Please use this identifier to cite or link to this item: https://hdl.handle.net/11147/6372
Title: Synthesis and anticancer activity evaluation of new isoindole analogues
Authors: Köse, Aytekin
Bal, Yıldız
Şanlı Mohamed, Gülşah
Kara, Yunus
Keywords: Anticancer activity
Cancer cell lines
Cytotoxicity
Ether cleavage
Norcantharimide
Issue Date: Apr-2017
Publisher: Birkhauser Verlag
Source: Köse, A., Bal, Y., Şanlı Mohamed, G. and Kara, Y. (2017). Synthesis and anticancer activity evaluation of new isoindole analogues. Medicinal Chemistry Research, 26(4), 779-786. doi:10.1007/s00044-017-1793-1
Abstract: We have developed a versatile synthetic approach for the synthesis of new isoindole derivatives via the cleavage of ethers from tricyclic imide skeleton compounds. An exo-cycloadduct prepared from the Diels–Alder reaction of furan and maleic anhydride furnished imide derivatives. The epoxide ring was opened with Ac2O in the presence of a catalytic amount of H2SO4 in order to yield new isoindole derivatives (8a and 8b). The anticancer activity of these compounds was evaluated against MCF-7 (breast adenocarcinoma) and A549 (adenocarcinomic human alveolar basal epithelial) cell lines. The synthesized compounds showed concentration- and time-dependent inhibitory effects on the viability of both cell lines. Compound 8a was more toxic compared to 8b in both cancer cell lines, having higher cytotoxicity against A549 cells. Testing the toxicity properties of these compounds on the BEAS 2B (human bronchial epithelial) cell line indicated that while both compounds decreased the cell viability of cancer cells, they were less toxic on healthy lung cells. Microscopy images of A549 cells after treatment with the new isoindole derivatives displayed characteristic apoptotic morphology compared to BEAS 2B cells. The results demonstrated here suggest that these new compounds might be considered as possible potential anticancer agents for the treatment of lung and breast cancer. © 2017, Springer Science+Business Media New York.
URI: http://hdl.handle.net/11147/6372
http://doi.org/10.1007/s00044-017-1793-1
ISSN: 1054-2523
1154-8520
Appears in Collections:Chemistry / Kimya
Scopus İndeksli Yayınlar Koleksiyonu / Scopus Indexed Publications Collection
WoS İndeksli Yayınlar Koleksiyonu / WoS Indexed Publications Collection

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