@inproceedings{MTMT:34831171,
	title = {Ciklodextrin-segített kapilláris elektroforézis: benzil-izokinolin alkaloidok enantiomer-elválasztása},
	url = {https://m2.mtmt.hu/api/publication/34831171},
	author = {Várnagy, Erzsébet and Tóth, Gergő and Hosztafi, Sándor and Fejős, Ida and Malanga, Milo and Béni, Szabolcs},
	booktitle = {Biotechnológus Napok 2024},
	unique-id = {34831171},
	year = {2024},
	pages = {22},
	orcid-numbers = {Várnagy, Erzsébet/0009-0004-8348-4545; Tóth, Gergő/0000-0001-5341-319X; Hosztafi, Sándor/0000-0003-3793-4651; Fejős, Ida/0000-0002-3458-0854; Béni, Szabolcs/0000-0001-7056-6825}
}

@article{MTMT:34804378,
	title = {Solving the puzzle of 2-hydroxypropyl β-cyclodextrin: Detailed assignment of the substituent distribution by NMR spectroscopy},
	url = {https://m2.mtmt.hu/api/publication/34804378},
	author = {Kalydi, Eszter and Malanga, Milo and Nielsen, Thorbjørn Terndrup and Wimmer, Reinhard and Béni, Szabolcs},
	doi = {10.1016/j.carbpol.2024.122167},
	journal-iso = {CARBOHYD POLYM},
	journal = {CARBOHYDRATE POLYMERS},
	unique-id = {34804378},
	issn = {0144-8617},
	year = {2024},
	eissn = {1879-1344},
	orcid-numbers = {Béni, Szabolcs/0000-0001-7056-6825}
}

@article{MTMT:34779108,
	title = {Diterpenes Isolated from Three Different Plectranthus Sensu Lato Species and Their Antiproliferative Activities against Gynecological and Glioblastoma Cancer Cells},
	url = {https://m2.mtmt.hu/api/publication/34779108},
	author = {Gáborová, Mária and Vágvölgyi, Máté and Tayeb, Bizhar Ahmed and Minorics, Renáta and Zupkó, István and Jurček, Ondřej and Béni, Szabolcs and Kubínová, Renata and Balogh, György Tibor and Hunyadi, Attila},
	doi = {10.1021/acsomega.4c00800},
	journal-iso = {ACS OMEGA},
	journal = {ACS OMEGA},
	volume = {9},
	unique-id = {34779108},
	issn = {2470-1343},
	year = {2024},
	eissn = {2470-1343},
	pages = {18495-18504},
	orcid-numbers = {Vágvölgyi, Máté/0000-0002-2233-9422; Tayeb, Bizhar Ahmed/0000-0001-5197-564X; Minorics, Renáta/0000-0001-9685-813X; Zupkó, István/0000-0003-3243-5300; Béni, Szabolcs/0000-0001-7056-6825; Balogh, György Tibor/0000-0003-3347-1880; Hunyadi, Attila/0000-0003-0074-3472}
}

@article{MTMT:34601420,
	title = {Cyclodextrin-Enabled Enantioselective Complexation Study of Cathinone Analogs},
	url = {https://m2.mtmt.hu/api/publication/34601420},
	author = {Dohárszky, András and Kalydi, Eszter and Völgyi, Gergely and Béni, Szabolcs and Fejős, Ida},
	doi = {10.3390/molecules29040876},
	journal-iso = {MOLECULES},
	journal = {MOLECULES},
	volume = {29},
	unique-id = {34601420},
	issn = {1420-3049},
	abstract = {The characteristic alkaloid component of the leaves of the catnip shrub (Catha edulis) is cathinone, and its synthetic analogs form a major group of recreational drugs. Cathinone derivatives are chiral compounds. In the literature, several chiral methods using cyclodextrins (CDs) have been achieved so far for diverse sets of analogs; however, a comprehensive investigation of the stability of their CD complexes has not been performed yet. To characterize the enantioselective complex formation, a systematic experimental design was developed in which a total number of 40 neutral, positively, and negatively charged CD derivatives were screened by affinity capillary electrophoresis and compared according to their cavity size, substituent type, and location. The functional groups responsible for the favorable interactions were identified in the case of para-substituted cathinone analog mephedrone, flephedrone, and 4-methylethcathinone (4-MEC) and in the case of 3,4-methylendioxy derivative butylone and methylenedioxypyrovalerone (MDPV). The succinylated-β-CD and subetadex exhibited the highest complex stabilities among the studied drugs. The complex stoichiometry was determined using the Job’s plot method, and the complex structures were further studied using ROESY NMR measurements. The results of our enantioselective complex formation study can facilitate chiral method development and may lead to evaluate potential CD-based antidotes for cathinone analogs.},
	year = {2024},
	eissn = {1420-3049},
	orcid-numbers = {Völgyi, Gergely/0000-0001-8990-3916; Béni, Szabolcs/0000-0001-7056-6825; Fejős, Ida/0000-0002-3458-0854}
}

@article{MTMT:34457258,
	title = {Anticholinesterase and Antityrosinase Secondary Metabolites from the Fungus Xylobolus subpileatus},
	url = {https://m2.mtmt.hu/api/publication/34457258},
	author = {Felegyi, Kristóf and Garádi, Zsófia and Elżbieta, Studzińska-Sroka and Papp, Viktor and Boldizsár, Imre and Dancsó, András and Béni, Szabolcs and Przemysław, Zalewski and Ványolós, Attila},
	doi = {10.3390/molecules29010213},
	journal-iso = {MOLECULES},
	journal = {MOLECULES},
	volume = {29},
	unique-id = {34457258},
	issn = {1420-3049},
	year = {2024},
	eissn = {1420-3049},
	orcid-numbers = {Garádi, Zsófia/0000-0002-0152-2746; Boldizsár, Imre/0000-0001-7852-8364; Dancsó, András/0000-0001-8460-217X; Béni, Szabolcs/0000-0001-7056-6825; Ványolós, Attila/0000-0002-4710-0004}
}

@CONFERENCE{MTMT:34562813,
	title = {The Contribution of NMR to the Characterization of Isomeric Human Milk Oligosaccharides},
	url = {https://m2.mtmt.hu/api/publication/34562813},
	author = {Garádi, Zsófia and Tóth, András and Gáti, Tamás and Dancsó, András and Béni, Szabolcs},
	booktitle = {PhD Scientific Days 2023},
	unique-id = {34562813},
	year = {2023},
	orcid-numbers = {Garádi, Zsófia/0000-0002-0152-2746; Béni, Szabolcs/0000-0001-7056-6825}
}

@{MTMT:34534824,
	title = {QUALITY REQUIREMENTS FOR HERBAL DRUGS; ANALYTICAL METHODS},
	url = {https://m2.mtmt.hu/api/publication/34534824},
	author = {Papp, Nóra and Kéry, Ágnes and Filep, Rita and Szőke, Éva and Lemberkovics, Éva and Bányai, Péter and Kalász, Huba and Szarka, Szabolcs and Béni, Szabolcs},
	booktitle = {From Herbs to Healing},
	unique-id = {34534824},
	year = {2023},
	pages = {5-48},
	orcid-numbers = {Kéry, Ágnes/0000-0001-6768-5057; Szőke, Éva/0000-0003-3433-8459; Lemberkovics, Éva/0000-0003-3530-8729; Bányai, Péter/0000-0001-7999-2230; Kalász, Huba/0000-0002-7242-2056; Béni, Szabolcs/0000-0001-7056-6825}
}

@CONFERENCE{MTMT:34165299,
	title = {Interactions of sugammadex with phytotoxins: Common modes of inclusion and a new potential for the old antidote},
	url = {https://m2.mtmt.hu/api/publication/34165299},
	author = {Kalydi, Eszter and Malanga, Milo and Yannakopoulou, Konstantina and Béni, Szabolcs},
	booktitle = {EUROCD 2023 7th European Cyclodextrin Conference},
	unique-id = {34165299},
	year = {2023},
	orcid-numbers = {Béni, Szabolcs/0000-0001-7056-6825}
}

@CONFERENCE{MTMT:34163446,
	title = {Unlocking the mysteries of 2-hydroxypropyl-beta-cyclodextrin:an NMR spectroscopy approach to deciphering substitution patterns},
	url = {https://m2.mtmt.hu/api/publication/34163446},
	author = {Kalydi, Eszter and Béni, Szabolcs and Malanga, Milo},
	booktitle = {EUROCD 2023 7th European Cyclodextrin Conference},
	unique-id = {34163446},
	year = {2023},
	orcid-numbers = {Béni, Szabolcs/0000-0001-7056-6825}
}

@CONFERENCE{MTMT:34163436,
	title = {Cyclodextrin polymers as versatile tools for innovation in the combination of chemo- and phototherapy under hypoxia},
	url = {https://m2.mtmt.hu/api/publication/34163436},
	author = {Manet, Ilse and Agnes, Marco and Mazza, Arianna and Kalydi, Eszter and Béni, Szabolcs and Malanga, Milo},
	booktitle = {EUROCD 2023 7th European Cyclodextrin Conference},
	unique-id = {34163436},
	year = {2023},
	orcid-numbers = {Béni, Szabolcs/0000-0001-7056-6825}
}