Synthesis and cytotoxicity studies of novel benzhydrylpiperazine carboxamide and thioamide derivatives
Date
2014
Authors
Gurdal, E. E.
Durmaz, I.
Cetin Atalay, R.
Yarim, M.
Editor(s)
Advisor
Supervisor
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Co-Supervisor
Instructor
Source Title
Journal of Enzyme Inhibition and Medicinal Chemistry
Print ISSN
1475-6366
Electronic ISSN
Publisher
Informa Healthcare
Volume
29
Issue
2
Pages
205 - 214
Language
English
Type
Journal Title
Journal ISSN
Volume Title
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Abstract
Synthesis and cytotoxic activities of 32 benzhydrylpiperazine derivatives with carboxamide and thioamide moieties were reported. In vitro cytotoxic activities of compounds were screened against hepatocellular (HUH-7), breast (MCF-7) and colorectal (HCT-116) cancer cell lines by sulphorhodamine B assay. In general, 4-chlorobenzhydrylpiperazine derivatives were more cytotoxic than other compounds. In addition, thioamide derivatives (6a-g) have higher growth inhibition than their carboxamide analogs. © 2014 Informa UK Ltd. All rights reserved.