Pregled bibliografske jedinice broj: 1159437
Antiproliferative properties of synthetic granulatamide B and its structural analogues
Antiproliferative properties of synthetic granulatamide B and its structural analogues // 27. hrvatski skup kemičara i kemijskih inženjera (27HSKIKI) / Marković, Dean, Meštrović, Ernest ; Namjesnik, Danijel ; Tomašić, Vesna (ur.).
Zagreb, 2021. str. 195-195 (poster, međunarodna recenzija, sažetak, znanstveni)
CROSBI ID: 1159437 Za ispravke kontaktirajte CROSBI podršku putem web obrasca
Naslov
Antiproliferative properties of synthetic
granulatamide B and its structural analogues
Autori
Matulja, Dario ; Grbčić, Petra ; Kraljević Pavelić, Sandra ; Marković, Dean
Vrsta, podvrsta i kategorija rada
Sažeci sa skupova, sažetak, znanstveni
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
Međunarodna recenzija
Ključne riječi
granulatamide B, structural analogues, antiproliferative
Sažetak
Gorgonian corals of the genus Eunicella have been shown as a rich source of various secondary metabolites differing in structural characteristic with promising biological activities. Among such is granulatamide B (1), a tryptamine-derived alkaloid, characterized by unsaturated N-fatty acyl moiety, which was found to exhibit high cytotoxicity against various cancer cell lines. Therefore, within the Bioprospecting of the Adriatic Sea project, we have synthesized granulatamide B following the procedure of Fürstner’s Fe-catalyzed synthesis as well as structural analogues by the modification of the side chain (number of C-atoms and saturation degree). Currently, total of 13 compounds have been prepared and examined for antiproliferative and cytotoxic activities applying MTT (3-(4, 5- dimethylthiazol-2-yl)-2, 5- diphenyltetrazolium bromide) assays. Granulatamide B (1) and 9 (analogue with retinoyl moiety) have exerted the most promising, non-selective anticancer activities against SW620, CFPAC-1, MCF-7 and HepG2 cancer cells with determined IC50 values in the range 20-39 µM. Finally, the presented results highlight the importance of the indole skeleton as the pharmacophore group in medicinal chemistry and potential of fatty acids to modulate pharmacological properties of target molecules.
Izvorni jezik
Engleski
Znanstvena područja
Kemija, Interdisciplinarne prirodne znanosti, Biotehnologija u biomedicini (prirodno područje, biomedicina i zdravstvo, biotehničko područje)
POVEZANOST RADA
Projekti:
EK-KF-KK.01.1.1.01.0002 - Bioprospecting Jadranskog mora (Jerković, Igor; Dragović-Uzelac, Verica; Šantek, Božidar; Čož-Rakovac, Rozelinda; Kraljević Pavelić, Sandra; Jokić, Stela, EK ) ( CroRIS)
IP-2019-04-8846 - In-silico potpomognut dizajn supstrata za hvatanje CO2 u katalitičkoj formaciji karbonata i karbamata (INDICATIOR) (Marković, Dean, HRZZ - 2019-04) ( CroRIS)
EK-EFRR-RC.2.2.06-0001 - Razvoj istraživačke infrastrukture na kampusu Sveučilišta u Rijeci (RISK) (Ožanić, Nevenka, EK - Operativni program Regionalna konkurentnost) ( CroRIS)
NadSve-Sveučilište u Rijeci-uniri-prirod-18-102 - Razvoj novih nanotehnološki unaprijeđenih materijala otpornih na stvaranje bakterijskih biofilmova (Marković, Dean, NadSve ) ( CroRIS)
Ustanove:
Sveučilište u Rijeci - Odjel za biotehnologiju,
Fakultet zdravstvenih studija u Rijeci
Profili:
Petra Grbčić
(autor)
Dean Marković
(autor)
Sandra Kraljević Pavelić
(autor)
Dario Matulja
(autor)