Zobrazeno 1 - 10
of 12
pro vyhledávání: '"Zuzana Čurillová"'
Autor:
Zuzana Čurillová, Peter Kutschy, Eva Solčániová, Martina Pilátová, Ján Mojžiš, and Vladimír Kováčik
Publikováno v:
ARKIVOC, Vol 2008, Iss 8, Pp 85-104 (2008)
Externí odkaz:
https://doaj.org/article/6813a96d72864b12958a995592a1a91c
Autor:
Tat’ána Gondová, Martin Fabián, Ján Petrovaj, Zuzana Čurillová, Aneta Salayová, Peter Kutschy, Daniel W. Armstrong
Publikováno v:
Chromatographia. 74:751-757
Direct chiral separation of the enantiomers of spirobrassinin, 1-methoxyspirobrassinin and ten novel cis- and trans-diastereoisomers of 2-amino analogs of indole phytoalexin 1-methoxyspirobrassinol methyl ether on macrocyclic glycopeptide-based chira
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::bee22eac1e7bd00de1bac9736700b37f
https://doi.org/10.1007/s10337-011-2143-y
https://doi.org/10.1007/s10337-011-2143-y
Autor:
Pavel Pazdera, Maria Repovska, Roman Mezencev, Zuzana Čurillová, Andrej Sýkora, Martina Pilátová, Tatiana Hromjáková, Ján Mojžiš, Peter Kutschy
Publikováno v:
Collection of Czechoslovak Chemical Communications. 75:887-903
Glyoxyl analogs of indole phytoalexins brassinin, 1-methoxybrassinin, brassitin, 1-methoxybrassitin and 1-methoxybrassenin B were prepared, using (1H-indol-3-yl)-, (1-methoxyindol-3-yl)- and [1-(2,3,4,6-tetra-O-acetyl-β-D-glucopyranosyl)indol-3-yl]g
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::8e53d939f3213cde1e6b5a22c9b6e104
https://doi.org/10.1135/cccc2010048
https://doi.org/10.1135/cccc2010048
Publikováno v:
Tetrahedron Letters. 48:8200-8204
Stereoselective synthesis of cruciferous indole phytoalexin (R)-(+)-1-methoxyspirobrassinin and its unnatural (S)-(−)-enantiomer was achieved by spirocyclization of 1-methoxybrassinin in the presence of (+)- and (−)-menthol and subsequent oxidati
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::5cf7a99de040c1776d35ff4bf265c8fe
https://doi.org/10.1016/j.tetlet.2007.09.080
https://doi.org/10.1016/j.tetlet.2007.09.080
Autor:
Nobuaki Miura, Zuzana Čurillová, Tohru Taniguchi, Martina Pilátová, Jan Mojzis, Kenji Monde, Peter Kutschy
Publikováno v:
Bioorganic & Medicinal Chemistry. 13:5206-5212
Synthesized by an efficient one-pot spirocyclization method, two chiral cruciferous phytoalexins, 1-methoxyspirobrassinin (2) and 1-methoxyspirobrassinol methyl ether (4a), were prepared through optical resolution using the chiral HPLC method of corr
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::06035baba08231748fa2428d8e8af241
https://doi.org/10.1016/j.bmc.2005.06.001
https://doi.org/10.1016/j.bmc.2005.06.001
Autor:
Roman Mezencev, Zuzana Čurillová, Renata Maruskova, Nobuyuki Harada, Mariana Miklosova, Peter Kutschy, Ján Mojžiš, Kenji Monde, Mojmír Suchý, Milan Dzurilla
Publikováno v:
Tetrahedron Letters. 43:9489-9492
The first syntheses of cruciferous indole phytoalexins (±)-1-methoxyspirobrassinin, (±)-1-methoxyspirobrassinol, (±)-1-methoxyspirobrassinol methyl ether as well as a new syntheses of phytoalexins (±)-spirobrassinin and cyclobrassinin were achiev
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::f419e7d4fb5f3e805361e11999185989
https://doi.org/10.1016/s0040-4039(02)02452-8
https://doi.org/10.1016/s0040-4039(02)02452-8
Autor:
Martina Pilátová, Pavel Pazdera, Maria Repovska, Zuzana Čurillová, Jan Mojzis, Roman Mezencev, Andrej Sykora, Peter Kutschy, Tatiana Hromjakova
Publikováno v:
ChemInform. 42
A series of analogues of indole phytoalexins is prepared and evaluated for their anticancer activity.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::9506e8fc8c2d6e5edf2cc6b628276394
https://doi.org/10.1002/chin.201102208
https://doi.org/10.1002/chin.201102208
Autor:
Martina Pilátová, Roman Mezencev, Peter Kutschy, Zuzana Čurillová, Aneta Salayová, Ján Mojžiš, John F. McDonald
Publikováno v:
Chemotherapy. 54(5)
Background: Several indole phytoalexins exhibit antiproliferative and/or cancer chemopreventive properties in vitro. However, the potency and selectivity of their anticancer effects were reported to be relatively weak. In order to improve the antican
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::754df0b1d2a7762f7235ec1ef6f0d7d9
https://pubmed.ncbi.nlm.nih.gov/18769026
https://pubmed.ncbi.nlm.nih.gov/18769026
Autor:
Renata Maruskova, Imrich Geci, Milan Dzurilla, Zuzana Čurillová, Vladimír Kováčik, Juraj Alföldi, Marian Sabol, Peter Kutschy
Publikováno v:
ChemInform. 35
The first synthesis of 1-(β-D-glucopyranosyl)brassinin, 1-(β-D-glucopyranosyl)brassenin A, 1-(β-D-glucopyranosyl)brassenin B and 9-(β-D-glucopyranosyl)cyclobrassinin, nucleoside analogs derived from indole phytoalexins, was achieved by linear app
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::67c2a6ca30da651abde0a4a6bfdefa37
https://doi.org/10.1002/chin.200435211
https://doi.org/10.1002/chin.200435211
Autor:
Mojmír Suchý, P. Kutschy, Andrej Mirossay, Roman Mezencev, Zuzana Čurillová, Ján Mojžiš, Kenji Monde, Martina Pilátová, L. Mirossay, Marek Šarišský
Publikováno v:
Leukemia research. 29(4)
We tested antiproliferative activity of selected cruciferous phytoalexins including brassinin, 1-methoxybrassinin, (+/-)-spirobrassin, (+/-)-1-methoxyspirobrassinin and (+/-)-1-methoxyspirobrassinol, in leukemic Jurkat cell. The most effective of the
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5c40c7f60ad73c105efe78279b6e570a
https://pubmed.ncbi.nlm.nih.gov/15725476
https://pubmed.ncbi.nlm.nih.gov/15725476