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Pregled bibliografske jedinice broj: 670861

Synthesis and biological activity of new diazenedicarboxamides as potential anticancer agents


Vajs, Jure; Soviček, Sanja; Kureljak, Petra; Stojanović, NIkolina; Steiner, Ivana; Eljuga, Domagoj; Urankar, Damijana; Kočevar, Marijan; Košmrlj, Janez; Polanc, Slovenko; Osmak, Maja
Synthesis and biological activity of new diazenedicarboxamides as potential anticancer agents // Acta chimica Slovenica, 60 (2013), 4; 842-852 (međunarodna recenzija, članak, znanstveni)


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Naslov
Synthesis and biological activity of new diazenedicarboxamides as potential anticancer agents

Autori
Vajs, Jure ; Soviček, Sanja ; Kureljak, Petra ; Stojanović, NIkolina ; Steiner, Ivana ; Eljuga, Domagoj ; Urankar, Damijana ; Kočevar, Marijan ; Košmrlj, Janez ; Polanc, Slovenko ; Osmak, Maja

Izvornik
Acta chimica Slovenica (1318-0207) 60 (2013), 4; 842-852

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

Ključne riječi
diazenedicarboxamides; tumor cells; anticancer drugs

Sažetak
To increase the effectiveness of cancer treatment, more effective anti-cancer drugs, as well as the new improved strategies of cancer treatment, are urgently needed. Our previous results have shown that various diazenes are cytotoxic to different tumor cells and can even revert the resistance to cisplatin and vincristine. We also demonstrated that unsymmetrical diazenedicarboxamides 1 and 2 exhibited promising cytotoxicity. The aim of the present study was to synthesize new diazenedicarboxamides with acceptable solubility and good cytotoxicity. Here we report the synthesis and biological evaluation of new N, N’-disubstituted diazenedicarboxamides. We found that a modification of either 1 or 2 led to the more active compounds. The most effective among them was diazenedicarboxamide 11, which can be considered as a new potential anticancer agent for the tumors of different origin, as well as for the drug resistant tumors.

Izvorni jezik
Engleski

Znanstvena područja
Biologija



POVEZANOST RADA


Projekti:
098-0982913-2748 - Stanični odgovor na citotoksične spojeve i razvoj otpornosti (Osmak, Maja, MZOS ) ( POIROT)
098-0982913-2850 - Povećanje transdukcije adenovirusnih vektora i otpornost stanica na citostatike (Ambriović Ristov, Andreja, MZOS ) ( POIROT)

Ustanove:
Institut "Ruđer Bošković", Zagreb,
Klinički bolnički centar Zagreb

Profili:

Avatar Url Nikolina Stojanović (autor)

Avatar Url Maja Osmak (autor)

Citiraj ovu publikaciju

Vajs, Jure; Soviček, Sanja; Kureljak, Petra; Stojanović, NIkolina; Steiner, Ivana; Eljuga, Domagoj; Urankar, Damijana; Kočevar, Marijan; Košmrlj, Janez; Polanc, Slovenko; Osmak, Maja
Synthesis and biological activity of new diazenedicarboxamides as potential anticancer agents // Acta chimica Slovenica, 60 (2013), 4; 842-852 (međunarodna recenzija, članak, znanstveni)
Vajs, J., Soviček, S., Kureljak, P., Stojanović, N., Steiner, I., Eljuga, D., Urankar, D., Kočevar, M., Košmrlj, J., Polanc, S. & Osmak, M. (2013) Synthesis and biological activity of new diazenedicarboxamides as potential anticancer agents. Acta chimica Slovenica, 60 (4), 842-852.
@article{article, year = {2013}, pages = {842-852}, keywords = {diazenedicarboxamides, tumor cells, anticancer drugs}, journal = {Acta chimica Slovenica}, volume = {60}, number = {4}, issn = {1318-0207}, title = {Synthesis and biological activity of new diazenedicarboxamides as potential anticancer agents}, keyword = {diazenedicarboxamides, tumor cells, anticancer drugs} }
@article{article, year = {2013}, pages = {842-852}, keywords = {diazenedicarboxamides, tumor cells, anticancer drugs}, journal = {Acta chimica Slovenica}, volume = {60}, number = {4}, issn = {1318-0207}, title = {Synthesis and biological activity of new diazenedicarboxamides as potential anticancer agents}, keyword = {diazenedicarboxamides, tumor cells, anticancer drugs} }

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





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