About: Lukasz Kaczmarek

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

researcher

Attributes	Values
rdf:type	Item
description	ikertzailea (eu) researcher (en) 연구원 (ko) wetenschapper (nl) дослідник (uk) изилдөөчү (ky) polski chemik (1949-2020) (pl)
rdfs:label	Łukasz Kaczmarek (pl) Kaczmarek L (nl) Lukasz Kaczmarek (en)
skos:prefLabel	Łukasz Kaczmarek (pl) Kaczmarek L (nl) Lukasz Kaczmarek (en)
name	Łukasz Kaczmarek (pl) Kaczmarek L (nl) Lukasz Kaczmarek (en)
Polish scientist ID (deprecated)	wds:Q71951370-335C48B7-3C72-4F5F-A241-DF1CE540A283
Polish scientist ID (deprecated)	23414
Scopus author ID	wds:Q71951370-92393FAD-8CD7-4602-B23F-0414626A1232 wds:Q71951370-E4582A5E-9046-40E5-9544-5AB8CA5C0F20
Scopus author ID	35918400700 7101654249
given name	wds:Q71951370-48EE5ED9-7A2D-4A16-B8FE-069C84C6F330 wds:Q71951370-E5F911B9-6264-4BAC-8103-4B2ABB1C1587
given name	Łukasz Szymon
instance of	wds:Q71951370-7B1BAEC9-1C72-49DB-8C08-D2C948D1C032
instance of	Homo sapiens
doctoral advisor	wds:Q71951370-D661E370-37DD-4EF2-9E15-F3B81078E45C
doctoral advisor	Paweł Nantka-Namirski
skos:altLabel	Łukasz Kaczmarek (nl) L Kaczmarek (en) Łukasz Szymon Kaczmarek (en) Łukasz Szymon Kaczmarek (pl)
occupation	wds:Q71951370-D2FA63C0-03B9-4F2F-BD64-D70814BF3151 wds:Q71951370-FA363FDB-0CBE-4FA3-A19B-5F7DB532510B
different from	wds:Q71951370-4450e51f-4b83-189a-0102-71251b8bfc09
sex or gender	wds:Q71951370-144DD1C4-F3F8-4FDC-851A-C00D84FE1BD7
country of citizenship	wds:Q71951370-E0A597C7-0B4D-4FF6-80BE-48D29DF7273F
Prabook ID	wds:Q71951370-FD0DC5E7-2C26-4B40-BCFE-D70B841828A5
academic degree	wds:Q71951370-11E2C145-FDDC-41BF-A82D-556E6958907E wds:Q71951370-C7D30890-8DAD-4668-A332-5B4CF8A5E59F wds:Q71951370-E90856BD-0C81-48A7-A094-90EFF5BF8DD3
date of birth	wds:Q71951370-BC177720-83BA-40ED-9E4D-9C80000B99E4
date of death	wds:Q71951370-DED7BC6A-64A0-4D0C-AEBE-52D65EB0751B
educated at	wds:Q71951370-3FA47298-5DBF-46BA-83DA-7EEB508A7D80
family name	wds:Q71951370-52BD72D4-2DA1-41BF-BE58-762C5739DAA6
occupation	researcher chemist
different from	Łukasz Kaczmarek
sex or gender	male
country of citizenship	Poland
Prabook ID	702556
academic degree	professor doctorate habilitation
date of birth	1949-11-29 00:00:00Z (xsd:dateTime)
date of death	2020-10-31 00:00:00Z (xsd:dateTime)
educated at	Jagiellonian University
family name	Kaczmarek
ORCID iD	wds:Q71951370-6C4AF409-BC9B-4EC8-971A-E69BA320E7B0
ORCID iD	https://orcid.org/0000-0001-8222-8380
ORCID iD	0000-0001-8222-8380
is owl:sameAs of	Lukasz Kaczmarek
is about of	https://pl.wikipedia.org/wiki/%C5%81ukasz_Kaczmarek_(chemik) https://www.wikidata.org/wiki/Special:EntityData/Q71951370
is author of	Identification and physicochemical characteristics of temozolomide process-related impurities. Optimization of aripiprazole synthesis Use of the hyphenated LC-MS/MS technique and NMR/IR spectroscopy for the identification of exemestane stress degradation products during the drug development. A solution and solid state 15N NMR study of hydrogen bonding in a Schiffs base Synthesis and biological evaluation of new amino acid and dipeptide derivatives of neocryptolepine as anticancer agents. Liposomal formulation of DIMIQ, potential antitumor indolo[2,3-b]quinoline agent and its cytotoxicity on hepatoma Morris 5123 cells Azacarbazole n-3 and n-6 polyunsaturated fatty acids ethyl esters nanoemulsion with enhanced efficacy against Plasmodium falciparum Biological evaluation of omega-(dialkylamino)alkyl derivatives of 6H-indolo[2,3-b]quinoline--novel cytotoxic DNA topoisomerase II inhibitors. The synthesis of indolo[2,3-b]quinoline derivatives with a guanidine group: highly selective cytotoxic agents An efficient synthesis of indolo[2,3-b]quinoline guanidine derivatives with their in vitro and in vivo study Sequence-selectivity of 5,11-dimethyl-5H-indolo[2,3-b]quinoline binding to DNA. Footprinting and molecular modeling studies. Synthesis, and cytotoxic activity of some novel indolo[2,3-b]quinoline derivatives: DNA topoisomerase II inhibitors Searching for new derivatives of neocryptolepine: synthesis, antiproliferative, antimicrobial and antifungal activities. New derivatives of 11-methyl-6-[2-(dimethylamino)ethyl]-6H-indolo[2,3-b]quinoline as cytotoxic DNA topoisomerase II inhibitors. Identification and characterization of potential impurities of quetiapine fumarate. A derivative of 5-H-indolo[2,3-b]quinoline--a novel liposomally-formulated anticancer agent 1H, 13C and 15N NMR data for indolo[2,3-b]quinolines, a novel potent anticancer drug family. Membrane perturbations induced by new analogs of neocryptolepine. Complex formation in the indolo[2,3-b]quinolines--methylene blue systems in aqueous solutions. Imatinib Inhibits the Renewal and Tumorigenicity of CT-26 Colon Cancer Cells after Cytoreductive Treatment with Doxorubicin. SYNTHESIS AND CYTOTOXIC ACTIVITY OF NEW 5H-INDOLO[2,3-B]QUINOLINE O-AMINOGLYCOSIDES. Synthesis of 6-substituted 6H-indolo[2,3-b]quinolines as novel cytotoxic agents and topoisomerase II inhibitors.
is author of	wds:Q34108535-DBF682FE-7B57-4435-B7FC-D95E27B7F4C0 wds:Q48596416-6DB197A7-AD66-4191-9C1B-3F130D52C98A wds:Q71951374-138D654A-FF00-468F-9E81-7F151B4826EC wds:Q94681308-4492C0E1-D5FF-4651-8779-46C6FD761DBB wds:Q101146369-62F8B193-9594-4369-9CDE-CA6386C8A024 wds:Q44363018-3B4E2EB9-1B4A-4447-9786-773DB840F8D7 wds:Q38825596-F0C5C73E-14DB-4B55-A88F-12F37534D44C wds:Q30601035-5FD2B4D7-BF3E-489D-AF1C-14A7E8D3E5FA wds:Q39286224-36C1D93A-8351-4590-9C41-A9E174902468 wds:Q46348199-0ABFB0E5-D49B-4870-87F4-5301D3A81D94 wds:Q74412156-9FEA9A95-A834-406D-B0DD-E2BBAAEA888D

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