Pregled bibliografske jedinice broj: 876425
Synthesis and antiproliferative activity of amino substituted benzimidazo[1,2-a]quinolines as mesylate salts designed by 3D-QSAR analysis
Synthesis and antiproliferative activity of amino substituted benzimidazo[1,2-a]quinolines as mesylate salts designed by 3D-QSAR analysis // Molecular diversity, 21 (2017), 3; 621-636 doi:10.1007/s11030-017-9753-8 (međunarodna recenzija, članak, znanstveni)
CROSBI ID: 876425 Za ispravke kontaktirajte CROSBI podršku putem web obrasca
Naslov
Synthesis and antiproliferative activity of amino substituted benzimidazo[1,2-a]quinolines as mesylate salts designed by 3D-QSAR analysis
Autori
Vušak, Darko ; Perin, Nataša ; Martin-Kleiner, Irena ; Kralj, Marijeta ; Karminski-Zamola, Grace ; Hranjec, Marijana ; Bertoša, Branimir
Izvornik
Molecular diversity (1381-1991) 21
(2017), 3;
621-636
Vrsta, podvrsta i kategorija rada
Radovi u časopisima, članak, znanstveni
Ključne riječi
amines ; benzimidazo[1 ; 2-a]quinolines ; mesylate salts ; 3D-QSAR ; anticancer ; microwave
Sažetak
The experimental search for new benzimidazole derivatives with enhanced antiproliferative activity was successfully guided by QSAR modelling. Robust 3D-QSAR models were derived on the available database of the compounds with previously measured activities. The QSAR analysis revealed that the increase of the antiproliferative activities towards H460, HCT 116, MCF-7 cell lines and normal fibroblasts SW 620 cells will be obtained if new compounds are charged at a pH range from 5 to 7 and if their hydrophobicity is increased compared to the dataset compounds. Novel benzimidazo[1, 2- a]quinolines bearing quarter amino groups with corresponding aliphatic chains were designed and their antiproliferative activities were computationally predicted. Using uncatalyzed microwave assisted amination, 14 novel compounds were obtained to assess their antiproliferative activities towards H460, HCT 116, MCF-7, and SW 620 tumor cell lines in vitro. Novel compounds showed antiproliferative activities at micromolar and submicromolar inhibition concentrations. Experimental measurements of antiproliferative activities enabled validated the QSAR models showing very good agreement between experimentally measured activities and computational predictions. In an attempt to elucidate the mode of action through which benzimidazole derivatives accomplish their antiproliferative activities, thermal denaturation experiments were performed to test their DNA binding properties.
Izvorni jezik
Engleski
Znanstvena područja
Kemija, Temeljne medicinske znanosti
POVEZANOST RADA
Projekti:
HRZZ-IP-2013-11-5596 - Sinteza i citostatska ispitivanja biblioteke novih dušikovih heterocikla (SCIENcENTRY) (Raić-Malić, Silvana, HRZZ - 2013-11) ( CroRIS)
IP-2013-11-5660 - Mulitidisciplinarni pristup otkriću lijekova s ciljanim djelovanjem na matične stanice tumora – uloga transporta kalija (MultiCaST) (Kralj, Marijeta, HRZZ - 2013-11) ( CroRIS)
HRZZ-IP-2014-09-7309 - Razvoj supramolekulskih receptora kationa i aniona (SupraCAR) (Tomišić, Vladislav, HRZZ - 2014-09) ( CroRIS)
Ustanove:
Institut "Ruđer Bošković", Zagreb,
Prirodoslovno-matematički fakultet, Zagreb,
Fakultet kemijskog inženjerstva i tehnologije, Zagreb
Profili:
Marijana Hranjec
(autor)
Nataša Perin
(autor)
Darko Vusak
(autor)
Branimir Bertoša
(autor)
Grace Karminski-Zamola
(autor)
Marijeta Kralj
(autor)
Irena Martin-Kleiner
(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::
- CA Search (Chemical Abstracts)