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Pregled bibliografske jedinice broj: 825541

Synthesis and biological activity of novel benzimidazolyl and benzothiazolyl substituted isoindolines


Sović, Irena; Jambon, Samy; Kraljević-Pavelić, Sandra; Markova-Car, Elitza; Ilić, Nataša; Depauw, Sabine; David-Cordonnier, Marie-Hélène; Karminski-Zamola, Grace
Synthesis and biological activity of novel benzimidazolyl and benzothiazolyl substituted isoindolines // 17th Tetrahedron Symposium Challenges in Biological, Bioorganic, Organic & Medicinal Chemistry, Sitges, Španjolska 2016.
Sitges, Španjolska: Elsevier, 2016. str. 18-18 (poster, međunarodna recenzija, sažetak, znanstveni)


Naslov
Synthesis and biological activity of novel benzimidazolyl and benzothiazolyl substituted isoindolines

Autori
Sović, Irena ; Jambon, Samy ; Kraljević-Pavelić, Sandra ; Markova-Car, Elitza ; Ilić, Nataša ; Depauw, Sabine ; David-Cordonnier, Marie-Hélène ; Karminski-Zamola, Grace

Vrsta, podvrsta i kategorija rada
Sažeci sa skupova, sažetak, znanstveni

Izvornik
17th Tetrahedron Symposium Challenges in Biological, Bioorganic, Organic & Medicinal Chemistry, Sitges, Španjolska 2016. / - : Elsevier, 2016, 18-18

Skup
17th TETRAHEDRON SYMPOSIUM - Challenges in Biological, Bioorganic, Organic & Medicinal Chemistry

Mjesto i datum
Sitges, Španjolska, 28.06.-01.07.2016

Vrsta sudjelovanja
Poster

Vrsta recenzije
Međunarodna recenzija

Ključne riječi
Isoindoline; antitumor activity; DNA binding

Sažetak
At the present time, a great challenge for medicinal chemistry is finding new and more selective anticancer agents and therefore there is tremendous growth in the number and types of new compounds which exhibit antitumor activity. Derivatives of isoindoline have been found interesting due to their presence in number of natural and synthetic bioactive compounds. In this report we present, as a part of our continuous research to develop novel nitrogen containing heterocycles as potential anticancer agents, synthesis and biological activity of novel benzimidazolyl and benzothiazolyl substituted isoindolines. Target compounds were prepared by condensation of o-phthalaldehyde and heterocyclic amines in acidic conditions. The antiproliferative activity was assessed on a panel of tumor cell lines and normal human fibroblasts. The majority of tested compounds exerted concentration dependent antiproliferative effects and for several compounds selective effect at micromolar concentrations was observed. For selected compounds, further mechanistic studies involving analysis of cell cycle and cell death mechanisms were pursued on. Interaction with ct-DNA was also studied by use of thermal denaturation experiment, circular dichroism spectra method, topoisomerase I-induced DNA relaxation and DNase I footprinting experiment.

Izvorni jezik
Engleski

Znanstvena područja
Kemija



POVEZANOST RADA


Projekt / tema
HRZZ-IP-2013-11-5596 - SINTEZA I CITOSTATSKA ISPITIVANJA BIBLIOTEKE NOVIH DUŠIKOVIH HETEROCIKLA (Silvana Raić-Malić, )

Ustanove
Fakultet kemijskog inženjerstva i tehnologije, Zagreb,
Sveučilište u Rijeci - Odjel za biotehnologiju