TY  - DATA
AU  - Petrović, Zorica D.
AU  - Đorović, Jelena
AU  - Simijonović, Dušica
AU  - Trifunović, Snežana S.
AU  - Petrović, Vladimir P.
PY  - 2018
UR  - https://cherry.chem.bg.ac.rs/handle/123456789/3209
PB  - Springer International Publishing Ag, Cham
T2  - Chemical Papers = Chemicke Zvesti
T1  - Supplementary material for the article: Petrović, Z. D.; Đorović, J.; Simijonović, D.; Trifunović, S.; Petrović, V. P. In Vitro Study of  Iron Coordination Properties, Anti-Inflammatory Potential, and Cytotoxic Effects of N Salicylidene and N-Vanillidene Anil Schiff Bases. Chemical Papers 2018, 72 (9), 2171– 2180. https://doi.org/10.1007/s11696-018-0419-5
UR  - https://hdl.handle.net/21.15107/rcub_cherry_3209
ER  - 

@misc{
author = "Petrović, Zorica D. and Đorović, Jelena and Simijonović, Dušica and Trifunović, Snežana S. and Petrović, Vladimir P.",
year = "2018",
publisher = "Springer International Publishing Ag, Cham",
journal = "Chemical Papers = Chemicke Zvesti",
title = "Supplementary material for the article: Petrović, Z. D.; Đorović, J.; Simijonović, D.; Trifunović, S.; Petrović, V. P. In Vitro Study of  Iron Coordination Properties, Anti-Inflammatory Potential, and Cytotoxic Effects of N Salicylidene and N-Vanillidene Anil Schiff Bases. Chemical Papers 2018, 72 (9), 2171– 2180. https://doi.org/10.1007/s11696-018-0419-5",
url = "https://hdl.handle.net/21.15107/rcub_cherry_3209"
}

Petrović, Z. D., Đorović, J., Simijonović, D., Trifunović, S. S.,& Petrović, V. P.. (2018). Supplementary material for the article: Petrović, Z. D.; Đorović, J.; Simijonović, D.; Trifunović, S.; Petrović, V. P. In Vitro Study of  Iron Coordination Properties, Anti-Inflammatory Potential, and Cytotoxic Effects of N Salicylidene and N-Vanillidene Anil Schiff Bases. Chemical Papers 2018, 72 (9), 2171– 2180. https://doi.org/10.1007/s11696-018-0419-5. in Chemical Papers = Chemicke Zvesti
Springer International Publishing Ag, Cham..
https://hdl.handle.net/21.15107/rcub_cherry_3209

Petrović ZD, Đorović J, Simijonović D, Trifunović SS, Petrović VP. Supplementary material for the article: Petrović, Z. D.; Đorović, J.; Simijonović, D.; Trifunović, S.; Petrović, V. P. In Vitro Study of  Iron Coordination Properties, Anti-Inflammatory Potential, and Cytotoxic Effects of N Salicylidene and N-Vanillidene Anil Schiff Bases. Chemical Papers 2018, 72 (9), 2171– 2180. https://doi.org/10.1007/s11696-018-0419-5. in Chemical Papers = Chemicke Zvesti. 2018;.
https://hdl.handle.net/21.15107/rcub_cherry_3209 .

Petrović, Zorica D., Đorović, Jelena, Simijonović, Dušica, Trifunović, Snežana S., Petrović, Vladimir P., "Supplementary material for the article: Petrović, Z. D.; Đorović, J.; Simijonović, D.; Trifunović, S.; Petrović, V. P. In Vitro Study of  Iron Coordination Properties, Anti-Inflammatory Potential, and Cytotoxic Effects of N Salicylidene and N-Vanillidene Anil Schiff Bases. Chemical Papers 2018, 72 (9), 2171– 2180. https://doi.org/10.1007/s11696-018-0419-5" in Chemical Papers = Chemicke Zvesti (2018),
https://hdl.handle.net/21.15107/rcub_cherry_3209 .

TY  - JOUR
AU  - Petrović, Zorica D.
AU  - Đorović, Jelena
AU  - Simijonović, Dušica
AU  - Trifunović, Snežana S.
AU  - Petrović, Vladimir P.
PY  - 2018
UR  - https://cherry.chem.bg.ac.rs/handle/123456789/2190
AB  - N-Salicylidene and N-vanillidene anil Schiff bases SB-1-5 were evaluated for their iron-coordinating properties. For this purpose, reactions with Fe(III) chloride were performed. The obtained results showed that salicylaldehyde bases SB-1 and SB-2 are the best coordinating ligands among the investigated SBs. The corresponding complexes are obtained in good yield and investigated using UV-Vis spectrophotometry and IR spectroscopy. The inhibitory potential of SB-1-5 against iron-containing enzyme lipoxygenase (LOX) was also tested. Salicylidene bases exerted better activity then vanilliden. The cytotoxic in vitro activities against human breast carcinoma MDA-MB-231 and human colon carcinoma HCT-116 cell lines were determined. Based on these results, SB-1 and SB-2 can be considered as interesting compounds for further in vivo investigations.
PB  - Springer International Publishing Ag, Cham
T2  - Chemical Papers = Chemicke Zvesti
T1  - In vitro study of iron coordination properties, anti-inflammatory potential, and cytotoxic effects of N-salicylidene and N-vanillidene anil Schiff bases
VL  - 72
IS  - 9
SP  - 2171
EP  - 2180
DO  - 10.1007/s11696-018-0419-5
ER  - 

@article{
author = "Petrović, Zorica D. and Đorović, Jelena and Simijonović, Dušica and Trifunović, Snežana S. and Petrović, Vladimir P.",
year = "2018",
abstract = "N-Salicylidene and N-vanillidene anil Schiff bases SB-1-5 were evaluated for their iron-coordinating properties. For this purpose, reactions with Fe(III) chloride were performed. The obtained results showed that salicylaldehyde bases SB-1 and SB-2 are the best coordinating ligands among the investigated SBs. The corresponding complexes are obtained in good yield and investigated using UV-Vis spectrophotometry and IR spectroscopy. The inhibitory potential of SB-1-5 against iron-containing enzyme lipoxygenase (LOX) was also tested. Salicylidene bases exerted better activity then vanilliden. The cytotoxic in vitro activities against human breast carcinoma MDA-MB-231 and human colon carcinoma HCT-116 cell lines were determined. Based on these results, SB-1 and SB-2 can be considered as interesting compounds for further in vivo investigations.",
publisher = "Springer International Publishing Ag, Cham",
journal = "Chemical Papers = Chemicke Zvesti",
title = "In vitro study of iron coordination properties, anti-inflammatory potential, and cytotoxic effects of N-salicylidene and N-vanillidene anil Schiff bases",
volume = "72",
number = "9",
pages = "2171-2180",
doi = "10.1007/s11696-018-0419-5"
}

Petrović, Z. D., Đorović, J., Simijonović, D., Trifunović, S. S.,& Petrović, V. P.. (2018). In vitro study of iron coordination properties, anti-inflammatory potential, and cytotoxic effects of N-salicylidene and N-vanillidene anil Schiff bases. in Chemical Papers = Chemicke Zvesti
Springer International Publishing Ag, Cham., 72(9), 2171-2180.
https://doi.org/10.1007/s11696-018-0419-5

Petrović ZD, Đorović J, Simijonović D, Trifunović SS, Petrović VP. In vitro study of iron coordination properties, anti-inflammatory potential, and cytotoxic effects of N-salicylidene and N-vanillidene anil Schiff bases. in Chemical Papers = Chemicke Zvesti. 2018;72(9):2171-2180.
doi:10.1007/s11696-018-0419-5 .

Petrović, Zorica D., Đorović, Jelena, Simijonović, Dušica, Trifunović, Snežana S., Petrović, Vladimir P., "In vitro study of iron coordination properties, anti-inflammatory potential, and cytotoxic effects of N-salicylidene and N-vanillidene anil Schiff bases" in Chemical Papers = Chemicke Zvesti, 72, no. 9 (2018):2171-2180,
https://doi.org/10.1007/s11696-018-0419-5 . .

TY  - JOUR
AU  - Petrović, ZD
AU  - Konstantinovic, S
AU  - Scheffold, R
AU  - Milosavljevic, S
PY  - 1997
UR  - https://cherry.chem.bg.ac.rs/handle/123456789/363
AB  - Chemical and electrochemical reductions of some allyl type halides catalyzed by vitamin B-12 have been studied. Geranyl bromide 1 and methyl (2E, 6E) 8-bromo-3,7-dimethylocta-2,6-dienoate 2 have been used as substrates and subjected to chemical and electrochemical reduction. The formation and distribution of the reaction products of these substrates can be explained by free radical mechanisms, namely by reductive reactions of some functional groups, rearrangements and intermolecular coupling of intermediate radicals.
PB  - Natl Inst Science Communication & Information Resources-Niscair, New Delhi
T2  - Indian Journal of Chemistry. Section B: Organic and Medicinal Chemistry
T1  - Chemical and electrochemical reductions of some allyl type halides catalyzed by vitamin B-12
VL  - 36
IS  - 9
SP  - 765
EP  - 768
UR  - https://hdl.handle.net/21.15107/rcub_cherry_363
ER  - 

@article{
author = "Petrović, ZD and Konstantinovic, S and Scheffold, R and Milosavljevic, S",
year = "1997",
abstract = "Chemical and electrochemical reductions of some allyl type halides catalyzed by vitamin B-12 have been studied. Geranyl bromide 1 and methyl (2E, 6E) 8-bromo-3,7-dimethylocta-2,6-dienoate 2 have been used as substrates and subjected to chemical and electrochemical reduction. The formation and distribution of the reaction products of these substrates can be explained by free radical mechanisms, namely by reductive reactions of some functional groups, rearrangements and intermolecular coupling of intermediate radicals.",
publisher = "Natl Inst Science Communication & Information Resources-Niscair, New Delhi",
journal = "Indian Journal of Chemistry. Section B: Organic and Medicinal Chemistry",
title = "Chemical and electrochemical reductions of some allyl type halides catalyzed by vitamin B-12",
volume = "36",
number = "9",
pages = "765-768",
url = "https://hdl.handle.net/21.15107/rcub_cherry_363"
}

Petrović, Z., Konstantinovic, S., Scheffold, R.,& Milosavljevic, S.. (1997). Chemical and electrochemical reductions of some allyl type halides catalyzed by vitamin B-12. in Indian Journal of Chemistry. Section B: Organic and Medicinal Chemistry
Natl Inst Science Communication & Information Resources-Niscair, New Delhi., 36(9), 765-768.
https://hdl.handle.net/21.15107/rcub_cherry_363

Petrović Z, Konstantinovic S, Scheffold R, Milosavljevic S. Chemical and electrochemical reductions of some allyl type halides catalyzed by vitamin B-12. in Indian Journal of Chemistry. Section B: Organic and Medicinal Chemistry. 1997;36(9):765-768.
https://hdl.handle.net/21.15107/rcub_cherry_363 .

Petrović, ZD, Konstantinovic, S, Scheffold, R, Milosavljevic, S, "Chemical and electrochemical reductions of some allyl type halides catalyzed by vitamin B-12" in Indian Journal of Chemistry. Section B: Organic and Medicinal Chemistry, 36, no. 9 (1997):765-768,
https://hdl.handle.net/21.15107/rcub_cherry_363 .