Pregled bibliografske jedinice broj: 1145166
Synthesis and Cytotoxic Evaluation of a New Ferrocene Triacyl Derivative of Resveratrol
Synthesis and Cytotoxic Evaluation of a New Ferrocene Triacyl Derivative of Resveratrol // European Symposium on Organic Chemistry (ESOC 2021) Virtual Mini Symposium, Book of Abstracts and Programme
online, 2021. str. 78-78 (poster, međunarodna recenzija, sažetak, znanstveni)
CROSBI ID: 1145166 Za ispravke kontaktirajte CROSBI podršku putem web obrasca
Naslov
Synthesis and Cytotoxic Evaluation of a New
Ferrocene Triacyl Derivative of Resveratrol
Autori
Kovač, Veronika ; Kmetič, Ivana ; Murati, Teuta ; Miletić, Marina
Vrsta, podvrsta i kategorija rada
Sažeci sa skupova, sažetak, znanstveni
Izvornik
European Symposium on Organic Chemistry (ESOC 2021) Virtual Mini Symposium, Book of Abstracts and Programme
/ - , 2021, 78-78
Skup
European Symposium on Organic Chemistry (ESOC 2021)
Mjesto i datum
Online, 05.07.2021. - 06.07.2021
Vrsta sudjelovanja
Poster
Vrsta recenzije
Međunarodna recenzija
Ključne riječi
ferrocene-resveratrol conjugate, resveratrol, biological activity, ovary cells, apoptosis
Sažetak
Resveratrol (3, 5, 4′‐trihydroxy‐trans‐stilbene, RSV) is well known as a natural polyphenolic phytoalexin with a variety of biological benefits including antioxidant, anticancer, cardio- and neuroprotective, antimicrobial, antiviral, anti-inflammatory and other activities.1 With a view to overcoming drawbacks of resveratrol, such as low bioavailability and solubility, 2 and enhancing its biological potential, different structural modifications of the resveratrol have been made including modifications of hydroxyl groups, the presence of long alkyl chains or functionalized chains on the aromatic rings, conjugation etc.3, 4 Thereby, some of the prepared ferrocenyl-stilbene analogs with hidden phenolic function showed higher antitumor activity than resveratrol, most likely due to their lipophilicity and thus improved solubility in the cellular environment.4 In a continuation of our previous study on a ferrocene-resveratrol conjugates, 5 we have prepared resveratrol triester derivative I. The new compound (in concentrations 5 – 50µM) and RSV (in concentrations 2.5 – 100µM) have been tested for the possible cytotoxicity towards normal ovary cells (CHO-K1). After 48h of treatment with RSV, cell viability was significantly reduced determined with Neutral Red (in doses ≥50 µM) and MTT (in doses ≥10 µM) methods and dose-response pattern was clearly observed. Biological activity of resveratrol derivative I was notably modified compared to RSV, with new U-shaped dose-response curve (obtained with MTT method). Application of 50 µM compound I did not suppress cell viability (as observed with RSV), on the contrary – cell viability was induced which is confirmed by Neutral Red method. Flow cytometry also indicated lower cytotoxicity of derivative I vs. RSV. This work has been fully supported by Croatian Science Foundation under the project IP-2020-02-9162.
Izvorni jezik
Engleski
Znanstvena područja
Kemija, Biotehnologija
POVEZANOST RADA
Projekti:
--IP-2020-02-9162 - Ferocenski analozi biomolekula: strukturna karakterizacija i biološka evaluacija (FER-AN-BIOMOL) (Barišić, Lidija) ( CroRIS)
Ustanove:
Prehrambeno-biotehnološki fakultet, Zagreb