An efficient synthesis of novel di-heterocyclic benzazole derivatives and evaluation of their antiproliferative activities
Özet
© 2020 Informa UK Limited, trading as Taylor & Francis Group.A series of unsymmetrical nine di-heterocyclic compounds of benzazole derivatives were synthesized at one step via cyclization reaction. The compounds evaluated for in vitro cytotoxic activity against A549, A498, HeLa, and HepG2 cancer cell lines. The biological evaluation results show that 23, 26 and 29 exhibit better activity against HepG2 and HeLa cancer cell lines. Compound 23 also showed good activity against A549, and A498 cancer cell lines. The analogs were further performed molecular docking studies against human cytochrome P450 2C8 monooxygenase enzyme, calculated some theoretical quantum parameters, ADMET descriptor and molecular electrostatic potential analysis. The strategy applied in this research work may act as a perspective for the rational design of potential anticancer drugs. Communicated by Ramaswamy H. Sarma.
Anahtar kelimeler
Sürdürülebilir Kalkınma Amaçları
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SKA 3: Sağlıklı Bireyler
Atıf için künye
Algul, O., Ersan, R. H., Alagoz, M. A., Duran, N., & Burmaoğlu, S. (2021). An efficient synthesis of novel di-heterocyclic benzazole derivatives and evaluation of their antiproliferative activities. JOURNAL OF BIOMOLECULAR STRUCTURE & DYNAMICS, 39(18), 6926–6938. https://doi.org/10.1080/07391102.2020.1803966
BibTeX
@article{algul2021-79098,
author = {Algul, Oztekin and Ersan, Ronak Haj and Alagoz, Mehmet Abdullah and Duran, Nizami and Burmaoğlu, Serdar},
title = {An efficient synthesis of novel di-heterocyclic benzazole derivatives and evaluation of their antiproliferative activities},
journal = {JOURNAL OF BIOMOLECULAR STRUCTURE & DYNAMICS},
year = {2021},
volume = {39},
number = {18},
pages = {6926--6938},
issn = {0739-1102},
doi = {10.1080/07391102.2020.1803966},
url = {https://akademik.atauni.edu.tr/yayinlar/79098-an-efficient-synthesis-of-novel-di-heterocyclic-benzazole-derivatives-and}
}