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新型 7-氯喹啉-苯并咪唑杂合体的设计、合成、抗肿瘤和抗疟原虫活性评价。

Design, Synthesis, Antitumor, and Antiplasmodial Evaluation of New 7-Chloroquinoline-Benzimidazole Hybrids.

机构信息

Department of Chemistry and Biochemistry, Faculty of Veterinary Medicine, University of Zagreb, Heinzelova 55, HR-10000 Zagreb, Croatia.

Department of Agroecology and Environmental Protection, Faculty of Agrobiotechnical Sciences Osijek, Josip Juraj Strossmayer University of Osijek, Vladimira Preloga 1, HR-31000 Osijek, Croatia.

出版信息

Molecules. 2024 Jun 24;29(13):2997. doi: 10.3390/molecules29132997.

Abstract

Newly synthesized 7-chloro-4-aminoquinoline-benzimidazole hybrids were characterized by NMR and elemental analysis. Compounds were tested for their effects on the growth of the non-tumor cell line MRC-5 (human fetal lung fibroblasts) and carcinoma (HeLa and CaCo-2), leukemia, and lymphoma (Hut78, THP-1, and HL-60) cell lines. The obtained results, expressed as the concentration at which 50% inhibition of cell growth is achieved (IC value), show that the tested compounds affect cell growth differently depending on the cell line and the applied dose (IC ranged from 0.2 to >100 µM). Also, the antiplasmodial activity of these hybrids was evaluated against two strains (3D7 and Dd2). The tested compounds showed potent antiplasmodial activity, against both strains, at nanomolar concentrations. Quantitative structure-activity relationship (QSAR) analysis resulted in predictive models for antiplasmodial activity against the 3D7 strain ( = 0.886; = 0.937; = 41.589) and Dd2 strain ( = 0.859; = 0.878; = 32.525) of . QSAR models identified the structural features of these favorable effects on antiplasmodial activities.

摘要

新合成的 7-氯-4-氨基喹啉-苯并咪唑杂合体通过 NMR 和元素分析进行了表征。对化合物进行了测试,以评估它们对非肿瘤细胞系 MRC-5(人胎肺成纤维细胞)和癌细胞系(HeLa 和 CaCo-2)、白血病和淋巴瘤细胞系(Hut78、THP-1 和 HL-60)生长的影响。以达到 50%细胞生长抑制的浓度(IC 值)表示获得的结果表明,测试的化合物根据细胞系和应用剂量的不同,对细胞生长的影响也不同(IC 范围为 0.2 至 >100µM)。此外,还评估了这些杂合体对两种疟原虫株(3D7 和 Dd2)的抗疟原虫活性。测试的化合物在纳摩尔浓度下对两种株均表现出很强的抗疟原虫活性。定量构效关系(QSAR)分析得到了针对 3D7 株( = 0.886; = 0.937; = 41.589)和 Dd2 株( = 0.859; = 0.878; = 32.525)的抗疟原虫活性的预测模型。QSAR 模型确定了这些对抗疟原虫活性有利影响的结构特征。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3f89/11243327/d595d1176dda/molecules-29-02997-sch001.jpg

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