Beč, Anja; Mioč, Marija; Bertoša, Branimir; Kos, Marija; Debogović, Patricia; Kralj, Marijeta; Starčević, Kristina; Hranjec, Marijana (2022) Design, synthesis, biological evaluation and QSAR analysis of novel N-substituted benzimidazole derived carboxamides. Journal of Enzyme Inhibition and Medicinal Chemistry, 37 (1). pp. 1327-1339. ISSN 1475-6366
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Abstract
As a result of our previous research focussed on benzimidazoles, herein we present design, synthesis, QSAR analysis and biological activity of novel N-substituted benzimidazole derived carboxamides. Carboxamides were designed to study the influence of the number of methoxy groups, the type of the substituent placed at the benzimidazole core on biological activity. Pronounced antioxidative activity displayed unsubstituted 28 (IC50 ≈ 3.78 mM, 538.81 mmolFe2+/mmolC) and dimethoxy substituted derivative 34 (IC50 ≈ 5.68 mM, 618.10 mmolFe2+/mmolC). Trimethoxy substituted 43 and unsubstituted compound 40 with isobutyl side chain at N atom showed strong activity against HCT116 (IC50 ≈ 0.6 µM, both) and H 460 cells (IC50 ≈ 2.5 µM; 0.4 µM), being less cytotoxic towards non-tumour cell. Antioxidative activity in cell generally confirmed relatively modest antioxidant capacity obtained in DPPH/FRAP assays of derivatives 34 and 40. The 3D-QSAR models were generated to explore molecular properties that have the highest influence on antioxidative activity.
Item Type: | Article | ||||||||||||
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Uncontrolled Keywords: | Antioxidant activity; QSAR; ROS; antiproliferative activity; benzimidazoles; carboxamides | ||||||||||||
Subjects: | NATURAL SCIENCES > Chemistry BIOMEDICINE AND HEALTHCARE > Basic Medical Sciences |
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Divisions: | Division of Molecular Medicine | ||||||||||||
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Depositing User: | Diana Mikoč Radešić | ||||||||||||
Date Deposited: | 26 Jan 2024 13:50 | ||||||||||||
URI: | http://fulir.irb.hr/id/eprint/8397 | ||||||||||||
DOI: | 10.1080/14756366.2022.2070910 |
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