Pregled bibliografske jedinice broj: 1162002
Novel para N-aryl substituted 3-hydroxypyridin-4- ones and their adamantyl derivatives
Novel para N-aryl substituted 3-hydroxypyridin-4- ones and their adamantyl derivatives // 27th Croatian Meeting of Chemists and Chemical Engineers and 5th Symposium Vladimir Prelog : Book of Abstracts / Marković, Dean ; Meštrović, Ernest ; Namjesnik, Danijel ; Tomašić, Vesna (ur.).
Zagreb: Hrvatsko kemijsko društvo, 2021. str. 202-202 (poster, domaća recenzija, sažetak, znanstveni)
CROSBI ID: 1162002 Za ispravke kontaktirajte CROSBI podršku putem web obrasca
Naslov
Novel para N-aryl substituted 3-hydroxypyridin-4-
ones
and their adamantyl derivatives
Autori
Dandić, Andrea ; Car, Željka ; Petrović Peroković, Vesna
Vrsta, podvrsta i kategorija rada
Sažeci sa skupova, sažetak, znanstveni
Izvornik
27th Croatian Meeting of Chemists and Chemical Engineers and 5th Symposium Vladimir Prelog : Book of Abstracts
/ Marković, Dean ; Meštrović, Ernest ; Namjesnik, Danijel ; Tomašić, Vesna - Zagreb : Hrvatsko kemijsko društvo, 2021, 202-202
Skup
27. hrvatski skup kemičara i kemijskih inženjera (27HSKIKI)
Mjesto i datum
Veli Lošinj, Hrvatska, 05.10.2021. - 08.10.2021
Vrsta sudjelovanja
Poster
Vrsta recenzije
Domaća recenzija
Ključne riječi
3-hydroxypiridin-4-one, antiproliferative activity
Sažetak
3-Hydroxypyridin-4-ones are nowadays widely investigated for their broad spectrum of biological activities (antibacterial, antidiabetes, antiprotozoal, antineurodegenerative and anticancer).[1] In our previous work we investigated several para 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. 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.[2] Further structure-activity relationship study (SAR) of such and similar pyridinone derivatives as potential anticancer agents is now in progress. In this work, for the purpose of that study, novel para N-aryl substituted 3-hydroxy-2-methylpyridin- 4-ones containing different substituents on the same position of the aryl part as well as their adamantyl derivatives were prepared (Fig. 1). All compounds were prepared with the aim of evaluating their in vitro antitumor properties on the panel of cancer cell lines. Antitumor properties of novel compounds started to elucidate the key elements, primarily the nature of the substituent on the aryl part on the adamantyl pyridinones, needed for their high antiproliferative activity.
Izvorni jezik
Engleski
Znanstvena područja
Kemija
POVEZANOST RADA
Ustanove:
Prirodoslovno-matematički fakultet, Zagreb,
Sveučilište u Osijeku - Odjel za kemiju