Zobrazeno 1 - 10
of 28
pro vyhledávání: '"Renata Kubínová"'
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:
Dagmar Jankovská, Nikol Jurčová, Renata Kubínová, Jiří Václavík, Emil Švajdlenka, Anna Mascellani, Petr Maršík, Kateřina Bouzková, Milan Malaník
Publikováno v:
Plants, Vol 13, Iss 9, p 1181 (2024)
Five putrescine and spermidine derivatives (1–5) together with five rotenoids (6–10) were isolated from a methanolic extract of the flowers of A. fruticosa that displayed promising inhibition of 76.0 ± 1.9% for AChE and 90.0 ± 4.0% for BuChE at
Externí odkaz:
https://doaj.org/article/61bf581e134a45f0a29e9b9251446fb3
Publikováno v:
Molecules, Vol 27, Iss 1, p 166 (2021)
Plectranthus (Lamiaceae), which—according to the latest systematic revision—includes three separate genera (Coleus, Plectranthus sensu stricto, and Equilabium), is a genus widely used in traditional medicine—mainly in the treatment of various a
Externí odkaz:
https://doaj.org/article/065e688ece8747e79eeda8e9d41427e4
Autor:
Anna Hudcová, Aleš Kroutil, Renata Kubínová, Adriana D. Garro, Lucas J. Gutierrez, Daniel Enriz, Michal Oravec, Jozef Csöllei
Publikováno v:
Molecules, Vol 25, Iss 7, p 1751 (2020)
Neurodegenerative diseases in which the decrease of the acetylcholine is observed are growing worldwide. In the present study, a series of new arylaminopropanone derivatives with N-phenylcarbamate moiety (1–16) were prepared as potential acetylchol
Externí odkaz:
https://doaj.org/article/75c2efaa89bc453883a1fcfeb93512d2
Autor:
Karel Šmejkal, Tereza Šlapetová, Pavel Krmenčík, Renata Kubínová, Pavel Suchý, Stefano Dall´Acqua, Gabbriella Innocenti, Ján Vančo, Karolína Kalvarová, Margita Dvorská, Jiří Slanina, Eva Kramářová, Jan Muselík, Milan Žemlička
Publikováno v:
Molecules, Vol 15, Iss 3, Pp 1223-1231 (2010)
The in vitro antiradical activity of Schisandra chinensis lignans was investigated using DPPH, ABTS+, Fenton reaction inhibition and tyrosine-nitration inhibition assays, as were the in vivo antidiabetic activities of selected lignans in an animal mo
Externí odkaz:
https://doaj.org/article/e75754c05ead4b368ad7ea601a96cf77
Publikováno v:
4th International Symposium of Young Researchers on Medicinal Plants and Natural Product Research.
Publikováno v:
Molecules, Vol 27, Iss 166, p 166 (2022)
Plectranthus (Lamiaceae), which—according to the latest systematic revision—includes three separate genera (Coleus, Plectranthus sensu stricto, and Equilabium), is a genus widely used in traditional medicine—mainly in the treatment of various a
Autor:
Renata Kubínová, Marcela Nejezchlebová, Markéta Gazdová, Mária Gáborová, Ivana Várady, Lenka Molčanová
Publikováno v:
Česká a slovenská farmacie. 70:206-209
Fytochemická analýza methanolického extraktu Helichrysum petiolare Hilliard & B. L. (Asteraceae) prokázala přítomnost sekundárních metabolitů patřících mezi fenylpropanoidy a flavonoidy. Pomocí preparativní HPLC se podařilo vyizolovat
Autor:
Renata, Kubínová, Marcela, Nejezchlebová, Markéta, Gazdová, Mária, Gáborová, Ivana, Várady, Lenka, Molčanová
Publikováno v:
Ceska a Slovenska farmacie : casopis Ceske farmaceuticke spolecnosti a Slovenske farmaceuticke spolecnosti. 70(6)
The phytochemical analysis of a methanolic extract from Helichrysum petiolare HilliardB. L. (Asteraceae) confirmed the content of phenylpropanoids and flavonoids. Five secondary metabolites were isolated using preparative HPLC, namely coumarin scopol
Autor:
Jiří Pazourek, Pavlina Marvanova, Klara Odehnalova, Tereza Padrtova, Jozef Csöllei, Karel Šmejkal, Tomáš Goněc, Oldřich Farsa, Petr Mokrý, Radka Opatřilová, Renata Kubínová, Alice Sychrová
Publikováno v:
Current organic synthesis. 17(7)
Background: The indole derivatives and the N-phenylpiperazine fragment represent interesting molecular moieties suitable for the research of new potentially biologically active compounds. This study was undertaken to identify if indol-2-carboxylic ac