Zobrazeno 1 - 10
of 158
pro vyhledávání: '"Avarol"'
Autor:
Tatjana P. Stanojkovic, Marina Filimonova, Nadja Grozdanic, Slavica Petovic, Anna Shitova, Olga Soldatova, Alexander Filimonov, Jelena Vladic, Petr Shegay, Andrey Kaprin, Sergey Ivanov, Marina Nikitovic
Publikováno v:
Molecules, Vol 27, Iss 24, p 9048 (2022)
The goal of this study was to determine the activity in vitro and in vivo of avarol, a sesquiterpene hydroquinone originating from the Dysidea avara sponge from the south Adriatic Sea, against different cancer cell lines and two types of mouse carcin
Externí odkaz:
https://doaj.org/article/ddf7251b4bc54e29913fb5c94bbca59d
Autor:
Concetta Imperatore, Roberto Gimmelli, Marco Persico, Marcello Casertano, Alessandra Guidi, Fulvio Saccoccia, Giovina Ruberti, Paolo Luciano, Anna Aiello, Silvia Parapini, Sibel Avunduk, Nicoletta Basilico, Caterina Fattorusso, Marialuisa Menna
Publikováno v:
Marine Drugs, Vol 18, Iss 2, p 112 (2020)
The chemical analysis of the sponge Dysidea avara afforded the known sesquiterpene quinone avarone, along with its reduced form avarol. To further explore the role of the thiazinoquinone scaffold as an antiplasmodial, antileishmanial and antischistos
Externí odkaz:
https://doaj.org/article/c93580dc6a934fa8a1887ddb21cc1626
Akademický článek
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Autor:
Takushi Namba, Rika Kodama
Publikováno v:
Marine Drugs, Vol 13, Iss 4, Pp 2376-2389 (2015)
Avarol is a sesquiterpenoid hydroquinone with potent cytotoxicity. Although resolving endoplasmic reticulum (ER) stress is essential for intracellular homeostasis, erratic or excessive ER stress can lead to apoptosis. Here, we reported that avarol se
Externí odkaz:
https://doaj.org/article/fbe4da1f6afa4546ac646a82bec6a36c
Autor:
Stanojkovic, Tatjana P, Filimonova Marina, Grozdanić Nađa, Petović Slavica, Shitova Anna, Soldatova Olga, Filimonov Alexander, Vladić Jelena, Shegay Petr, Kaprin Andrey, Ivanov Sergey, Nikitović Marina
Publikováno v:
Molecules; Volume 27; Issue 24; Pages: 9048
The goal of this study was to determine the activity in vitro and in vivo of avarol, a sesquiterpene hydroquinone originating from theDysidea avarasponge from the south Adriatic Sea, against different cancer cell lines and two types of mouse carcinom
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3b641175653ee551a8653cd63b1e4f1d
Akademický článek
Tento výsledek nelze pro nepřihlášené uživatele zobrazit.
K zobrazení výsledku je třeba se přihlásit.
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Autor:
Marina Gordaliza
Publikováno v:
Marine Drugs, Vol 8, Iss 12, Pp 2849-2870 (2010)
The 1,4-benzoquinone moiety is a common structural feature in a large number of compounds that have received considerable attention owing to their broad spectrum of biological activities. The cytotoxic and antiproliferative properties of many natural
Externí odkaz:
https://doaj.org/article/844ffdff12d442ef839635ac0e870212
Publikováno v:
Journal of the Serbian Chemical Society, Vol 72, Iss 12, Pp 1265-1269 (2007)
Changes in electrophoresis pattern after interaction of supercoiled plasmid pBR322 DNA with avarol was studied at a micromolar concentration of reactants under mild reaction conditions. Interactions of avarol with linear high-molecular CT-DNA at mill
Externí odkaz:
https://doaj.org/article/dd06f07e8653403e8875f4ecbc3addf7
Autor:
Maria Tsoukatou, Jean Philippe Maréchal, Claire Hellio, Irena Novaković, Srdan Tufegdzic, Dusan Sladić, Miroslav J Gašić, Anthony S Clare, Constantinos Vagias, Vassilios Roussis
Publikováno v:
Molecules, Vol 12, Iss 5, Pp 1022-1034 (2007)
The sesquiterpene hydroquinone avarol (1) was isolated from the marine sponge Dysidea avara, whereas the corresponding quinone, avarone (2), was obtained by oxidation of avarol, and the significantly more lipophilic compounds [3’-(p-chloro-phenyl)a
Externí odkaz:
https://doaj.org/article/b95e64c9fb864bdf84d75d9b7c39d8d8
Publikováno v:
Journal of the Serbian Chemical Society, Vol 72, Iss 12, Pp 1265-1269 (2007)
Changes in electrophoresis pattern after interaction of supercoiled plasmid pBR322 DNA with avarol was studied at a micromolar concentration of reactants under mild reaction conditions. Interactions of avarol with linear high-molecular CT-DNA at mill
Externí odkaz:
https://doaj.org/article/70fce68b645344e88873b32ec8249440