TY - JOUR AU - Pálla, Tamás AU - Kolompár, Z. AU - Mazák, Károly AU - Mirzahosseini, Arash AU - Noszál, Béla TI - Estimating the Bias of Model Compounds for the Determination of Species-Specific Protonation Constants JF - ACS OMEGA J2 - ACS OMEGA VL - 9 PY - 2024 IS - 1 SP - 896 EP - 902 PG - 7 SN - 2470-1343 DO - 10.1021/acsomega.3c06994 UR - https://m2.mtmt.hu/api/publication/34509318 ID - 34509318 LA - English DB - MTMT ER - TY - CONF AU - Tűz, Boglárka AU - Noszál, Béla AU - Hosztafi, Sándor AU - Mazák, Károly TI - β-cyclodextrin complex formation and protonation equilibria of morphine and other opioid compounds of therapeutic interest T2 - EUROCD 2023 7th European Cyclodextrin Conference PY - 2023 UR - https://m2.mtmt.hu/api/publication/34163635 ID - 34163635 LA - English DB - MTMT ER - TY - JOUR AU - Pálla, Tamás AU - Mirzahosseini, Arash AU - Noszál, Béla TI - Properties of Selenolate-Diselenide Redox Equilibria in View of Their Thiolate-Disulfide Counterparts JF - ANTIOXIDANTS J2 - ANTIOXIDANTS-BASEL VL - 12 PY - 2023 IS - 4 PG - 16 SN - 2076-3921 DO - 10.3390/antiox12040822 UR - https://m2.mtmt.hu/api/publication/33720076 ID - 33720076 N1 - Department of Pharmaceutical Chemistry, Semmelweis University, Hőgyes Endre utca 9, Budapest, 1092, Hungary Research Group of Drugs of Abuse and Doping Agents, Hungarian Academy of Sciences, Széchenyi István tér 9, Budapest, 1051, Hungary Export Date: 15 May 2023 Correspondence Address: Noszál, B.; Department of Pharmaceutical Chemistry, Hőgyes Endre utca 9, Hungary; email: noszal.bela@pharma.semmelweis-univ.hu LA - English DB - MTMT ER - TY - JOUR AU - Mirzahosseini, Arash AU - Molaeit, Mirsadra AU - Mazák, Károly AU - Pálla, Tamás AU - Köteles, István AU - Varró, Nikolett AU - Mándity, István AU - Noszál, Béla TI - Species-specific acid-base characterization of carnosine and homocarnosine using nuclear magnetic resonance JF - CHEMICAL PHYSICS LETTERS J2 - CHEM PHYS LETT VL - 808 PY - 2022 PG - 6 SN - 0009-2614 DO - 10.1016/j.cplett.2022.140128 UR - https://m2.mtmt.hu/api/publication/33207317 ID - 33207317 LA - English DB - MTMT ER - TY - JOUR AU - Ferreira de Santana, Juliana AU - Mirzahosseini, Arash AU - Noszál, Béla TI - Correlation between the NMR Chemical Shifts and Thiolate Protonation Constants of Cysteamine, Homocysteine, and Penicillamine JF - JOURNAL OF SPECTROSCOPY J2 - J SPECTROSC VL - 2022 PY - 2022 PG - 8 SN - 2314-4920 DO - 10.1155/2022/9491360 UR - https://m2.mtmt.hu/api/publication/33071534 ID - 33071534 N1 - Department of Pharmaceutical Chemistry, Semmelweis University, Budapest, Hungary Research Group of Drugs of Abuse and Doping Agents, Hungarian Academy of Sciences, Budapest, Hungary Export Date: 15 May 2023 Correspondence Address: Noszál, B.; Department of Pharmaceutical Chemistry, Hungary; email: noszal.bela@pharma.semmelweis-univ.hu LA - English DB - MTMT ER - TY - JOUR AU - Ferreira de Santana, Juliana AU - Mirzahosseini, Arash AU - Mándity, B. AU - Bogdán, Dóra AU - Mándity, István AU - Noszál, Béla TI - Close correlation between thiolate basicity and certain NMR parameters in cysteine and cystine microspecies JF - PLOS ONE J2 - PLOS ONE VL - 17 PY - 2022 IS - 3 PG - 13 SN - 1932-6203 DO - 10.1371/journal.pone.0264866 UR - https://m2.mtmt.hu/api/publication/32764077 ID - 32764077 LA - English DB - MTMT ER - TY - JOUR AU - Tűz, Boglárka AU - Noszál, Béla AU - Hosztafi, Sándor AU - Mazák, Károly TI - β-cyclodextrin complex formation and protonation equilibria of morphine and other opioid compounds of therapeutic interest JF - EUROPEAN JOURNAL OF PHARMACEUTICAL SCIENCES J2 - EUR J PHARM SCI VL - 171 PY - 2022 PG - 11 SN - 0928-0987 DO - 10.1016/j.ejps.2022.106120 UR - https://m2.mtmt.hu/api/publication/32630183 ID - 32630183 N1 - Export Date: 27 May 2022 CODEN: EPSCE LA - English DB - MTMT ER - TY - JOUR AU - Pálla, Tamás AU - Herbath, Laura AU - Mazák, Károly AU - Mirzahosseini, Arash AU - Noszál, Béla TI - Selenate – An internal chemical shift standard for aqueous 77 Se NMR spectroscopy JF - MAGNETIC RESONANCE IN CHEMISTRY J2 - MAGN RESON CHEM VL - 60 PY - 2022 IS - 1 SP - 148 EP - 156 PG - 9 SN - 0749-1581 DO - 10.1002/mrc.5196 UR - https://m2.mtmt.hu/api/publication/32111667 ID - 32111667 LA - English DB - MTMT ER - TY - JOUR AU - Faragó, Zoltán AU - Mirzahosseini, Arash AU - Horváth, Dániel AU - Pálla, Tamás AU - Horváth, Péter AU - Perczel, András AU - Noszál, Béla TI - Solution Structure and Acid-Base Properties of Reduced α-Conotoxin MI JF - CHEMISTRY & BIODIVERSITY J2 - CHEM BIODIVERS VL - 18 PY - 2021 IS - 10 PG - 9 SN - 1612-1872 DO - 10.1002/cbdv.202100464 UR - https://m2.mtmt.hu/api/publication/32173833 ID - 32173833 AB - The reduced derivative of α-conotoxin MI, a 14 amino acid peptide is characterized by NMR-pH titrations and molecular dynamics simulations to determine the protonation constants of the nine basic moieties, including four cysteine thiolates, and the charge-dependent structural properties. The peptide conformation at various protonation states was determined. The results show that the disulfide motifs in the native globular α-conotoxin MI occur between those cysteine moieties that exhibit the most similar thiolate basicities. Since the basicity of thiolates correlates to its redox potential, this phenomenon can be explained by the higher reactivity of the two thiolates with higher basicities. The folding of the oxidized peptide is further facilitated by the loop-like structure of the reduced form, which brings the thiolate groups into sufficient proximity. The 9 group-specific protonation constants and the related, charge-dependent, species-specific peptide structures are presented. LA - English DB - MTMT ER - TY - JOUR AU - Zürn, Moritz AU - Tóth, Gergő AU - Ausbüttel, Tim AU - Mucsi, Zoltán AU - Horváti, Kata AU - Bősze, Szilvia AU - Sütöriné Diószegi, Magdolna AU - Pályi, Bernadett AU - Kis, Zoltán AU - Noszál, Béla AU - Boldizsár, Imre TI - Tissue-Specific Accumulation and Isomerization of Valuable Phenylethanoid Glycosides from Plantago and Forsythia Plants JF - INTERNATIONAL JOURNAL OF MOLECULAR SCIENCES J2 - INT J MOL SCI VL - 22 PY - 2021 IS - 8 PG - 18 SN - 1661-6596 DO - 10.3390/ijms22083880 UR - https://m2.mtmt.hu/api/publication/31962099 ID - 31962099 N1 - Department of Plant Anatomy, Institute of Biology, Eötvös Loránd University, Pázmány Péter Sétány 1/C, Budapest, 1117, Hungary Department of Pharmaceutical Chemistry, Semmelweis University, Hőgyes Endre u. 9, Budapest, 1092, Hungary Department of Pharmacognosy, Semmelweis University, Üllői út 26, Budapest, 1085, Hungary Femtonics Ltd, Tűzoltó u. 59, Budapest, 1094, Hungary Research Group of Peptide Chemistry, Eötvös Loránd University, Eötvös Loránd Research Network (ELKH), Pázmány Péter Sétány 1/A, Budapest, 1117, Hungary Department of Floriculture and Dendrology, Faculty of Horticultural Science, Szent István University, Villányi út 29-43, Budapest, 1119, Hungary National Biosafety Laboratory, National Public Health Center, Albert Flórián út 2-6, Budapest, 1097, Hungary Cited By :1 Export Date: 11 April 2023 Correspondence Address: Boldizsár, I.; Department of Plant Anatomy, Pázmány Péter Sétány 1/C, Hungary; email: boldizsar.imre@ttk.elte.hu LA - English DB - MTMT ER -