Zobrazeno 1 - 10
of 23
pro vyhledávání: '"Zsófia Dubrovay"'
Autor:
Anita Horváth, Kristóf Bolla, Alexandra Wachtler, Lilla Maksó, Máté Papp, Sándor Mahó, Zsófia Dubrovay, János Kóti, Rita Skoda-Földes
Publikováno v:
ACS Omega, Vol 6, Iss 41, Pp 26846-26856 (2021)
Externí odkaz:
https://doaj.org/article/8c597458d1624363a543d60f78b3486e
Autor:
Alexandra Wachtler, Rita Skoda-Földes, Sándor Mahó, Máté Papp, Anita Horváth, Zsófia Dubrovay, Kristóf Bolla, Lilla Maksó, János Kóti
Publikováno v:
ACS Omega, Vol 6, Iss 41, Pp 26846-26856 (2021)
ACS Omega
ACS Omega
The ring opening of 2α,3α- and 2β,3β-epoxy-5α-androstan-17-one with halide reagents (AlCl3, TMSCl, LiCl, and LiBr) was investigated using imidazolium ionic liquids in the dual role of solvent and catalyst. The application of the ionic liquid was
Publikováno v:
Letters in Drug Design & Discovery. 16:1248-1257
Background: Aryl-methoxybenzaldehydes substituted in various positions may serve as valuable starting materials for the synthesis of biologically active compounds. Methods: Biaryl-methoxybenzaldehydes and pyridyl-aryl-methoxybenzaldehydes were synthe
Autor:
Andrea Német-Hanzelik, Zsófia Dubrovay, György Keglevich, István Greiner, Hedvig Bölcskei, Viktor Háda
Publikováno v:
Letters in Drug Design & Discovery. 14:233-239
The benzyloxy-benzyl moiety is a valuable building block in medicinal chemistry, e.g. in case of the voltage gated sodium channel blockers Safinamide and Ralfinamide. To prepare further derivatives a series of (iodobenzyl)oxybenzaldehydes (3a-3i) use
Autor:
András Keglevich, József Molnár, Ana Martins, Péter Keglevich, Zsófia Dubrovay, Áron Szigetvári, Laszlo Hegedus, Judit Gyenese, Csaba Szántay, Lilla Péter, Attila Hunyadi, Miklós Dékány, László Hazai
Publikováno v:
Current Organic Chemistry. 20:2639-2646
Autor:
András Keglevich, Zita Hegedüs, László Hazai, Zoltán Bánóczi, Ildikò Szabò, József Tóvári, Péter Keglevich, Áron Szigetvári, Zsófia Lengyel, Csaba Szántay, Zsófia Dubrovay, Ivan Ranđelović, Ferenc Hudecz, Viktor Háda, Fruzsina L. Regenbach, Álmos Gorka-Kereskényi
Publikováno v:
Journal of peptide science : an official publication of the European Peptide Society. 24(10)
Some Vinca alkaloids (eg, vinblastine, vincristine) have been widely used as antitumor drugs for a long time. Unfortunately, vindoline, a main alkaloid component of Catharanthus roseus (L.) G. Don, itself, has no antitumor activity. In our novel rese
Autor:
Viktor Háda, Zsófia Dubrovay, Janos Galambos, Zoltán Gulyás, Csaba Szántay, Antal Aranyi, Ágnes Lakó-Futó
Publikováno v:
Journal of Pharmaceutical and Biomedical Analysis. 84:309-322
In the course of exploring the possibilities of developing a new, improved process at Gedeon Richter for the production of the "bisindole" alkaloids vinblastine (VLB) and vincristine (VCR), some novel VLB/VCR-related trace impurities were detected by
Autor:
Zsófia Dubrovay, Viktor Háda
In this chapter, we describe the NMR- and MS-based structure elucidation of a new impurity of the bisindole alkaloid vincristine (VCR). Owing to its size and internal conformational dynamics, VCR and its derivatives are highly “NMR-unfriendly” ev
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::1c6c9c8a7aa1424ef62a679d198c541d
https://doi.org/10.1016/b978-0-12-419963-7.00011-0
https://doi.org/10.1016/b978-0-12-419963-7.00011-0
Autor:
Zoltán Béni, Ádám Demeter, Miklós Dékány, Zsófia Dubrovay, Lars G. Hanson, Viktor Háda, János Kóti, Zsuzsanna Sánta, Zoltán Szakács, Csaba Szántay
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::0d3f649b3cda36bebc47cd782e0c1f30
https://doi.org/10.1016/b978-0-12-419963-7.09990-9
https://doi.org/10.1016/b978-0-12-419963-7.09990-9
Autor:
Tímea Imre, Pál Szabó, Eniko Takacs, V. Pongracz, Júlia Kovári, Angéla Békési, Zsófia Dubrovay, Imre Zagyva, Beáta G. Vértessy, Orsolya Barabas
Publikováno v:
Journal of Biological Chemistry. 279:17932-17944
dUTPase is responsible for preventive DNA repair via exclusion of uracil. Developmental regulation of the Drosophila enzyme is suggested to be involved in thymine-less apoptosis. Here we show that in addition to conserved dUTPase sequence motifs, the