About: Krzysztof Sztanke

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An Entity of Type : wikibase:Item, within Data Space : wikidata.demo.openlinksw.com associated with source document(s)

Polish biochemist

Attributes	Values
rdf:type	Item
description	Forscher (de) ikertzailea (eu) investigador (es) chercheur (fr) дослідник (uk) 研究者 (zh) 研究員 (ja) onderzoeker (nl) polski biochemik (pl) Polish biochemist (en)
rdfs:label	Krzysztof Sztanke (en) Krzysztof Sztanke (it) Krzysztof Sztanke (nl) Krzysztof Sztanke (pl)
skos:prefLabel	Krzysztof Sztanke (en) Krzysztof Sztanke (it) Krzysztof Sztanke (nl) Krzysztof Sztanke (pl)
name	Krzysztof Sztanke (en) Krzysztof Sztanke (it) Krzysztof Sztanke (nl) Krzysztof Sztanke (pl)
Polish scientist ID (deprecated)	wds:Q104734019-8a3dea88-4c54-2e14-d8e0-84f84d01ad3e
Polish scientist ID (deprecated)	26579
given name	wds:Q104734019-51BDE811-2B20-4F32-B971-C0AFA02281AE
given name	Krzysztof
instance of	wds:Q104734019-70AE4725-F4EE-4B72-92A9-9361997635BC
instance of	Homo sapiens
doctoral student	wds:Q104734019-145A03F9-0554-4BDE-933D-6A1DE962C3F9
doctoral student	Anna Osinka
occupation	wds:Q104734019-4A19FC3C-8E72-4927-A866-A2A975FA9B6E
employer	wds:Q104734019-252D4F85-9740-491B-BEA6-3702DBBBB3A0
sex or gender	wds:Q104734019-AF7A19BF-BCC4-47C2-83B9-97E13F11CAC3
academic degree	wds:Q104734019-267DD5B5-F55E-410B-B004-08918D77DDEC wds:Q104734019-39A0D761-EE1E-40C6-AF09-D899C21A4997 wds:Q104734019-B27D2BEB-0E94-466C-9F6C-0A8AC754D516
educated at	wds:Q104734019-2F346A06-C4C3-436D-AE6D-FFC1C94D1162
family name	wds:q104734019-de856b92-49f6-601b-6924-9d3966852a03
occupation	researcher
employer	Medical University of Lublin
sex or gender	male
academic degree	doctorate habilitation scientific professorship degree
educated at	Medical University of Lublin
family name	Sztanke
ORCID iD	wds:Q104734019-D19C64BB-44A9-41DA-BFAA-5DDAF88E33A0
Dimensions author ID	wds:Q104734019-336994A6-4D35-4A30-A7A9-8584D3A493B0
ORCID iD	https://orcid.org/0000-0002-1898-5245
ORCID iD	0000-0002-1898-5245
Dimensions author ID	01000671664.22
is about of	https://www.wikidata.org/wiki/Special:EntityData/Q104734019
is author of	Antinociceptive activity of new imidazolidine carbonyl derivatives. Part 4. Synthesis and pharmacological activity of 8-aryl-3,4-dioxo-2H,8H-6,7-dihydroimidazo[2,1-c] [1,2,4]triazines Reversed-phase liquid chromatography with octadecylsilyl, immobilized artificial membrane and cholesterol columns in correlation studies with in silico biological descriptors of newly synthesized antiproliferative and analgesic active compounds Lipophilicity of novel antitumour and analgesic active 8-aryl-2,6,7,8-tetrahydroimidazo[2,1-c][1,2,4]triazine-3,4-dione derivatives determined by reversed-phase HPLC and computational methods. Synthesis, determination of the lipophilicity, anticancer and antimicrobial properties of some fused 1,2,4-triazole derivatives. Synthesis, structure elucidation and identification of antitumoural properties of novel fused 1,2,4-triazine aryl derivatives Volatile anesthetics reduce biochemical markers of brain injury and brain magnesium disorders in patients undergoing coronary artery bypass graft surgery. Synthesis, structure elucidation and identification of antiproliferative activities of a novel class of thiophene bioisosteres bearing the privileged 7,8-dihydroimidazo[2,1-c][1,2,4]triazin-4(6H)-one scaffold Crystal structure, antitumour and antimetastatic activities of disubstituted fused 1,2,4-triazinones Identification of antibacterial and antiviral activities of novel fused 1,2,4-triazine esters. Identification of antitumour activity of novel derivatives of 8-aryl-2,6,7,8-tetrahydroimidazo[2,1-c][1,2,4]triazine-3,4-dione and 8-aryl-4-imino-2,3,7,8-tetrahydroimidazo[2,1-c][1,2,4]triazin-3(6H)-one Synthesis, crystal structure and anticancer activity of novel derivatives of ethyl 1-(4-oxo-8-aryl-4,6,7,8-tetrahydroimidazo[2,1-c][1,2,4]triazin-3-yl)formate Synthesis of imidazoline and imidazo[2,1-c][1,2,4]triazole aryl derivatives containing the methylthio group as possible antibacterial agents. The influence of some promising fused azaisocytosine-containing congeners on zebrafish (Danio rerio) embryos/larvae and their antihaemolytic, antitumour and antiviral activities An insight into synthetic Schiff bases revealing antiproliferative activities in vitro Two novel classes of fused azaisocytosine-containing congeners as promising drug candidates: Design, synthesis as well as in vitro, ex vivo and in silico studies Structure-retention behaviour of biologically active fused 1,2,4-triazinones--correlation with in silico molecular properties. A novel fused 1,2,4-triazine aryl derivative as antioxidant and nonselective antagonist of adenosine A(2A) receptors in ethanol-activated liver stellate cells Synthesis of new derivatives of 3-methyl-8-aryl-7,8-dihydro-6H-imidazo[2,1-c][1,2,4] triazin-4-one Synthesis of new derivatives of 8-aryl-3-phenyl-6,7-dihydro-4H-imidazo[2, 1-c][1,2,4]triazin-4-one. The Maillard reaction and its consequences for a living body. The susceptibility of certain bacterial strains to imidazotriazine derivatives Thermal behaviour of antiproliferative active 3-(2-furanyl)-8-aryl-7,8-dihydroimidazo[2,1-c][1,2,4]triazin-4(6H)-ones Electron ionization mass spectra of 8-aryl-3,4-dioxo-2H,8H-6,7-dihydroimidazo[2,1-c][1,2,4]triazines. Do they exhibit tautomerism in the gas phase? Biologically and chemically important hydrazino-containing imidazolines as antioxidant agents The susceptibility of certain microbial strains to some imidazoline derivatives Synthesis, structure elucidation, determination of the lipophilicity and identification of antitumour activities in vitro of novel 3-(2-furanyl)-8-aryl-7,8-dihydroimidazo[2,1-c][1,2,4]triazin-4(6H)-ones with a low cytotoxicity towards normal [...] Square-wave adsorptive stripping voltammetric approaches at two in situ modified electrodes as first analytical methods for the quantitative determination of a new anticancer drug candidate Synthesis, structure elucidation and in vitro anticancer activities of novel derivatives of diethyl (2E)-2-[(2E)-(1-arylimidazolidin-2-ylidene)hydrazono]succinate and ethyl (4-oxo-8-aryl-4,6,7,8-tetrahydroimidazo[2,1-c][1,2,4]triazin-3-yl)acetate In vitro effects of a new fused azaisocytosine-like congener on relative cell proliferation, necrosis and cell cycle in cancer and normal cell cultures. Exclusion of antimicrobial activity of some analgesic active imidazo[2,1-c]triazines. Biologically important hydrazide-containing fused azaisocytosines as antioxidant agents. Exclusion of antimicrobial activity of some analgesic active imidazo[2,1-c][1,2,4]triazines Anticancer active trifluoromethylated fused triazinones are safe for early-life stages of zebrafish (<i>Danio rerio</i>) and reveal a proapoptotic action The Maillard reaction inhibitors and their biological and therapeutic significance Oxazolidinones--a new class of broad-spectrum chemotherapeutics. A simple stripping voltammetric method for the determination of a new anticancer prodrug in serum. Studies on the synthesis of new derivatives of 8-aryl-4-imino-2,3,7,8-tetrahydro-imidazo [2,1-c][1,2,4] triazin-3 (6H)-one with an expected biological activity. Synthesis, structure confirmation, identification of in vitro antiproliferative activities and correlation of determined lipophilicity parameters with in silico bioactivity descriptors of two novel classes of fused azaisocytosine-like congeners The susceptibility of certain microbial strains to fused 1,2,4-triazole derivatives. Novel derivatives of methyl and ethyl 2-(4-oxo-8-aryl-2H-3,4,6,7-tetrahydroimidazo[2,1-c][1,2,4]triazin-3-yl)acetates from biologically active 1-aryl-2-hydrazinoimidazolines: synthesis, crystal structure and antiproliferative activity Antimicrobial screening of certain fused 1,2,4-triazine derivatives. Current trends in asthma therapy. Plasma matrix metalloproteinase 9 correlates with disorders of brain magnesium homeostasis in patients undergoing coronary artery bypass surgery. Predicting the Blood-Brain Barrier Permeability of New Drug-Like Compounds via HPLC with Various Stationary Phases A Screen-Printed Sensor Coupled with Flow System for Quantitative Determination of a Novel Promising Anticancer Agent Candidate
is author of	wds:Q40080392-F62FDDB5-E51F-4443-8FB9-358B55EFD38F wds:Q45253110-B098AA58-8C69-40F8-BEE4-A62F35FBE498

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