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An efficient synthesis of novel di-heterocyclic benzazole derivatives and evaluation of their antiproliferative activities

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dc.contributor.author Algul, O.
dc.contributor.author Ersan, R.H.
dc.contributor.author Alagoz, M.A.
dc.contributor.author Duran, N.
dc.contributor.author Burmaoglu, S.
dc.date.accessioned 2022-10-06T12:50:49Z
dc.date.available 2022-10-06T12:50:49Z
dc.date.issued 2021
dc.identifier.issn 07391102 (ISSN)
dc.identifier.uri http://hdl.handle.net/11616/71939
dc.description.abstract 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. © 2020 Informa UK Limited, trading as Taylor & Francis Group.
dc.source Journal of Biomolecular Structure and Dynamics
dc.title An efficient synthesis of novel di-heterocyclic benzazole derivatives and evaluation of their antiproliferative activities


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