Zobrazeno 1 - 10
of 40
pro vyhledávání: '"Máté Vágvölgyi"'
Autor:
Mária Gáborová, Máté Vágvölgyi, Bizhar Ahmed Tayeb, Renáta Minorics, István Zupkó, Ondřej Jurček, Szabolcs Béni, Renata Kubínová, György Tibor Balogh, Attila Hunyadi
Publikováno v:
ACS Omega, Vol 9, Iss 16, Pp 18495-18504 (2024)
Externí odkaz:
https://doaj.org/article/7fbece91a8724e5fae69ba49cb526264
Autor:
Máté Vágvölgyi, Dávid Laczkó, Ana Raquel Santa-Maria, Judit P. Vigh, Fruzsina R. Walter, Róbert Berkecz, Mária A. Deli, Gábor Tóth, Attila Hunyadi
Publikováno v:
PLoS ONE, Vol 19, Iss 2 (2024)
Externí odkaz:
https://doaj.org/article/a51fd285e1124fe18c4800a15ad4a943
Autor:
Gordana Krstić, Muhammad Bello Saidu, Anita Barta, Máté Vágvölgyi, Hazhmat Ali, István Zupkó, Róbert Berkecz, Umar Shehu Gallah, Dóra Rédei, Judit Hohmann
Publikováno v:
ACS Omega, Vol 8, Iss 34, Pp 31389-31398 (2023)
Externí odkaz:
https://doaj.org/article/e294224370c14d3aa49b71c8c2202081
Autor:
Bettina Szerencsés, Mónika Vörös, Kristóf Bagi, Márton B. Háznagy, Attila Hunyadi, Csaba Vágvölgyi, Ilona Pfeiffer, Máté Vágvölgyi
Publikováno v:
Microbiology Research, Vol 13, Iss 4, Pp 985-994 (2022)
Cryptococcosis, a life-threatening fungal infection, frequently occurs in patients suffering from AIDS. The treatment of the disease is hampered by the limited number of the effective drugs and the increasing resistance; therefore, to find new active
Externí odkaz:
https://doaj.org/article/e35650da48474db5be9f1a861a717443
Autor:
Erzsébet Mernyák, Sándor Bartha, Lili Kóczán, Rebeka Jójárt, Vivien Resch, Gábor Paragi, Máté Vágvölgyi, Attila Hunyadi, Bella Bruszel, István Zupkó, Renáta Minorics
Publikováno v:
Journal of Enzyme Inhibition and Medicinal Chemistry, Vol 36, Iss 1, Pp 1931-1937 (2021)
Microwave-assisted phospha-Michael addition reactions were carried out in the 13α-oestrone series. The exocyclic 16-methylene-17-ketones as α,β-unsaturated ketones were reacted with secondary phosphine oxides as nucleophilic partners. The addition
Externí odkaz:
https://doaj.org/article/cf583eaeec9e45a3aa656d5aef85ad16
Autor:
Muhammad Bello Saidu, Norbert Kúsz, Yu-Chi Tsai, Máté Vágvölgyi, Róbert Berkecz, Dávid Kókai, Katalin Burián, Judit Hohmann, Dóra Rédei
Publikováno v:
Plants, Vol 11, Iss 6, p 764 (2022)
Two undescribed compounds, 3β,7β-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-
Externí odkaz:
https://doaj.org/article/6de03454b37a484cab8e243a5f8452a7
Autor:
Máté Vágvölgyi, Endre Kocsis, Márta Nové, Nikoletta Szemerédi, Gabriella Spengler, Zoltán Kele, Róbert Berkecz, Tamás Gáti, Gábor Tóth, Attila Hunyadi
Publikováno v:
International Journal of Molecular Sciences, Vol 23, Iss 7, p 3447 (2022)
Fluorine represents a privileged building block in pharmaceutical chemistry. Diethylaminosulfur-trifluoride (DAST) is a reagent commonly used for replacement of alcoholic hydroxyl groups with fluorine and is also known to catalyze water elimination a
Externí odkaz:
https://doaj.org/article/868bcde88d844a48933c7431c54cbcf2
Autor:
Máté Vágvölgyi, Péter Bélteky, Dóra Bogdán, Márta Nové, Gabriella Spengler, Ahmed D. Latif, István Zupkó, Tamás Gáti, Gábor Tóth, Zoltán Kónya, Attila Hunyadi
Publikováno v:
Frontiers in Pharmacology, Vol 11 (2020)
Several ecdysteroid acetonides act as adjuvant chemo-sensitizing agents against various cancer cell lines, and they can be formulated to self-assembling nanoparticle (NP) pro-drugs through a hydrolysable conjugation with squalene. In the bloodstream
Externí odkaz:
https://doaj.org/article/b9fbb432dbbd4321afce66970cf9fd0b
Autor:
Ahmed Dhahir Latif, Tamás Jernei, Ana Podolski-Renić, Ching-Ying Kuo, Máté Vágvölgyi, Gábor Girst, István Zupkó, Sedef Develi, Engin Ulukaya, Hui-Chun Wang, Milica Pešić, Antal Csámpai, Attila Hunyadi
Publikováno v:
Antioxidants, Vol 9, Iss 6, p 519 (2020)
Hybrid compounds combine fragments with complementary targets to achieve a common pharmacological goal. This approach represents an increasingly popular strategy for drug discovery. In this work, we aimed to design antitumor hybrid compounds based on
Externí odkaz:
https://doaj.org/article/31cfd7612c754272a12853f2531b14a3
Autor:
Ahmed Dhahir Latif, Tímea Gonda, Máté Vágvölgyi, Norbert Kúsz, Ágnes Kulmány, Imre Ocsovszki, Zoltán Péter Zomborszki, István Zupkó, Attila Hunyadi
Publikováno v:
International Journal of Molecular Sciences, Vol 20, Iss 9, p 2184 (2019)
Naringenin is one of the most abundant dietary flavonoids exerting several beneficial biological activities. Synthetic modification of naringenin is of continuous interest. During this study our aim was to synthesize a compound library of oxime and o
Externí odkaz:
https://doaj.org/article/f46070facb774c2fb535d0cb3f79c604