@article{MTMT:33695599,
	title = {Monoterpenoid 5-methylcoumarins from Centrapalus pauciflorus with antiproliferative activity},
	url = {https://m2.mtmt.hu/api/publication/33695599},
	author = {Saidu, Muhammad Bello and Krstić, Gordana and Todorović, Nina and Berkecz, Róbert and Ali, Hazhmat and Zupkó, István and Hohmann, Judit and Rédei, Dóra},
	doi = {10.1016/j.arabjc.2023.104777},
	journal-iso = {ARAB J CHEM},
	journal = {ARABIAN JOURNAL OF CHEMISTRY},
	volume = {16},
	unique-id = {33695599},
	issn = {1878-5352},
	year = {2023},
	eissn = {1878-5379},
	orcid-numbers = {Krstić, Gordana/0000-0001-6945-6178; Todorović, Nina/0000-0002-7798-9449; Berkecz, Róbert/0000-0002-9076-2177; Zupkó, István/0000-0003-3243-5300; Hohmann, Judit/0000-0002-2887-6392; Rédei, Dóra/0000-0002-5013-247X}
}

@article{MTMT:34103969,
	title = {Anticancer Meroterpenoids from Centrapalus pauciflorus leaves: Chromone- and 2,4-Chromadione-Monoterpene Derivatives},
	url = {https://m2.mtmt.hu/api/publication/34103969},
	author = {Krstić, Gordana and Saidu, Muhammad Bello and Barta, Anita and Vágvölgyi, Máté and Ali, Hazhmat and Zupkó, István and Berkecz, Róbert and Gallah, Umar Shehu and Rédei, Dóra and Hohmann, Judit},
	doi = {10.1021/acsomega.3c03884},
	journal-iso = {ACS OMEGA},
	journal = {ACS OMEGA},
	volume = {8},
	unique-id = {34103969},
	issn = {2470-1343},
	year = {2023},
	eissn = {2470-1343},
	pages = {31389-31398},
	orcid-numbers = {Krstić, Gordana/0000-0001-6945-6178; Vágvölgyi, Máté/0000-0002-2233-9422; Zupkó, István/0000-0003-3243-5300; Berkecz, Róbert/0000-0002-9076-2177; Rédei, Dóra/0000-0002-5013-247X; Hohmann, Judit/0000-0002-2887-6392}
}

@article{MTMT:33709446,
	title = {Pauciflorins A–E, Unexpected Chromone–Monoterpene-Derived Meroterpenoids from Centrapalus pauciflorus},
	url = {https://m2.mtmt.hu/api/publication/33709446},
	author = {Krstić, Gordana and Saidu, Muhammad Bello and Bombicz, Petra and De, Sourav and Ali, Hazhmat and Zupkó, István and Berkecz, Róbert and Gallah, Umar Shehu and Rédei, Dóra and Hohmann, Judit},
	doi = {10.1021/acs.jnatprod.2c01132},
	journal-iso = {J NAT PROD},
	journal = {JOURNAL OF NATURAL PRODUCTS},
	volume = {86},
	unique-id = {33709446},
	issn = {0163-3864},
	year = {2023},
	eissn = {1520-6025},
	pages = {891-896},
	orcid-numbers = {Krstić, Gordana/0000-0001-6945-6178; Bombicz, Petra/0000-0002-5509-1515; De, Sourav/0000-0003-3014-8084; Zupkó, István/0000-0003-3243-5300; Berkecz, Róbert/0000-0002-9076-2177; Rédei, Dóra/0000-0002-5013-247X; Hohmann, Judit/0000-0002-2887-6392}
}

@CONFERENCE{MTMT:33963610,
	title = {Phytochemical investigations of Euphorbia desmondii},
	url = {https://m2.mtmt.hu/api/publication/33963610},
	author = {Saidu, Muhammad Bello and Barta, Anita and Rédei, Dóra},
	booktitle = {4th Symposium of Young Researchers on Pharmacognosy},
	doi = {10.14232/syrmpnpr.2023.15},
	unique-id = {33963610},
	year = {2023},
	pages = {22-22},
	orcid-numbers = {Rédei, Dóra/0000-0002-5013-247X}
}

@misc{MTMT:32900661,
	title = {Fiatal Gyógynövénykutatók Fóruma: a Magyar Gyógyszerésztudományi Társaság Gyógynövény Szakosztályának rendezvénye},
	url = {https://m2.mtmt.hu/api/publication/32900661},
	doi = {10.14232/fgykf.2022.af},
	editor = {Rédei, Dóra},
	publisher = {Magyar Gyógyszerésztudományi Társaság Gyógynövény Szakosztálya},
	unique-id = {32900661},
	year = {2022},
	orcid-numbers = {Rédei, Dóra/0000-0002-5013-247X}
}

@article{MTMT:33049861,
	title = {Ingol, ent-atisane, and stachane-type diterpenoids from Euphorbia deightonii with multidrug resistance reversing activity},
	url = {https://m2.mtmt.hu/api/publication/33049861},
	author = {Saidu, Muhammad Bello and Kúsz, Norbert and Berkecz, Róbert and Rácz, Bálint and Spengler, Gabriella and Hohmann, Judit and Rédei, Dóra},
	doi = {10.1016/j.phytochem.2022.113344},
	journal-iso = {PHYTOCHEMISTRY},
	journal = {PHYTOCHEMISTRY},
	volume = {204},
	unique-id = {33049861},
	issn = {0031-9422},
	abstract = {Nine previously undescribed ingol-type diterpenoid polyesters with eighteen known ingol esters, two ent-atisane, and one stachane diterpenoid were isolated from the methanol extract of Euphorbia deightonii Croizat. The structures were established by extensive spectroscopic analysis involving 1D (1H, 13C J-modulation) and 2D NMR experiments, HRESIMS measurements, and the comparison of the spectroscopic data with reported literature values. The cytotoxic concentrations of 13 isolated compounds were determined, and the compounds were investigated for multidrug resistance modulating activity on an L5178 mouse lymphoma cell line using a rho-damin 123 accumulation assay. Six ingol esters demonstrated the significant inhibition of P-glycoprotein, while the two ent-atisane diterpenoids were found to be inactive. The measured activities allowed to establish some structure-activity relationships. Notably, lower and higher-type diterpenoids simultaneously occurred in E. deightonii.},
	year = {2022},
	eissn = {1873-3700},
	orcid-numbers = {Kúsz, Norbert/0000-0002-9973-6442; Berkecz, Róbert/0000-0002-9076-2177; Rácz, Bálint/0000-0003-0088-3408; Spengler, Gabriella/0000-0001-8085-0950; Hohmann, Judit/0000-0002-2887-6392; Rédei, Dóra/0000-0002-5013-247X}
}

@article{MTMT:32765771,
	title = {Triterpenes and Phenolic Compounds from Euphorbia deightonii with Antiviral Activity against Herpes Simplex Virus Type-2},
	url = {https://m2.mtmt.hu/api/publication/32765771},
	author = {Saidu, Muhammad Bello and Kúsz, Norbert and Tsai, Yu-Chi and Vágvölgyi, Máté and Berkecz, Róbert and Kókai, Dávid and Burián, Katalin and Hohmann, Judit and Rédei, Dóra},
	doi = {10.3390/plants11060764},
	journal-iso = {PLANTS-BASEL},
	journal = {PLANTS-BASEL},
	volume = {11},
	unique-id = {32765771},
	abstract = {Two undescribed compounds, 3 beta,7 beta-dihydroxy-24-methylenelanosta-8-ene-11-one (1) and neolignane deightonin (4) were isolated from the aerial parts of Euphorbia deightonii Croizat together with six known compounds, namely, kansenone (2), euphorbol-7-one (3), dehydrodiconiferyl diacetate (5), marylaurencinol D (6), scoparon (7), and 3,4,3'-tri-O-methylellagic acid (8). The structures of the isolated compounds were determined by HRESIMS, 1D (H-1, C-13 JMOD) and 2D NMR (HSQC, HMBC, H-1-H-1 COSY, NOESY) spectroscopic analysis, and by comparison of the assignments with literature data. The anti-herpes simplex virus type-2 activity of the isolated compounds were investigated by qRT-PCR assay on Vero cells after determining cytotoxic concentration 50% (CC50). Compounds 1, 3, 4, and 7 exhibited inhibitory effects with respective IC50 values of 7.05, 2.42, 11.73, and 0.032 mu M. Scoparon (7) showed the strongest anti-HSV activity with a selectivity index of 10.93.},
	year = {2022},
	eissn = {2223-7747},
	orcid-numbers = {Kúsz, Norbert/0000-0002-9973-6442; Vágvölgyi, Máté/0000-0002-2233-9422; Berkecz, Róbert/0000-0002-9076-2177; Burián, Katalin/0000-0003-1300-2374; Hohmann, Judit/0000-0002-2887-6392; Rédei, Dóra/0000-0002-5013-247X}
}

@article{MTMT:32100393,
	title = {Bioactive Compounds from Euphorbia usambarica Pax. with HIV-1 Latency Reversal Activity},
	url = {https://m2.mtmt.hu/api/publication/32100393},
	author = {Tsai, Yu-Chi and Nell, Racheal A. and Buckendorf, Jonathan E. and Kúsz, Norbert and Mwangi, Peter Waweru and Berkecz, Róbert and Rédei, Dóra and Vasas, Andrea and Spivak, Adam M. and Hohmann, Judit},
	doi = {10.3390/ph14070653},
	journal-iso = {PHARMACEUTICALS-BASE},
	journal = {PHARMACEUTICALS},
	volume = {14},
	unique-id = {32100393},
	year = {2021},
	eissn = {1424-8247},
	orcid-numbers = {Nell, Racheal A./0000-0002-0324-7522; Kúsz, Norbert/0000-0002-9973-6442; Berkecz, Róbert/0000-0002-9076-2177; Rédei, Dóra/0000-0002-5013-247X; Vasas, Andrea/0000-0002-1818-7702; Hohmann, Judit/0000-0002-2887-6392}
}

@article{MTMT:31784472,
	title = {Bíbor kasvirág - az Év Gyógynövénye 2020-ban},
	url = {https://m2.mtmt.hu/api/publication/31784472},
	author = {Tóth, Barbara and Rédei, Dóra and Fekete, Orsolya and Csupor, Dezső},
	journal-iso = {GYÓGYSZERÉSZET},
	journal = {GYÓGYSZERÉSZET},
	volume = {2020},
	unique-id = {31784472},
	issn = {0017-6036},
	year = {2020},
	pages = {643-648},
	orcid-numbers = {Tóth, Barbara/0000-0002-6086-8819; Rédei, Dóra/0000-0002-5013-247X; Csupor, Dezső/0000-0002-4088-3333}
}

@article{MTMT:31629692,
	title = {12-Deoxyphorbol Esters Induce Growth Arrest and Apoptosis in Human Lung Cancer A549 Cells via Activation of PKC-δ/PKD/ERK Signaling Pathway},
	url = {https://m2.mtmt.hu/api/publication/31629692},
	author = {Tsai, Yu-Chi and Rédei, Dóra and Hohmann, Judit and Wu, Chin-Chung},
	doi = {10.3390/ijms21207579},
	journal-iso = {INT J MOL SCI},
	journal = {INTERNATIONAL JOURNAL OF MOLECULAR SCIENCES},
	volume = {21},
	unique-id = {31629692},
	issn = {1661-6596},
	year = {2020},
	eissn = {1422-0067},
	orcid-numbers = {Rédei, Dóra/0000-0002-5013-247X; Hohmann, Judit/0000-0002-2887-6392}
}