TY  - JOUR
AU  - Vučković, Ivan
AU  - Stiković, Sonja
AU  - Stešević, Danijela
AU  - Jadranin, Milka
AU  - Trifunović, Snežana S.
PY  - 2021
UR  - http://cherry.chem.bg.ac.rs/handle/123456789/5040
AB  - The plant species Pimpinella serbica (Vis.) Drude, endemic to West
Balkans, belongs to the genus Pimpinella L. (Apiaceae) according to newer
botanical classification. Initially, the plant was described as Pancicia serbica Vis.
and long considered as a monotypic genus. Previous phytochemical investigations
of this plant were limited to the essential oil analysis by the GC–MS method. This
is first study that includes LC-DAD–MS screening of the extracts of the roots and
aerial parts, followed by isolation of secondary metabolites using chromatographic
techniques. Five compounds belonging to phenylpropanoids and polyacetylenes,
well known for their bioactivities, were isolated and structurally determined by
combined spectroscopic methods (UV, NMR, MS). Dillapiole (1), nothoapiole (2)
and oplopantriol A 18-acetate (4) were found in both extracts, while falcarindiol (3)
was isolated from the roots and dendrotrifidol (5) from the aerial parts only. The
phytochemical profile of P. serbica L. supports its position in the Pimpinella L.
genus.
PB  - Belgrade : Serbian Chemical Society
T2  - Journal of the Serbian Chemical Society
T1  - Phytochemical investigation of Pimpinella serbica
VL  - 86
IS  - 12
SP  - 1241
EP  - 1247
DO  - 10.2298/JSC210816081V
ER  - 

@article{
author = "Vučković, Ivan and Stiković, Sonja and Stešević, Danijela and Jadranin, Milka and Trifunović, Snežana S.",
year = "2021",
abstract = "The plant species Pimpinella serbica (Vis.) Drude, endemic to West
Balkans, belongs to the genus Pimpinella L. (Apiaceae) according to newer
botanical classification. Initially, the plant was described as Pancicia serbica Vis.
and long considered as a monotypic genus. Previous phytochemical investigations
of this plant were limited to the essential oil analysis by the GC–MS method. This
is first study that includes LC-DAD–MS screening of the extracts of the roots and
aerial parts, followed by isolation of secondary metabolites using chromatographic
techniques. Five compounds belonging to phenylpropanoids and polyacetylenes,
well known for their bioactivities, were isolated and structurally determined by
combined spectroscopic methods (UV, NMR, MS). Dillapiole (1), nothoapiole (2)
and oplopantriol A 18-acetate (4) were found in both extracts, while falcarindiol (3)
was isolated from the roots and dendrotrifidol (5) from the aerial parts only. The
phytochemical profile of P. serbica L. supports its position in the Pimpinella L.
genus.",
publisher = "Belgrade : Serbian Chemical Society",
journal = "Journal of the Serbian Chemical Society",
title = "Phytochemical investigation of Pimpinella serbica",
volume = "86",
number = "12",
pages = "1241-1247",
doi = "10.2298/JSC210816081V"
}

Vučković, I., Stiković, S., Stešević, D., Jadranin, M.,& Trifunović, S. S.. (2021). Phytochemical investigation of Pimpinella serbica. in Journal of the Serbian Chemical Society
Belgrade : Serbian Chemical Society., 86(12), 1241-1247.
https://doi.org/10.2298/JSC210816081V

Vučković I, Stiković S, Stešević D, Jadranin M, Trifunović SS. Phytochemical investigation of Pimpinella serbica. in Journal of the Serbian Chemical Society. 2021;86(12):1241-1247.
doi:10.2298/JSC210816081V .

Vučković, Ivan, Stiković, Sonja, Stešević, Danijela, Jadranin, Milka, Trifunović, Snežana S., "Phytochemical investigation of Pimpinella serbica" in Journal of the Serbian Chemical Society, 86, no. 12 (2021):1241-1247,
https://doi.org/10.2298/JSC210816081V . .

TY  - DATA
AU  - Vučković, Ivan
AU  - Stiković, Sonja
AU  - Stešević, Danijela
AU  - Jadranin, Milka
AU  - Trifunović, Snežana S.
PY  - 2021
UR  - http://cherry.chem.bg.ac.rs/handle/123456789/5117
PB  - Belgrade : Serbian Chemical Society
T2  - Journal of the Serbian Chemical Society
T1  - Supplementary data for the article: Vučković, I.; Stiković, S.; Stešević, D.; Jadranin, M.; Trifunović, S. Phytochemical Investigation of Pimpinella Serbica. Journal of the Serbian Chemical Society 2021, 86 (12), 1241–1247. https://doi.org/10.2298/JSC210816081V.
UR  - https://hdl.handle.net/21.15107/rcub_cherry_5117
ER  - 

@misc{
author = "Vučković, Ivan and Stiković, Sonja and Stešević, Danijela and Jadranin, Milka and Trifunović, Snežana S.",
year = "2021",
publisher = "Belgrade : Serbian Chemical Society",
journal = "Journal of the Serbian Chemical Society",
title = "Supplementary data for the article: Vučković, I.; Stiković, S.; Stešević, D.; Jadranin, M.; Trifunović, S. Phytochemical Investigation of Pimpinella Serbica. Journal of the Serbian Chemical Society 2021, 86 (12), 1241–1247. https://doi.org/10.2298/JSC210816081V.",
url = "https://hdl.handle.net/21.15107/rcub_cherry_5117"
}

Vučković, I., Stiković, S., Stešević, D., Jadranin, M.,& Trifunović, S. S.. (2021). Supplementary data for the article: Vučković, I.; Stiković, S.; Stešević, D.; Jadranin, M.; Trifunović, S. Phytochemical Investigation of Pimpinella Serbica. Journal of the Serbian Chemical Society 2021, 86 (12), 1241–1247. https://doi.org/10.2298/JSC210816081V.. in Journal of the Serbian Chemical Society
Belgrade : Serbian Chemical Society..
https://hdl.handle.net/21.15107/rcub_cherry_5117

Vučković I, Stiković S, Stešević D, Jadranin M, Trifunović SS. Supplementary data for the article: Vučković, I.; Stiković, S.; Stešević, D.; Jadranin, M.; Trifunović, S. Phytochemical Investigation of Pimpinella Serbica. Journal of the Serbian Chemical Society 2021, 86 (12), 1241–1247. https://doi.org/10.2298/JSC210816081V.. in Journal of the Serbian Chemical Society. 2021;.
https://hdl.handle.net/21.15107/rcub_cherry_5117 .

Vučković, Ivan, Stiković, Sonja, Stešević, Danijela, Jadranin, Milka, Trifunović, Snežana S., "Supplementary data for the article: Vučković, I.; Stiković, S.; Stešević, D.; Jadranin, M.; Trifunović, S. Phytochemical Investigation of Pimpinella Serbica. Journal of the Serbian Chemical Society 2021, 86 (12), 1241–1247. https://doi.org/10.2298/JSC210816081V." in Journal of the Serbian Chemical Society (2021),
https://hdl.handle.net/21.15107/rcub_cherry_5117 .

TY  - JOUR
AU  - Stanković, Nada
AU  - Šenerović, Lidija
AU  - Bojić-Trbojević, Žanka
AU  - Vučković, Ivan
AU  - Vicovac, Ljiljana
AU  - Vasiljević, Branka
AU  - Nikodinović-Runić, Jasmina
PY  - 2013
UR  - https://cherry.chem.bg.ac.rs/handle/123456789/1438
AB  - AimsThe aim of this study was to improve production of pentaene 32,33-didehydroroflamycoin (DDHR) in Streptomyces durmitorensis MS405 strain to obtain quantities sufficient for in depth analysis of antimicrobial properties. Methods and ResultsThrough classical medium optimization conditions for stable growth, DDHR production within 7days of incubation was established. Yields of 215mgl(-1) were achieved in shake flask experiments in complex medium with mannitol as the primary carbon source. DDHR had poor antibacterial activity with minimal inhibitory concentrations (MIC) of 400gml(-1) for Staphylococcus aureus and Bacillus subtilis, while MIC of 70gml(-1) was determined for Candida albicans. Using flow cytometry and fluorescent microscopy, it was demonstrated that DDHR induced membrane damage in C.albicans followed by cell death. Combination studies with known antifungal nystatin showed that DDHR is a promising agent for the development of novel antimycotic treatments potentially less toxic for human cells. ConclusionsPentaene didehydroroflamycoin has no antibacterial activity but can be further developed for the application in antifungal therapy. Significance and Impact of the StudyThis study is the first report on the stable and production in high yields of a novel pentaene family that acts on Candida cell membranes and can be used in combination with known antifungals. Polyenes are still antifungal antibiotics of choice, and therefore, isolation and production of new lead structures are highly significant.
PB  - Wiley, Hoboken
T2  - Journal of Applied Microbiology
T1  - Didehydroroflamycoin pentaene macrolide family from Streptomyces durmitorensis MS405(T): production optimization and antimicrobial activity
VL  - 115
IS  - 6
SP  - 1297
EP  - 1306
DO  - 10.1111/jam.12326
ER  - 

@article{
author = "Stanković, Nada and Šenerović, Lidija and Bojić-Trbojević, Žanka and Vučković, Ivan and Vicovac, Ljiljana and Vasiljević, Branka and Nikodinović-Runić, Jasmina",
year = "2013",
abstract = "AimsThe aim of this study was to improve production of pentaene 32,33-didehydroroflamycoin (DDHR) in Streptomyces durmitorensis MS405 strain to obtain quantities sufficient for in depth analysis of antimicrobial properties. Methods and ResultsThrough classical medium optimization conditions for stable growth, DDHR production within 7days of incubation was established. Yields of 215mgl(-1) were achieved in shake flask experiments in complex medium with mannitol as the primary carbon source. DDHR had poor antibacterial activity with minimal inhibitory concentrations (MIC) of 400gml(-1) for Staphylococcus aureus and Bacillus subtilis, while MIC of 70gml(-1) was determined for Candida albicans. Using flow cytometry and fluorescent microscopy, it was demonstrated that DDHR induced membrane damage in C.albicans followed by cell death. Combination studies with known antifungal nystatin showed that DDHR is a promising agent for the development of novel antimycotic treatments potentially less toxic for human cells. ConclusionsPentaene didehydroroflamycoin has no antibacterial activity but can be further developed for the application in antifungal therapy. Significance and Impact of the StudyThis study is the first report on the stable and production in high yields of a novel pentaene family that acts on Candida cell membranes and can be used in combination with known antifungals. Polyenes are still antifungal antibiotics of choice, and therefore, isolation and production of new lead structures are highly significant.",
publisher = "Wiley, Hoboken",
journal = "Journal of Applied Microbiology",
title = "Didehydroroflamycoin pentaene macrolide family from Streptomyces durmitorensis MS405(T): production optimization and antimicrobial activity",
volume = "115",
number = "6",
pages = "1297-1306",
doi = "10.1111/jam.12326"
}

Stanković, N., Šenerović, L., Bojić-Trbojević, Ž., Vučković, I., Vicovac, L., Vasiljević, B.,& Nikodinović-Runić, J.. (2013). Didehydroroflamycoin pentaene macrolide family from Streptomyces durmitorensis MS405(T): production optimization and antimicrobial activity. in Journal of Applied Microbiology
Wiley, Hoboken., 115(6), 1297-1306.
https://doi.org/10.1111/jam.12326

Stanković N, Šenerović L, Bojić-Trbojević Ž, Vučković I, Vicovac L, Vasiljević B, Nikodinović-Runić J. Didehydroroflamycoin pentaene macrolide family from Streptomyces durmitorensis MS405(T): production optimization and antimicrobial activity. in Journal of Applied Microbiology. 2013;115(6):1297-1306.
doi:10.1111/jam.12326 .

Stanković, Nada, Šenerović, Lidija, Bojić-Trbojević, Žanka, Vučković, Ivan, Vicovac, Ljiljana, Vasiljević, Branka, Nikodinović-Runić, Jasmina, "Didehydroroflamycoin pentaene macrolide family from Streptomyces durmitorensis MS405(T): production optimization and antimicrobial activity" in Journal of Applied Microbiology, 115, no. 6 (2013):1297-1306,
https://doi.org/10.1111/jam.12326 . .

TY  - JOUR
AU  - Stanković, Nada
AU  - Šenerović, Lidija
AU  - Bojić-Trbojević, Žanka
AU  - Vučković, Ivan
AU  - Vicovac, Ljiljana
AU  - Vasiljević, Branka
AU  - Nikodinović-Runić, Jasmina
PY  - 2013
UR  - https://cherry.chem.bg.ac.rs/handle/123456789/3486
AB  - AimsThe aim of this study was to improve production of pentaene 32,33-didehydroroflamycoin (DDHR) in Streptomyces durmitorensis MS405 strain to obtain quantities sufficient for in depth analysis of antimicrobial properties. Methods and ResultsThrough classical medium optimization conditions for stable growth, DDHR production within 7days of incubation was established. Yields of 215mgl(-1) were achieved in shake flask experiments in complex medium with mannitol as the primary carbon source. DDHR had poor antibacterial activity with minimal inhibitory concentrations (MIC) of 400gml(-1) for Staphylococcus aureus and Bacillus subtilis, while MIC of 70gml(-1) was determined for Candida albicans. Using flow cytometry and fluorescent microscopy, it was demonstrated that DDHR induced membrane damage in C.albicans followed by cell death. Combination studies with known antifungal nystatin showed that DDHR is a promising agent for the development of novel antimycotic treatments potentially less toxic for human cells. ConclusionsPentaene didehydroroflamycoin has no antibacterial activity but can be further developed for the application in antifungal therapy. Significance and Impact of the StudyThis study is the first report on the stable and production in high yields of a novel pentaene family that acts on Candida cell membranes and can be used in combination with known antifungals. Polyenes are still antifungal antibiotics of choice, and therefore, isolation and production of new lead structures are highly significant.
PB  - Wiley, Hoboken
T2  - Journal of Applied Microbiology
T1  - Didehydroroflamycoin pentaene macrolide family from Streptomyces durmitorensis MS405(T): production optimization and antimicrobial activity
VL  - 115
IS  - 6
SP  - 1297
EP  - 1306
DO  - 10.1111/jam.12326
ER  - 

@article{
author = "Stanković, Nada and Šenerović, Lidija and Bojić-Trbojević, Žanka and Vučković, Ivan and Vicovac, Ljiljana and Vasiljević, Branka and Nikodinović-Runić, Jasmina",
year = "2013",
abstract = "AimsThe aim of this study was to improve production of pentaene 32,33-didehydroroflamycoin (DDHR) in Streptomyces durmitorensis MS405 strain to obtain quantities sufficient for in depth analysis of antimicrobial properties. Methods and ResultsThrough classical medium optimization conditions for stable growth, DDHR production within 7days of incubation was established. Yields of 215mgl(-1) were achieved in shake flask experiments in complex medium with mannitol as the primary carbon source. DDHR had poor antibacterial activity with minimal inhibitory concentrations (MIC) of 400gml(-1) for Staphylococcus aureus and Bacillus subtilis, while MIC of 70gml(-1) was determined for Candida albicans. Using flow cytometry and fluorescent microscopy, it was demonstrated that DDHR induced membrane damage in C.albicans followed by cell death. Combination studies with known antifungal nystatin showed that DDHR is a promising agent for the development of novel antimycotic treatments potentially less toxic for human cells. ConclusionsPentaene didehydroroflamycoin has no antibacterial activity but can be further developed for the application in antifungal therapy. Significance and Impact of the StudyThis study is the first report on the stable and production in high yields of a novel pentaene family that acts on Candida cell membranes and can be used in combination with known antifungals. Polyenes are still antifungal antibiotics of choice, and therefore, isolation and production of new lead structures are highly significant.",
publisher = "Wiley, Hoboken",
journal = "Journal of Applied Microbiology",
title = "Didehydroroflamycoin pentaene macrolide family from Streptomyces durmitorensis MS405(T): production optimization and antimicrobial activity",
volume = "115",
number = "6",
pages = "1297-1306",
doi = "10.1111/jam.12326"
}

Stanković, N., Šenerović, L., Bojić-Trbojević, Ž., Vučković, I., Vicovac, L., Vasiljević, B.,& Nikodinović-Runić, J.. (2013). Didehydroroflamycoin pentaene macrolide family from Streptomyces durmitorensis MS405(T): production optimization and antimicrobial activity. in Journal of Applied Microbiology
Wiley, Hoboken., 115(6), 1297-1306.
https://doi.org/10.1111/jam.12326

Stanković N, Šenerović L, Bojić-Trbojević Ž, Vučković I, Vicovac L, Vasiljević B, Nikodinović-Runić J. Didehydroroflamycoin pentaene macrolide family from Streptomyces durmitorensis MS405(T): production optimization and antimicrobial activity. in Journal of Applied Microbiology. 2013;115(6):1297-1306.
doi:10.1111/jam.12326 .

Stanković, Nada, Šenerović, Lidija, Bojić-Trbojević, Žanka, Vučković, Ivan, Vicovac, Ljiljana, Vasiljević, Branka, Nikodinović-Runić, Jasmina, "Didehydroroflamycoin pentaene macrolide family from Streptomyces durmitorensis MS405(T): production optimization and antimicrobial activity" in Journal of Applied Microbiology, 115, no. 6 (2013):1297-1306,
https://doi.org/10.1111/jam.12326 . .

TY  - DATA
AU  - Stanković, Nada
AU  - Šenerović, Lidija
AU  - Bojić-Trbojević, Žanka
AU  - Vučković, Ivan
AU  - Vicovac, Ljiljana
AU  - Vasiljević, Branka
AU  - Nikodinović-Runić, Jasmina
PY  - 2013
UR  - https://cherry.chem.bg.ac.rs/handle/123456789/3487
PB  - Wiley, Hoboken
T2  - Journal of Applied Microbiology
T1  - Supplementary data for article: Stanković, N.; Šenerović, L.; Bojic-Trbojevic, Z.; Vuckovic, I.; Vicovac, L.; Vasiljevic, B.; Nikodinović-Runić, J. Didehydroroflamycoin Pentaene Macrolide Family from Streptomyces Durmitorensis MS405(T): Production Optimization and Antimicrobial Activity. Journal of Applied Microbiology 2013, 115 (6), 1297–1306. https://doi.org/10.1111/jam.12326
UR  - https://hdl.handle.net/21.15107/rcub_cherry_3487
ER  - 

@misc{
author = "Stanković, Nada and Šenerović, Lidija and Bojić-Trbojević, Žanka and Vučković, Ivan and Vicovac, Ljiljana and Vasiljević, Branka and Nikodinović-Runić, Jasmina",
year = "2013",
publisher = "Wiley, Hoboken",
journal = "Journal of Applied Microbiology",
title = "Supplementary data for article: Stanković, N.; Šenerović, L.; Bojic-Trbojevic, Z.; Vuckovic, I.; Vicovac, L.; Vasiljevic, B.; Nikodinović-Runić, J. Didehydroroflamycoin Pentaene Macrolide Family from Streptomyces Durmitorensis MS405(T): Production Optimization and Antimicrobial Activity. Journal of Applied Microbiology 2013, 115 (6), 1297–1306. https://doi.org/10.1111/jam.12326",
url = "https://hdl.handle.net/21.15107/rcub_cherry_3487"
}

Stanković, N., Šenerović, L., Bojić-Trbojević, Ž., Vučković, I., Vicovac, L., Vasiljević, B.,& Nikodinović-Runić, J.. (2013). Supplementary data for article: Stanković, N.; Šenerović, L.; Bojic-Trbojevic, Z.; Vuckovic, I.; Vicovac, L.; Vasiljevic, B.; Nikodinović-Runić, J. Didehydroroflamycoin Pentaene Macrolide Family from Streptomyces Durmitorensis MS405(T): Production Optimization and Antimicrobial Activity. Journal of Applied Microbiology 2013, 115 (6), 1297–1306. https://doi.org/10.1111/jam.12326. in Journal of Applied Microbiology
Wiley, Hoboken..
https://hdl.handle.net/21.15107/rcub_cherry_3487

Stanković N, Šenerović L, Bojić-Trbojević Ž, Vučković I, Vicovac L, Vasiljević B, Nikodinović-Runić J. Supplementary data for article: Stanković, N.; Šenerović, L.; Bojic-Trbojevic, Z.; Vuckovic, I.; Vicovac, L.; Vasiljevic, B.; Nikodinović-Runić, J. Didehydroroflamycoin Pentaene Macrolide Family from Streptomyces Durmitorensis MS405(T): Production Optimization and Antimicrobial Activity. Journal of Applied Microbiology 2013, 115 (6), 1297–1306. https://doi.org/10.1111/jam.12326. in Journal of Applied Microbiology. 2013;.
https://hdl.handle.net/21.15107/rcub_cherry_3487 .

Stanković, Nada, Šenerović, Lidija, Bojić-Trbojević, Žanka, Vučković, Ivan, Vicovac, Ljiljana, Vasiljević, Branka, Nikodinović-Runić, Jasmina, "Supplementary data for article: Stanković, N.; Šenerović, L.; Bojic-Trbojevic, Z.; Vuckovic, I.; Vicovac, L.; Vasiljevic, B.; Nikodinović-Runić, J. Didehydroroflamycoin Pentaene Macrolide Family from Streptomyces Durmitorensis MS405(T): Production Optimization and Antimicrobial Activity. Journal of Applied Microbiology 2013, 115 (6), 1297–1306. https://doi.org/10.1111/jam.12326" in Journal of Applied Microbiology (2013),
https://hdl.handle.net/21.15107/rcub_cherry_3487 .

TY  - JOUR
AU  - Vujisić, Ljubodrag V.
AU  - Vučković, Ivan
AU  - Vajs, Vlatka
AU  - Tešević, Vele
AU  - Janaćković, Peđa T.
AU  - Milosavljević, Slobodan M.
PY  - 2011
UR  - https://cherry.chem.bg.ac.rs/handle/123456789/1188
PB  - Springer, New York
T2  - Chemistry of Natural Compounds
T1  - Sesquiterpene Lactones and Flavonoids from  Anthemis Ruthenica Growing Wild in Serbia
VL  - 47
IS  - 3
SP  - 459
EP  - 460
DO  - 10.1007/s10600-011-9963-8
ER  - 

@article{
author = "Vujisić, Ljubodrag V. and Vučković, Ivan and Vajs, Vlatka and Tešević, Vele and Janaćković, Peđa T. and Milosavljević, Slobodan M.",
year = "2011",
publisher = "Springer, New York",
journal = "Chemistry of Natural Compounds",
title = "Sesquiterpene Lactones and Flavonoids from  Anthemis Ruthenica Growing Wild in Serbia",
volume = "47",
number = "3",
pages = "459-460",
doi = "10.1007/s10600-011-9963-8"
}

Vujisić, L. V., Vučković, I., Vajs, V., Tešević, V., Janaćković, P. T.,& Milosavljević, S. M.. (2011). Sesquiterpene Lactones and Flavonoids from  Anthemis Ruthenica Growing Wild in Serbia. in Chemistry of Natural Compounds
Springer, New York., 47(3), 459-460.
https://doi.org/10.1007/s10600-011-9963-8

Vujisić LV, Vučković I, Vajs V, Tešević V, Janaćković PT, Milosavljević SM. Sesquiterpene Lactones and Flavonoids from  Anthemis Ruthenica Growing Wild in Serbia. in Chemistry of Natural Compounds. 2011;47(3):459-460.
doi:10.1007/s10600-011-9963-8 .

Vujisić, Ljubodrag V., Vučković, Ivan, Vajs, Vlatka, Tešević, Vele, Janaćković, Peđa T., Milosavljević, Slobodan M., "Sesquiterpene Lactones and Flavonoids from  Anthemis Ruthenica Growing Wild in Serbia" in Chemistry of Natural Compounds, 47, no. 3 (2011):459-460,
https://doi.org/10.1007/s10600-011-9963-8 . .

TY  - JOUR
AU  - Vujisić, Ljubodrag V.
AU  - Vučković, Ivan
AU  - Tešević, Vele
AU  - Dokovic, D
AU  - Ristic, MS
AU  - Janaćković, Peđa T.
AU  - Milosavljevic, S
PY  - 2006
UR  - https://cherry.chem.bg.ac.rs/handle/123456789/778
AB  - The essential oils from the aerial parts of Anthemis ruthenica and Anthemis arvensis, wild-growing in Serbia, obtained by hydrodistillation were analyzed using GC and GC/MS. A total of 75 and 81 components were identified in A. ruthenica and A. arvensis, respectively. The major constituents of A. ruthenica oil were ss-pinene (3.6%), 1,8-cineol (6.8%), 4-terpineol (6.2%), alpha-terpineol (3.6%), isophyllocladene (5.4%) and palmitic acid (9.9%). The oil of A. arvensis showed a high content of non-terpenic compounds. The main components were palmitic acid (21.2%) and linoleic acid (6.5%). The most abundant terpenic compounds in the oil of A. arvensis were pinocarvone (5.4%) and isospathulenol (4.6%). Copyright (c) 2006 John Wiley & Sons, Ltd.
PB  - John Wiley & Sons Ltd, Chichester
T2  - Flavour and Fragrance Journal
T1  - Comparative examination of the essential oils of Anthemis ruthenica and A-arvensis wild-growing in Serbia
VL  - 21
IS  - 3
SP  - 458
EP  - 461
DO  - 10.1002/ffj.1681
ER  - 

@article{
author = "Vujisić, Ljubodrag V. and Vučković, Ivan and Tešević, Vele and Dokovic, D and Ristic, MS and Janaćković, Peđa T. and Milosavljevic, S",
year = "2006",
abstract = "The essential oils from the aerial parts of Anthemis ruthenica and Anthemis arvensis, wild-growing in Serbia, obtained by hydrodistillation were analyzed using GC and GC/MS. A total of 75 and 81 components were identified in A. ruthenica and A. arvensis, respectively. The major constituents of A. ruthenica oil were ss-pinene (3.6%), 1,8-cineol (6.8%), 4-terpineol (6.2%), alpha-terpineol (3.6%), isophyllocladene (5.4%) and palmitic acid (9.9%). The oil of A. arvensis showed a high content of non-terpenic compounds. The main components were palmitic acid (21.2%) and linoleic acid (6.5%). The most abundant terpenic compounds in the oil of A. arvensis were pinocarvone (5.4%) and isospathulenol (4.6%). Copyright (c) 2006 John Wiley & Sons, Ltd.",
publisher = "John Wiley & Sons Ltd, Chichester",
journal = "Flavour and Fragrance Journal",
title = "Comparative examination of the essential oils of Anthemis ruthenica and A-arvensis wild-growing in Serbia",
volume = "21",
number = "3",
pages = "458-461",
doi = "10.1002/ffj.1681"
}

Vujisić, L. V., Vučković, I., Tešević, V., Dokovic, D., Ristic, M., Janaćković, P. T.,& Milosavljevic, S.. (2006). Comparative examination of the essential oils of Anthemis ruthenica and A-arvensis wild-growing in Serbia. in Flavour and Fragrance Journal
John Wiley & Sons Ltd, Chichester., 21(3), 458-461.
https://doi.org/10.1002/ffj.1681

Vujisić LV, Vučković I, Tešević V, Dokovic D, Ristic M, Janaćković PT, Milosavljevic S. Comparative examination of the essential oils of Anthemis ruthenica and A-arvensis wild-growing in Serbia. in Flavour and Fragrance Journal. 2006;21(3):458-461.
doi:10.1002/ffj.1681 .

Vujisić, Ljubodrag V., Vučković, Ivan, Tešević, Vele, Dokovic, D, Ristic, MS, Janaćković, Peđa T., Milosavljevic, S, "Comparative examination of the essential oils of Anthemis ruthenica and A-arvensis wild-growing in Serbia" in Flavour and Fragrance Journal, 21, no. 3 (2006):458-461,
https://doi.org/10.1002/ffj.1681 . .

TY  - JOUR
AU  - Vučković, Ivan
AU  - Vujisić, Ljubodrag V.
AU  - Vajs, Vlatka
AU  - Tešević, Vele
AU  - Janaćković, Peđa T.
AU  - Milosavljevic, S
PY  - 2006
UR  - https://cherry.chem.bg.ac.rs/handle/123456789/760
AB  - The investigation of roots of Anthemis cotula (Asteraceae) from cast Serbia revealed, in addition to polyacetylenes previously isolated from the same species, three prenylated 4-hydroxyacetophenones, detected for the first time in any Anthemis species. It is possible that they act as phytoalexins in the plant. From the aerial parts, six linear sesquiterpene lactones (four known and two new ones), as well as two known flavones, apigenin and hispidulin, were isolated.
AB  - Novo ispitivanje korena biljke A. cotula (Asteraceae) pokazalo je, pored četiri već izolovana poliacetilena, i prisustvo tri prenilovana 4-hidroksiacetofenona koji do sada nisu bili izolovani iz ovog roda. Iz nadzemnog dela biljke izolovano je šest linearnih seskviterpenskih laktona, od koji su dva nova, dok su preostali ranije nađeni u istoj biljci. Takođe su u nadzemnom delu identifikovana dva poznata flavona, apigenin i hispidulin.
PB  - Serbian Chemical Soc, Belgrade
T2  - Journal of the Serbian Chemical Society
T1  - Phytochemical investigation of Anthemis cotula
T1  - Fitohemijsko ispitivanje biljne vrste Anthemis cotula
VL  - 71
IS  - 2
SP  - 127
EP  - 133
DO  - 10.2298/JSC0602127V
ER  - 

@article{
author = "Vučković, Ivan and Vujisić, Ljubodrag V. and Vajs, Vlatka and Tešević, Vele and Janaćković, Peđa T. and Milosavljevic, S",
year = "2006",
abstract = "The investigation of roots of Anthemis cotula (Asteraceae) from cast Serbia revealed, in addition to polyacetylenes previously isolated from the same species, three prenylated 4-hydroxyacetophenones, detected for the first time in any Anthemis species. It is possible that they act as phytoalexins in the plant. From the aerial parts, six linear sesquiterpene lactones (four known and two new ones), as well as two known flavones, apigenin and hispidulin, were isolated., Novo ispitivanje korena biljke A. cotula (Asteraceae) pokazalo je, pored četiri već izolovana poliacetilena, i prisustvo tri prenilovana 4-hidroksiacetofenona koji do sada nisu bili izolovani iz ovog roda. Iz nadzemnog dela biljke izolovano je šest linearnih seskviterpenskih laktona, od koji su dva nova, dok su preostali ranije nađeni u istoj biljci. Takođe su u nadzemnom delu identifikovana dva poznata flavona, apigenin i hispidulin.",
publisher = "Serbian Chemical Soc, Belgrade",
journal = "Journal of the Serbian Chemical Society",
title = "Phytochemical investigation of Anthemis cotula, Fitohemijsko ispitivanje biljne vrste Anthemis cotula",
volume = "71",
number = "2",
pages = "127-133",
doi = "10.2298/JSC0602127V"
}

Vučković, I., Vujisić, L. V., Vajs, V., Tešević, V., Janaćković, P. T.,& Milosavljevic, S.. (2006). Phytochemical investigation of Anthemis cotula. in Journal of the Serbian Chemical Society
Serbian Chemical Soc, Belgrade., 71(2), 127-133.
https://doi.org/10.2298/JSC0602127V

Vučković I, Vujisić LV, Vajs V, Tešević V, Janaćković PT, Milosavljevic S. Phytochemical investigation of Anthemis cotula. in Journal of the Serbian Chemical Society. 2006;71(2):127-133.
doi:10.2298/JSC0602127V .

Vučković, Ivan, Vujisić, Ljubodrag V., Vajs, Vlatka, Tešević, Vele, Janaćković, Peđa T., Milosavljevic, S, "Phytochemical investigation of Anthemis cotula" in Journal of the Serbian Chemical Society, 71, no. 2 (2006):127-133,
https://doi.org/10.2298/JSC0602127V . .

TY  - JOUR
AU  - Tešević, Vele
AU  - Nikićević, Ninoslav
AU  - Jovanovic, A
AU  - Đoković, Dejan
AU  - Vujisić, Ljubodrag V.
AU  - Vučković, Ivan
AU  - Bonic, M
PY  - 2005
UR  - https://cherry.chem.bg.ac.rs/handle/123456789/745
AB  - Gas chromatography and GC/MS methods were used to detect volatile components of three home-made natural old plum brandy samples and one sample of industrially-produced plum brandy. Gas chromatography and gas chromatography-mass spectrometric analysis of this extracts led to the identification of 99 components, including 46 esters, 7 hydrocarbons (alkanes and alkenes), 3 aldehydes, 9 alcohols, 1 lactone, 1 ketone, 8 acetals, 14 terpenes, 8 acids and 2 phenols. Ethyl esters of C-8-C-18 acids were the most abundant in all samples. In addition, the content of methanol, ethanol and higher alcohols (C-3-C-5) was determined.
PB  - Faculty Food Technology Biotechnology, Zagreb
T2  - Food Technology and Biotechnology
T1  - Volatile components from old plum brandies
VL  - 43
IS  - 4
SP  - 367
EP  - 372
UR  - https://hdl.handle.net/21.15107/rcub_cherry_745
ER  - 

@article{
author = "Tešević, Vele and Nikićević, Ninoslav and Jovanovic, A and Đoković, Dejan and Vujisić, Ljubodrag V. and Vučković, Ivan and Bonic, M",
year = "2005",
abstract = "Gas chromatography and GC/MS methods were used to detect volatile components of three home-made natural old plum brandy samples and one sample of industrially-produced plum brandy. Gas chromatography and gas chromatography-mass spectrometric analysis of this extracts led to the identification of 99 components, including 46 esters, 7 hydrocarbons (alkanes and alkenes), 3 aldehydes, 9 alcohols, 1 lactone, 1 ketone, 8 acetals, 14 terpenes, 8 acids and 2 phenols. Ethyl esters of C-8-C-18 acids were the most abundant in all samples. In addition, the content of methanol, ethanol and higher alcohols (C-3-C-5) was determined.",
publisher = "Faculty Food Technology Biotechnology, Zagreb",
journal = "Food Technology and Biotechnology",
title = "Volatile components from old plum brandies",
volume = "43",
number = "4",
pages = "367-372",
url = "https://hdl.handle.net/21.15107/rcub_cherry_745"
}

Tešević, V., Nikićević, N., Jovanovic, A., Đoković, D., Vujisić, L. V., Vučković, I.,& Bonic, M.. (2005). Volatile components from old plum brandies. in Food Technology and Biotechnology
Faculty Food Technology Biotechnology, Zagreb., 43(4), 367-372.
https://hdl.handle.net/21.15107/rcub_cherry_745

Tešević V, Nikićević N, Jovanovic A, Đoković D, Vujisić LV, Vučković I, Bonic M. Volatile components from old plum brandies. in Food Technology and Biotechnology. 2005;43(4):367-372.
https://hdl.handle.net/21.15107/rcub_cherry_745 .

Tešević, Vele, Nikićević, Ninoslav, Jovanovic, A, Đoković, Dejan, Vujisić, Ljubodrag V., Vučković, Ivan, Bonic, M, "Volatile components from old plum brandies" in Food Technology and Biotechnology, 43, no. 4 (2005):367-372,
https://hdl.handle.net/21.15107/rcub_cherry_745 .