XPS and AFM characterization of aminosilanes with different numbers of bonding sites on a silicon wafer
- G. Jaksa, B. Štefane, J. Kováč
- Chemistry
- 1 November 2013
The aim of this work was the preparation and characterization of a silicon surface modified by different self‐assembled aminopropylsilanes with the purpose of using them in sensor applications.…
A study of the thermal decomposition of adulterated cocaine samples under optimized aerobic pyrolytic conditions.
- T. Gostic, S. Klemenc, B. Štefane
- ChemistryForensic Science International
- 30 May 2009
Thiazole orange-induced c-di-GMP quadruplex formation facilitates a simple fluorescent detection of this ubiquitous biofilm regulating molecule.
- Shizuka Nakayama, Ilana Kelsey, H. Sintim
- Biology, ChemistryJournal of the American Chemical Society
- 8 March 2011
It is demonstrated that c-di-GMP can form G-quadruplexes at low micromolar concentrations when aromatic molecules such as thiazole orange template the quadruplex formation, and this property of aromatic molecule-induced G- quadruplex formation is used to design a thiazoles orange-based fluorescent detection of this important signaling molecule.
Influence of different solvents on the morphology of APTMS-modified silicon surfaces
- G. Jaksa, B. Štefane, J. Kováč
- Materials Science
- 1 October 2014
C–H Bond Functionalization of Arylpyrimidines Catalyzed by an in situ Generated Ruthenium(II) Carboxylate System and the Construction of Tris(heteroaryl)‐Substituted Benzenes
- B. Štefane, Jan Fabris, F. Požgan
- Chemistry
- 1 July 2011
A ruthenium(II) carboxylate catalyst, generated in situ from [RuCl 2 (p-cymene)] 2 and 1-phenyl-1-cyclopentanecarboxylic acid (PCCA) in the presence of K 2 CO 3 , allowed activation of the C―H bond…
Antioxidant activity of natural and modified phenolic extracts from Satureja montana L.
- Sanja Ćavar Zeljković, A. Topčagić, F. Požgan, B. Štefane, P. Tarkowski, M. Maksimović
- Chemistry
- 15 December 2015
New cyclopentane derivatives as inhibitors of steroid metabolizing enzymes AKR1C1 and AKR1C3.
- B. Štefane, P. Brožič, Matej Vehovc, T. Rižner, S. Gobec
- Chemistry, BiologyEuropean journal of medicinal chemistry
- 1 June 2009
Synthesis and biological evaluation of 7-(aminoalkyl)pyrazolo[1,5-a]pyrimidine derivatives as cathepsin K inhibitors.
- Nejc Petek, B. Štefane, Marko Novinec, J. Svete
- Chemistry, BiologyBioorganic chemistry (Print)
- 1 March 2019
Acetylcholinesterase Inhibition and Antioxidant Activity of N-trans-Caffeoyldopamine and N-trans-Feruloyldopamine
- Muamer Dizdar, Danijela Vidic, F. Požgan, B. Štefane, M. Maksimović
- ChemistryScientia Pharmaceutica
- 4 April 2018
Both synthesized hydroxycinnamates were found to be better antioxidants than the parent acids in in vitro tests applied, and N-trans-Caffeoyldopamine showed the best antioxidant activity in the three tested methods.
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