Secondary metabolites of three endemic Centaurea L. species
2014
Аутори
Tešević, VeleAljančić, Ivana
Milosavljević, Slobodan M.
Vajs, Vlatka
Đorđević, Iris
Jadranin, Milka
Menkovic, Nebojsa
Matevski, Vlado
Чланак у часопису (Објављена верзија)
Метаподаци
Приказ свих података о документуАпстракт
The aerial parts of three endemic Centaurea L. species, namely C. tomorosii Micevski, C. soskae Hayek and C. galicicae Micevski, afforded the sesquiterpene lactone cnicin (1) and seven flavonoids: apigenin (2), isokaempferide (3), hispidulin (4), eupatorin (5), cirsimaritin (6), santoflavone (7) and salvigenin (8). The structures of the isolated compounds were determined by UV, H-1-NMR and C-13-NMR spectroscopy and HR-ESI-MS spectrometry. H-1-NMR spectroscopy was used as a method for the quantitative analysis of cnicin.
Кључне речи:
Centaurea / cnicin / flavonoidsИзвор:
Journal of the Serbian Chemical Society, 2014, 79, 11, 1355-1362Издавач:
- Serbian Chemical Soc, Belgrade
Финансирање / пројекти:
- Биоактивни природни производи самониклих, гајених и јестивих биљака: одређивање структура и активности (RS-172053)
DOI: 10.2298/JSC140318048T
ISSN: 0352-5139
WoS: 000346879000003
Scopus: 2-s2.0-84986889441
Колекције
Институција/група
Hemijski fakultet / Faculty of ChemistryTY - JOUR AU - Tešević, Vele AU - Aljančić, Ivana AU - Milosavljević, Slobodan M. AU - Vajs, Vlatka AU - Đorđević, Iris AU - Jadranin, Milka AU - Menkovic, Nebojsa AU - Matevski, Vlado PY - 2014 UR - https://cherry.chem.bg.ac.rs/handle/123456789/1890 AB - The aerial parts of three endemic Centaurea L. species, namely C. tomorosii Micevski, C. soskae Hayek and C. galicicae Micevski, afforded the sesquiterpene lactone cnicin (1) and seven flavonoids: apigenin (2), isokaempferide (3), hispidulin (4), eupatorin (5), cirsimaritin (6), santoflavone (7) and salvigenin (8). The structures of the isolated compounds were determined by UV, H-1-NMR and C-13-NMR spectroscopy and HR-ESI-MS spectrometry. H-1-NMR spectroscopy was used as a method for the quantitative analysis of cnicin. PB - Serbian Chemical Soc, Belgrade T2 - Journal of the Serbian Chemical Society T1 - Secondary metabolites of three endemic Centaurea L. species VL - 79 IS - 11 SP - 1355 EP - 1362 DO - 10.2298/JSC140318048T ER -
@article{ author = "Tešević, Vele and Aljančić, Ivana and Milosavljević, Slobodan M. and Vajs, Vlatka and Đorđević, Iris and Jadranin, Milka and Menkovic, Nebojsa and Matevski, Vlado", year = "2014", abstract = "The aerial parts of three endemic Centaurea L. species, namely C. tomorosii Micevski, C. soskae Hayek and C. galicicae Micevski, afforded the sesquiterpene lactone cnicin (1) and seven flavonoids: apigenin (2), isokaempferide (3), hispidulin (4), eupatorin (5), cirsimaritin (6), santoflavone (7) and salvigenin (8). The structures of the isolated compounds were determined by UV, H-1-NMR and C-13-NMR spectroscopy and HR-ESI-MS spectrometry. H-1-NMR spectroscopy was used as a method for the quantitative analysis of cnicin.", publisher = "Serbian Chemical Soc, Belgrade", journal = "Journal of the Serbian Chemical Society", title = "Secondary metabolites of three endemic Centaurea L. species", volume = "79", number = "11", pages = "1355-1362", doi = "10.2298/JSC140318048T" }
Tešević, V., Aljančić, I., Milosavljević, S. M., Vajs, V., Đorđević, I., Jadranin, M., Menkovic, N.,& Matevski, V.. (2014). Secondary metabolites of three endemic Centaurea L. species. in Journal of the Serbian Chemical Society Serbian Chemical Soc, Belgrade., 79(11), 1355-1362. https://doi.org/10.2298/JSC140318048T
Tešević V, Aljančić I, Milosavljević SM, Vajs V, Đorđević I, Jadranin M, Menkovic N, Matevski V. Secondary metabolites of three endemic Centaurea L. species. in Journal of the Serbian Chemical Society. 2014;79(11):1355-1362. doi:10.2298/JSC140318048T .
Tešević, Vele, Aljančić, Ivana, Milosavljević, Slobodan M., Vajs, Vlatka, Đorđević, Iris, Jadranin, Milka, Menkovic, Nebojsa, Matevski, Vlado, "Secondary metabolites of three endemic Centaurea L. species" in Journal of the Serbian Chemical Society, 79, no. 11 (2014):1355-1362, https://doi.org/10.2298/JSC140318048T . .