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Oral Administration of Polymyxin B Modulates the Activity of Lipooligosaccharide E. coli B against Lung Metastases in Murine Tumor ModelsSynthesis and Biological Evaluation of Novel Phosphatidylcholine Analogues Containing Monoterpene Acids as Potent Antiproliferative AgentsIsoprenoid-phospholipid conjugates as potential therapeutic agents: Synthesis, characterization and antiproliferative studiesThe effects of 1,4-dimethylpyridine in metastatic prostate cancer in miceNovel phosphonate analogs of sulforaphane: Synthesis, in vitro and in vivo anticancer activity.Vitamin D Analogs Potentiate the Antitumor Effect of Imatinib Mesylate in a Human A549 Lung Tumor Model.Effectiveness of CO2 laser in an experimental mammary gland adenocarcinoma model.1-methylnicotinamide and its structural analog 1,4-dimethylpyridine for the prevention of cancer metastasisSynthesis and biological evaluation of 4'-O-acetyl-isoxanthohumol and its analogues as antioxidant and antiproliferative agents.Dehalogenation Activity of Selected Fungi Toward δ-Iodo-γ-Lactone Derived from trans,trans-Farnesol.The synthesis of indolo[2,3-b]quinoline derivatives with a guanidine group: highly selective cytotoxic agents.Design, synthesis, and biological evaluation of artemisinin-indoloquinoline hybrids as potent antiproliferative agents.Synthesis and in vitro antiproliferative activity of thiazole-based nitrogen mustards: the hydrogen bonding interaction between model systems and nucleobases.Synthesis and in vitro cytotoxic effect of 6-amino-substituted 11H- and 11Me-indolo[3,2-c]quinolines.Searching for new derivatives of neocryptolepine: synthesis, antiproliferative, antimicrobial and antifungal activities.Design, synthesis, and in vitro cancer cell growth inhibition evaluation and antimalarial testing of trioxanes installed in cyclic 2-enoate substructures.Synthesis and in vitro antiproliferative activity of new 11-aminoalkylamino-substituted chromeno[2,3-b]indoles.New derivatives of 11-methyl-6-[2-(dimethylamino)ethyl]-6H-indolo[2,3-b]quinoline as cytotoxic DNA topoisomerase II inhibitors.Synthesis and in vitro antiproliferative activity of new 11-aminoalkylamino-substituted 5H- and 6H-indolo[2,3-b]quinolines; structure-activity relationships of neocryptolepines and 6-methyl congeners.Synthesis and biological evaluation of new amino acid and dipeptide derivatives of neocryptolepine as anticancer agents.An efficient synthesis of indolo[2,3-b]quinoline guanidine derivatives with their in vitro and in vivo study.Synthesis and In Vitro Antiproliferative Activity of 11-Substituted Neocryptolepines with a Branched ω-Aminoalkylamino Chain.Clopidogrel in a combined therapy with anticancer drugs-effect on tumor growth, metastasis, and treatment toxicity: Studies in animal models.Design, Synthesis, and Evaluation of ω-(Isothiocyanato)alkylphosphinates and Phosphine Oxides as Antiproliferative Agents.Molecular basis for the DNA damage induction and anticancer activity of asymmetrically substituted anthrapyridazone PDZ-7.Cell density-dependent cytological stage profile and its application for a screen of cytostatic agents active towards Leukemic Stem Cells.Synthesis and biological evaluation of acyl derivatives of hydroxyflavones as potent antiproliferative agents against drug resistance cell lines.Synthesis, molecular docking, ctDNA interaction, DFT calculation and evaluation of antiproliferative and anti-Toxoplasma gondii activities of 2,4-diaminotriazine-thiazole derivatives.Efficient glycosylation of natural Danshensu and its enantiomer by sugar and 2-deoxy sugar donors.Phosphorus-containing isothiocyanate-derived mercapturic acids as a useful alternative for parental isothiocyanates in experimental oncologySynthesis, Characterization, and In Vitro Cancer Cell Growth Inhibition Evaluation of Novel Phosphatidylcholines with Anisic and Veratric AcidsSynthesis and cytotoxicity studies of bifunctional hybrids of nitrogen mustards with potential enzymes inhibitors based on melamine frameworkDiscovery of tropinone-thiazole derivatives as potent caspase 3/7 activators, and noncompetitive tyrosinase inhibitors with high antiproliferative activity: Rational design, one-pot tricomponent synthesis, and lipophilicity determinationInfluence of amide versus ester linkages on the anticancer properties of the new flavone-biotin conjugatesStructural Modifications of Nature-Inspired Indoloquinolines: A Mini Review of Their Potential Antiproliferative ActivityThe halogenation of natural flavonoids, baicalein and chrysin, enhances their affinity to human protein kinase CK2
P50
Q35909845-7C5623C1-75DE-4F20-A605-169BBF13D749Q36054396-98F3D301-7880-4878-B889-234DF2967D7BQ36280086-53A5BEA5-C882-486C-9E31-5274E0333EE0Q36300102-F66A233B-1EF4-4F50-82E7-08016739221FQ36323022-82724880-1FA2-4741-9AA5-20931C882520Q36324677-9EA388A2-1FC1-4CC5-BCD1-F780098A6D1BQ36332693-076AAA25-7D90-4A26-AD99-4E15A6EB0099Q37093441-33815E2F-1607-4623-8E24-04A81739BBD5Q38695029-A15EF324-0E51-4CBA-9813-FDA403C68948Q38790397-58A03B3B-AD0E-47E9-BF94-BFCEC06C3711Q38825596-4360294B-0C04-44BF-A4A4-F363750EEF80Q38938953-07BA3025-3415-4086-B675-AF22B3CBCBCEQ38971861-D293867D-E4AE-47FF-9165-FA59888A0E61Q39009784-38EF685A-AB23-497D-A556-9763556A21DEQ39009788-2D98D98D-13B5-4A36-9CD5-BD3B81E9F0D8Q39093311-9DA14B9B-3ADA-4C24-8C40-3BCE4EADF4E5Q39244989-68CD44B5-1164-4AF9-B367-F050045DCE62Q39286224-22F5CDC0-7310-4647-907C-E863CA4F90C5Q39322504-A4058522-0C4F-46C5-BECC-13122F7AD188Q39350836-307386EC-DE15-4DC7-84F6-7E26280D0F4EQ44363018-827239AD-023A-4CCC-9D3F-41A004A4A818Q46901604-0D7207CD-65EF-4A9D-8E16-8264DE06CC30Q47094540-D80E3421-20EE-4729-98F8-91E8022E67E8Q48240219-42B549B8-233A-4B66-8358-C1FE36911D79Q49236261-236A825B-A3E4-477E-8A4F-B5B4C583B2B2Q50070056-3DCA94AF-C2F6-4E8A-B5AE-99C4571F0434Q50106868-10E5BBF7-9AF1-4D9B-8D29-DB3C0294F2FCQ52342512-655CFF05-8D28-4F7A-ABB1-8B0D2A80A41DQ52675703-75BFAA9A-400E-4907-A282-ED1466B8A841Q57169174-D0895AF2-84D0-42F4-93FD-101958EF08ADQ58692554-CB024F58-C064-4F83-B5DF-D654842366CAQ64028965-B9358646-50FB-4E41-A70C-818AEABA1A1AQ91977371-FA7E7098-C570-4C17-A3F6-18C0AEE8DBCFQ92112978-659400CF-3533-4866-B0F5-34283AE32260Q92723562-3E617F4E-0206-4FE5-8D23-6311ADCDEC70Q94510064-86DEB219-B937-44E4-B03E-6DBC34C1F75D
P50
description
investigador
@es
researcher
@en
wetenschapper
@nl
name
Marta Switalska
@en
Marta Switalska
@nl
type
label
Marta Switalska
@en
Marta Switalska
@nl
prefLabel
Marta Switalska
@en
Marta Switalska
@nl
P31
P496
0000-0001-7920-2251