Zobrazeno 1 - 9
of 9
pro vyhledávání: '"Ana Cikos"'
Autor:
Mladenka Jurin, Ana Čikoš, Višnja Stepanić, Marcin Górecki, Gennaro Pescitelli, Darko Kontrec, Andreja Jakas, Tonko Dražić, Marin Roje
Publikováno v:
Pharmaceuticals, Vol 17, Iss 10, p 1259 (2024)
Hydantoins, a class of five-membered heterocyclic compounds, exhibit diverse biological activities. The aim of this study was to synthesize and characterize a series of novel 3,5-disubstituted hydantoins and to investigate their antiproliferative act
Externí odkaz:
https://doaj.org/article/1f091d752c254b9f837e2296ffa5b003
Publikováno v:
Marine Drugs, Vol 22, Iss 7, p 310 (2024)
The total synthesis of two new marine natural products, (±)-marinoaziridine B 7 and (±)-N-methyl marinoaziridine A 8, was accomplished. The (±)-marinoaziridine 7 was prepared in a six-step linear sequence with a 2% overall yield. The key steps in
Externí odkaz:
https://doaj.org/article/f9c5298509cf491eaf21c11aa2ebfd57
Autor:
Ana Mandura Jarić, Ana Čikoš, Marijana Pocrnić, Krunoslav Aladić, Stela Jokić, Danijela Šeremet, Aleksandra Vojvodić Cebin, Draženka Komes
Publikováno v:
Antioxidants, Vol 12, Iss 11, p 1903 (2023)
Health-oriented preferences, a demand for innovative food concepts, and technological advances have greatly influenced changes in the food industry and led to remarkable development of the functional food market. Incorporating herbal extracts as a ri
Externí odkaz:
https://doaj.org/article/aa2e5dc6db3a49bfb6894696d6db3295
Autor:
Biljana Arsic, Jill Barber, Ana Cikos, Manikandan Kadirvel, Emilija Kostic, Andrew J. McBain, Jelena Milicevic, Angela Oates, Andrew Regan
Publikováno v:
Molecules, Vol 27, Iss 21, p 7280 (2022)
Although many antibiotics are active against Gram-positive bacteria, fewer also show activity against Gram-negative bacteria. Here, we present a combination of in silico (electron ion-interaction potential, molecular docking, ADMET), NMR, and microbi
Externí odkaz:
https://doaj.org/article/6e59cbb94b5942ef9cc0601635fdd2a8
Autor:
Goran Kragol, Victoria A. Steadman, Zorica Marušić Ištuk, Ana Čikoš, Martina Bosnar, Dubravko Jelić, Gabrijela Ergović, Marija Trzun, Berislav Bošnjak, Ana Bokulić, Jasna Padovan, Ines Glojnarić, Vesna Eraković Haber
Publikováno v:
Molecules, Vol 27, Iss 3, p 1034 (2022)
Certain macrolide antibiotics, azithromycin included, possess anti-inflammatory properties that are considered fundamental for their efficacy in the treatment of chronic inflammatory diseases, such as diffuse pan-bronchiolitis and cystic fibrosis. In
Externí odkaz:
https://doaj.org/article/3265db1c9f2b4ba6bcffd1ed6fb3b886
Publikováno v:
Chemosensors, Vol 10, Iss 1, p 21 (2022)
We present the synthesis and analytical, spectroscopic and computational characterization of three amino-substituted benzo[b]thieno[2,3-b]pyrido[1,2-a]benzimidazoles as novel pH probes with a potential application in pH-sensing materials. The designe
Externí odkaz:
https://doaj.org/article/1c19bea55ef5419781190baca1c42fc7
Publikováno v:
Molecules, Vol 27, Iss 2, p 432 (2022)
Unprecedented tandem allylic alkylation/intermolecular Michael addition was used in the preparation of novel bicyclic azalides. NMR spectroscopy was used not only to unambiguously determine and characterize the structures of these unexpected products
Externí odkaz:
https://doaj.org/article/518a86c847de4bdf903df01b809308b2
Autor:
Leo Štefan, Ana Čikoš, Robert Vianello, Ivica Đilović, Dubravka Matković-Čalogović, Miljenko Dumić
Publikováno v:
Molecules, Vol 26, Iss 22, p 7032 (2021)
Spontaneous S-alkylation of methimazole (1) with 1,2-dichloroethane (DCE) into 1,2-bis[(1-methyl-1H-imidazole-2-yl)thio]ethane (2), that we have described recently, opened the question about its formation pathway(s). Results of the synthetic, NMR spe
Externí odkaz:
https://doaj.org/article/fd49ec461dd54c97a020001764d53e54
Autor:
Ana Čikoš, Irena Ćaleta, Dinko Žiher, Mark B. Vine, Ivaylo J. Elenkov, Marko Dukši, Dubravka Gembarovski, Marina Ilijaš, Snježana Dragojević, Ivica Malnar, Sulejman Alihodžić
Publikováno v:
Beilstein Journal of Organic Chemistry, Vol 11, Iss 1, Pp 1447-1457 (2015)
Three novel spiroketals were prepared by a one-pot transformation of 6-O-methyl-9(E)-hydroxyiminoerythronolide A. We present the formation of a [4.5]spiroketal moiety within the macrolide lactone ring, but also the unexpected formation of a 10-C=11-C
Externí odkaz:
https://doaj.org/article/089280259e35471f8f9793ad37804522