Pregled bibliografske jedinice broj: 1034130
Antiproliferative activity and mode of action analysis of novel amino and amido substituted phenantrene and naphtho[2,1-b]thiophene derivatives
Antiproliferative activity and mode of action analysis of novel amino and amido substituted phenantrene and naphtho[2,1-b]thiophene derivatives // European journal of medicinal chemistry, 185 (2020), 111833, 13 doi:10.1016/j.ejmech.2019.111833 (međunarodna recenzija, članak, znanstveni)
CROSBI ID: 1034130 Za ispravke kontaktirajte CROSBI podršku putem web obrasca
Naslov
Antiproliferative activity and mode of action
analysis of novel amino and amido substituted
phenantrene and naphtho[2,1-b]thiophene
derivatives
Autori
Perin, Nataša ; Rep, Valentina ; Sović, Irena ; Juričić, Štefica ; Selgrad, Danijel ; Klobučar, Marko ; Pržulj, Nataša ; Gupta, Chhedi Lal ; Malod-Dognin, Noël ; Kraljević Pavelić, Sandra ; Hranjec, Marijana
Izvornik
European journal of medicinal chemistry (0223-5234) 185
(2020);
111833, 13
Vrsta, podvrsta i kategorija rada
Radovi u časopisima, članak, znanstveni
Ključne riječi
amines ; amides ; antiproliferative activity ; phenatrenes ; mode of action analysis ; naphtho[2 ; 1-b]thiophenes
Sažetak
Herein we present and describe the design and synthesis of novel phenantrene derivatives substituted with either amino or amido side chains and their biological activity. Antiproliferative activities were assessed in vitro on a panel of human cancer cell lines. Tested compounds showed moderate activity against cancer cells in comparison with 5- fluorouracile. Among all tested compounds, some compounds substituted with cyano groups showed a pronounced and selective activity in the nanomolar range of inhibitory concentrations against HeLa and HepG2. The strongest selective activity against HeLa cells was observed for acrylonitriles 8 and 11 and their cyclic analogues 15 and 17 substituted with two cyano groups with a corresponding IC50 = 0.33, 0.21, 0.65 and 0.45 M, respectively. Compounds 11 showed the most pronounced selectivity being almost non cytotoxic to normal fibroblasts. Additionally, mode of biological action analysis was performed in silico and in vitro by Western blot analysis of HIF-1-α relative expression for compounds 8 and 11.
Izvorni jezik
Engleski
Znanstvena područja
Kemija, Biologija, Temeljne medicinske znanosti
POVEZANOST RADA
Projekti:
HRZZ-IP-2018-01-4379 - Istraživanje antioksidativnog djelovanja benzazolskog skeleta u dizajnu novih antitumorskih agensa (AntioxPot) (Hranjec, Marijana, HRZZ - 2018-01) ( CroRIS)
Ustanove:
Fakultet kemijskog inženjerstva i tehnologije, Zagreb,
Sveučilište u Rijeci - Odjel za biotehnologiju
Profili:
Irena Sović
(autor)
Marijana Hranjec
(autor)
Nataša Perin
(autor)
Sandra Kraljević Pavelić
(autor)
Marko Klobučar
(autor)
Valentina Rep Kaulić
(autor)
Citiraj ovu publikaciju:
Časopis indeksira:
- Current Contents Connect (CCC)
- Web of Science Core Collection (WoSCC)
- Science Citation Index Expanded (SCI-EXP)
- SCI-EXP, SSCI i/ili A&HCI
- Scopus
- MEDLINE
Uključenost u ostale bibliografske baze podataka::
- BIOSIS Previews (Biological Abstracts)
- CA Search (Chemical Abstracts)