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Pregled bibliografske jedinice broj: 825476

Amino substituted benzimidazo[1, 2-a]quinolines: Antiproliferative potency, 3D QSAR study and DNA binding properties


Perin, Nataša; Nhili, Raja; Cindrić, Maja; Bertoša, Branimir; Vušak, Darko; Martin-Kleiner, Irena; Laine, William; Karminski-Zamola, Grace; Kralj, Marijeta; David-Cordonnier, Marie-Hélène; Hranjec, Marijana
Amino substituted benzimidazo[1, 2-a]quinolines: Antiproliferative potency, 3D QSAR study and DNA binding properties // European journal of medicinal chemistry, 122 (2016), 530-545 doi:10.1016/j.ejmech.2016.07.007 (međunarodna recenzija, članak, znanstveni)


Naslov
Amino substituted benzimidazo[1, 2-a]quinolines: Antiproliferative potency, 3D QSAR study and DNA binding properties

Autori
Perin, Nataša ; Nhili, Raja ; Cindrić, Maja ; Bertoša, Branimir ; Vušak, Darko ; Martin-Kleiner, Irena ; Laine, William ; Karminski-Zamola, Grace ; Kralj, Marijeta ; David-Cordonnier, Marie-Hélène ; Hranjec, Marijana

Izvornik
European journal of medicinal chemistry (0223-5234) 122 (2016); 530-545

Vrsta, podvrsta i kategorija rada
Radovi u časopisima, članak, znanstveni

Ključne riječi
Benzimidazoles ; benzimidazo[1 ; 2-a]quinolines ; 3D-QSAR ; antiproliferative activity ; DNA binding properties

Sažetak
We describe the synthesis, 3D-derived quantitative structure-activity relationship (QSAR), antiproliferative activity and DNA binding properties of a series of 2-amino, 5-amino and 2, 5-diamino substituted benzimidazo[1, 2-a]quinolines prepared by environmentally friendly uncatalyzed microwave assisted amination. The antiproliferative activities were assessed in vitro against colon, lung and breast carcinoma cell lines ; activities ranged from submicromolar to micromolar. The strongest antiproliferative activity was demonstrated by 2-amino-substituted analogues, whereas 5-amino and or 2, 5-diamino substituted derivatives resulted in much less activity. Derivatives bearing 4-methyl- or 3, 5-dimethyl-1-piperazinyl substitutents emerged as the most active. DNA binding properties and the mode of interaction of chosen substituted benzimidazo[1, 2-a]quinolines prepared herein were studied using melting temperature studies, a series of spectroscopic studies (UV/Visible, fluorescence, and circular dichroism), and biochemical experiments (topoisomerase I-mediated DNA relaxation and DNase I footprinting experiments). Both compound 36 and its bis-quaternary iodide salt 37 intercalate between adjacent base pairs of the DNA helix while compound 33 presented a very weak topoisomerase I poisoning activity. A 3D-QSAR analysis was performed to identify hydrogen bonding properties, hydrophobicity, molecular flexibility and distribution of hydrophobic regions as these molecular properties had the highest impact on the antiproliferative activity against the three cell lines.

Izvorni jezik
Engleski

Znanstvena područja
Kemija, Temeljne medicinske znanosti



POVEZANOST RADA


Projekt / tema
HRZZ-IP-2013-11-5596 - SINTEZA I CITOSTATSKA ISPITIVANJA BIBLIOTEKE NOVIH DUŠIKOVIH HETEROCIKLA (Silvana Raić-Malić, )
HRZZ-IP-2013-11-5660 - Mulitidisciplinarni pristup otkriću lijekova s ciljanim djelovanjem na matične stanice tumora – uloga transporta kalija (Marijeta Kralj, )

Ustanove
Institut "Ruđer Bošković", Zagreb,
Fakultet kemijskog inženjerstva i tehnologije, Zagreb

Časopis indeksira:


  • Current Contents Connect (CCC)
  • Web of Science Core Collection (WoSCC)
    • Science Citation Index Expanded (SCI-EXP)
    • Arts & Humanities Citation Index (A&HCI)
    • SCI-EXP, SSCI i/ili A&HCI
  • Scopus
  • MEDLINE


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