Zobrazeno 1 - 10
of 41
pro vyhledávání: '"Roberto Antolović"'
Autor:
Dubravko Jelić, Roberto Antolović
Publikováno v:
Antibiotics, Vol 5, Iss 3, p 29 (2016)
Macrolides, as a class of natural or semisynthetic products, express their antibacterial activity primarily by reversible binding to the bacterial 50S ribosomal subunits and by blocking nascent proteins’ progression through their exit tunnel in bac
Externí odkaz:
https://doaj.org/article/7ce7d9d5105a47759a96d1cf61163f19
Autor:
Lara Saftić Martinović, Nada Birkic, Vedran Miletić, Roberto Antolović, Danijela Štanfel, Karlo Wittine
Publikováno v:
International Journal of Molecular Sciences; Volume 24; Issue 2; Pages: 1410
The antioxidant activity and chemical stability of 6-amino-6-deoxy-L-ascorbic acid (D1) and N-methyl-6-amino-6-deoxy-L-ascorbic acid (D2) were examined with ABTS and DPPH assays and compared with the reference L-ascorbic acid (AA). In addition, the o
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d86e3937460d28c3f60f4bb996164016
https://doi.org/10.3390/ijms24021410
https://doi.org/10.3390/ijms24021410
Autor:
Mario Cetina, Dubravko Jelić, Adrijana Vinter, Sara Bracanović, Roberto Antolović, Uroš Andjelković, Ozren Wittine, Karlo Wittine, Sandra Kraljević Pavelić
Publikováno v:
Bioorganic & Medicinal Chemistry Letters
Furanocoumarins, particularly furo[3,2-c]coumarins, are found in many natural products. However, coumarins annulated to a thiophene ring have received scarce attention to date in the literature. Therefore, we synthesized 4-oxo-4H-thieno[3,2-c]chromen
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6a5a15446cde9f7ed290f3f445200873
https://doi.org/10.1016/j.bmcl.2020.127415
https://doi.org/10.1016/j.bmcl.2020.127415
Autor:
Zrinka Ivezić Schoenfeld, Jasna Padovan, Sulejman Alihodžić, Samra Kapić, Adrijana Vinter, Ivana Palej Jakopović, Darko Filic, Radan Spaventi, Marina Modrić, Hana Čipčić Paljetak, Andrea Fajdetić, Vesna Eraković Haber, Roberto Antolović, Stjepan Mutak, Nada Košutić-Hulita
Publikováno v:
European Journal of Medicinal Chemistry. 46:3388-3397
Synthesis, antibacterial activity and pharmacokinetic properties of a novel class of macrolide antibiotics—macrolones—derived from azithromycin, comprising oxygen atom(s) in the linker and either free or esterified quinolone 3-carboxylic group, a
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3f9ac21f7da9a1bbe6928e6c2ca1ba52
https://doi.org/10.1016/j.ejmech.2011.05.002
https://doi.org/10.1016/j.ejmech.2011.05.002
Autor:
John Broskey, Sulejman Alihodžić, David J. Holmes, Samra Kapić, Vesna Eraković Haber, Eric Hunt, Roberto Antolović, Hana Čipčić Paljetak, Richard L. Jarvest
Publikováno v:
Bioorganic & Medicinal Chemistry. 18:6569-6577
Two series of clarithromycin and azithromycin derivatives with terminal 6-alkylquinolone-3-carboxylic unit with central ether bond in the linker were prepared and tested for antimicrobial activity. Quinolonelinker intermediates were prepared by Sonog
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::691dc8bdf9ad277d50d1a99bf5e0cda8
https://doi.org/10.1016/j.bmc.2010.06.048
https://doi.org/10.1016/j.bmc.2010.06.048
Autor:
Zrinka Kovarik, Dubravko Jelić, Jelena Domaćinović Barović, Goran Šinko, Gordana Rusak, Roberto Antolović, Maja Katalinić
Publikováno v:
European Journal of Medicinal Chemistry. 45:186-192
Selected flavonoids: galangin, kaempferol, quercetin, myricetin, fisetin, apigenin, luteolin and rutin, reversibly inhibited human butyrylcholinesterase (BChE, EC 3.1.1.8). Inhibition potency of the flavonoids we attributed to their chemical structur
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::bd668367fee7d4d074f281fcd0e7d288
https://doi.org/10.1016/j.ejmech.2009.09.041
https://doi.org/10.1016/j.ejmech.2009.09.041
Autor:
Holger Kost, Ernst-Günther Grünbaum, Ulrike Kirch, Maryam Mohadjerani, H. Neu, Roberto Antolović, Wilhelm Schoner, Natali Bauer
Publikováno v:
Scopus-Elsevier
Ouabain, that has been isolated from bovine adrenals and hypothalamus, is a new cardiotonic steroid hormone, which is either synthesized in the adrenals or stored there after it has absorbed from the diet. Little is known in vivo which events may lea
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::fb7d6dd35d051476ee2a36e16d1f8435
https://doi.org/10.1291/hypres.23.supplement_s93
https://doi.org/10.1291/hypres.23.supplement_s93
Autor:
Engin Halit Serpersu, Holger Linnertz, Wilhelm Schoner, Evelyn Hamer, Zeljka Kovarik, Roberto Antolović, Holger Kost
Publikováno v:
European Journal of Biochemistry. 261:181-189
To test the hypothesis that Na+/K+-ATPase works as an (alpha beta)2-diprotomer with interacting catalytic alpha-subunits, tryptic digestion of pig kidney enzyme, that had been inactivated with substitution-inert MgATP complex analogues, was performed
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::53812f4fda782d0a69c320250da591fd
https://doi.org/10.1046/j.1432-1327.1999.00260.x
https://doi.org/10.1046/j.1432-1327.1999.00260.x
Autor:
Roberto Antolović, Wilhelm Schoner, Jan Slavík, Zeljka Kovarik, Holger Linnertz, Evzen Amler, Rita Krumscheid, Tomas Obsil, Martin Gregor, Edvard Lanz
Publikováno v:
Biochemical and Biophysical Research Communications. 254:215-221
Fluorescein-5'-isothiocyanate (FITC) was used to study the high-affinity ATP-binding site of Na+/K+-ATPase. The molar ratio of specifically bound FITC per alpha-subunit of Na+/K+-ATPase was found to be 0.5 as followed from pretreatment experiments wi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::81b5f523a7be9d08bce8508f8b401b7c
https://doi.org/10.1006/bbrc.1998.9874
https://doi.org/10.1006/bbrc.1998.9874
Autor:
Roberto Antolović, Bernard C. Rossier, Käthi Geering, Wilhelm Schoner, Cecilia M. Canessa, Jean-Daniel Horisberger
Publikováno v:
FEBS Letters. 368:169-172
The digoxigenin derivative N-hydroxysuccinimidyl digoxigenin-3-O-methylcarbonyl-epsilon- aminocaproate (HDMA) has been shown to covalently label the ouabain binding site of the Na, K-ATPase epsilon subunit [Antolovic et al. (1995) Eur. J. Biochem. 22
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d2bda8110b976aaa07bff553d6256110
https://doi.org/10.1016/0014-5793(95)00637-o
https://doi.org/10.1016/0014-5793(95)00637-o