Nalazite se na CroRIS probnoj okolini. Ovdje evidentirani podaci neće biti pohranjeni u Informacijskom sustavu znanosti RH. Ako je ovo greška, CroRIS produkcijskoj okolini moguće je pristupi putem poveznice www.croris.hr
izvor podataka: crosbi !

Synthesis and Antiproliferative in vitro Study of Novel Lipophilic 3-Hydroxypyridin-4-ones (CROSBI ID 647092)

Prilog sa skupa u zborniku | sažetak izlaganja sa skupa | međunarodna recenzija

Car, Željka ; Fržić, Ivana ; Petrović Peroković, Vesna ; Opačak-Bernardi, Teuta ; Tomić, Srđanka Synthesis and Antiproliferative in vitro Study of Novel Lipophilic 3-Hydroxypyridin-4-ones // 25th CROATIAN MEETING OF CHEMISTS AND CHEMICAL ENGINEERS with international participation, 3rd symposium “VLADIMIR PRELOG” 19-22 April 2017, Poreč, Croatia, Book of abstracts / Đaković, Marijana ; Šantić, Ana (ur.). Zagreb, 2017. str. 192-192

Podaci o odgovornosti

Car, Željka ; Fržić, Ivana ; Petrović Peroković, Vesna ; Opačak-Bernardi, Teuta ; Tomić, Srđanka

engleski

Synthesis and Antiproliferative in vitro Study of Novel Lipophilic 3-Hydroxypyridin-4-ones

3-Hydroxypyridin-4-ones are nowadays widely investigated for their broad spectrum of biological activities (antibacterial, antidiabetes, antiprotozoal, antineurodegenerative and anticancer) [1]. Recently, we prepared and investigated several N-aryl substituted 3-hydroxy-2-methylpyridin-4- ones as well as their ester adamantyl derivatives for their in vitro antitumor properties on several cancer cell lines [2]. All tested compounds showed antiproliferative activity ranging from moderate to strong on all inspected cell lines with lipophilic adamantane containing derivatives being active at low micromolar IC50 concentrations. Further studies of those derivatives in terms of their mechanism of action is now in progress. In this work, for the purpose of the structure-activity relationship study (SAR), novel lipophilic ether (adamantyl and cyclohexyl) derivatives of N-aryl substituted 3- hydroxy-2-methylpyridin- 4-ones were prepared (Figure 1) and their in vitro antitumor properties evaluated on the related panel of cancer and leukemia cell lines. The compounds were synthesized starting from corresponding pyridinones and adamant-1-yl or cyclohexyl bromoacetates by Williamson synthesis. Antitumor properties of novel compounds will start to elucidate the key elements (ester or ether bond between lipophilic unit and pyridinone part, the nature and/or the position of lipophilic unit) needed for high antiproliferative activity of observed pyridinone derivatives. In vitro testing included cytotoxicity evaluation and additional testing of the most potent candidates to determine the mechanism of action more precisely.

3-hydroxypyridin-4-ones ; in vitro antitumor study, SAR, adamantan-1-yl, cyclohexyl

nije evidentirano

nije evidentirano

nije evidentirano

nije evidentirano

nije evidentirano

nije evidentirano

Podaci o prilogu

192-192.

2017.

objavljeno

Podaci o matičnoj publikaciji

25th CROATIAN MEETING OF CHEMISTS AND CHEMICAL ENGINEERS with international participation, 3rd symposium “VLADIMIR PRELOG” 19-22 April 2017, Poreč, Croatia, Book of abstracts

Đaković, Marijana ; Šantić, Ana

Zagreb:

Podaci o skupu

25. HRVATSKI SKUP KEMIČARA I KEMIJSKIH INŽENJERA s međunarodnim sudjelovanjem, 3.simpozij „VLADIMIR PRELOG“

poster

19.04.2017-22.04.2017

Zagreb, Hrvatska; Poreč, Hrvatska

Povezanost rada

Kemija

Poveznice