidmar R, Prislan I, Tufegdžić S, Fonovic M, Lah J, Turk B, Sladić D. A new lectin from coral Gerardia savaglia: purification, physico-chemical characterization and thermodynamics of saccharide binding. in FEBS Journal. 2013;280 (Supp. 1):531-531.
https://hdl.handle.net/21.15107/rcub_cherry_1419 .

Anđelković, Uroš, Pajic, I., Vizovisek, M., Vidmar, R., Prislan, I., Tufegdžić, Srđan, Fonovic, M., Lah, Jurij, Turk, B., Sladić, Dušan, "A new lectin from coral Gerardia savaglia: purification, physico-chemical characterization and thermodynamics of saccharide binding" in FEBS Journal, 280 (Supp. 1) (2013):531-531,
https://hdl.handle.net/21.15107/rcub_cherry_1419 .

TY  - JOUR
AU  - Vujčić, Miroslava
AU  - Tufegdžić, Srđan
AU  - Novaković, Irena
AU  - Djikanovic, Daniela
AU  - Gašić, Miroslav J.
AU  - Sladić, Dušan
PY  - 2013
UR  - https://cer.ihtm.bg.ac.rs/handle/123456789/1237
AB  - The interactions of avarone, a quinone from the marine sponge Dysideaavara, and the methylamino derivatives of avarone (2), 3'-(methylamino)avarone (3) and 4'-(methylamino)avarone (4) with calf thymus DNA (CT-DNA) were studied. Agarose gel electrophoreticanalysis showed that binding of the quinones quenched fluorescence of ethidium bromide (EB). The extent of fluorescence quenching of intercalator EB by competitive displacement from EB-CT-DNA system and of groove binder Hoechst 33258 (H) from H-CT-DNA system with the quinones was analyzed by fluorescence spectroscopy. The obtained results demonstrated that the quinones reduced binding of both the intercalator EB and the minor groove binder H, indicating possible degradation of DNA. The substituent on the quinone moiety determined the extent of DNA damaging effect of the quinone, which was the most extensive with 3'-(methylamino)avarone and the least extensive with its regioisomer 4'-(methylamino)avarone. The results were confirmed by the observed hyperchromic effects in UV-visible spectra measured after interactions of the derivatives with CT-DNA.
PB  - Elsevier
T2  - International Journal of Biological Macromolecules
T1  - Studies on the interactions of bioactive quinone avarone and its methylamino derivatives with calf thymus DNA
VL  - 62
SP  - 405
EP  - 410
DO  - 10.1016/j.ijbiomac.2013.09.013
ER  - 

@article{
author = "Vujčić, Miroslava and Tufegdžić, Srđan and Novaković, Irena and Djikanovic, Daniela and Gašić, Miroslav J. and Sladić, Dušan",
year = "2013",
abstract = "The interactions of avarone, a quinone from the marine sponge Dysideaavara, and the methylamino derivatives of avarone (2), 3'-(methylamino)avarone (3) and 4'-(methylamino)avarone (4) with calf thymus DNA (CT-DNA) were studied. Agarose gel electrophoreticanalysis showed that binding of the quinones quenched fluorescence of ethidium bromide (EB). The extent of fluorescence quenching of intercalator EB by competitive displacement from EB-CT-DNA system and of groove binder Hoechst 33258 (H) from H-CT-DNA system with the quinones was analyzed by fluorescence spectroscopy. The obtained results demonstrated that the quinones reduced binding of both the intercalator EB and the minor groove binder H, indicating possible degradation of DNA. The substituent on the quinone moiety determined the extent of DNA damaging effect of the quinone, which was the most extensive with 3'-(methylamino)avarone and the least extensive with its regioisomer 4'-(methylamino)avarone. The results were confirmed by the observed hyperchromic effects in UV-visible spectra measured after interactions of the derivatives with CT-DNA.",
publisher = "Elsevier",
journal = "International Journal of Biological Macromolecules",
title = "Studies on the interactions of bioactive quinone avarone and its methylamino derivatives with calf thymus DNA",
volume = "62",
pages = "405-410",
doi = "10.1016/j.ijbiomac.2013.09.013"
}

Vujčić, M., Tufegdžić, S., Novaković, I., Djikanovic, D., Gašić, M. J.,& Sladić, D.. (2013). Studies on the interactions of bioactive quinone avarone and its methylamino derivatives with calf thymus DNA. in International Journal of Biological Macromolecules
Elsevier., 62, 405-410.
https://doi.org/10.1016/j.ijbiomac.2013.09.013

Vujčić M, Tufegdžić S, Novaković I, Djikanovic D, Gašić MJ, Sladić D. Studies on the interactions of bioactive quinone avarone and its methylamino derivatives with calf thymus DNA. in International Journal of Biological Macromolecules. 2013;62:405-410.
doi:10.1016/j.ijbiomac.2013.09.013 .

Vujčić, Miroslava, Tufegdžić, Srđan, Novaković, Irena, Djikanovic, Daniela, Gašić, Miroslav J., Sladić, Dušan, "Studies on the interactions of bioactive quinone avarone and its methylamino derivatives with calf thymus DNA" in International Journal of Biological Macromolecules, 62 (2013):405-410,
https://doi.org/10.1016/j.ijbiomac.2013.09.013 . .

TY  - JOUR
AU  - Filipovic, Nenad
AU  - Todorović, Tamara
AU  - Marković, Rade
AU  - Marinković, Aleksandar D.
AU  - Tufegdžić, Srđan
AU  - Gođevac, Dejan
AU  - Anđelković, Katarina
PY  - 2010
UR  - https://cer.ihtm.bg.ac.rs/handle/123456789/662
AB  - Condensation derivatives of ethyl hydrazinoacetate with 2-formylpyridine and quinoline-2-carboxaldehyde were synthesized. Pd(II), Pt(II) and Cd(II) complexes with the 2-formylpyridine derivative and a Cd(II) complex with the quinoline-2-carboxaldehyde derivative were synthesized and characterized by spectroscopic techniques. In the complexes, both ligands are coordinated in neutral NN bidentate modes, while the remaining two coordination sites are occupied by chloride. All compounds showed biological activity when tested against Escherichia coli, Bacillus subtilis and Staphylococcus aureus.
PB  - Springer, Dordrecht
T2  - Transition Metal Chemistry
T1  - Synthesis, characterization and biological activities of N-heteroaromatic hydrazones and their complexes with Pd(II), Pt(II) and Cd(II)
VL  - 35
IS  - 6
SP  - 765
EP  - 772
DO  - 10.1007/s11243-010-9391-9
ER  - 

@article{
author = "Filipovic, Nenad and Todorović, Tamara and Marković, Rade and Marinković, Aleksandar D. and Tufegdžić, Srđan and Gođevac, Dejan and Anđelković, Katarina",
year = "2010",
abstract = "Condensation derivatives of ethyl hydrazinoacetate with 2-formylpyridine and quinoline-2-carboxaldehyde were synthesized. Pd(II), Pt(II) and Cd(II) complexes with the 2-formylpyridine derivative and a Cd(II) complex with the quinoline-2-carboxaldehyde derivative were synthesized and characterized by spectroscopic techniques. In the complexes, both ligands are coordinated in neutral NN bidentate modes, while the remaining two coordination sites are occupied by chloride. All compounds showed biological activity when tested against Escherichia coli, Bacillus subtilis and Staphylococcus aureus.",
publisher = "Springer, Dordrecht",
journal = "Transition Metal Chemistry",
title = "Synthesis, characterization and biological activities of N-heteroaromatic hydrazones and their complexes with Pd(II), Pt(II) and Cd(II)",
volume = "35",
number = "6",
pages = "765-772",
doi = "10.1007/s11243-010-9391-9"
}

Filipovic, N., Todorović, T., Marković, R., Marinković, A. D., Tufegdžić, S., Gođevac, D.,& Anđelković, K.. (2010). Synthesis, characterization and biological activities of N-heteroaromatic hydrazones and their complexes with Pd(II), Pt(II) and Cd(II). in Transition Metal Chemistry
Springer, Dordrecht., 35(6), 765-772.
https://doi.org/10.1007/s11243-010-9391-9

Filipovic N, Todorović T, Marković R, Marinković AD, Tufegdžić S, Gođevac D, Anđelković K. Synthesis, characterization and biological activities of N-heteroaromatic hydrazones and their complexes with Pd(II), Pt(II) and Cd(II). in Transition Metal Chemistry. 2010;35(6):765-772.
doi:10.1007/s11243-010-9391-9 .

Filipovic, Nenad, Todorović, Tamara, Marković, Rade, Marinković, Aleksandar D., Tufegdžić, Srđan, Gođevac, Dejan, Anđelković, Katarina, "Synthesis, characterization and biological activities of N-heteroaromatic hydrazones and their complexes with Pd(II), Pt(II) and Cd(II)" in Transition Metal Chemistry, 35, no. 6 (2010):765-772,
https://doi.org/10.1007/s11243-010-9391-9 . .

TY  - JOUR
AU  - Božić, Tatjana T.
AU  - Novaković, Irena
AU  - Gašić, Miroslav J.
AU  - Juranić, Zorica
AU  - Stanojković, Tatjana
AU  - Tufegdžić, Srđan
AU  - Kljajić, Zoran
AU  - Sladić, Dušan
PY  - 2010
UR  - https://cer.ihtm.bg.ac.rs/handle/123456789/730
AB  - Nine alkyl(aryl)thio derivatives of the marine sesquiterpene quinone avarone were synthesized by nucleophilic addition of thiols or thiophenol to avarone. In most cases only one regioisomer was obtained. Their cytotoxic activities, brine shrimp lethality and antibacterial activity were evaluated, as well as those of some previously synthesized avarone derivatives. Anti-HIV activity of two derivatives was tested. Electrochemical properties were determined for all the derivatives in Order to obtain more accurate information on structure-activity relationships. Most derivatives showed cytotoxic activity against tumor cell lines, with IC50 values less than 10 mu M for some of them, in particular those with electron-donating substituents. The most active Compound was 4'-(methylamino)avarone, with IC50 value of 2.4 mu M to melanoma Fem-X cells, and no cytotoxicity to normal lymphocytes.
PB  - Elsevier France-Editions Scientifiques Medicales Elsevier, Paris
T2  - European Journal of Medicinal Chemistry
T1  - Synthesis and biological activity of derivatives of the marine quinone avarone
VL  - 45
IS  - 3
SP  - 923
EP  - 929
DO  - 10.1016/j.ejmech.2009.11.033
ER  - 

@article{
author = "Božić, Tatjana T. and Novaković, Irena and Gašić, Miroslav J. and Juranić, Zorica and Stanojković, Tatjana and Tufegdžić, Srđan and Kljajić, Zoran and Sladić, Dušan",
year = "2010",
abstract = "Nine alkyl(aryl)thio derivatives of the marine sesquiterpene quinone avarone were synthesized by nucleophilic addition of thiols or thiophenol to avarone. In most cases only one regioisomer was obtained. Their cytotoxic activities, brine shrimp lethality and antibacterial activity were evaluated, as well as those of some previously synthesized avarone derivatives. Anti-HIV activity of two derivatives was tested. Electrochemical properties were determined for all the derivatives in Order to obtain more accurate information on structure-activity relationships. Most derivatives showed cytotoxic activity against tumor cell lines, with IC50 values less than 10 mu M for some of them, in particular those with electron-donating substituents. The most active Compound was 4'-(methylamino)avarone, with IC50 value of 2.4 mu M to melanoma Fem-X cells, and no cytotoxicity to normal lymphocytes.",
publisher = "Elsevier France-Editions Scientifiques Medicales Elsevier, Paris",
journal = "European Journal of Medicinal Chemistry",
title = "Synthesis and biological activity of derivatives of the marine quinone avarone",
volume = "45",
number = "3",
pages = "923-929",
doi = "10.1016/j.ejmech.2009.11.033"
}

Božić, T. T., Novaković, I., Gašić, M. J., Juranić, Z., Stanojković, T., Tufegdžić, S., Kljajić, Z.,& Sladić, D.. (2010). Synthesis and biological activity of derivatives of the marine quinone avarone. in European Journal of Medicinal Chemistry
Elsevier France-Editions Scientifiques Medicales Elsevier, Paris., 45(3), 923-929.
https://doi.org/10.1016/j.ejmech.2009.11.033

Božić TT, Novaković I, Gašić MJ, Juranić Z, Stanojković T, Tufegdžić S, Kljajić Z, Sladić D. Synthesis and biological activity of derivatives of the marine quinone avarone. in European Journal of Medicinal Chemistry. 2010;45(3):923-929.
doi:10.1016/j.ejmech.2009.11.033 .

Božić, Tatjana T., Novaković, Irena, Gašić, Miroslav J., Juranić, Zorica, Stanojković, Tatjana, Tufegdžić, Srđan, Kljajić, Zoran, Sladić, Dušan, "Synthesis and biological activity of derivatives of the marine quinone avarone" in European Journal of Medicinal Chemistry, 45, no. 3 (2010):923-929,
https://doi.org/10.1016/j.ejmech.2009.11.033 . .

TY  - JOUR
AU  - Harhaji-Trajković, Ljubica
AU  - Mijatović, Sanja
AU  - Maksimović-Ivanić, Danijela D.
AU  - Stojanovic, I.D.
AU  - Momcilovic, M.B.
AU  - Tufegdžić, Srđan
AU  - Maksimović, Vesna M.
AU  - Marjanovi, Z.S.
AU  - Stosic-Grujicic, S.D.
PY  - 2009
UR  - https://cer.ihtm.bg.ac.rs/handle/123456789/616
AB  - Anticancer activities of various extracts of the medicinal mushroom, Ganoderma lucidum, have been widely demonstrated and are mainly associated with the presence of different bioactive polysaccharides and triterpenoids. We have evaluated and compared in vitro and in vivo the antitumor effects of two preparations from Ganoderma lucidum: a methanol extract containing total terpenoids (GLme) and a purified methanol extract containing mainly acidic terpenoids (GLpme). Both extracts inhibited tumor growth of B16 mouse melanoma cells inoculated subcutaneously into syngeneic C57BL/6 mice and reduced viability of B16 cells in vitro, whereby GLme exhibited stronger effect. Furthermore, anticancer activity of GLme was demonstrated for the first time against two other rodent tumor cell lines, L929-mouse fibrosarcoma and C6-rat astrocytoma. The mechanism of antitumor activity of GLme comprised inhibition of cell proliferation and induction of caspase-dependent apoptotic cell death mediated by upregulated p53 and inhibited Bcl-2 expression. Moreover, the antitumor effect of the GLme was associated with intensified production of reactive oxygen species, whereas their neutralization by the antioxidant, N-acetyl cysteine, resulted in partial recovery of cell viability. Thus, our results suggest that GLme might be a good candidate for treatment of diverse forms of cancers.
T2  - Nutrition and Cancer
T1  - Anticancer properties of ganoderma lucidum methanol extracts in vitro and in vivo
VL  - 61
IS  - 5
SP  - 696
EP  - 707
DO  - 10.1080/01635580902898743
ER  - 

@article{
author = "Harhaji-Trajković, Ljubica and Mijatović, Sanja and Maksimović-Ivanić, Danijela D. and Stojanovic, I.D. and Momcilovic, M.B. and Tufegdžić, Srđan and Maksimović, Vesna M. and Marjanovi, Z.S. and Stosic-Grujicic, S.D.",
year = "2009",
abstract = "Anticancer activities of various extracts of the medicinal mushroom, Ganoderma lucidum, have been widely demonstrated and are mainly associated with the presence of different bioactive polysaccharides and triterpenoids. We have evaluated and compared in vitro and in vivo the antitumor effects of two preparations from Ganoderma lucidum: a methanol extract containing total terpenoids (GLme) and a purified methanol extract containing mainly acidic terpenoids (GLpme). Both extracts inhibited tumor growth of B16 mouse melanoma cells inoculated subcutaneously into syngeneic C57BL/6 mice and reduced viability of B16 cells in vitro, whereby GLme exhibited stronger effect. Furthermore, anticancer activity of GLme was demonstrated for the first time against two other rodent tumor cell lines, L929-mouse fibrosarcoma and C6-rat astrocytoma. The mechanism of antitumor activity of GLme comprised inhibition of cell proliferation and induction of caspase-dependent apoptotic cell death mediated by upregulated p53 and inhibited Bcl-2 expression. Moreover, the antitumor effect of the GLme was associated with intensified production of reactive oxygen species, whereas their neutralization by the antioxidant, N-acetyl cysteine, resulted in partial recovery of cell viability. Thus, our results suggest that GLme might be a good candidate for treatment of diverse forms of cancers.",
journal = "Nutrition and Cancer",
title = "Anticancer properties of ganoderma lucidum methanol extracts in vitro and in vivo",
volume = "61",
number = "5",
pages = "696-707",
doi = "10.1080/01635580902898743"
}

Harhaji-Trajković, L., Mijatović, S., Maksimović-Ivanić, D. D., Stojanovic, I.D., Momcilovic, M.B., Tufegdžić, S., Maksimović, V. M., Marjanovi, Z.S.,& Stosic-Grujicic, S.D.. (2009). Anticancer properties of ganoderma lucidum methanol extracts in vitro and in vivo. in Nutrition and Cancer, 61(5), 696-707.
https://doi.org/10.1080/01635580902898743

Harhaji-Trajković L, Mijatović S, Maksimović-Ivanić DD, Stojanovic I, Momcilovic M, Tufegdžić S, Maksimović VM, Marjanovi Z, Stosic-Grujicic S. Anticancer properties of ganoderma lucidum methanol extracts in vitro and in vivo. in Nutrition and Cancer. 2009;61(5):696-707.
doi:10.1080/01635580902898743 .

Harhaji-Trajković, Ljubica, Mijatović, Sanja, Maksimović-Ivanić, Danijela D., Stojanovic, I.D., Momcilovic, M.B., Tufegdžić, Srđan, Maksimović, Vesna M., Marjanovi, Z.S., Stosic-Grujicic, S.D., "Anticancer properties of ganoderma lucidum methanol extracts in vitro and in vivo" in Nutrition and Cancer, 61, no. 5 (2009):696-707,
https://doi.org/10.1080/01635580902898743 . .

TY  - JOUR
AU  - Tsoukatou, M.
AU  - Maréchal, J.P.
AU  - Hellio, C.
AU  - Novaković, Irena
AU  - Tufegdžić, Srđan
AU  - Sladić, Dušan
AU  - Gašić, Miroslav J.
AU  - Clare, A.S.
AU  - Vagias, C.
AU  - Roussis, V.
PY  - 2007
UR  - https://cer.ihtm.bg.ac.rs/handle/123456789/359
AB  - The sesquiterpene hydroquinone avarol (1) was isolated from the marine sponge Dysidea avara, whereas the corresponding quinone, avarone (2), was obtained by oxidation of avarol, and the significantly more lipophilic compounds [3′-(p-chlorophenyl) avarone (3), 3′,4′-ethylenedithioavarone (4), 4′-isopropylthioavarone (5), 4′-tert-butylthioavarone (6), 4′-propylthioavarone (7), 4′-octylthioavarone (8)] were obtained by nucleophilic addition of thiols or p-chloroaniline to avarone. All these compounds were tested, at concentrations ranging from 0.5 to 50 μg/mL, for their effect on the settlement of the cyprid stage of Balanus amphitrite, for toxicity to both nauplii and cyprids and for their growth inhibitory activity on marine bacteria (Cobetia marina, Marinobacterium stanieri, Vibrio fischeri and Pseudoalteromonas haloplanktis) and marine fungi (Halosphaeriopsis mediosetigera, Asteromyces cruciatus, Lulworthia uniseptata and Monodictys pelagica).
PB  - MDPI
T2  - Molecules
T1  - Evaluation of the activity of the sponge metabolites avarol and avarone and their synthetic derivatives against fouling micro- and macroorganisms
VL  - 12
IS  - 5
SP  - 1022
EP  - 1034
DO  - 10.3390/12051022
ER  - 

@article{
author = "Tsoukatou, M. and Maréchal, J.P. and Hellio, C. and Novaković, Irena and Tufegdžić, Srđan and Sladić, Dušan and Gašić, Miroslav J. and Clare, A.S. and Vagias, C. and Roussis, V.",
year = "2007",
abstract = "The sesquiterpene hydroquinone avarol (1) was isolated from the marine sponge Dysidea avara, whereas the corresponding quinone, avarone (2), was obtained by oxidation of avarol, and the significantly more lipophilic compounds [3′-(p-chlorophenyl) avarone (3), 3′,4′-ethylenedithioavarone (4), 4′-isopropylthioavarone (5), 4′-tert-butylthioavarone (6), 4′-propylthioavarone (7), 4′-octylthioavarone (8)] were obtained by nucleophilic addition of thiols or p-chloroaniline to avarone. All these compounds were tested, at concentrations ranging from 0.5 to 50 μg/mL, for their effect on the settlement of the cyprid stage of Balanus amphitrite, for toxicity to both nauplii and cyprids and for their growth inhibitory activity on marine bacteria (Cobetia marina, Marinobacterium stanieri, Vibrio fischeri and Pseudoalteromonas haloplanktis) and marine fungi (Halosphaeriopsis mediosetigera, Asteromyces cruciatus, Lulworthia uniseptata and Monodictys pelagica).",
publisher = "MDPI",
journal = "Molecules",
title = "Evaluation of the activity of the sponge metabolites avarol and avarone and their synthetic derivatives against fouling micro- and macroorganisms",
volume = "12",
number = "5",
pages = "1022-1034",
doi = "10.3390/12051022"
}

Tsoukatou, M., Maréchal, J.P., Hellio, C., Novaković, I., Tufegdžić, S., Sladić, D., Gašić, M. J., Clare, A.S., Vagias, C.,& Roussis, V.. (2007). Evaluation of the activity of the sponge metabolites avarol and avarone and their synthetic derivatives against fouling micro- and macroorganisms. in Molecules
MDPI., 12(5), 1022-1034.
https://doi.org/10.3390/12051022

Tsoukatou M, Maréchal J, Hellio C, Novaković I, Tufegdžić S, Sladić D, Gašić MJ, Clare A, Vagias C, Roussis V. Evaluation of the activity of the sponge metabolites avarol and avarone and their synthetic derivatives against fouling micro- and macroorganisms. in Molecules. 2007;12(5):1022-1034.
doi:10.3390/12051022 .

Tsoukatou, M., Maréchal, J.P., Hellio, C., Novaković, Irena, Tufegdžić, Srđan, Sladić, Dušan, Gašić, Miroslav J., Clare, A.S., Vagias, C., Roussis, V., "Evaluation of the activity of the sponge metabolites avarol and avarone and their synthetic derivatives against fouling micro- and macroorganisms" in Molecules, 12, no. 5 (2007):1022-1034,
https://doi.org/10.3390/12051022 . .

TY  - JOUR
AU  - Vujčić, Miroslava
AU  - Tufegdžić, Srđan
AU  - Vujčić, Zoran
AU  - Gašić, Miroslav J.
AU  - Sladić, Dušan
PY  - 2007
UR  - https://cer.ihtm.bg.ac.rs/handle/123456789/302
AB  - Changes in electrophoresis pattern after interaction of supercoiled plasmid pBR322 DNA with avarol was studied at a micromolar concentration of reactants under mild reaction conditions. Interactions of avarol with linear high-molecular CT-DNA at millimolar concentrations were analyzed by electrophoresis and UV spectrophotometry. It was observed that avarol is capable of quenching ethidium bromide fluorescence in DNA bands. An increase in the absorbance of DNA was detected. The results indicate the binding of avarol to DNA and/or modification of nucleotide bases.
AB  - Proučavane su promene elektroforetskog ponašanja DNA posle interakcija superhelikoidalnog plazmida pBR322 s avarolom pri mikromolarnim koncentracijama reaktanata pod blagim reakcionim uslovima. Interakcije avarola sa linearnom visokomolekulskom CT-DNA pri milimolarnim koncentracijama analizirane su elektroforezom i UV spektrofotometrijom. Uočeno je da je avarol u stanju da gasi fluorescenciju etidijum-bromida u trakama koje potiču od DNA. Detektovan je porast apsorbancije DNA. Rezultati ukazuju na vezivanje avarona za DNA i/ili modifikaciju nukleotidnih baza.
PB  - Serbian Chemical Society
T2  - Journal of the Serbian Chemical Society
T1  - Interactions of the anti-tumor sesquiterpene hydroquinone avarol with DNA in vitro
T1  - Interakcije antitumorskog seskviterpenskog hidrohinona avarola sa DNA in vitro
VL  - 72
IS  - 12
SP  - 1265
EP  - 1269
DO  - 10.2298/JSC0712265V
ER  - 

@article{
author = "Vujčić, Miroslava and Tufegdžić, Srđan and Vujčić, Zoran and Gašić, Miroslav J. and Sladić, Dušan",
year = "2007",
abstract = "Changes in electrophoresis pattern after interaction of supercoiled plasmid pBR322 DNA with avarol was studied at a micromolar concentration of reactants under mild reaction conditions. Interactions of avarol with linear high-molecular CT-DNA at millimolar concentrations were analyzed by electrophoresis and UV spectrophotometry. It was observed that avarol is capable of quenching ethidium bromide fluorescence in DNA bands. An increase in the absorbance of DNA was detected. The results indicate the binding of avarol to DNA and/or modification of nucleotide bases., Proučavane su promene elektroforetskog ponašanja DNA posle interakcija superhelikoidalnog plazmida pBR322 s avarolom pri mikromolarnim koncentracijama reaktanata pod blagim reakcionim uslovima. Interakcije avarola sa linearnom visokomolekulskom CT-DNA pri milimolarnim koncentracijama analizirane su elektroforezom i UV spektrofotometrijom. Uočeno je da je avarol u stanju da gasi fluorescenciju etidijum-bromida u trakama koje potiču od DNA. Detektovan je porast apsorbancije DNA. Rezultati ukazuju na vezivanje avarona za DNA i/ili modifikaciju nukleotidnih baza.",
publisher = "Serbian Chemical Society",
journal = "Journal of the Serbian Chemical Society",
title = "Interactions of the anti-tumor sesquiterpene hydroquinone avarol with DNA in vitro, Interakcije antitumorskog seskviterpenskog hidrohinona avarola sa DNA in vitro",
volume = "72",
number = "12",
pages = "1265-1269",
doi = "10.2298/JSC0712265V"
}

Vujčić, M., Tufegdžić, S., Vujčić, Z., Gašić, M. J.,& Sladić, D.. (2007). Interactions of the anti-tumor sesquiterpene hydroquinone avarol with DNA in vitro. in Journal of the Serbian Chemical Society
Serbian Chemical Society., 72(12), 1265-1269.
https://doi.org/10.2298/JSC0712265V

Vujčić M, Tufegdžić S, Vujčić Z, Gašić MJ, Sladić D. Interactions of the anti-tumor sesquiterpene hydroquinone avarol with DNA in vitro. in Journal of the Serbian Chemical Society. 2007;72(12):1265-1269.
doi:10.2298/JSC0712265V .

Vujčić, Miroslava, Tufegdžić, Srđan, Vujčić, Zoran, Gašić, Miroslav J., Sladić, Dušan, "Interactions of the anti-tumor sesquiterpene hydroquinone avarol with DNA in vitro" in Journal of the Serbian Chemical Society, 72, no. 12 (2007):1265-1269,
https://doi.org/10.2298/JSC0712265V . .

TY  - JOUR
AU  - Bogdanović, J.
AU  - Dikanović, D.
AU  - Maksimović, V.
AU  - Tufegdžić, Srđan
AU  - Doković, D.
AU  - Isajev, V.
AU  - Radotić, Ksenija
PY  - 2006
UR  - https://cer.ihtm.bg.ac.rs/handle/123456789/286
AB  - We analyzed low molecular mass phenolics, lignin content and both soluble and cell wall bound peroxidase activity in the needles of three Picea omorika (Pancic) Purkyne lines grown in the generative seed orchard. The highest values of the total phenol content as well as of catechine, caffeic acid, coniferyl alcohol, isoferulic acid and lignin concentration were detected in B5 line ("semidichotomy" line). The soluble guaiacol peroxidase activity was the highest in A3 line (line "borealis"). The highest activity of cell wall bound peroxidases was measured in B5 line, and it was in correlation with lignin content.
T2  - Biologia Plantarum
T1  - Phenolics, lignin content and peroxidase activity in Picea omorika lines
VL  - 50
IS  - 3
SP  - 461
EP  - 464
DO  - 10.1007/s10535-006-0071-8
ER  - 

@article{
author = "Bogdanović, J. and Dikanović, D. and Maksimović, V. and Tufegdžić, Srđan and Doković, D. and Isajev, V. and Radotić, Ksenija",
year = "2006",
abstract = "We analyzed low molecular mass phenolics, lignin content and both soluble and cell wall bound peroxidase activity in the needles of three Picea omorika (Pancic) Purkyne lines grown in the generative seed orchard. The highest values of the total phenol content as well as of catechine, caffeic acid, coniferyl alcohol, isoferulic acid and lignin concentration were detected in B5 line ("semidichotomy" line). The soluble guaiacol peroxidase activity was the highest in A3 line (line "borealis"). The highest activity of cell wall bound peroxidases was measured in B5 line, and it was in correlation with lignin content.",
journal = "Biologia Plantarum",
title = "Phenolics, lignin content and peroxidase activity in Picea omorika lines",
volume = "50",
number = "3",
pages = "461-464",
doi = "10.1007/s10535-006-0071-8"
}

Bogdanović, J., Dikanović, D., Maksimović, V., Tufegdžić, S., Doković, D., Isajev, V.,& Radotić, K.. (2006). Phenolics, lignin content and peroxidase activity in Picea omorika lines. in Biologia Plantarum, 50(3), 461-464.
https://doi.org/10.1007/s10535-006-0071-8

Bogdanović J, Dikanović D, Maksimović V, Tufegdžić S, Doković D, Isajev V, Radotić K. Phenolics, lignin content and peroxidase activity in Picea omorika lines. in Biologia Plantarum. 2006;50(3):461-464.
doi:10.1007/s10535-006-0071-8 .

Bogdanović, J., Dikanović, D., Maksimović, V., Tufegdžić, Srđan, Doković, D., Isajev, V., Radotić, Ksenija, "Phenolics, lignin content and peroxidase activity in Picea omorika lines" in Biologia Plantarum, 50, no. 3 (2006):461-464,
https://doi.org/10.1007/s10535-006-0071-8 . .

TY  - JOUR
AU  - Tufegdžić, Srđan
AU  - Bogdanovic, J
AU  - Maksimović, Vuk
AU  - Vucinic, Z
PY  - 2005
UR  - https://cer.ihtm.bg.ac.rs/handle/123456789/167
AB  - Horseradish peroxidase was used to synthesize diferulates by a procedure in which ethyl ferulate was used as substrate. Four different forms were obtained, of which two dominant were the 5-5' and 8-5' diferulate. Fluorescence emission spectra of the diferulates (excited at 284 nm) indicate that they contain two chromophores, as opposed to the substrate molecule. Fluorescence excitation spectra with emission at 417 run further demonstrate the difference between the synthesized diferulates and starting substrates.
PB  - New York Acad Sciences, New York
T2  - Biophysics From Molecules To Brain: in Memory of Radoslav K. Andjus
T1  - Characterization of enzymatically synthesized diferulate
VL  - 1048
SP  - 466
EP  - 470
DO  - 10.1196/annals.1342.068
ER  - 

@article{
author = "Tufegdžić, Srđan and Bogdanovic, J and Maksimović, Vuk and Vucinic, Z",
year = "2005",
abstract = "Horseradish peroxidase was used to synthesize diferulates by a procedure in which ethyl ferulate was used as substrate. Four different forms were obtained, of which two dominant were the 5-5' and 8-5' diferulate. Fluorescence emission spectra of the diferulates (excited at 284 nm) indicate that they contain two chromophores, as opposed to the substrate molecule. Fluorescence excitation spectra with emission at 417 run further demonstrate the difference between the synthesized diferulates and starting substrates.",
publisher = "New York Acad Sciences, New York",
journal = "Biophysics From Molecules To Brain: in Memory of Radoslav K. Andjus",
title = "Characterization of enzymatically synthesized diferulate",
volume = "1048",
pages = "466-470",
doi = "10.1196/annals.1342.068"
}

Tufegdžić, S., Bogdanovic, J., Maksimović, V.,& Vucinic, Z.. (2005). Characterization of enzymatically synthesized diferulate. in Biophysics From Molecules To Brain: in Memory of Radoslav K. Andjus
New York Acad Sciences, New York., 1048, 466-470.
https://doi.org/10.1196/annals.1342.068

Tufegdžić S, Bogdanovic J, Maksimović V, Vucinic Z. Characterization of enzymatically synthesized diferulate. in Biophysics From Molecules To Brain: in Memory of Radoslav K. Andjus. 2005;1048:466-470.
doi:10.1196/annals.1342.068 .

Tufegdžić, Srđan, Bogdanovic, J, Maksimović, Vuk, Vucinic, Z, "Characterization of enzymatically synthesized diferulate" in Biophysics From Molecules To Brain: in Memory of Radoslav K. Andjus, 1048 (2005):466-470,
https://doi.org/10.1196/annals.1342.068 . .