Pavol Mártonfi

Prof. Dr. Pavol Mártonfi

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Research Focus & Metrics

Academic Career Length

35Years (1992-Present)

(Calculated once Scilit publication data is synced: current year − year of first publication + 1)

Representative Publications

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29 April 2010 in Plant Species Biology
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Journal Article
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LMLenka Mártonfiová
Lenka Mártonfiová
PMPavol Mártonfi
Pavol Mártonfi
RŠRóbert Šuvada
Róbert Šuvada

1 January 2012 in Industrial Crops and Products
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Journal Article
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EBEdita Bagdonaitė
Edita Bagdonaitė
PMPavol Mártonfi
Pavol Mártonfi
MRMiroslav Repčák
Miroslav Repčák
JLJuozas Labokas
Juozas Labokas


1 January 2017 in Pharmaceutical Biology
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Journal Article
Open access
Stefano Dall'acquaStefano Dall'acqua
Stefano Dall'acqua
Gregorio PeronGregorio Peron
Gregorio Peron
SFSara Ferrari
Sara Ferrari
Valentina GandinValentina Gandin
Valentina Gandin
MBMassimo Bramucci
Massimo Bramucci
Filippo MaggiFilippo Maggi
Filippo Maggi
Context: Thymus alternans Klokov (Lamiaceae) is a neglected species of the genus Thymus (Sect. Serpyllum) endemic to Carpathian area, where it is used as a flavouring agent and for medicinal purposes. Objective: The aim of the work was to identify antiproliferative constituents from the flowering aerial parts of this plant. Materials and methods: Thymus alternans extracts were analyzed by HPLC-MSn and subjected to extensive chromatographic separations. The isolated compounds (phenolics and triterpenes) were structurally elucidated by MS and 1D and 2D NMR experiments. Essential oil (EO) composition was determined by GC-FID and GC-MS. Six purified triterpenes and EO were assayed for in vitro antiproliferative activity against a panel of human cancer cells, namely, breast (MDA-MB 231), colon (HCT-15 and HCT116), lung (U1810), pancreatic (BxPC3), melanoma (A375) and cervical carcinoma (A431) cells. Results: The structures of the isolated compounds were achieved on the basis of H-NMR and MS experiments. Luteolin-4′-O-β-d-glucopyranoside (P1), chrysoeriol-7-O-β-d-glucopyranoside (P2), chrysoeriol-5-O-β-d-glucopyranoside (P3), apigenin-7-O-β-d-glucopyranoside (P4), rosmarinic acid (P5), rosmarinic acid-3′-O-β-d-glucopyranoside (P6), caffeic acid-3-O-β-d-glucopyranoside (P7), 3α-hydroxy-urs-12,15-diene (T1), α-amyrin (T2), β-amyrin (T3), isoursenol (T4), epitaraxerol (T5), and oleanolic acid (T6). GC-MS analysis revealed that the EO of T. alternans was devoid of phenols and belonged to the nerolidol-chemotype, that is typical of the Sect. Serpyllum. The six purified triterpenes (T1-T6) were active with IC50 ranging from 0.5 to 5 μM being comparable or better than those of reference compounds betulinic acid and cisplatin. The EO exhibited significant effects on A375, MDA-MB 231 and HCT116 cell lines with IC50 in the range of 5–8 μg/mL. Conclusion: The reported results suggest that T. alternans can be considered as a good source of phytoconstituents with possible importance in the pharmaceutical field.

1 November 2016 in Environmental Pollution
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Journal Article
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Jozef KovacikJozef Kovacik
Jozef Kovacik
MDMatej Dudáš
Matej Dudáš
JHJosef Hedbavny
Josef Hedbavny
PMPavol Mártonfi
Pavol Mártonfi

1 December 1994 in Biochemical Systematics and Ecology
Verified
Journal Article
Closed access
PMPavol Mártonfi
Pavol Mártonfi
AGAnton Grejtovský
Anton Grejtovský
MRMiroslav Repčák
Miroslav Repčák