Pretražite po imenu i prezimenu autora, mentora, urednika, prevoditelja

Napredna pretraga

Pregled bibliografske jedinice broj: 510141

Synthesis and biological evaluation of 4-nitro-substituted 1, 3-diaryltriazenes as a novel class of potent antitumor agents


Čimbora-Zovko, Tamara; Brozović, Anamaria; Piantanida, Ivo; Fritz, Gerhard; Virag, Andrej; Alič, Branko; Majce, Vita; Kočevar, Marjan; Polanc, Slovenko; Osmak, Maja
Synthesis and biological evaluation of 4-nitro-substituted 1, 3-diaryltriazenes as a novel class of potent antitumor agents // European journal of medicinal chemistry, 46 (2011), 7; 2971-2983 doi:10.1016/j.ejmech.2011.04.024 (međunarodna recenzija, članak, znanstveni)


CROSBI ID: 510141 Za ispravke kontaktirajte CROSBI podršku putem web obrasca

Naslov
Synthesis and biological evaluation of 4-nitro-substituted 1, 3-diaryltriazenes as a novel class of potent antitumor agents

Autori
Čimbora-Zovko, Tamara ; Brozović, Anamaria ; Piantanida, Ivo ; Fritz, Gerhard ; Virag, Andrej ; Alič, Branko ; Majce, Vita ; Kočevar, Marjan ; Polanc, Slovenko ; Osmak, Maja

Izvornik
European journal of medicinal chemistry (0223-5234) 46 (2011), 7; 2971-2983

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

Ključne riječi
1 ; 3-diaryltriazenes ; synthesis ; cytotoxicity ; ROS induction ; apoptosis

Sažetak
We describe the synthesis and biological activity of a new class of 1, 3-diaryltriazenes, namely 4-nitro-substituted 1, 3-diaryltriazenes. Structure-activity relationship analysis reveals that 1, 3-diaryltriazenes can be modified from inactive to highly cytotoxic compounds by the introduction of two nitro groups at the para positions of benzene rings and two additional electron-withdrawing groups (bromo, chloro, trifluoromethyl or fluoro substituents) at their ortho position. In order to increase the solubility of the modified compounds, we introduced various acyl groups to their triazene nitrogen. The results of LC-MS/MS analysis showed that N-acyltriazenes can be considered as prodrugs of non-acylated triazenes. Selected 3-acetyl-1, 3-bis(2-chloro-4-nitrophenyl)-1-triazene (8b) is highly cytotoxic against different tumor cell lines, including cisplatin-resistant laryngeal carcinoma cells. Notably, its antiproliferative activity is significantly higher against tumor cells than against normal cells. DNA binding analysis suggests that neither 8b nor its non-acylated derivative 8a bind into the minor groove of DNA. Instead, 8b induces reactive oxygen species that could provoke endoplasmic reticulum (ER) stress finally leading to apoptosis. Our data suggest that 4-nitro-substituted 1, 3-diaryltriazenes are a new class of anticancer molecules which preferentially target malignant cells and may serve as potential antitumor agents.

Izvorni jezik
Engleski

Znanstvena područja
Kemija, Biologija



POVEZANOST RADA


Projekti:
098-0982913-2748 - Stanični odgovor na citotoksične spojeve i razvoj otpornosti (Osmak, Maja, MZOS ) ( CroRIS)
098-0982913-2850 - Povećanje transdukcije adenovirusnih vektora i otpornost stanica na citostatike (Ambriović Ristov, Andreja, MZOS ) ( CroRIS)
098-0982914-2918 - Dizajn, sinteza i ispitivanje interakcija malih molekula s DNA, RNA i proteinima (Piantanida, Ivo, MZOS ) ( CroRIS)

Ustanove:
Institut "Ruđer Bošković", Zagreb

Poveznice na cjeloviti tekst rada:

doi dx.doi.org www.sciencedirect.com

Citiraj ovu publikaciju:

Čimbora-Zovko, Tamara; Brozović, Anamaria; Piantanida, Ivo; Fritz, Gerhard; Virag, Andrej; Alič, Branko; Majce, Vita; Kočevar, Marjan; Polanc, Slovenko; Osmak, Maja
Synthesis and biological evaluation of 4-nitro-substituted 1, 3-diaryltriazenes as a novel class of potent antitumor agents // European journal of medicinal chemistry, 46 (2011), 7; 2971-2983 doi:10.1016/j.ejmech.2011.04.024 (međunarodna recenzija, članak, znanstveni)
Čimbora-Zovko, T., Brozović, A., Piantanida, I., Fritz, G., Virag, A., Alič, B., Majce, V., Kočevar, M., Polanc, S. & Osmak, M. (2011) Synthesis and biological evaluation of 4-nitro-substituted 1, 3-diaryltriazenes as a novel class of potent antitumor agents. European journal of medicinal chemistry, 46 (7), 2971-2983 doi:10.1016/j.ejmech.2011.04.024.
@article{article, author = {\v{C}imbora-Zovko, Tamara and Brozovi\'{c}, Anamaria and Piantanida, Ivo and Fritz, Gerhard and Virag, Andrej and Ali\v{c}, Branko and Majce, Vita and Ko\v{c}evar, Marjan and Polanc, Slovenko and Osmak, Maja}, year = {2011}, pages = {2971-2983}, DOI = {10.1016/j.ejmech.2011.04.024}, keywords = {1, 3-diaryltriazenes, synthesis, cytotoxicity, ROS induction, apoptosis}, journal = {European journal of medicinal chemistry}, doi = {10.1016/j.ejmech.2011.04.024}, volume = {46}, number = {7}, issn = {0223-5234}, title = {Synthesis and biological evaluation of 4-nitro-substituted 1, 3-diaryltriazenes as a novel class of potent antitumor agents}, keyword = {1, 3-diaryltriazenes, synthesis, cytotoxicity, ROS induction, apoptosis} }
@article{article, author = {\v{C}imbora-Zovko, Tamara and Brozovi\'{c}, Anamaria and Piantanida, Ivo and Fritz, Gerhard and Virag, Andrej and Ali\v{c}, Branko and Majce, Vita and Ko\v{c}evar, Marjan and Polanc, Slovenko and Osmak, Maja}, year = {2011}, pages = {2971-2983}, DOI = {10.1016/j.ejmech.2011.04.024}, keywords = {1, 3-diaryltriazenes, synthesis, cytotoxicity, ROS induction, apoptosis}, journal = {European journal of medicinal chemistry}, doi = {10.1016/j.ejmech.2011.04.024}, volume = {46}, number = {7}, issn = {0223-5234}, title = {Synthesis and biological evaluation of 4-nitro-substituted 1, 3-diaryltriazenes as a novel class of potent antitumor agents}, keyword = {1, 3-diaryltriazenes, synthesis, cytotoxicity, ROS induction, apoptosis} }

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


Citati:





    Contrast
    Increase Font
    Decrease Font
    Dyslexic Font