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  1. Article

    Open Access

    Topical dura mater application of CFA induces enhanced expression of c-fos and glutamate in rat trigeminal nucleus caudalis: attenuated by KYNA derivate (SZR72)

    Migraine is a debilitating neurological disorder where trigeminovascular activation plays a key role. We have previously reported that local application of Complete Freund’s Adjuvant (CFA) onto the dura mater ...

    M. Lukács, K. Warfvinge, J. Tajti, F. Fülöp, J. Toldi in The Journal of Headache and Pain (2017)

  2. Article

    Open Access

    KYNA analogue SZR72 modifies CFA-induced dural inflammation- regarding expression of pERK1/2 and IL-1β in the rat trigeminal ganglion

    Neurogenic inflammation has for decades been considered an important part of migraine pathophysiology. In the present study, we asked the question if administration of a novel kynurenic acid analogue (SZR72), ...

    M. Lukács, K. Warfvinge, L. S. Kruse, J. Tajti in The Journal of Headache and Pain (2016)

  3. Article

    Open Access

    Kynurenic acid modulates experimentally induced inflammation in the trigeminal ganglion

    The trigeminal ganglion (TG) plays a central role in cranial pain. Administration of complete Freund’s adjuvant (CFA) into the temporomandibular joint (TMJ) elicits activation of TG. Kynurenic acid (KYNA) is a...

    A. Csáti, L. Edvinsson, L. Vécsei, J. Toldi, F. Fülöp in The Journal of Headache and Pain (2015)

  4. No Access

    Article

    Application of a Ball Milling Technique for the Condensation of Anthranilic Hydrazides with Aromatic Aldehydes Towards 4-Quinazolinone Derivatives*

    An environmentally friendly method was applied to prepare anthranilic hydrazones and quinazolin-4(1H)-ones from anthranilic hydrazides and a number of aldehydes in solventless medium. The condensations proceed...

    T. Magyar, F. Miklós, L. Lázár, F. Fülöp in Chemistry of Heterocyclic Compounds (2015)

  5. Article

    Open Access

    In vitro and in vivo multidrug resistance reversal activity by a Betti-base derivative of tylosin

    The multidrug resistance (MDR) proteins are present in a majority of human tumours. Their activity is important to understand the chemotherapeutic failure. A search for MDR-reversing compounds was conducted am...

    N Gyémánt, H Engi, Z Schelz, I Szatmári, D Tóth, F Fülöp in British Journal of Cancer (2010)

  6. No Access

    Article

    Kynurenines in chronic neurodegenerative disorders: future therapeutic strategies

    Parkinson’s, Alzheimer’s and Huntington’s diseases are chronic neurodegenerative disorders of a progressive nature which lead to a considerable deterioration of the quality of life. Their pathomechanisms displ...

    D. Zádori, P. Klivényi, E. Vámos, F. Fülöp, J. Toldi in Journal of Neural Transmission (2009)

  7. No Access

    Article

    HPLC Enantioseparation of 1-(α-Aminobenzyl)-2-naphthol and 2-(α-Aminobenzyl)-1-naphthol Analogs on a β-Cyclodextrin-Based Chiral Stationary Phase

    The enantiomers of 1-(α-aminobenzyl)-2-naphthol and 2-(α-aminobenzyl)-1-naphthol analogs were separated isothermally on a 3,5-dimethylphenylcarbamoylated β-cyclodextrin-based chiral stationary phase (Cyclobond DM...

    R. Berkecz, I. Ilisz, A. Ivanov-Sztojkov, I. Szatmári, F. Fülöp in Chromatographia (2007)

  8. No Access

    Article

    Comparison of Separation Efficiency of Macrocyclic Glycopeptide-Based Chiral Stationary Phases for the LC Enantioseparation of β-Amino Acids

    Direct reversed-phase high-performance liquid chromatographic methods were developed for the separation of enantiomers of eighteen unnatural β-amino acids, including several β-3-homo-amino acids. The direct separ...

    A. Sztojkov-Ivanov, L. Lázár, F. Fülöp, D. W. Armstrong, A. Péter in Chromatographia (2006)

  9. No Access

    Article

    LC Enantioseparation of β-Lactam and β-Amino Acid Stereoisomers and a Comparison of Macrocyclic Glycopeptide- and β-Cyclodextrin-Based Columns

    Direct reversed-phase high-performance liquid chromatographic methods were developed for the separation of the enantiomers of tricyclic β-lactams, cis-3,4-benzo-6-azabicyclo[3.2.0]heptan-7-one, cis-4,5-benzo-7-az...

    R. Berkecz, R. Török, I. Ilisz, E. Forró, F. Fülöp, D. W. Armstrong in Chromatographia (2006)

  10. No Access

    Article

    LC Enantioseparation of Aryl-Substituted β-Lactams Using Variable-Temperature Conditions

    Direct reversed-phase high-performance liquid chromatographic methods were developed for the separation of enantiomers of β-lactams. The enantiomers of 7 aryl-substituted β-lactams were separated on chiral statio...

    R. Berkecz, I. Ilisz, E. Forró, F. Fülöp, D. W. Armstrong, A. Péter in Chromatographia (2006)

  11. No Access

    Article

    High-Performance Liquid Chromatographic Separation of Stereoisomers of β-Amino Acids and a Comparison of Separation Efficiencies on Chirobiotic T and TAG Columns

    Direct and indirect reversed-phase high-performance liquid chromatographic methods were developed for the separation of enantiomers of seventeen unnatural β-amino acids, including several β-3-homo amino acids....

    A. Árki, D. Tourwé, M. Solymár, F. Fülöp, D. W. Armstrong, A. Péter in Chromatographia (2004)

  12. No Access

    Article

    Comparison of isothiocyanate chiral derivatizing reagents for high-performance liquid chromatography

    This paper describes the synthesis of a new chiral derivatizing reagent, (1S, 2R)-1-acetoxy-1-phenyl-2-propyl isothiocyanate ((S,R)-APPI), which is readily available in both enantiomeric forms after a straightfor...

    M. Péter, F. Fülöp in Chromatographia (2002)

  13. No Access

    Chapter

    Synthesis and pharmacological properties of oxytocin antagonists containing conformationally constrained amino acids

    G. K. Tóth, K. Bakos, I. Zupkóo, F. FüLöP, I. Pávó in Peptide Science — Present and Future (2002)

  14. No Access

    Article

    High-performance liquid chromatographic separation of unusual amino acid enantiomers derivatized with (1S,2S)-1,3-diacetoxy-1-(4-nitrophenyl)-2-propyl-isothiocyanate

    A new chiral derivatizing agent (CDA), (1S,2S)-1,3-diacetoxy-1-(4-nitrophenyl)-2-propylisothiocyanate, (S,S)-DANI, was applied to the separation of the enantiomers of unusual amino acids containing two chiral cen...

    A. Péter, M. Péter, F. Fülöp, G. Török, G. Tóth, D. Tourwé, J. Sápi in Chromatographia (2000)

  15. No Access

    Article

    Development of new isothiocyanate-based chiral derivatizing agent for amino acids

    (1S,2S)-1,3-Diacetoxy-1-(4-nitrophenyl)-2-propylisothiocyanate [(S,S)-DANI] has been developed as a new chiral derivatizing agent for resolution of compounds containing an amino group. The reagent is readily avai...

    M. Peter, A. Peter, F. Fülöp in Chromatographia (1999)

  16. No Access

    Article

    High-Performance liquid chromatographic separation of enantiomers of unusual amino acids possessing cycloalkane or cycloalkene skeletons on a chiral crown ether containing stationary phase

    Direct reversed-phase high-performance liquid chromatographic methods were developed for the separation and identification of the enantiomers of mono- and bicyclic racemic β-amino acids:cis- andtrans-2-aminocyclo...

    G. Török, A. Péter, F. Fülöp in Chromatographia (1998)

  17. No Access

    Article

    An operated case of Holt-Oram syndrome with autosomal dominant inheritance

    This report is concerned with a patient successfully operated forHolt-Oram syndrome. The disorder is inherited dominantly with complete penetrance and variable expressivity. It is pointed out that in cases of con...

    Z. Czakó, A. Gömöry, P. Homolay, S. Bacsa, S. Kiss in Basic Research in Cardiology (1976)