TY  - JOUR
AU  - Krstić, Gordana
AU  - Aljančić, Ivana
AU  - Stanković, Jovana
AU  - Cvetković, Mirjana
AU  - Marin, Petar D.
AU  - Janaćković, Peđa T.
AU  - Tešević, Vele
PY  - 2019
UR  - https://cer.ihtm.bg.ac.rs/handle/123456789/2923
AB  - The presence of n-alkanes, free alcohols and free acids in leaf epicuticular wax extracts of 22 samples of 11 Euphorbia L. species belonging to the sections Paralias, Esula, Myrsiniteae and Helioscopia, 10 of which were never examined before, were analyzed by gas chromatography (GC) and gas chromatography/mass spectrometry (GC/MS), and n-alkane C27 was detected as the principal component of leaf epicuticular waxes in the majority of the examined species, while the most abundant free alcohol was C26. Three Euphorbia species belonging to section Helioscopia were characterized by a predominance of alcohol C28. Free acid (C16) was the major component in 21 investigated samples. The usefulness of n-alkanes and free alcohols and free acids as potential chemotaxonomic markers is briefly discussed.
T2  - Archives of Biological Sciences
T1  - Leaf epicuticular waxes of eleven Euphorbia species (Euphorbiaceae) from the central Balkans: Impact on chemotaxonomy
VL  - 71
IS  - 1
SP  - 21
EP  - 26
DO  - 10.2298/ABS180608041K
ER  - 

@article{
author = "Krstić, Gordana and Aljančić, Ivana and Stanković, Jovana and Cvetković, Mirjana and Marin, Petar D. and Janaćković, Peđa T. and Tešević, Vele",
year = "2019",
abstract = "The presence of n-alkanes, free alcohols and free acids in leaf epicuticular wax extracts of 22 samples of 11 Euphorbia L. species belonging to the sections Paralias, Esula, Myrsiniteae and Helioscopia, 10 of which were never examined before, were analyzed by gas chromatography (GC) and gas chromatography/mass spectrometry (GC/MS), and n-alkane C27 was detected as the principal component of leaf epicuticular waxes in the majority of the examined species, while the most abundant free alcohol was C26. Three Euphorbia species belonging to section Helioscopia were characterized by a predominance of alcohol C28. Free acid (C16) was the major component in 21 investigated samples. The usefulness of n-alkanes and free alcohols and free acids as potential chemotaxonomic markers is briefly discussed.",
journal = "Archives of Biological Sciences",
title = "Leaf epicuticular waxes of eleven Euphorbia species (Euphorbiaceae) from the central Balkans: Impact on chemotaxonomy",
volume = "71",
number = "1",
pages = "21-26",
doi = "10.2298/ABS180608041K"
}

Krstić, G., Aljančić, I., Stanković, J., Cvetković, M., Marin, P. D., Janaćković, P. T.,& Tešević, V.. (2019). Leaf epicuticular waxes of eleven Euphorbia species (Euphorbiaceae) from the central Balkans: Impact on chemotaxonomy. in Archives of Biological Sciences, 71(1), 21-26.
https://doi.org/10.2298/ABS180608041K

Krstić G, Aljančić I, Stanković J, Cvetković M, Marin PD, Janaćković PT, Tešević V. Leaf epicuticular waxes of eleven Euphorbia species (Euphorbiaceae) from the central Balkans: Impact on chemotaxonomy. in Archives of Biological Sciences. 2019;71(1):21-26.
doi:10.2298/ABS180608041K .

Krstić, Gordana, Aljančić, Ivana, Stanković, Jovana, Cvetković, Mirjana, Marin, Petar D., Janaćković, Peđa T., Tešević, Vele, "Leaf epicuticular waxes of eleven Euphorbia species (Euphorbiaceae) from the central Balkans: Impact on chemotaxonomy" in Archives of Biological Sciences, 71, no. 1 (2019):21-26,
https://doi.org/10.2298/ABS180608041K . .

TY  - JOUR
AU  - Rajčević, Nemanja
AU  - Marin, Petar D.
AU  - Vujisić, Ljubodrag V.
AU  - Krivosej, Zoran
AU  - Vajs, Vlatka
AU  - Janaćković, Peđa T.
PY  - 2015
UR  - https://cer.ihtm.bg.ac.rs/handle/123456789/2724
AB  - The composition of essential oil isolated from the areal parts of Aster albanicus Deg, an endemic species of the central Balkans, was analyzed. In total, 111 compounds were identified, representing 98% of the essential oil. The essential oil was dominated by sesquiterpene (69.3%) and monoterpene hydrocarbons (15.9%), with germacrene D as the most abundant compound (34.7%). Several multivariant statistical methods (HCA, NJ, PCoA) were deployed to infer the relation between A. albanicus and other species belonging to this genus. Taxonomical implications are discussed.
PB  - Inst Bioloska Istrazivanja Sinisa Stankovic, Beograd
T2  - Archives of biological sciences
T1  - Chemical Composition of Aster Albanicus Deg. (Asteraceae) Essential Oil: Taxonomical Implications
VL  - 67
IS  - 3
SP  - 1055
EP  - 1061
DO  - 10.2298/ABS150223068R
ER  - 

@article{
author = "Rajčević, Nemanja and Marin, Petar D. and Vujisić, Ljubodrag V. and Krivosej, Zoran and Vajs, Vlatka and Janaćković, Peđa T.",
year = "2015",
abstract = "The composition of essential oil isolated from the areal parts of Aster albanicus Deg, an endemic species of the central Balkans, was analyzed. In total, 111 compounds were identified, representing 98% of the essential oil. The essential oil was dominated by sesquiterpene (69.3%) and monoterpene hydrocarbons (15.9%), with germacrene D as the most abundant compound (34.7%). Several multivariant statistical methods (HCA, NJ, PCoA) were deployed to infer the relation between A. albanicus and other species belonging to this genus. Taxonomical implications are discussed.",
publisher = "Inst Bioloska Istrazivanja Sinisa Stankovic, Beograd",
journal = "Archives of biological sciences",
title = "Chemical Composition of Aster Albanicus Deg. (Asteraceae) Essential Oil: Taxonomical Implications",
volume = "67",
number = "3",
pages = "1055-1061",
doi = "10.2298/ABS150223068R"
}

Rajčević, N., Marin, P. D., Vujisić, L. V., Krivosej, Z., Vajs, V.,& Janaćković, P. T.. (2015). Chemical Composition of Aster Albanicus Deg. (Asteraceae) Essential Oil: Taxonomical Implications. in Archives of biological sciences
Inst Bioloska Istrazivanja Sinisa Stankovic, Beograd., 67(3), 1055-1061.
https://doi.org/10.2298/ABS150223068R

Rajčević N, Marin PD, Vujisić LV, Krivosej Z, Vajs V, Janaćković PT. Chemical Composition of Aster Albanicus Deg. (Asteraceae) Essential Oil: Taxonomical Implications. in Archives of biological sciences. 2015;67(3):1055-1061.
doi:10.2298/ABS150223068R .

Rajčević, Nemanja, Marin, Petar D., Vujisić, Ljubodrag V., Krivosej, Zoran, Vajs, Vlatka, Janaćković, Peđa T., "Chemical Composition of Aster Albanicus Deg. (Asteraceae) Essential Oil: Taxonomical Implications" in Archives of biological sciences, 67, no. 3 (2015):1055-1061,
https://doi.org/10.2298/ABS150223068R . .

TY  - JOUR
AU  - Janaćković, Peđa T.
AU  - Soković, Marina
AU  - Vujisić, Ljubodrag V.
AU  - Vajs, Vlatka
AU  - Vučković, Ivan
AU  - Krivosej, Zoran
AU  - Marin, Petar D.
PY  - 2011
UR  - https://cer.ihtm.bg.ac.rs/handle/123456789/2739
AB  - The essential oil from aerial parts of Seseli globiferum Vis. obtained by hydrodistillation with Clevenger-type apparatus was analyzed by GC-MS. Twenty-eight compounds were identified, representing 99.4% of the total oil. The main components of the oil were sabinene (38.0%), alpha-pinene (21.2%) and beta-phellandrene (13.5%). The microbial growth inhibitory properties of the isolated essential oil were determined using the broth microdilution method against seven bacterial species: Salmonella typhimurium (ATCC 13311), Escherichia coli (ATCC 25922), Pseudomonas aeruginosa (ATCC 27853), Enterobacter cloacae (clinical isolates), Bacillus cereus (clinical isolates), Staphylococcus aureus (ATCC 25923), Staphylococcus epidermidis (ATCC 12228), Micrococcus flaw's (ATCC 10240) and three fungal species: Aspergillus niger (ATCC 6275), Aspergillus versicolor (ATCC 11730), Trichoderma viride (IAM 5061) and Penicillium funiculosum (ATCC 36839). The essential oil showed activity against bacteria P. aeruginosa, followed by M flavus, L. monocytigenes and E. coli, and all investigated fungal species.
PB  - Natural Products Inc, Westerville
T2  - Natural Product Communications
T1  - Composition and Antimicrobial Activity of Seseli globiferum Essential Oil
VL  - 6
IS  - 8
SP  - 1163
EP  - 1166
DO  - 10.1177/1934578X1100600831
ER  - 

@article{
author = "Janaćković, Peđa T. and Soković, Marina and Vujisić, Ljubodrag V. and Vajs, Vlatka and Vučković, Ivan and Krivosej, Zoran and Marin, Petar D.",
year = "2011",
abstract = "The essential oil from aerial parts of Seseli globiferum Vis. obtained by hydrodistillation with Clevenger-type apparatus was analyzed by GC-MS. Twenty-eight compounds were identified, representing 99.4% of the total oil. The main components of the oil were sabinene (38.0%), alpha-pinene (21.2%) and beta-phellandrene (13.5%). The microbial growth inhibitory properties of the isolated essential oil were determined using the broth microdilution method against seven bacterial species: Salmonella typhimurium (ATCC 13311), Escherichia coli (ATCC 25922), Pseudomonas aeruginosa (ATCC 27853), Enterobacter cloacae (clinical isolates), Bacillus cereus (clinical isolates), Staphylococcus aureus (ATCC 25923), Staphylococcus epidermidis (ATCC 12228), Micrococcus flaw's (ATCC 10240) and three fungal species: Aspergillus niger (ATCC 6275), Aspergillus versicolor (ATCC 11730), Trichoderma viride (IAM 5061) and Penicillium funiculosum (ATCC 36839). The essential oil showed activity against bacteria P. aeruginosa, followed by M flavus, L. monocytigenes and E. coli, and all investigated fungal species.",
publisher = "Natural Products Inc, Westerville",
journal = "Natural Product Communications",
title = "Composition and Antimicrobial Activity of Seseli globiferum Essential Oil",
volume = "6",
number = "8",
pages = "1163-1166",
doi = "10.1177/1934578X1100600831"
}

Janaćković, P. T., Soković, M., Vujisić, L. V., Vajs, V., Vučković, I., Krivosej, Z.,& Marin, P. D.. (2011). Composition and Antimicrobial Activity of Seseli globiferum Essential Oil. in Natural Product Communications
Natural Products Inc, Westerville., 6(8), 1163-1166.
https://doi.org/10.1177/1934578X1100600831

Janaćković PT, Soković M, Vujisić LV, Vajs V, Vučković I, Krivosej Z, Marin PD. Composition and Antimicrobial Activity of Seseli globiferum Essential Oil. in Natural Product Communications. 2011;6(8):1163-1166.
doi:10.1177/1934578X1100600831 .

Janaćković, Peđa T., Soković, Marina, Vujisić, Ljubodrag V., Vajs, Vlatka, Vučković, Ivan, Krivosej, Zoran, Marin, Petar D., "Composition and Antimicrobial Activity of Seseli globiferum Essential Oil" in Natural Product Communications, 6, no. 8 (2011):1163-1166,
https://doi.org/10.1177/1934578X1100600831 . .

TY  - JOUR
AU  - Milosavljević, Slobodan
AU  - Tešević, Vele
AU  - Vučković, Ivan
AU  - Jadranin, Milka
AU  - Vajs, Vlatka
AU  - Soković, Marina
AU  - Janaćković, Peđa T.
AU  - Jovanovic, Anka
PY  - 2007
UR  - https://cer.ihtm.bg.ac.rs/handle/123456789/2712
AB  - The essential oil from the aerial parts of Seseli annuum, wild-growing in Serbia, was obtained by hydrodistillation and analyzed using GC and GC/MS. A total of 43 components were identified representing 96.5% of S. annuum oil. The most abundant compounds were germacrene D (29.8%), sabinene (10.3%), beta-ocimene Z (9.8%) and limonene (8.6%). The essential oil showed antifungal activity against fifteen fungi with MICs between 12.5 to 50 mu l/ml. (c) 2007 Elsevier B.V. All rights reserved.
PB  - Elsevier
T2  - Fitoterapia
T1  - Composition and antifungal activity of the essential oil of Seseli annuum wild-growing in Serbia
VL  - 78
IS  - 4
SP  - 319
EP  - 322
DO  - 10.1016/j.fitote.2007.03.014
ER  - 

@article{
author = "Milosavljević, Slobodan and Tešević, Vele and Vučković, Ivan and Jadranin, Milka and Vajs, Vlatka and Soković, Marina and Janaćković, Peđa T. and Jovanovic, Anka",
year = "2007",
abstract = "The essential oil from the aerial parts of Seseli annuum, wild-growing in Serbia, was obtained by hydrodistillation and analyzed using GC and GC/MS. A total of 43 components were identified representing 96.5% of S. annuum oil. The most abundant compounds were germacrene D (29.8%), sabinene (10.3%), beta-ocimene Z (9.8%) and limonene (8.6%). The essential oil showed antifungal activity against fifteen fungi with MICs between 12.5 to 50 mu l/ml. (c) 2007 Elsevier B.V. All rights reserved.",
publisher = "Elsevier",
journal = "Fitoterapia",
title = "Composition and antifungal activity of the essential oil of Seseli annuum wild-growing in Serbia",
volume = "78",
number = "4",
pages = "319-322",
doi = "10.1016/j.fitote.2007.03.014"
}

Milosavljević, S., Tešević, V., Vučković, I., Jadranin, M., Vajs, V., Soković, M., Janaćković, P. T.,& Jovanovic, A.. (2007). Composition and antifungal activity of the essential oil of Seseli annuum wild-growing in Serbia. in Fitoterapia
Elsevier., 78(4), 319-322.
https://doi.org/10.1016/j.fitote.2007.03.014

Milosavljević S, Tešević V, Vučković I, Jadranin M, Vajs V, Soković M, Janaćković PT, Jovanovic A. Composition and antifungal activity of the essential oil of Seseli annuum wild-growing in Serbia. in Fitoterapia. 2007;78(4):319-322.
doi:10.1016/j.fitote.2007.03.014 .

Milosavljević, Slobodan, Tešević, Vele, Vučković, Ivan, Jadranin, Milka, Vajs, Vlatka, Soković, Marina, Janaćković, Peđa T., Jovanovic, Anka, "Composition and antifungal activity of the essential oil of Seseli annuum wild-growing in Serbia" in Fitoterapia, 78, no. 4 (2007):319-322,
https://doi.org/10.1016/j.fitote.2007.03.014 . .

TY  - JOUR
AU  - Tešević, Vele
AU  - Milosavljević, Slobodan
AU  - Vajs, Vlatka
AU  - Janaćković, Peđa
AU  - Đorđević, Iris
AU  - Jadranin, Milka
AU  - Vučković, Ivan
PY  - 2007
UR  - https://cer.ihtm.bg.ac.rs/handle/123456789/301
AB  - 1H-NMR spectroscopy was applied for the quantitative analysis of cnicin, a bioactive germacranolide type sesquiterpene lactone, in the aerial parts of seven wild-growing Centaurea species collected in Serbia and Montenegro. The analysis was performed by comparison of the integral of the one-proton signal of cnicin (H-13, δ 5.75) with that of the two-proton singlet ( δ 6.98) of 2,6-bis(1,1-dimethylethyl)-4-methylphenol (BHT), used as the internal standard. Cnicin, within the concentration range 1.06-6.12 mg/g, calculated per weight of the fresh plant material was detected in six species, the exception being C. salonitana. This method allows the rapid and simple quantification of cnicin without any pre-purification step.
AB  - 1H-NMR spektrometrija je primenjena za kvantitativnu analizu knicina, bioaktivnog seskviterpenskog laktona germakranolidnog tipa, u nadzemnom delu sedam samoniklih biljnih vrsta roda Centaurea sakupljenih u Srbiji i Crnoj Gori. Analiza je izvršena poređenjem integrala signala jednog protona knicina (H-13, δ 5.75) sa singletom koji potiče od dva protona ( δ 6.98) internog standarda, 2,6-bis(1,1-dimetiletil)-4-metilfenola (BHT). Knicin je detektovan u svim vrstama, osim u C. salonitana, u koncentracijama u opsegu od 1,06 do 6,12 mg/g, računato na masu svežeg biljnog materijala. Ovaj metod omogućava brzu i jednostavnu kvantifikaciju knicina bez prethodnog prečišćavanja.
PB  - Serbian Chemical Society
T2  - Journal of the Serbian Chemical Society
T1  - Quantitative analysis of sesquiterpene lactone cnicin in seven Centaurea species wild-growing in Serbia and Montenegro using 1H-NMR spectroscopy
T1  - Kvantitativna analiza seskviterpenskog laktona knicina u sedam samoniklih biljnih vrsta roda Centaurea, koje rastu u Srbiji i Crnoj Gori, korišćenjem 1H-NMR
VL  - 72
IS  - 12
SP  - 1275
EP  - 1280
DO  - 10.2298/JSC0712275T
ER  - 

@article{
author = "Tešević, Vele and Milosavljević, Slobodan and Vajs, Vlatka and Janaćković, Peđa and Đorđević, Iris and Jadranin, Milka and Vučković, Ivan",
year = "2007",
abstract = "1H-NMR spectroscopy was applied for the quantitative analysis of cnicin, a bioactive germacranolide type sesquiterpene lactone, in the aerial parts of seven wild-growing Centaurea species collected in Serbia and Montenegro. The analysis was performed by comparison of the integral of the one-proton signal of cnicin (H-13, δ 5.75) with that of the two-proton singlet ( δ 6.98) of 2,6-bis(1,1-dimethylethyl)-4-methylphenol (BHT), used as the internal standard. Cnicin, within the concentration range 1.06-6.12 mg/g, calculated per weight of the fresh plant material was detected in six species, the exception being C. salonitana. This method allows the rapid and simple quantification of cnicin without any pre-purification step., 1H-NMR spektrometrija je primenjena za kvantitativnu analizu knicina, bioaktivnog seskviterpenskog laktona germakranolidnog tipa, u nadzemnom delu sedam samoniklih biljnih vrsta roda Centaurea sakupljenih u Srbiji i Crnoj Gori. Analiza je izvršena poređenjem integrala signala jednog protona knicina (H-13, δ 5.75) sa singletom koji potiče od dva protona ( δ 6.98) internog standarda, 2,6-bis(1,1-dimetiletil)-4-metilfenola (BHT). Knicin je detektovan u svim vrstama, osim u C. salonitana, u koncentracijama u opsegu od 1,06 do 6,12 mg/g, računato na masu svežeg biljnog materijala. Ovaj metod omogućava brzu i jednostavnu kvantifikaciju knicina bez prethodnog prečišćavanja.",
publisher = "Serbian Chemical Society",
journal = "Journal of the Serbian Chemical Society",
title = "Quantitative analysis of sesquiterpene lactone cnicin in seven Centaurea species wild-growing in Serbia and Montenegro using 1H-NMR spectroscopy, Kvantitativna analiza seskviterpenskog laktona knicina u sedam samoniklih biljnih vrsta roda Centaurea, koje rastu u Srbiji i Crnoj Gori, korišćenjem 1H-NMR",
volume = "72",
number = "12",
pages = "1275-1280",
doi = "10.2298/JSC0712275T"
}

Tešević, V., Milosavljević, S., Vajs, V., Janaćković, P., Đorđević, I., Jadranin, M.,& Vučković, I.. (2007). Quantitative analysis of sesquiterpene lactone cnicin in seven Centaurea species wild-growing in Serbia and Montenegro using 1H-NMR spectroscopy. in Journal of the Serbian Chemical Society
Serbian Chemical Society., 72(12), 1275-1280.
https://doi.org/10.2298/JSC0712275T

Tešević V, Milosavljević S, Vajs V, Janaćković P, Đorđević I, Jadranin M, Vučković I. Quantitative analysis of sesquiterpene lactone cnicin in seven Centaurea species wild-growing in Serbia and Montenegro using 1H-NMR spectroscopy. in Journal of the Serbian Chemical Society. 2007;72(12):1275-1280.
doi:10.2298/JSC0712275T .

Tešević, Vele, Milosavljević, Slobodan, Vajs, Vlatka, Janaćković, Peđa, Đorđević, Iris, Jadranin, Milka, Vučković, Ivan, "Quantitative analysis of sesquiterpene lactone cnicin in seven Centaurea species wild-growing in Serbia and Montenegro using 1H-NMR spectroscopy" in Journal of the Serbian Chemical Society, 72, no. 12 (2007):1275-1280,
https://doi.org/10.2298/JSC0712275T . .

TY  - JOUR
AU  - Novaković, Miroslav
AU  - Vučković, Ivan
AU  - Janaćković, Peđa
AU  - Soković, Marina
AU  - Filipović, Anka
AU  - Tešević, Vele
AU  - Milosavljević, Slobodan
PY  - 2007
UR  - https://cer.ihtm.bg.ac.rs/handle/123456789/305
AB  - Essential oils from leaves with young branches of Cotinus coggygria Scop. from two localities in Serbia (Deliblatska peščara and Zemun), obtained by hydrodistillation, were analyzed by GC-MS. Thirty-one component were identified from both oils and among them monoterpenic hydrocarbons were the dominant class (87.4 and 93.1 %). The dominant constituent in both essential oils was limonene (47.0 and 39.2 %). Both oils were also tested for antibacterial and antifungal activities. In comparison to streptomycin, both oils showed slightly higher activity (against most Gram-positive bacteria) in the disc diffusion method and slightly lower activity when the microdilution method was employed. They also exhibited antifungal potential higher than that of the commercial fungicide bifonazole.
AB  - Primenom GC-MS metode identifikovana je ukupno 31 komponenta u oba etarska ulja izolovana destilacijom vodenom parom iz lišća i mladih grančica biljne vrste Cotinus coggygria Scop. sa dva lokaliteta u Srbiji (Deliblatska peščara i Zemun). Takođe je ispitana antibakterijska i antifungalna aktivnost oba uzorka. U oba ulja najzastupljeniji su bili monoterpenski ugljovodonici (87,4 i 93,1 %), među kojima je dominantna komponenta limonen (47,0 i 39,2 %). Antibakterijska aktivnost je određena difuzionom i mikrodilucionom metodom, a antifungalna aktivnost modifikovanom mikrodilucionom metodom. Prema dufuzionoj metodi, oba ulja su pokazala nešto bolje antibakterijsko dejstvo (prvenstveno na gram-pozitivne bakterije) nego streptomicin, dok je na osnovu mikrodilucione metode njihova aktivnost bila nešto slabija. U poređenju sa bifonazolom, oba testirana ulja su pokazala nešto bolje antifungalno dejstvo.
PB  - Serbian Chemical Society
T2  - Journal of the Serbian Chemical Society
T1  - Chemical composition, antibacterial and antifungal activity of the essential oils of Cotinus coggygria from Serbia
T1  - Hemijski sastav, antibakterijska i antifungalna aktivnost etarskih ulja biljne vrste Cotinus coggygria iz Srbije
VL  - 72
IS  - 11
SP  - 1045
EP  - 1051
DO  - 10.2298/JSC0711045N
ER  - 

@article{
author = "Novaković, Miroslav and Vučković, Ivan and Janaćković, Peđa and Soković, Marina and Filipović, Anka and Tešević, Vele and Milosavljević, Slobodan",
year = "2007",
abstract = "Essential oils from leaves with young branches of Cotinus coggygria Scop. from two localities in Serbia (Deliblatska peščara and Zemun), obtained by hydrodistillation, were analyzed by GC-MS. Thirty-one component were identified from both oils and among them monoterpenic hydrocarbons were the dominant class (87.4 and 93.1 %). The dominant constituent in both essential oils was limonene (47.0 and 39.2 %). Both oils were also tested for antibacterial and antifungal activities. In comparison to streptomycin, both oils showed slightly higher activity (against most Gram-positive bacteria) in the disc diffusion method and slightly lower activity when the microdilution method was employed. They also exhibited antifungal potential higher than that of the commercial fungicide bifonazole., Primenom GC-MS metode identifikovana je ukupno 31 komponenta u oba etarska ulja izolovana destilacijom vodenom parom iz lišća i mladih grančica biljne vrste Cotinus coggygria Scop. sa dva lokaliteta u Srbiji (Deliblatska peščara i Zemun). Takođe je ispitana antibakterijska i antifungalna aktivnost oba uzorka. U oba ulja najzastupljeniji su bili monoterpenski ugljovodonici (87,4 i 93,1 %), među kojima je dominantna komponenta limonen (47,0 i 39,2 %). Antibakterijska aktivnost je određena difuzionom i mikrodilucionom metodom, a antifungalna aktivnost modifikovanom mikrodilucionom metodom. Prema dufuzionoj metodi, oba ulja su pokazala nešto bolje antibakterijsko dejstvo (prvenstveno na gram-pozitivne bakterije) nego streptomicin, dok je na osnovu mikrodilucione metode njihova aktivnost bila nešto slabija. U poređenju sa bifonazolom, oba testirana ulja su pokazala nešto bolje antifungalno dejstvo.",
publisher = "Serbian Chemical Society",
journal = "Journal of the Serbian Chemical Society",
title = "Chemical composition, antibacterial and antifungal activity of the essential oils of Cotinus coggygria from Serbia, Hemijski sastav, antibakterijska i antifungalna aktivnost etarskih ulja biljne vrste Cotinus coggygria iz Srbije",
volume = "72",
number = "11",
pages = "1045-1051",
doi = "10.2298/JSC0711045N"
}

Novaković, M., Vučković, I., Janaćković, P., Soković, M., Filipović, A., Tešević, V.,& Milosavljević, S.. (2007). Chemical composition, antibacterial and antifungal activity of the essential oils of Cotinus coggygria from Serbia. in Journal of the Serbian Chemical Society
Serbian Chemical Society., 72(11), 1045-1051.
https://doi.org/10.2298/JSC0711045N

Novaković M, Vučković I, Janaćković P, Soković M, Filipović A, Tešević V, Milosavljević S. Chemical composition, antibacterial and antifungal activity of the essential oils of Cotinus coggygria from Serbia. in Journal of the Serbian Chemical Society. 2007;72(11):1045-1051.
doi:10.2298/JSC0711045N .

Novaković, Miroslav, Vučković, Ivan, Janaćković, Peđa, Soković, Marina, Filipović, Anka, Tešević, Vele, Milosavljević, Slobodan, "Chemical composition, antibacterial and antifungal activity of the essential oils of Cotinus coggygria from Serbia" in Journal of the Serbian Chemical Society, 72, no. 11 (2007):1045-1051,
https://doi.org/10.2298/JSC0711045N . .

TY  - JOUR
AU  - Gođevac, Dejan
AU  - Mandić, Boris
AU  - Vajs, Vlatka
AU  - Tešević, Vele
AU  - Menković, Nebojša
AU  - Janaćković, Peđa T.
AU  - Milosavljević, Slobodan
PY  - 2006
UR  - https://cer.ihtm.bg.ac.rs/handle/123456789/2716
PB  - Oxford : Pergamon-Elsevier Science Ltd
T2  - Biochemical Systematics and Ecology
T1  - Triterpenoid saponins and iridoid glycosides from the aerial parts of Cephalaria pastricensis
VL  - 34
IS  - 12
SP  - 890
EP  - 893
DO  - 10.1016/j.bse.2006.05.015
ER  - 

@article{
author = "Gođevac, Dejan and Mandić, Boris and Vajs, Vlatka and Tešević, Vele and Menković, Nebojša and Janaćković, Peđa T. and Milosavljević, Slobodan",
year = "2006",
publisher = "Oxford : Pergamon-Elsevier Science Ltd",
journal = "Biochemical Systematics and Ecology",
title = "Triterpenoid saponins and iridoid glycosides from the aerial parts of Cephalaria pastricensis",
volume = "34",
number = "12",
pages = "890-893",
doi = "10.1016/j.bse.2006.05.015"
}

Gođevac, D., Mandić, B., Vajs, V., Tešević, V., Menković, N., Janaćković, P. T.,& Milosavljević, S.. (2006). Triterpenoid saponins and iridoid glycosides from the aerial parts of Cephalaria pastricensis. in Biochemical Systematics and Ecology
Oxford : Pergamon-Elsevier Science Ltd., 34(12), 890-893.
https://doi.org/10.1016/j.bse.2006.05.015

Gođevac D, Mandić B, Vajs V, Tešević V, Menković N, Janaćković PT, Milosavljević S. Triterpenoid saponins and iridoid glycosides from the aerial parts of Cephalaria pastricensis. in Biochemical Systematics and Ecology. 2006;34(12):890-893.
doi:10.1016/j.bse.2006.05.015 .

Gođevac, Dejan, Mandić, Boris, Vajs, Vlatka, Tešević, Vele, Menković, Nebojša, Janaćković, Peđa T., Milosavljević, Slobodan, "Triterpenoid saponins and iridoid glycosides from the aerial parts of Cephalaria pastricensis" in Biochemical Systematics and Ecology, 34, no. 12 (2006):890-893,
https://doi.org/10.1016/j.bse.2006.05.015 . .

TY  - JOUR
AU  - Janaćković, Peđa T.
AU  - Tešević, Vele
AU  - Milosavljević, Slobodan
AU  - Vajs, Vlatka
AU  - Marin, Petar D.
PY  - 2004
UR  - https://cer.ihtm.bg.ac.rs/handle/123456789/4147
AB  - Aerial parts of Centaurea affinis Friv. were collected at Vlasina (east Serbia) in September 1998.
PB  - Oxford : Pergamon-Elsevier Science Ltd
T2  - Biochemical Systematics and Ecology
T1  - Sesquiterpene lactones, lignans and flavones of Centaurea affinis
VL  - 32
IS  - 3
SP  - 355
EP  - 357
DO  - 10.1016/j.bse.2003.08.008
ER  - 

@article{
author = "Janaćković, Peđa T. and Tešević, Vele and Milosavljević, Slobodan and Vajs, Vlatka and Marin, Petar D.",
year = "2004",
abstract = "Aerial parts of Centaurea affinis Friv. were collected at Vlasina (east Serbia) in September 1998.",
publisher = "Oxford : Pergamon-Elsevier Science Ltd",
journal = "Biochemical Systematics and Ecology",
title = "Sesquiterpene lactones, lignans and flavones of Centaurea affinis",
volume = "32",
number = "3",
pages = "355-357",
doi = "10.1016/j.bse.2003.08.008"
}

Janaćković, P. T., Tešević, V., Milosavljević, S., Vajs, V.,& Marin, P. D.. (2004). Sesquiterpene lactones, lignans and flavones of Centaurea affinis. in Biochemical Systematics and Ecology
Oxford : Pergamon-Elsevier Science Ltd., 32(3), 355-357.
https://doi.org/10.1016/j.bse.2003.08.008

Janaćković PT, Tešević V, Milosavljević S, Vajs V, Marin PD. Sesquiterpene lactones, lignans and flavones of Centaurea affinis. in Biochemical Systematics and Ecology. 2004;32(3):355-357.
doi:10.1016/j.bse.2003.08.008 .

Janaćković, Peđa T., Tešević, Vele, Milosavljević, Slobodan, Vajs, Vlatka, Marin, Petar D., "Sesquiterpene lactones, lignans and flavones of Centaurea affinis" in Biochemical Systematics and Ecology, 32, no. 3 (2004):355-357,
https://doi.org/10.1016/j.bse.2003.08.008 . .

TY  - JOUR
AU  - Đorđević, Iris
AU  - Vajs, Vlatka
AU  - Bulatović, V.
AU  - Menkovic, N
AU  - Tešević, Vele
AU  - Macura, S
AU  - Janaćković, Peđa T.
AU  - Milosavljević, Slobodan
PY  - 2004
UR  - https://cer.ihtm.bg.ac.rs/handle/123456789/4148
AB  - Quantitative H-1 NMR measurements revealed Delta(11(13)) sesquiterpene gamma-lactones as the main constituents (greater than or equal to 1% per weight of dried plant material) in the crude extracts of the aerial parts of Amphoricarpos neumayeri ssp. neumayeri and ssp. murbeckii from mountains Orjen and Visitor (Montenegro), respectively. Preparative silica gel chromatography afforded thirteen guai-11(13)-en-12,6alpha-olides, named amphoricarpolides (1-13), with the same relative (1alphaH,4PH,5alphaH,7betaH) configuration of the basic skeleton. The common structural feature of lactones 2-13 was 3beta,15-dioxygenation pattern. The only exception was 1 (3-deoxyamphoricarpolide), containing a single oxygen substituent (15-OH). Eight of them exhibited an additional oxygen substituent, 9beta-OH (5 and 6), 2alpha-OH (8-12), or 2alpha-OAc (13). Compound 7 was epoxydated at 10alpha(14)-position, whereas the remaining lactones contained a 10(14) double bond. (C) 2004 Elsevier Ltd. All rights reserved.
PB  - Oxford : Pergamon-Elsevier Science Ltd
T2  - Phytochemistry
T1  - Guaianolides from two subspecies of Amphoricarpos neumayeri from Montenegro
VL  - 65
IS  - 16
SP  - 2337
EP  - 2345
DO  - 10.1016/j.phytochem.2004.07.014
ER  - 

@article{
author = "Đorđević, Iris and Vajs, Vlatka and Bulatović, V. and Menkovic, N and Tešević, Vele and Macura, S and Janaćković, Peđa T. and Milosavljević, Slobodan",
year = "2004",
abstract = "Quantitative H-1 NMR measurements revealed Delta(11(13)) sesquiterpene gamma-lactones as the main constituents (greater than or equal to 1% per weight of dried plant material) in the crude extracts of the aerial parts of Amphoricarpos neumayeri ssp. neumayeri and ssp. murbeckii from mountains Orjen and Visitor (Montenegro), respectively. Preparative silica gel chromatography afforded thirteen guai-11(13)-en-12,6alpha-olides, named amphoricarpolides (1-13), with the same relative (1alphaH,4PH,5alphaH,7betaH) configuration of the basic skeleton. The common structural feature of lactones 2-13 was 3beta,15-dioxygenation pattern. The only exception was 1 (3-deoxyamphoricarpolide), containing a single oxygen substituent (15-OH). Eight of them exhibited an additional oxygen substituent, 9beta-OH (5 and 6), 2alpha-OH (8-12), or 2alpha-OAc (13). Compound 7 was epoxydated at 10alpha(14)-position, whereas the remaining lactones contained a 10(14) double bond. (C) 2004 Elsevier Ltd. All rights reserved.",
publisher = "Oxford : Pergamon-Elsevier Science Ltd",
journal = "Phytochemistry",
title = "Guaianolides from two subspecies of Amphoricarpos neumayeri from Montenegro",
volume = "65",
number = "16",
pages = "2337-2345",
doi = "10.1016/j.phytochem.2004.07.014"
}

Đorđević, I., Vajs, V., Bulatović, V., Menkovic, N., Tešević, V., Macura, S., Janaćković, P. T.,& Milosavljević, S.. (2004). Guaianolides from two subspecies of Amphoricarpos neumayeri from Montenegro. in Phytochemistry
Oxford : Pergamon-Elsevier Science Ltd., 65(16), 2337-2345.
https://doi.org/10.1016/j.phytochem.2004.07.014

Đorđević I, Vajs V, Bulatović V, Menkovic N, Tešević V, Macura S, Janaćković PT, Milosavljević S. Guaianolides from two subspecies of Amphoricarpos neumayeri from Montenegro. in Phytochemistry. 2004;65(16):2337-2345.
doi:10.1016/j.phytochem.2004.07.014 .

Đorđević, Iris, Vajs, Vlatka, Bulatović, V., Menkovic, N, Tešević, Vele, Macura, S, Janaćković, Peđa T., Milosavljević, Slobodan, "Guaianolides from two subspecies of Amphoricarpos neumayeri from Montenegro" in Phytochemistry, 65, no. 16 (2004):2337-2345,
https://doi.org/10.1016/j.phytochem.2004.07.014 . .

TY  - JOUR
AU  - Đorđević, Iris
AU  - Tešević, Vele
AU  - Janaćković, Peđa T.
AU  - Milosavljević, Slobodan
AU  - Vajs, Vlatka
PY  - 2004
UR  - https://cer.ihtm.bg.ac.rs/handle/123456789/4149
AB  - The roots of Cicerbita alpina (L.) Wallr. were collected from Mt. Komovi, Montenegro.
PB  - Oxford : Pergamon-Elsevier Science Ltd
T2  - Biochemical Systematics and Ecology
T1  - Sesquiterpene lactones from Cicerbita alpina
VL  - 32
IS  - 2
SP  - 209
EP  - 210
DO  - 10.1016/S0305-1978(03)00159-5
ER  - 

@article{
author = "Đorđević, Iris and Tešević, Vele and Janaćković, Peđa T. and Milosavljević, Slobodan and Vajs, Vlatka",
year = "2004",
abstract = "The roots of Cicerbita alpina (L.) Wallr. were collected from Mt. Komovi, Montenegro.",
publisher = "Oxford : Pergamon-Elsevier Science Ltd",
journal = "Biochemical Systematics and Ecology",
title = "Sesquiterpene lactones from Cicerbita alpina",
volume = "32",
number = "2",
pages = "209-210",
doi = "10.1016/S0305-1978(03)00159-5"
}

Đorđević, I., Tešević, V., Janaćković, P. T., Milosavljević, S.,& Vajs, V.. (2004). Sesquiterpene lactones from Cicerbita alpina. in Biochemical Systematics and Ecology
Oxford : Pergamon-Elsevier Science Ltd., 32(2), 209-210.
https://doi.org/10.1016/S0305-1978(03)00159-5

Đorđević I, Tešević V, Janaćković PT, Milosavljević S, Vajs V. Sesquiterpene lactones from Cicerbita alpina. in Biochemical Systematics and Ecology. 2004;32(2):209-210.
doi:10.1016/S0305-1978(03)00159-5 .

Đorđević, Iris, Tešević, Vele, Janaćković, Peđa T., Milosavljević, Slobodan, Vajs, Vlatka, "Sesquiterpene lactones from Cicerbita alpina" in Biochemical Systematics and Ecology, 32, no. 2 (2004):209-210,
https://doi.org/10.1016/S0305-1978(03)00159-5 . .

TY  - JOUR
AU  - Tešević, Vele
AU  - Milosavljević, Slobodan
AU  - Vajs, Vlatka
AU  - Janaćković, Peđa T.
AU  - Jovic, DJ
AU  - Vujisić, Ljubodrag V.
PY  - 2004
UR  - https://cer.ihtm.bg.ac.rs/handle/123456789/2715
PB  - Oxford : Pergamon-Elsevier Science Ltd
T2  - Biochemical Systematics and Ecology
T1  - Tetrahydrofuran-type sesquiterpenes from Artemisia lobelii All. var. canescens (DC.) Briqu. and Artemisia lobelii All. var. biasolettiana (Vis.) K. Maly
VL  - 32
IS  - 5
SP  - 525
EP  - 527
DO  - 10.1016/j.bse.2003.09.008
ER  - 

@article{
author = "Tešević, Vele and Milosavljević, Slobodan and Vajs, Vlatka and Janaćković, Peđa T. and Jovic, DJ and Vujisić, Ljubodrag V.",
year = "2004",
publisher = "Oxford : Pergamon-Elsevier Science Ltd",
journal = "Biochemical Systematics and Ecology",
title = "Tetrahydrofuran-type sesquiterpenes from Artemisia lobelii All. var. canescens (DC.) Briqu. and Artemisia lobelii All. var. biasolettiana (Vis.) K. Maly",
volume = "32",
number = "5",
pages = "525-527",
doi = "10.1016/j.bse.2003.09.008"
}

Tešević, V., Milosavljević, S., Vajs, V., Janaćković, P. T., Jovic, D.,& Vujisić, L. V.. (2004). Tetrahydrofuran-type sesquiterpenes from Artemisia lobelii All. var. canescens (DC.) Briqu. and Artemisia lobelii All. var. biasolettiana (Vis.) K. Maly. in Biochemical Systematics and Ecology
Oxford : Pergamon-Elsevier Science Ltd., 32(5), 525-527.
https://doi.org/10.1016/j.bse.2003.09.008

Tešević V, Milosavljević S, Vajs V, Janaćković PT, Jovic D, Vujisić LV. Tetrahydrofuran-type sesquiterpenes from Artemisia lobelii All. var. canescens (DC.) Briqu. and Artemisia lobelii All. var. biasolettiana (Vis.) K. Maly. in Biochemical Systematics and Ecology. 2004;32(5):525-527.
doi:10.1016/j.bse.2003.09.008 .

Tešević, Vele, Milosavljević, Slobodan, Vajs, Vlatka, Janaćković, Peđa T., Jovic, DJ, Vujisić, Ljubodrag V., "Tetrahydrofuran-type sesquiterpenes from Artemisia lobelii All. var. canescens (DC.) Briqu. and Artemisia lobelii All. var. biasolettiana (Vis.) K. Maly" in Biochemical Systematics and Ecology, 32, no. 5 (2004):525-527,
https://doi.org/10.1016/j.bse.2003.09.008 . .

TY  - JOUR
AU  - Gođevac, Dejan
AU  - Vajs, Vlatka
AU  - Menković, Nebojša
AU  - Tešević, Vele
AU  - Janaćković, Peđa T.
AU  - Milosavljević, Slobodan
PY  - 2004
UR  - https://cer.ihtm.bg.ac.rs/handle/123456789/137
AB  - Two flavonoid glycosides 1 and 2 having the luteolin structure were isolated from flowers of the endemic plant species Cephalaria pastricensis. They were identified by 1H and 13C NMR, as well as UV/Vis spectroscopy. The structures of 1 and 2 were also confirmed by the spectral data of aglycones and TLC of the sugars obtained after acid hydrolysis. Flavones 1 and 2 showed significant antiradical activity in the 1,1-diphenyl-2-picrylhydrazyl (DPPH) assay.
AB  - Iz cvetova Cephalaria pastricensis izolovana su dva heterozidna flavonoida sa luteolinskim aglikonom (1 i 2). Wihova struktura je određena primenom 1H i 13C-NMR i UV spektroskopije. Strukture flavona 1 i 2 su potvrđene i spektrima aglikona, odnosno tankoslojnom hromatografijom oslobođenih šećera nakon kisele hidrolize. Jedinjenja 1 i 2 su pokazala značajnu antiradikalsku aktivnost u 1,1-difenil-2 pikrilhidrazil (DPPH) testu.
PB  - Serbian Chemical Society
T2  - Journal of the Serbian Chemical Society
T1  - Flavonoids from flowers of Cephalaria pastricenis and their antiradical activity
T1  - Flavonoidi iz cvetova Cephalaria pastricensis i njihova antiradikalska aktivnost
VL  - 69
IS  - 11
SP  - 883
EP  - 886
DO  - 10.2298/JSC0411883G
ER  - 

@article{
author = "Gođevac, Dejan and Vajs, Vlatka and Menković, Nebojša and Tešević, Vele and Janaćković, Peđa T. and Milosavljević, Slobodan",
year = "2004",
abstract = "Two flavonoid glycosides 1 and 2 having the luteolin structure were isolated from flowers of the endemic plant species Cephalaria pastricensis. They were identified by 1H and 13C NMR, as well as UV/Vis spectroscopy. The structures of 1 and 2 were also confirmed by the spectral data of aglycones and TLC of the sugars obtained after acid hydrolysis. Flavones 1 and 2 showed significant antiradical activity in the 1,1-diphenyl-2-picrylhydrazyl (DPPH) assay., Iz cvetova Cephalaria pastricensis izolovana su dva heterozidna flavonoida sa luteolinskim aglikonom (1 i 2). Wihova struktura je određena primenom 1H i 13C-NMR i UV spektroskopije. Strukture flavona 1 i 2 su potvrđene i spektrima aglikona, odnosno tankoslojnom hromatografijom oslobođenih šećera nakon kisele hidrolize. Jedinjenja 1 i 2 su pokazala značajnu antiradikalsku aktivnost u 1,1-difenil-2 pikrilhidrazil (DPPH) testu.",
publisher = "Serbian Chemical Society",
journal = "Journal of the Serbian Chemical Society",
title = "Flavonoids from flowers of Cephalaria pastricenis and their antiradical activity, Flavonoidi iz cvetova Cephalaria pastricensis i njihova antiradikalska aktivnost",
volume = "69",
number = "11",
pages = "883-886",
doi = "10.2298/JSC0411883G"
}

Gođevac, D., Vajs, V., Menković, N., Tešević, V., Janaćković, P. T.,& Milosavljević, S.. (2004). Flavonoids from flowers of Cephalaria pastricenis and their antiradical activity. in Journal of the Serbian Chemical Society
Serbian Chemical Society., 69(11), 883-886.
https://doi.org/10.2298/JSC0411883G

Gođevac D, Vajs V, Menković N, Tešević V, Janaćković PT, Milosavljević S. Flavonoids from flowers of Cephalaria pastricenis and their antiradical activity. in Journal of the Serbian Chemical Society. 2004;69(11):883-886.
doi:10.2298/JSC0411883G .

Gođevac, Dejan, Vajs, Vlatka, Menković, Nebojša, Tešević, Vele, Janaćković, Peđa T., Milosavljević, Slobodan, "Flavonoids from flowers of Cephalaria pastricenis and their antiradical activity" in Journal of the Serbian Chemical Society, 69, no. 11 (2004):883-886,
https://doi.org/10.2298/JSC0411883G . .

TY  - JOUR
AU  - Vajs, Vlatka
AU  - Trifunović, Snežana
AU  - Janaćković, Peđa T.
AU  - Soković, Marina
AU  - Milpsavljevic, S
AU  - Tešević, Vele
PY  - 2004
UR  - https://cer.ihtm.bg.ac.rs/handle/123456789/2717
AB  - Five tetrahydrofuran sesquiterpenes, so-called davanones, and coumarin umbelliferone isolated from Artemisia lobelii All. var. canescens (DC.) Briqu, were tested for antifungal activity. All the compounds inhibited the growth of the applied fungi. The overall activity of one of them, 2-hydroxy-2,6,10-trimethyl-7,10-epoxy-dodeca-3,11-dien-5-on, was comparable to that of the antibiotic bifonazole.
AB  - Pet tetrahidrofuranskih terpenoida davanonskog tipa i kumarin umbeliferon koji su prethodno izolovani iz biljne vrste Aretemisia lobelii var. conescens ispitivani su na antifungalnu aktivnost. Sva testirana jedinjenja inhibiraju rast primenjenih kultura gljiva. Najveću aktivnost, koja se može meriti sa aktivnošću komercijalnog antibiotika bifonazola, pokazuje 2-hidroksi-2,6,10-trimetil-7,10-epoksidodeka-3,11-dien-5-on.
PB  - Serbian Chemical Soc, Belgrade
T2  - Journal of the Serbian Chemical Society
T1  - Antifungal activity of davanone-type sesquiterpenes from Artemisia lobelii var. conescens
T1  - Antifungalna aktivnost terpenoida davanonskog tipa izolovanih iz Artemisia lobelii Var. canescens
VL  - 69
IS  - 11
SP  - 969
EP  - 972
DO  - 10.2298/JSC0411969V
ER  - 

@article{
author = "Vajs, Vlatka and Trifunović, Snežana and Janaćković, Peđa T. and Soković, Marina and Milpsavljevic, S and Tešević, Vele",
year = "2004",
abstract = "Five tetrahydrofuran sesquiterpenes, so-called davanones, and coumarin umbelliferone isolated from Artemisia lobelii All. var. canescens (DC.) Briqu, were tested for antifungal activity. All the compounds inhibited the growth of the applied fungi. The overall activity of one of them, 2-hydroxy-2,6,10-trimethyl-7,10-epoxy-dodeca-3,11-dien-5-on, was comparable to that of the antibiotic bifonazole., Pet tetrahidrofuranskih terpenoida davanonskog tipa i kumarin umbeliferon koji su prethodno izolovani iz biljne vrste Aretemisia lobelii var. conescens ispitivani su na antifungalnu aktivnost. Sva testirana jedinjenja inhibiraju rast primenjenih kultura gljiva. Najveću aktivnost, koja se može meriti sa aktivnošću komercijalnog antibiotika bifonazola, pokazuje 2-hidroksi-2,6,10-trimetil-7,10-epoksidodeka-3,11-dien-5-on.",
publisher = "Serbian Chemical Soc, Belgrade",
journal = "Journal of the Serbian Chemical Society",
title = "Antifungal activity of davanone-type sesquiterpenes from Artemisia lobelii var. conescens, Antifungalna aktivnost terpenoida davanonskog tipa izolovanih iz Artemisia lobelii Var. canescens",
volume = "69",
number = "11",
pages = "969-972",
doi = "10.2298/JSC0411969V"
}

Vajs, V., Trifunović, S., Janaćković, P. T., Soković, M., Milpsavljevic, S.,& Tešević, V.. (2004). Antifungal activity of davanone-type sesquiterpenes from Artemisia lobelii var. conescens. in Journal of the Serbian Chemical Society
Serbian Chemical Soc, Belgrade., 69(11), 969-972.
https://doi.org/10.2298/JSC0411969V

Vajs V, Trifunović S, Janaćković PT, Soković M, Milpsavljevic S, Tešević V. Antifungal activity of davanone-type sesquiterpenes from Artemisia lobelii var. conescens. in Journal of the Serbian Chemical Society. 2004;69(11):969-972.
doi:10.2298/JSC0411969V .

Vajs, Vlatka, Trifunović, Snežana, Janaćković, Peđa T., Soković, Marina, Milpsavljevic, S, Tešević, Vele, "Antifungal activity of davanone-type sesquiterpenes from Artemisia lobelii var. conescens" in Journal of the Serbian Chemical Society, 69, no. 11 (2004):969-972,
https://doi.org/10.2298/JSC0411969V . .

TY  - JOUR
AU  - Tešević, Vele
AU  - Milosavljević, Slobodan
AU  - Vajs, Vlatka
AU  - Janaćković, Peđa T.
AU  - Popsavin, M
PY  - 2003
UR  - https://cer.ihtm.bg.ac.rs/handle/123456789/4153
AB  - Centaurea nicolai Bald. is an endemic species found in the Mediterranean part of Montenegro, and in Albania. Roots of C. nicolai were collected on the south slopes of mountain Rumija on the Adriatic coast of Montenegro.
PB  - Oxford : Pergamon-Elsevier Science Ltd
T2  - Biochemical Systematics and Ecology
T1  - Dithiophenes and other constituents of roots of Centaurea nicolai
VL  - 31
IS  - 1
SP  - 89
EP  - 90
DO  - 10.1016/S0305-1978(02)00067-4
ER  - 

@article{
author = "Tešević, Vele and Milosavljević, Slobodan and Vajs, Vlatka and Janaćković, Peđa T. and Popsavin, M",
year = "2003",
abstract = "Centaurea nicolai Bald. is an endemic species found in the Mediterranean part of Montenegro, and in Albania. Roots of C. nicolai were collected on the south slopes of mountain Rumija on the Adriatic coast of Montenegro.",
publisher = "Oxford : Pergamon-Elsevier Science Ltd",
journal = "Biochemical Systematics and Ecology",
title = "Dithiophenes and other constituents of roots of Centaurea nicolai",
volume = "31",
number = "1",
pages = "89-90",
doi = "10.1016/S0305-1978(02)00067-4"
}

Tešević, V., Milosavljević, S., Vajs, V., Janaćković, P. T.,& Popsavin, M.. (2003). Dithiophenes and other constituents of roots of Centaurea nicolai. in Biochemical Systematics and Ecology
Oxford : Pergamon-Elsevier Science Ltd., 31(1), 89-90.
https://doi.org/10.1016/S0305-1978(02)00067-4

Tešević V, Milosavljević S, Vajs V, Janaćković PT, Popsavin M. Dithiophenes and other constituents of roots of Centaurea nicolai. in Biochemical Systematics and Ecology. 2003;31(1):89-90.
doi:10.1016/S0305-1978(02)00067-4 .

Tešević, Vele, Milosavljević, Slobodan, Vajs, Vlatka, Janaćković, Peđa T., Popsavin, M, "Dithiophenes and other constituents of roots of Centaurea nicolai" in Biochemical Systematics and Ecology, 31, no. 1 (2003):89-90,
https://doi.org/10.1016/S0305-1978(02)00067-4 . .