Pregled bibliografske jedinice broj: 977375
Design, synthesis and antitumor activity of novel quinoline-benzimidazolamidine hybrids
Design, synthesis and antitumor activity of novel quinoline-benzimidazolamidine hybrids // Book of Abstracts, International Symposium on Medicinal Chemistry
Ljubljana: EFMC, 2018. str. 143-143 (poster, međunarodna recenzija, sažetak, znanstveni)
CROSBI ID: 977375 Za ispravke kontaktirajte CROSBI podršku putem web obrasca
Naslov
Design, synthesis and antitumor activity of novel quinoline-benzimidazolamidine hybrids
Autori
Krstulović, Luka ; Starčević, Kristina ; Opačak- Bernardi, Teuta ; Bajić, Miroslav ; Glavaš- Obrovac, Ljubica
Vrsta, podvrsta i kategorija rada
Sažeci sa skupova, sažetak, znanstveni
Izvornik
Book of Abstracts, International Symposium on Medicinal Chemistry
/ - Ljubljana : EFMC, 2018, 143-143
Skup
International Symposium on Medicinal Chemistry
Mjesto i datum
Ljubljana, Slovenija, 02.09.2018. - 06.09.2018
Vrsta sudjelovanja
Poster
Vrsta recenzije
Međunarodna recenzija
Ključne riječi
Quinoline, benzimidazolamidine, hybrids, antitumor activity
Sažetak
Cancer is one of the most prominent health issues responsible for more than 1 million deaths per year in EU, costing annually more than billion euros. One of the emerging strategies for overcoming the drawbacks of the available anticancer therapeutics is the development of hybrid agents, composed of two distinct pharmocophores [1]. In continuing our work on the synthesis and evaluation of hybrid molecules [2] we have synthesized two series of new hybrids in which 7-chloro-4-aminoquinoline is linked with two different linkers to a benzimidazole amidine moiety. Moieties have been chosen, because both of them show anticancer activity. Several 7- chloro-4- aminoquinoline based antimalarial therapeutics are tested for their anticancer activity, two of them (chloroquine and hydroxychloroquine) are currently investigated in clinical trials for cancer therapy [3]. On the other hand benzimidazole moiety is found in many known pharmaceuticals, displaying besides anticancer a variety of biological effects, also positively charged amidine groups are known for their cellular and nuclear uptake. Novel compounds were evaluated for their in vitro cytotoxic activity against normal epithelial (MDCK1), cervix adenocarcinoma (HeLa), colon adenocarcinoma (CaCo2), and leukemia (K562 and RaJi) cell lines using MTT assay.
Izvorni jezik
Engleski
Znanstvena područja
Kemija, Temeljne medicinske znanosti
POVEZANOST RADA
Ustanove:
Veterinarski fakultet, Zagreb,
Medicinski fakultet, Osijek
Profili:
Miroslav Bajić
(autor)
Kristina Starčević
(autor)
Ljubica Glavaš Obrovac
(autor)
Luka Krstulović
(autor)
Teuta Opačak-Bernardi
(autor)