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Wyszukujesz frazę ""Filipić, Slavica"" wg kryterium: Autor


Tytuł :
3D-QSAR, Virtual Screening, Docking and Design of Dual PI3K/mTOR Inhibitors with Enhanced Antiproliferative Activity.
Autorzy :
Oluić J; Institute of Pharmaceutical Chemistry, Faculty of Pharmacy, University of Belgrade, Vojvode Stepe 450, 11000 Belgrade. Serbia.
Nikolic K; Institute of Pharmaceutical Chemistry, Faculty of Pharmacy, University of Belgrade, Vojvode Stepe 450, 11000 Belgrade. Serbia.
Vucicevic J; Institute of Pharmaceutical Chemistry, Faculty of Pharmacy, University of Belgrade, Vojvode Stepe 450, 11000 Belgrade. Serbia.
Gagic Z; Department of Pharmacy, Faculty of Medicine, Save Mrkalja 14, University of Banja Luka, 78000 Banja Luka. Bosnia and Herzegovina.
Filipic S; Institute of Pharmaceutical Chemistry, Faculty of Pharmacy, University of Belgrade, Vojvode Stepe 450, 11000 Belgrade. Serbia.
Agbaba D; Institute of Pharmaceutical Chemistry, Faculty of Pharmacy, University of Belgrade, Vojvode Stepe 450, 11000 Belgrade. Serbia.
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Źródło :
Combinatorial chemistry & high throughput screening [Comb Chem High Throughput Screen] 2017 Aug 10; Vol. 20 (4), pp. 292-303.
Typ publikacji :
Journal Article
MeSH Terms :
Drug Design*
Molecular Docking Simulation*
Phosphoinositide-3 Kinase Inhibitors*
Protein Kinase Inhibitors/*chemistry
Protein Kinase Inhibitors/*pharmacology
TOR Serine-Threonine Kinases/*antagonists & inhibitors
Cell Proliferation/drug effects ; Humans ; Ligands ; Phosphatidylinositol 3-Kinases/metabolism ; Quantitative Structure-Activity Relationship ; TOR Serine-Threonine Kinases/metabolism
Czasopismo naukowe
Tytuł :
Multitarget compounds bearing tacrine- and donepezil-like structural and functional motifs for the potential treatment of Alzheimer's disease.
Autorzy :
Ismaili L; Neurosciences Intégratives et Cliniques EA 481, Laboratoire de Chimie Organique et Thérapeutique, UFR SMP, 19 rue Ambroise Paré, Université de Franche-Comté, Université Bourgogne Franche-Comté, CHRU Besançon, F-25000 Besançon, France. Electronic address: .
Refouvelet B; Neurosciences Intégratives et Cliniques EA 481, Laboratoire de Chimie Organique et Thérapeutique, UFR SMP, 19 rue Ambroise Paré, Université de Franche-Comté, Université Bourgogne Franche-Comté, CHRU Besançon, F-25000 Besançon, France.
Benchekroun M; Neurosciences Intégratives et Cliniques EA 481, Laboratoire de Chimie Organique et Thérapeutique, UFR SMP, 19 rue Ambroise Paré, Université de Franche-Comté, Université Bourgogne Franche-Comté, CHRU Besançon, F-25000 Besançon, France.
Brogi S; European Research Centre for Drug Discovery and Development (NatSynDrugs) and Department of Biotechnology, Chemistry and Pharmacy, Università di Siena, Via A. Moro, 53100 Siena, Italy.
Brindisi M; European Research Centre for Drug Discovery and Development (NatSynDrugs) and Department of Biotechnology, Chemistry and Pharmacy, Università di Siena, Via A. Moro, 53100 Siena, Italy.
Gemma S; European Research Centre for Drug Discovery and Development (NatSynDrugs) and Department of Biotechnology, Chemistry and Pharmacy, Università di Siena, Via A. Moro, 53100 Siena, Italy.
Campiani G; European Research Centre for Drug Discovery and Development (NatSynDrugs) and Department of Biotechnology, Chemistry and Pharmacy, Università di Siena, Via A. Moro, 53100 Siena, Italy.
Filipic S; Institute of Pharmaceutical Chemistry, Faculty of Pharmacy, University of Belgrade, Vojvode Stepe 450, 11000 Belgrade, Serbia.
Agbaba D; Institute of Pharmaceutical Chemistry, Faculty of Pharmacy, University of Belgrade, Vojvode Stepe 450, 11000 Belgrade, Serbia.
Esteban G; Departament de Bioquímica i Biologia Molecular, Facultat de Medicina, Institut de Neurociències, Universitat Autònoma de Barcelona, 08193 Bellaterra, Barcelona, Spain.
Unzeta M; Departament de Bioquímica i Biologia Molecular, Facultat de Medicina, Institut de Neurociències, Universitat Autònoma de Barcelona, 08193 Bellaterra, Barcelona, Spain.
Nikolic K; Institute of Pharmaceutical Chemistry, Faculty of Pharmacy, University of Belgrade, Vojvode Stepe 450, 11000 Belgrade, Serbia. Electronic address: .
Butini S; European Research Centre for Drug Discovery and Development (NatSynDrugs) and Department of Biotechnology, Chemistry and Pharmacy, Università di Siena, Via A. Moro, 53100 Siena, Italy. Electronic address: .
Marco-Contelles J; Laboratory of Medicinal Chemistry (IQOG, CSIC), C/ Juan de la Cierva 3, 28006 Madrid, Spain. Electronic address: .
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Źródło :
Progress in neurobiology [Prog Neurobiol] 2017 Apr; Vol. 151, pp. 4-34. Date of Electronic Publication: 2016 Jan 18.
Typ publikacji :
Journal Article; Review
MeSH Terms :
Alzheimer Disease/*drug therapy
Cholinesterase Inhibitors/*therapeutic use
Indans/*therapeutic use
Piperidines/*therapeutic use
Tacrine/*therapeutic use
Animals ; Donepezil ; Humans ; Indans/chemistry ; Ligands ; Piperidines/chemistry ; Tacrine/chemistry
Czasopismo naukowe
Tytuł :
Quantitative structure-retention relationship of selected imidazoline derivatives on α1-acid glycoprotein column.
Autorzy :
Filipic S; University of Belgrade, Faculty of Pharmacy, Department of Pharmaceutical Chemistry, Vojvode Stepe 450, 11000 Belgrade, Serbia. Electronic address: .
Ruzic D; University of Belgrade, Faculty of Pharmacy, Department of Pharmaceutical Chemistry, Vojvode Stepe 450, 11000 Belgrade, Serbia.
Vucicevic J; University of Belgrade, Faculty of Pharmacy, Department of Pharmaceutical Chemistry, Vojvode Stepe 450, 11000 Belgrade, Serbia.
Nikolic K; University of Belgrade, Faculty of Pharmacy, Department of Pharmaceutical Chemistry, Vojvode Stepe 450, 11000 Belgrade, Serbia.
Agbaba D; University of Belgrade, Faculty of Pharmacy, Department of Pharmaceutical Chemistry, Vojvode Stepe 450, 11000 Belgrade, Serbia.
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Źródło :
Journal of pharmaceutical and biomedical analysis [J Pharm Biomed Anal] 2016 Aug 05; Vol. 127, pp. 101-11. Date of Electronic Publication: 2016 Mar 03.
Typ publikacji :
Journal Article
MeSH Terms :
Models, Chemical*
Quantitative Structure-Activity Relationship*
Chromatography, High Pressure Liquid/*methods
Imidazolines/*chemistry
Orosomucoid/*chemistry
Pharmaceutical Preparations/*chemistry
2-Propanol/chemistry ; Linear Models ; Molecular Structure ; Protein Binding
Czasopismo naukowe
Tytuł :
A Comparative Study of Chromatographic Behavior and Lipophilicity of Selected Imidazoline Derivatives.
Autorzy :
Filipic S; Department of Pharmaceutical Chemistry, Faculty of Pharmacy, University of Belgrade, Vojvode Stepe 450, 11000 Belgrade, Serbia .
Antic A; Department of Pharmaceutical Chemistry, Faculty of Pharmacy, University of Belgrade, Vojvode Stepe 450, 11000 Belgrade, Serbia.
Vujovic M; Department of Pharmaceutical Chemistry, Faculty of Pharmacy, University of Belgrade, Vojvode Stepe 450, 11000 Belgrade, Serbia.
Nikolic K; Department of Pharmaceutical Chemistry, Faculty of Pharmacy, University of Belgrade, Vojvode Stepe 450, 11000 Belgrade, Serbia.
Agbaba D; Department of Pharmaceutical Chemistry, Faculty of Pharmacy, University of Belgrade, Vojvode Stepe 450, 11000 Belgrade, Serbia.
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Źródło :
Journal of chromatographic science [J Chromatogr Sci] 2016 Aug; Vol. 54 (7), pp. 1137-45.
Typ publikacji :
Journal Article
Czasopismo naukowe
Tytuł :
Development of Hydrophilic Interaction Liquid Chromatography Method for the Analysis of Moxonidine and Its Impurities.
Autorzy :
Filipic S; Department of Pharmaceutical Chemistry, University of Belgrade, Vojvode Stepe 450, Belgrade, Serbia.
Elek M; Department of Pharmaceutical Chemistry, University of Belgrade, Vojvode Stepe 450, Belgrade, Serbia.
Popović M; Department of Pharmaceutical Chemistry, University of Belgrade, Vojvode Stepe 450, Belgrade, Serbia.
Nikolic K; Department of Pharmaceutical Chemistry, University of Belgrade, Vojvode Stepe 450, Belgrade, Serbia.
Agbaba D; Department of Pharmaceutical Chemistry, University of Belgrade, Vojvode Stepe 450, Belgrade, Serbia.
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Źródło :
Journal of analytical methods in chemistry [J Anal Methods Chem] 2016; Vol. 2016, pp. 3715972. Date of Electronic Publication: 2016 Oct 26.
Typ publikacji :
Journal Article
Czasopismo naukowe
Tytuł :
Polypharmacology of dopamine D1-like receptor antagonists
Autorzy :
Nikolić Katarina
Filipić Slavica
Agbaba Danica
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Temat :
polypharmacology
multitarget drugs
dopamine receptors
Pharmacy and materia medica
RS1-441
Źródło :
Arhiv za farmaciju, Vol 65, Iss 5, Pp 287-303 (2015)
Opis pliku :
electronic resource
Relacje :
https://scindeks-clanci.ceon.rs/data/pdf/0004-1963/2015/0004-19631505287N.pdf; https://doaj.org/toc/0004-1963; https://doaj.org/toc/2217-8767
Dostęp URL :
https://doaj.org/article/ae7a2ea78afd4136b5c4d0350d0f58fa
Czasopismo naukowe
Tytuł :
N-Methyl-N-((1-methyl-5-(3-(1-(2-methylbenzyl)piperidin-4-yl)propoxy)-1H-indol-2-yl)methyl)prop-2-yn-1-amine, a new cholinesterase and monoamine oxidase dual inhibitor.
Autorzy :
Bautista-Aguilera OM; Laboratorio de Química Médica, (IQOG, CSIC) , Juan de la Cierva 3, E-28006 Madrid, Spain.
Samadi A
Chioua M
Nikolic K
Filipic S
Agbaba D
Soriano E
de Andrés L
Rodríguez-Franco MI
Alcaro S
Ramsay RR
Ortuso F
Yañez M
Marco-Contelles J
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Źródło :
Journal of medicinal chemistry [J Med Chem] 2014 Dec 26; Vol. 57 (24), pp. 10455-63. Date of Electronic Publication: 2014 Dec 08.
Typ publikacji :
Journal Article; Research Support, Non-U.S. Gov't
MeSH Terms :
Cholinesterase Inhibitors/*pharmacology
Cholinesterases/*chemistry
Indoles/*pharmacology
Monoamine Oxidase/*chemistry
Monoamine Oxidase Inhibitors/*pharmacology
Piperidines/*pharmacology
Animals ; Blood-Brain Barrier/drug effects ; Brain/drug effects ; Brain/enzymology ; Cell Membrane Permeability/drug effects ; Cholinesterase Inhibitors/chemical synthesis ; Indoles/chemical synthesis ; Models, Molecular ; Molecular Structure ; Monoamine Oxidase Inhibitors/chemical synthesis ; Piperidines/chemical synthesis ; Swine
Czasopismo naukowe
Tytuł :
Procognitive properties of drugs with single and multitargeting H3 receptor antagonist activities.
Autorzy :
Nikolic K; Faculty of Pharmacy, Department of Pharmaceutical Chemistry, University of Belgrade, Belgrade, Serbia.
Filipic S
Agbaba D
Stark H
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Źródło :
CNS neuroscience & therapeutics [CNS Neurosci Ther] 2014 Jul; Vol. 20 (7), pp. 613-23. Date of Electronic Publication: 2014 May 19.
Typ publikacji :
Journal Article; Research Support, Non-U.S. Gov't; Review
MeSH Terms :
Drug Delivery Systems/*methods
Nootropic Agents/*administration & dosage
Nootropic Agents/*metabolism
Receptors, Histamine H3/*metabolism
Serotonin 5-HT3 Receptor Antagonists/*administration & dosage
Serotonin 5-HT3 Receptor Antagonists/*metabolism
Animals ; Humans ; Nootropic Agents/chemistry ; Serotonin 5-HT3 Receptor Antagonists/chemistry
Czasopismo naukowe

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