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Synthesis and Biological Evaluation of Novel Phosphatidylcholine Analogues Containing Monoterpene Acids as Potent Antiproliferative AgentsIsoprenoid-phospholipid conjugates as potential therapeutic agents: Synthesis, characterization and antiproliferative studiesOptically active stereoisomers of 5-(1-iodoethyl)-4-(4'-isopropylphenyl)dihydrofuran-2-one: The effect of the configuration of stereocenters on apoptosis induction in canine cancer cell lines.Dehalogenation Activity of Selected Fungi Toward δ-Iodo-γ-Lactone Derived from trans,trans-Farnesol.Lactones 46. Synthesis, antifeedant and antibacterial activity of γ-lactones with a p-methoxyphenyl substituent.Regio- and enantioselective microbial hydroxylation and evaluation of cytotoxic activity of β-cyclocitral-derived halolactones.Lipase-Catalyzed Transesterification of Egg-Yolk Phophatidylcholine with Concentrate of n-3 Polyunsaturated Fatty Acids from Cod Liver Oil.Chemoenzymatic Synthesis of trans-β-Aryl-δ-hydroxy-γ-lactones and Enzymatic Kinetic Resolution of Their Racemic Mixtures.Enantiomeric trans β-aryl-δ-iodo-γ-lactones derived from 2,5-dimethylbenzaldehyde induce apoptosis in canine lymphoma cell lines by downregulation of anti-apoptotic Bcl-2 family members Bcl-xL and Bcl-2.Lactones 43. New biologically active lactones: β-cyclocitral derivatives.Enantioselective Microbial Hydroxylation as a Useful Tool in the Production of Jasmonate Derivatives with Aphid Deterrent Activity.Positional analysis of phosphatidylcholine and phosphatidylethanolamine via LC with a charged aerosol detector.Preparation of Enantiomeric β-(2',5'-Dimethylphenyl)Bromolactones, Their Antiproliferative Activity and Effect on Biological MembranesMicrobial Asymmetric Functionalization of β-Cyclocitral-Derived Tetramethyl-Substituted γ-LactoneLactones 35 [1]. Metabolism of iodolactones with cyclohexane ring in Absidia cylindrospora cultureAn LC method for the analysis of phosphatidylcholine hydrolysis products and its application to the monitoring of the acyl migration processA simple method for positional analysis of phosphatidylcholineStereoselective yeast-mediated reduction of trans-5-(1'-oxo-3'-methylbutyl)-3-methyldihydrofuran-2-one: production of chiral intermediates for the synthesis of β-secretase inhibitorsMicrobial Hydrolysis of Racemic β-Aryl-γ-ethylidene-γ-lactones and Antifeedant Activity of the Products against Alphitobius diaperinus PanzerFree and Immobilized Lecitase™ Ultra as the Biocatalyst in the Kinetic Resolution of (E)-4-Arylbut-3-en-2-yl EstersSynthesis and Antimicrobial Activity of Methoxy- Substituted γ-Oxa-ε-lactones Derived from FlavanonesChemoenzymatic Synthesis of Enantiomeric, Bicyclic δ-Halo-γ-lactones with a Cyclohexane Ring, Their Biological Activity and Interaction with Biological Membranes
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description
onderzoeker
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researcher ORCID ID = 0000-0002-3271-779X
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Witold Gładkowski
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Witold Gładkowski
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Witold Gładkowski
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Witold Gładkowski
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Witold Gładkowski
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Witold Gładkowski
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Witold Gładkowski
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Witold Gładkowski
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Witold Gładkowski
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Witold Gładkowski
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Witold Gładkowski
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Witold Gładkowski
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Witold Gładkowski
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Witold Gładkowski
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Witold Gładkowski
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Witold Gładkowski
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Witold Gładkowski
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Witold Gładkowski
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Witold Gładkowski
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Witold Gładkowski
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Witold Przemysław Gładkowski
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Witold Gładkowski
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Witold Gładkowski
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Witold Gładkowski
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Witold Gładkowski
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Witold Gładkowski
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Witold Gładkowski
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Witold Gładkowski
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Witold Gładkowski
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Witold Gładkowski
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Witold Gładkowski
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Witold Gładkowski
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0000-0002-3271-779X