TY - JOUR AU - Kovács, Z AU - Jernei, Tamás AU - Katona, D AU - Kocsis, László AU - Csámpai, Antal TI - Synthesis and structure of novel ferrocene-containing β-carbolines including polycondensed derivatives with the elements of planar-, central- and conformational chirality JF - JOURNAL OF ORGANOMETALLIC CHEMISTRY J2 - J ORGANOMET CHEM VL - 794 PY - 2015 SP - 125 EP - 135 PG - 11 SN - 0022-328X DO - 10.1016/j.jorganchem.2015.07.004 UR - https://m2.mtmt.hu/api/publication/2923890 ID - 2923890 N1 - Institute of Chemistry, Eötvös Loránd University, P. O. B. 32Budapest-112 H-1518, Hungary MTA-ELTE Research Group of Peptide Chemistry, P. O. B. 32Budapest-112 H-1518, Hungary Cited By :3 Export Date: 5 June 2020 CODEN: JORCA Correspondence Address: Csámpai, A.; Institute of Chemistry, Eötvös Loránd University, P. O. B. 32, Hungary AB - Abstract Employing tryptamine or tryptophane methylester hydrochloride and (Sp)-2-formylferrocene-1-carboxylate as precursors by means of Pictet-Spengler reactions and subsequent intramolecular acylation effected by cyanuricfluoride or carbonyldiimidazole (CDI), the first representatives of ferrocene-containing β-carboline derivatives including polycyclic ferroceno/fused lactames, were prepared. In the course of CDI-mediated tandem cyclization of a tryptophane-derived carboxyferrocenyl-substituted β-carboline, a ring enlargement simultaneously taking place with the loss of the η5-C5H5Fe+ fragment of the fused ferrocene moiety, effected by the coordinating imidazole released from the reagent, led to a 4H-cyclopenta[7,8]azonino[5,4-b]indole as a minor product. The constitution and relative configuration of the new compounds with the elements of planar-, central- and conformational chirality were established by NMR methods including HMQC, HMBC and NOESY measurements supported by DFT modeling studies. © 2015 Published by Elsevier B.V. LA - English DB - MTMT ER - TY - CONF AU - Szabó, Ildikó AU - Bősze, Szilvia AU - Kocsis, László AU - Hudecz, Ferenc AU - Csámpai, Antal ED - EvamarieHey-Hawkins, null TI - Synthesis and invitro cytostaticeffect of diverseferrocene-conjugateson human celllines T2 - 13th Ferrocene Colloquium PY - 2015 SP - 76 UR - https://m2.mtmt.hu/api/publication/2893991 ID - 2893991 LA - English DB - MTMT ER - TY - CONF AU - Csámpai, Antal AU - Kovács, Zoltán AU - Csókás, Dániel AU - Gyömöre, Ádám AU - Jernei, Tamás AU - Kocsis, László AU - Szabó, Ildikó AU - Bősze, Szilvia AU - Hudecz, Ferenc ED - EvamarieHey-Hawkins, null TI - Synthesis of ferrocene - based bis heterocycles with biological relevance employing sequential degradation and reconstruction of the metallocene structure T2 - 13th Ferrocene Colloquium PY - 2015 SP - 20 UR - https://m2.mtmt.hu/api/publication/2893986 ID - 2893986 LA - English DB - MTMT ER - TY - JOUR AU - Castillo, G AU - Pribransky, Kinga AU - Mező, Gábor AU - Kocsis, László AU - Csámpai, Antal AU - Németh, Krisztina AU - Keresztes, Zsófia AU - Hianik, T TI - Electrochemical and Photometric Detection of Plasmin by Specific Peptide Substrate. JF - ELECTROANALYSIS J2 - ELECTROANAL VL - 27 PY - 2015 IS - 3 SP - 789 EP - 798 PG - 10 SN - 1040-0397 DO - 10.1002/elan.201400622 UR - https://m2.mtmt.hu/api/publication/2863245 ID - 2863245 N1 - Special Issue: Mátrafüred 2014 – International Conference on Electrochemical Sensors AB - We report a comparative analysis of plasmin detection by means of electrochemical biosensor and photometric assays. The biosensor has been based on ferrocene-modified peptide (Fc-P) specific to plasmin. Fc-P substrate is enzymatically cleaved by plasmin and the short fragment of peptide contained Fc is released causing decrease of redox current measured by cyclic voltammetry. The biosensor was tested in the range 1–20 nM of freshly prepared plasmin and it was highly selective (LOD=0.56±0.03 nM) demonstrating lower reaction to other proteins such as thrombin and β-casein. The concentration of plasmin has been determined also by a photometric analysis based on UV-vis spectroscopy (LOD=3.68±0.04 nM). The assay has been validated in milk samples. LA - English DB - MTMT ER - TY - CHAP AU - Kocsis, László AU - Patik, Márta AU - Szabó, Ildikó AU - Bősze, Szilvia AU - Csámpai, Antal AU - Hudecz, Ferenc ED - Uray, Katalin ED - Szabó, Ildikó ED - Kóczán, György TI - Shynthesis of novel ferrocene, chalcone and triazole containing molecules with promising results in anticancer chemotherapy T2 - COST Action - Chemical Approaches to Targeting Drug Resistance in Cancer Stem Cells PB - MTA-ELTE Peptidkémiai Kutatócsoport CY - Budapest SN - 9789632845005 PY - 2014 UR - https://m2.mtmt.hu/api/publication/2730897 ID - 2730897 LA - English DB - MTMT ER - TY - CONF AU - Kolos, Kiss AU - Kocsis, László AU - Holczbauer, Tamás AU - Mátyás, Czugler AU - Luminita, Silaghi-Dumitrescu AU - Antal, Csámpai ED - Holger, Butenschön TI - 2-Arylideneferroceno[e]cyclohexanones and related 3-aryl-3,3a,4,5-tetrahydroferroceno[g]indazoles: synthesis, NMR-, DFT- and x-ray analysis T2 - 2-Arylideneferroceno[e]cyclohexanones and related 3-aryl-3,3a,4,5-tetrahydroferroceno[g]indazoles: synthesis, NMR-, DFT- and x-ray analysis C1 - Hannover PY - 2013 SP - 4 EP - 4 PG - 1 UR - https://m2.mtmt.hu/api/publication/2525033 ID - 2525033 N1 - http://www.ak-renz.uni-hannover.de/ferrocene.html LA - English DB - MTMT ER - TY - CONF AU - Kocsis, László AU - Kolos, KISS AU - Kinga, FODOR AU - Antal, CSÁMPAI AU - Luminiţa, SILAGHI-DUMITRESCU ED - Majdik, Cornelia TI - Synthesis and Spectroscopic Structure Analysis of Novel C2-Chiral Diphenothiazinyl- Salen Complexes T2 - XVIII. Nemzetközi Vegyészkonferencia PB - Erdélyi Magyar Műszaki Tudományos Társaság (EMT) C1 - Kolozsvár T3 - Nemzetközi Vegyészkonferencia, ISSN 1843-6293 PY - 2012 SP - 22 EP - 22 PG - 1 UR - https://m2.mtmt.hu/api/publication/2525044 ID - 2525044 LA - English DB - MTMT ER - TY - CONF AU - Kocsis, László AU - Kiss, Kolos AU - FODOR, Kinga AU - KÁROLYI, Benedek-Imre AU - CSÁMPAI, Antal AU - LOVÁSZ, Tamás AU - SILAGHI-DUMITRESCU, Lum ini ţ a ED - Majdik, Kornélia TI - Synthesis and Characterization of New Phenothiazine Derivatives T2 - 17th International Conference on Chemistry C1 - Cluj-Napoca PY - 2011 UR - https://m2.mtmt.hu/api/publication/2525036 ID - 2525036 LA - English DB - MTMT ER - TY - CONF AU - ifj, VÁRHELYI Csaba AU - Pokol, György AU - Izvekov, Vladiszlav AU - GÖMÖRY, Ágnes AU - VÁRHELYI, Csaba AU - Kocsis, László ED - Majdik, Cornelia TI - Aszimmetrikus kobalt(III)-komplexek etil-metil-dioximmal T2 - XV. Nemzetközi Vegyészkonferencia PB - Erdélyi Magyar Műszaki Tudományos Társaság (EMT) C1 - Kolozsvár T3 - Nemzetközi Vegyészkonferencia, ISSN 1843-6293 PY - 2009 UR - https://m2.mtmt.hu/api/publication/2525041 ID - 2525041 LA - English DB - MTMT ER - TY - JOUR AU - Rónai, András AU - Szemenyei, Erzsébet AU - Kató, Erzsébet AU - Kocsis, László AU - Orosz, György AU - Al-Khrasani, Mahmoud AU - Tóth, Géza TI - Endomorphin synthesis in rat brain from intracerebroventricularly injected [H-3]-Tyr-Pro: A possible biosynthetic route for endomorphins JF - REGULATORY PEPTIDES J2 - REGUL PEPTIDES VL - 134 PY - 2006 IS - 1 SP - 54 EP - 60 PG - 7 SN - 0167-0115 DO - 10.1016/j.regpep.2005.12.004 UR - https://m2.mtmt.hu/api/publication/1626916 ID - 1626916 N1 - Cited By :17 Export Date: 29 May 2022 CODEN: REPPD AB - in spite of concentrated efforts, the biosynthetic route of mu-opioid receptor agonist brain tetrapeptide endomorphins (Tyr-Pro-Trp-Phe-NH2 and Tyr-Pro-Phe-Phe-NH2), discovered in 1997, is still obscure. We report presently that 30 min after intracerebroventricular injection of 20 or 200 mu Ci [H-3]Tyr-Pro (49.9 Ci mmol(-1)) the incorporated radioactivity was found in endomorphin-related tetra- and tripeptides in rat brain extracts. As detected by the combination of HPLC with radiodetection, a peak corresponding to endomorphin-2-OH could be identified in two of four extracts of "20 mu Ci" series. Radioactive peaks in position of Tyr, Tyr-Pro, Tyr-Pro-Phe or Tyr-Pro-Trp appeared regularly in both series and also in the "tetrapeptide cluster" constituted by endomorphins and their free carboxylic forms. In one of the four extracts in the "200 mu Ci" series a robust active peak in the position of endomorphin 2 could be detected. Intracerebroventricularly injected 100 mmol, but not 10 or 1000 nmol cold Tyr-Pro (devoid of opioid activity in vitro), caused a naloxone-reversible prolongation of tail-flick latency in rats, peaking between 15 and 30 min. We suggest that Tyr-Pro may serve as a biosynthetic precursor to endomorphin synthesis. (C) 2006 Elsevier B.V. All rights reserved. LA - English DB - MTMT ER -