Vuković, Nenad L.

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  • Vuković, Nenad L. (5)
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Antibacterial and Cytotoxic Activities of Naphthoquinone Pigments from Onosma Visianii Clem

Vukic, Milena D.; Vuković, Nenad L.; Djelic, Gorica T.; Popovic, Suzana Lj.; Zarić, Milan M.; Baskic, Dejan D.; Krstić, Gordana B.; Tešević, Vele; Kacaniova, Miroslava M.

(Excli Journal Managing Office, Dortmund, 2017)

TY  - JOUR
AU  - Vukic, Milena D.
AU  - Vuković, Nenad L.
AU  - Djelic, Gorica T.
AU  - Popovic, Suzana Lj.
AU  - Zarić, Milan M.
AU  - Baskic, Dejan D.
AU  - Krstić, Gordana B.
AU  - Tešević, Vele
AU  - Kacaniova, Miroslava M.
PY  - 2017
UR  - https://cherry.chem.bg.ac.rs/handle/123456789/2422
AB  - In this study, the antibacterial and cytotoxic activities of isolated compounds from the roots of Onosma visianii were investigated. By using different chromatographic techniques and appropriate spectroscopic methods, the seven naphthoquinones were described: deoxyshikonin (1), isobutyrylshikonin (2), alpha-methylbutyrylshikonin (3), acetylshikonin (4), beta-hydroxyisovalerylshikonin (5), 5,8-O-dimethyl isobutyrylshikonin (6) and 5,8-O-dimethyl deoxyshikonin (7). Among the tested compounds, 3 and 4 exhibited the highest antibacterial activities toward all tested bacterial species (MIC50 and MIC90 for gram positive bacteria: 6.40 mu g/mL-12.79 mu g/mL and 6.82 mu g/mL-13.60 mu g/mL, respectively; for gram negative bacteria: 4.27. mu g/mL-8.53 mu g/mL and 4.77 mu g/mL-9.54 mu g/mL, respectively). Also, naphthoquinones 3 and 4 exhibited strong cytotoxic activity against MDA-MB-231 cells (IC50 values 86.0 mu g/mL and 80.2 mu g/mL, respectively), while compounds 1, 3, 4 and 5 significantly decreased viability of HCT116 cells (IC50 values of 97.8 mu g/mL, 15.2 mu g/mL, 24.6 mu g/mL and 30.9 mu g/mL, respectively). Our results indicated that all tested naphthoquinone pigments are potential candidates for clinical uses as antibacterial and cytotoxic agents.
PB  - Excli Journal Managing Office, Dortmund
T2  - EXCLI Journal
T1  - Antibacterial and Cytotoxic Activities of Naphthoquinone Pigments from  Onosma Visianii Clem
VL  - 16
SP  - 73
EP  - 88
DO  - 10.17179/excli2016-762
ER  - 
@article{
author = "Vukic, Milena D. and Vuković, Nenad L. and Djelic, Gorica T. and Popovic, Suzana Lj. and Zarić, Milan M. and Baskic, Dejan D. and Krstić, Gordana B. and Tešević, Vele and Kacaniova, Miroslava M.",
year = "2017",
abstract = "In this study, the antibacterial and cytotoxic activities of isolated compounds from the roots of Onosma visianii were investigated. By using different chromatographic techniques and appropriate spectroscopic methods, the seven naphthoquinones were described: deoxyshikonin (1), isobutyrylshikonin (2), alpha-methylbutyrylshikonin (3), acetylshikonin (4), beta-hydroxyisovalerylshikonin (5), 5,8-O-dimethyl isobutyrylshikonin (6) and 5,8-O-dimethyl deoxyshikonin (7). Among the tested compounds, 3 and 4 exhibited the highest antibacterial activities toward all tested bacterial species (MIC50 and MIC90 for gram positive bacteria: 6.40 mu g/mL-12.79 mu g/mL and 6.82 mu g/mL-13.60 mu g/mL, respectively; for gram negative bacteria: 4.27. mu g/mL-8.53 mu g/mL and 4.77 mu g/mL-9.54 mu g/mL, respectively). Also, naphthoquinones 3 and 4 exhibited strong cytotoxic activity against MDA-MB-231 cells (IC50 values 86.0 mu g/mL and 80.2 mu g/mL, respectively), while compounds 1, 3, 4 and 5 significantly decreased viability of HCT116 cells (IC50 values of 97.8 mu g/mL, 15.2 mu g/mL, 24.6 mu g/mL and 30.9 mu g/mL, respectively). Our results indicated that all tested naphthoquinone pigments are potential candidates for clinical uses as antibacterial and cytotoxic agents.",
publisher = "Excli Journal Managing Office, Dortmund",
journal = "EXCLI Journal",
title = "Antibacterial and Cytotoxic Activities of Naphthoquinone Pigments from  Onosma Visianii Clem",
volume = "16",
pages = "73-88",
doi = "10.17179/excli2016-762"
}
Vukic, M. D., Vuković, N. L., Djelic, G. T., Popovic, S. Lj., Zarić, M. M., Baskic, D. D., Krstić, G. B., Tešević, V.,& Kacaniova, M. M.. (2017). Antibacterial and Cytotoxic Activities of Naphthoquinone Pigments from  Onosma Visianii Clem. in EXCLI Journal
Excli Journal Managing Office, Dortmund., 16, 73-88.
https://doi.org/10.17179/excli2016-762
Vukic MD, Vuković NL, Djelic GT, Popovic SL, Zarić MM, Baskic DD, Krstić GB, Tešević V, Kacaniova MM. Antibacterial and Cytotoxic Activities of Naphthoquinone Pigments from  Onosma Visianii Clem. in EXCLI Journal. 2017;16:73-88.
doi:10.17179/excli2016-762 .
Vukic, Milena D., Vuković, Nenad L., Djelic, Gorica T., Popovic, Suzana Lj., Zarić, Milan M., Baskic, Dejan D., Krstić, Gordana B., Tešević, Vele, Kacaniova, Miroslava M., "Antibacterial and Cytotoxic Activities of Naphthoquinone Pigments from  Onosma Visianii Clem" in EXCLI Journal, 16 (2017):73-88,
https://doi.org/10.17179/excli2016-762 . .
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Supplementary data for the article: Stojković, D. L. J.; Bacchi, A.; Capucci, D.; Milenković, M. R.; Čobeljić, B.; Trifunović, S. R.; Andelković, K.; Jevtić, V. V.; Vuković, N.; Vukić, M.; et al. Synthesis and Characterization of Palladium(II) Complexes with Glycine Coumarin Derivatives. Journal of the Serbian Chemical Society 2016, 81 (12), 1383–1392. https://doi.org/10.2298/JSC160915087S

Stojković, Danijela; Bacchi, Alessia; Capucci, Davide; Milenković, Milica R.; Čobeljić, Božidar; Trifunović, Srećko R.; Anđelković, Katarina K.; Jevtic, Verica V.; Vuković, Nenad L.; Vukic, Milena; Sladić, Dušan

(Serbian Chemical Soc, Belgrade, 2016)

TY  - DATA
AU  - Stojković, Danijela
AU  - Bacchi, Alessia
AU  - Capucci, Davide
AU  - Milenković, Milica R.
AU  - Čobeljić, Božidar
AU  - Trifunović, Srećko R.
AU  - Anđelković, Katarina K.
AU  - Jevtic, Verica V.
AU  - Vuković, Nenad L.
AU  - Vukic, Milena
AU  - Sladić, Dušan
PY  - 2016
UR  - https://cherry.chem.bg.ac.rs/handle/123456789/3626
PB  - Serbian Chemical Soc, Belgrade
T2  - Journal of the Serbian Chemical Society
T1  - Supplementary data for the article: Stojković, D. L. J.; Bacchi, A.; Capucci, D.; Milenković, M. R.; Čobeljić, B.; Trifunović, S. R.; Andelković, K.; Jevtić, V. V.; Vuković, N.; Vukić, M.; et al. Synthesis and Characterization of Palladium(II) Complexes with Glycine Coumarin Derivatives. Journal of the Serbian Chemical Society 2016, 81 (12), 1383–1392. https://doi.org/10.2298/JSC160915087S
UR  - https://hdl.handle.net/21.15107/rcub_cherry_3626
ER  - 
@misc{
author = "Stojković, Danijela and Bacchi, Alessia and Capucci, Davide and Milenković, Milica R. and Čobeljić, Božidar and Trifunović, Srećko R. and Anđelković, Katarina K. and Jevtic, Verica V. and Vuković, Nenad L. and Vukic, Milena and Sladić, Dušan",
year = "2016",
publisher = "Serbian Chemical Soc, Belgrade",
journal = "Journal of the Serbian Chemical Society",
title = "Supplementary data for the article: Stojković, D. L. J.; Bacchi, A.; Capucci, D.; Milenković, M. R.; Čobeljić, B.; Trifunović, S. R.; Andelković, K.; Jevtić, V. V.; Vuković, N.; Vukić, M.; et al. Synthesis and Characterization of Palladium(II) Complexes with Glycine Coumarin Derivatives. Journal of the Serbian Chemical Society 2016, 81 (12), 1383–1392. https://doi.org/10.2298/JSC160915087S",
url = "https://hdl.handle.net/21.15107/rcub_cherry_3626"
}
Stojković, D., Bacchi, A., Capucci, D., Milenković, M. R., Čobeljić, B., Trifunović, S. R., Anđelković, K. K., Jevtic, V. V., Vuković, N. L., Vukic, M.,& Sladić, D.. (2016). Supplementary data for the article: Stojković, D. L. J.; Bacchi, A.; Capucci, D.; Milenković, M. R.; Čobeljić, B.; Trifunović, S. R.; Andelković, K.; Jevtić, V. V.; Vuković, N.; Vukić, M.; et al. Synthesis and Characterization of Palladium(II) Complexes with Glycine Coumarin Derivatives. Journal of the Serbian Chemical Society 2016, 81 (12), 1383–1392. https://doi.org/10.2298/JSC160915087S. in Journal of the Serbian Chemical Society
Serbian Chemical Soc, Belgrade..
https://hdl.handle.net/21.15107/rcub_cherry_3626
Stojković D, Bacchi A, Capucci D, Milenković MR, Čobeljić B, Trifunović SR, Anđelković KK, Jevtic VV, Vuković NL, Vukic M, Sladić D. Supplementary data for the article: Stojković, D. L. J.; Bacchi, A.; Capucci, D.; Milenković, M. R.; Čobeljić, B.; Trifunović, S. R.; Andelković, K.; Jevtić, V. V.; Vuković, N.; Vukić, M.; et al. Synthesis and Characterization of Palladium(II) Complexes with Glycine Coumarin Derivatives. Journal of the Serbian Chemical Society 2016, 81 (12), 1383–1392. https://doi.org/10.2298/JSC160915087S. in Journal of the Serbian Chemical Society. 2016;.
https://hdl.handle.net/21.15107/rcub_cherry_3626 .
Stojković, Danijela, Bacchi, Alessia, Capucci, Davide, Milenković, Milica R., Čobeljić, Božidar, Trifunović, Srećko R., Anđelković, Katarina K., Jevtic, Verica V., Vuković, Nenad L., Vukic, Milena, Sladić, Dušan, "Supplementary data for the article: Stojković, D. L. J.; Bacchi, A.; Capucci, D.; Milenković, M. R.; Čobeljić, B.; Trifunović, S. R.; Andelković, K.; Jevtić, V. V.; Vuković, N.; Vukić, M.; et al. Synthesis and Characterization of Palladium(II) Complexes with Glycine Coumarin Derivatives. Journal of the Serbian Chemical Society 2016, 81 (12), 1383–1392. https://doi.org/10.2298/JSC160915087S" in Journal of the Serbian Chemical Society (2016),
https://hdl.handle.net/21.15107/rcub_cherry_3626 .

Synthesis and characterization of palladium(II) complexes with glycine coumarin derivatives

Stojković, Danijela; Bacchi, Alessia; Capucci, Davide; Milenković, Milica R.; Čobeljić, Božidar; Trifunović, Srećko R.; Anđelković, Katarina K.; Jevtic, Verica V.; Vuković, Nenad L.; Vukic, Milena; Sladić, Dušan

(Serbian Chemical Soc, Belgrade, 2016)

TY  - JOUR
AU  - Stojković, Danijela
AU  - Bacchi, Alessia
AU  - Capucci, Davide
AU  - Milenković, Milica R.
AU  - Čobeljić, Božidar
AU  - Trifunović, Srećko R.
AU  - Anđelković, Katarina K.
AU  - Jevtic, Verica V.
AU  - Vuković, Nenad L.
AU  - Vukic, Milena
AU  - Sladić, Dušan
PY  - 2016
UR  - https://cherry.chem.bg.ac.rs/handle/123456789/2392
AB  - A Pd(II) complex with methyl 2-([1-{2,4-dioxochroman-3-ylidene}ethyl]amino)acetate was synthesized. The structures of both the ligand and its Pd(II) complex were determined by elemental analysis, and IR and NMR spectroscopy. Recrystallization of the Pd(II) complex from DMF/water solution resulted in its hydrolysis and the formation of the dimethylamine (2-[{1-(2,4-dioxochroman-3-ylidene) ethyl} amino] acetato) palladium(II) complex, the structure of which was determined by elemental analysis, IR, H-1- and C-13-NMR spectroscopy and X-ray analysis.
PB  - Serbian Chemical Soc, Belgrade
T2  - Journal of the Serbian Chemical Society
T1  - Synthesis and characterization of palladium(II) complexes with glycine coumarin derivatives
VL  - 81
IS  - 12
SP  - 1383
EP  - 1392
DO  - 10.2298/JSC160915087S
ER  - 
@article{
author = "Stojković, Danijela and Bacchi, Alessia and Capucci, Davide and Milenković, Milica R. and Čobeljić, Božidar and Trifunović, Srećko R. and Anđelković, Katarina K. and Jevtic, Verica V. and Vuković, Nenad L. and Vukic, Milena and Sladić, Dušan",
year = "2016",
abstract = "A Pd(II) complex with methyl 2-([1-{2,4-dioxochroman-3-ylidene}ethyl]amino)acetate was synthesized. The structures of both the ligand and its Pd(II) complex were determined by elemental analysis, and IR and NMR spectroscopy. Recrystallization of the Pd(II) complex from DMF/water solution resulted in its hydrolysis and the formation of the dimethylamine (2-[{1-(2,4-dioxochroman-3-ylidene) ethyl} amino] acetato) palladium(II) complex, the structure of which was determined by elemental analysis, IR, H-1- and C-13-NMR spectroscopy and X-ray analysis.",
publisher = "Serbian Chemical Soc, Belgrade",
journal = "Journal of the Serbian Chemical Society",
title = "Synthesis and characterization of palladium(II) complexes with glycine coumarin derivatives",
volume = "81",
number = "12",
pages = "1383-1392",
doi = "10.2298/JSC160915087S"
}
Stojković, D., Bacchi, A., Capucci, D., Milenković, M. R., Čobeljić, B., Trifunović, S. R., Anđelković, K. K., Jevtic, V. V., Vuković, N. L., Vukic, M.,& Sladić, D.. (2016). Synthesis and characterization of palladium(II) complexes with glycine coumarin derivatives. in Journal of the Serbian Chemical Society
Serbian Chemical Soc, Belgrade., 81(12), 1383-1392.
https://doi.org/10.2298/JSC160915087S
Stojković D, Bacchi A, Capucci D, Milenković MR, Čobeljić B, Trifunović SR, Anđelković KK, Jevtic VV, Vuković NL, Vukic M, Sladić D. Synthesis and characterization of palladium(II) complexes with glycine coumarin derivatives. in Journal of the Serbian Chemical Society. 2016;81(12):1383-1392.
doi:10.2298/JSC160915087S .
Stojković, Danijela, Bacchi, Alessia, Capucci, Davide, Milenković, Milica R., Čobeljić, Božidar, Trifunović, Srećko R., Anđelković, Katarina K., Jevtic, Verica V., Vuković, Nenad L., Vukic, Milena, Sladić, Dušan, "Synthesis and characterization of palladium(II) complexes with glycine coumarin derivatives" in Journal of the Serbian Chemical Society, 81, no. 12 (2016):1383-1392,
https://doi.org/10.2298/JSC160915087S . .
1

Chemical composition, cytotoxic and antioxidative activities of ethanolic extracts of propolis on HCT-116 cell line

Žižić, Jovana B.; Vuković, Nenad L.; Jadranin, Milka; Anđelković, Boban D.; Tešević, Vele; Kacaniova, Miroslava M.; Sukdolak, Slobodan B.; Marković, Snežana D.

(Wiley, Hoboken, 2013)

TY  - JOUR
AU  - Žižić, Jovana B.
AU  - Vuković, Nenad L.
AU  - Jadranin, Milka
AU  - Anđelković, Boban D.
AU  - Tešević, Vele
AU  - Kacaniova, Miroslava M.
AU  - Sukdolak, Slobodan B.
AU  - Marković, Snežana D.
PY  - 2013
UR  - https://cherry.chem.bg.ac.rs/handle/123456789/3472
AB  - BACKGROUND Propolis is a complex resinous sticky substance that honeybees collect from buds and exudates of various plants. Owing to its versatile biological and pharmacological activities, propolis is widely used in medicines, cosmetics and foods. The aim of this study was to evaluate the cytotoxic and antioxidative effects of various ethanolic extracts of propolis (EEPs) on human colon cancer cell line HCT-116 and compare them with their composition determined by HPLC-DAD. RESULTS The most abundant flavonoids in all samples were chrysin, pinocembrin and galangin (12.697-40.811 mu gmg(-1)), while the main phenolic acids were caffeic acid, ferulic acid and isoferulic acid. Dose- and time-dependent inhibition of growth of HCT-116 cells was observed for all propolis samples, with IC50 values ranging from 26.33 to 143.09 mu gmL(-1). Differences in cytotoxic activity of propolis samples were associated with differences in their composition. All EEP samples reduced both superoxide anion radical and nitrite levels and also had strong DPPH-scavenging activity. CONCLUSION All tested propolis samples had pronounced cytotoxic and antioxidative activities.
PB  - Wiley, Hoboken
T2  - Journal of the Science of Food and Agriculture
T1  - Chemical composition, cytotoxic and antioxidative activities of ethanolic extracts of propolis on HCT-116 cell line
VL  - 93
IS  - 12
SP  - 3001
EP  - 3009
DO  - 10.1002/jsfa.6132
ER  - 
@article{
author = "Žižić, Jovana B. and Vuković, Nenad L. and Jadranin, Milka and Anđelković, Boban D. and Tešević, Vele and Kacaniova, Miroslava M. and Sukdolak, Slobodan B. and Marković, Snežana D.",
year = "2013",
abstract = "BACKGROUND Propolis is a complex resinous sticky substance that honeybees collect from buds and exudates of various plants. Owing to its versatile biological and pharmacological activities, propolis is widely used in medicines, cosmetics and foods. The aim of this study was to evaluate the cytotoxic and antioxidative effects of various ethanolic extracts of propolis (EEPs) on human colon cancer cell line HCT-116 and compare them with their composition determined by HPLC-DAD. RESULTS The most abundant flavonoids in all samples were chrysin, pinocembrin and galangin (12.697-40.811 mu gmg(-1)), while the main phenolic acids were caffeic acid, ferulic acid and isoferulic acid. Dose- and time-dependent inhibition of growth of HCT-116 cells was observed for all propolis samples, with IC50 values ranging from 26.33 to 143.09 mu gmL(-1). Differences in cytotoxic activity of propolis samples were associated with differences in their composition. All EEP samples reduced both superoxide anion radical and nitrite levels and also had strong DPPH-scavenging activity. CONCLUSION All tested propolis samples had pronounced cytotoxic and antioxidative activities.",
publisher = "Wiley, Hoboken",
journal = "Journal of the Science of Food and Agriculture",
title = "Chemical composition, cytotoxic and antioxidative activities of ethanolic extracts of propolis on HCT-116 cell line",
volume = "93",
number = "12",
pages = "3001-3009",
doi = "10.1002/jsfa.6132"
}
Žižić, J. B., Vuković, N. L., Jadranin, M., Anđelković, B. D., Tešević, V., Kacaniova, M. M., Sukdolak, S. B.,& Marković, S. D.. (2013). Chemical composition, cytotoxic and antioxidative activities of ethanolic extracts of propolis on HCT-116 cell line. in Journal of the Science of Food and Agriculture
Wiley, Hoboken., 93(12), 3001-3009.
https://doi.org/10.1002/jsfa.6132
Žižić JB, Vuković NL, Jadranin M, Anđelković BD, Tešević V, Kacaniova MM, Sukdolak SB, Marković SD. Chemical composition, cytotoxic and antioxidative activities of ethanolic extracts of propolis on HCT-116 cell line. in Journal of the Science of Food and Agriculture. 2013;93(12):3001-3009.
doi:10.1002/jsfa.6132 .
Žižić, Jovana B., Vuković, Nenad L., Jadranin, Milka, Anđelković, Boban D., Tešević, Vele, Kacaniova, Miroslava M., Sukdolak, Slobodan B., Marković, Snežana D., "Chemical composition, cytotoxic and antioxidative activities of ethanolic extracts of propolis on HCT-116 cell line" in Journal of the Science of Food and Agriculture, 93, no. 12 (2013):3001-3009,
https://doi.org/10.1002/jsfa.6132 . .
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Chemical composition, cytotoxic and antioxidative activities of ethanolic extracts of propolis on HCT-116 cell line

Žižić, Jovana B.; Vuković, Nenad L.; Jadranin, Milka; Anđelković, Boban D.; Tešević, Vele; Kacaniova, Miroslava M.; Sukdolak, Slobodan B.; Marković, Snežana D.

(Wiley, Hoboken, 2013)

TY  - JOUR
AU  - Žižić, Jovana B.
AU  - Vuković, Nenad L.
AU  - Jadranin, Milka
AU  - Anđelković, Boban D.
AU  - Tešević, Vele
AU  - Kacaniova, Miroslava M.
AU  - Sukdolak, Slobodan B.
AU  - Marković, Snežana D.
PY  - 2013
UR  - https://cherry.chem.bg.ac.rs/handle/123456789/1387
AB  - BACKGROUND Propolis is a complex resinous sticky substance that honeybees collect from buds and exudates of various plants. Owing to its versatile biological and pharmacological activities, propolis is widely used in medicines, cosmetics and foods. The aim of this study was to evaluate the cytotoxic and antioxidative effects of various ethanolic extracts of propolis (EEPs) on human colon cancer cell line HCT-116 and compare them with their composition determined by HPLC-DAD. RESULTS The most abundant flavonoids in all samples were chrysin, pinocembrin and galangin (12.697-40.811 mu gmg(-1)), while the main phenolic acids were caffeic acid, ferulic acid and isoferulic acid. Dose- and time-dependent inhibition of growth of HCT-116 cells was observed for all propolis samples, with IC50 values ranging from 26.33 to 143.09 mu gmL(-1). Differences in cytotoxic activity of propolis samples were associated with differences in their composition. All EEP samples reduced both superoxide anion radical and nitrite levels and also had strong DPPH-scavenging activity. CONCLUSION All tested propolis samples had pronounced cytotoxic and antioxidative activities.
PB  - Wiley, Hoboken
T2  - Journal of the Science of Food and Agriculture
T1  - Chemical composition, cytotoxic and antioxidative activities of ethanolic extracts of propolis on HCT-116 cell line
VL  - 93
IS  - 12
SP  - 3001
EP  - 3009
DO  - 10.1002/jsfa.6132
ER  - 
@article{
author = "Žižić, Jovana B. and Vuković, Nenad L. and Jadranin, Milka and Anđelković, Boban D. and Tešević, Vele and Kacaniova, Miroslava M. and Sukdolak, Slobodan B. and Marković, Snežana D.",
year = "2013",
abstract = "BACKGROUND Propolis is a complex resinous sticky substance that honeybees collect from buds and exudates of various plants. Owing to its versatile biological and pharmacological activities, propolis is widely used in medicines, cosmetics and foods. The aim of this study was to evaluate the cytotoxic and antioxidative effects of various ethanolic extracts of propolis (EEPs) on human colon cancer cell line HCT-116 and compare them with their composition determined by HPLC-DAD. RESULTS The most abundant flavonoids in all samples were chrysin, pinocembrin and galangin (12.697-40.811 mu gmg(-1)), while the main phenolic acids were caffeic acid, ferulic acid and isoferulic acid. Dose- and time-dependent inhibition of growth of HCT-116 cells was observed for all propolis samples, with IC50 values ranging from 26.33 to 143.09 mu gmL(-1). Differences in cytotoxic activity of propolis samples were associated with differences in their composition. All EEP samples reduced both superoxide anion radical and nitrite levels and also had strong DPPH-scavenging activity. CONCLUSION All tested propolis samples had pronounced cytotoxic and antioxidative activities.",
publisher = "Wiley, Hoboken",
journal = "Journal of the Science of Food and Agriculture",
title = "Chemical composition, cytotoxic and antioxidative activities of ethanolic extracts of propolis on HCT-116 cell line",
volume = "93",
number = "12",
pages = "3001-3009",
doi = "10.1002/jsfa.6132"
}
Žižić, J. B., Vuković, N. L., Jadranin, M., Anđelković, B. D., Tešević, V., Kacaniova, M. M., Sukdolak, S. B.,& Marković, S. D.. (2013). Chemical composition, cytotoxic and antioxidative activities of ethanolic extracts of propolis on HCT-116 cell line. in Journal of the Science of Food and Agriculture
Wiley, Hoboken., 93(12), 3001-3009.
https://doi.org/10.1002/jsfa.6132
Žižić JB, Vuković NL, Jadranin M, Anđelković BD, Tešević V, Kacaniova MM, Sukdolak SB, Marković SD. Chemical composition, cytotoxic and antioxidative activities of ethanolic extracts of propolis on HCT-116 cell line. in Journal of the Science of Food and Agriculture. 2013;93(12):3001-3009.
doi:10.1002/jsfa.6132 .
Žižić, Jovana B., Vuković, Nenad L., Jadranin, Milka, Anđelković, Boban D., Tešević, Vele, Kacaniova, Miroslava M., Sukdolak, Slobodan B., Marković, Snežana D., "Chemical composition, cytotoxic and antioxidative activities of ethanolic extracts of propolis on HCT-116 cell line" in Journal of the Science of Food and Agriculture, 93, no. 12 (2013):3001-3009,
https://doi.org/10.1002/jsfa.6132 . .
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