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具有独立于 HSP90 抑制的抗癌和抗疟原虫活性的新生霉素-二茂铁轭合物。

Novobiocin-ferrocene conjugates possessing anticancer and antiplasmodial activity independent of HSP90 inhibition.

机构信息

Department of Chemistry, Faculty of Science, Rhodes University, Grahamstown, 6140, South Africa.

Department of Biochemistry and Microbiology, Faculty of Science, Rhodes University, Grahamstown, 6140, South Africa.

出版信息

J Biol Inorg Chem. 2019 Mar;24(2):139-149. doi: 10.1007/s00775-018-1634-9. Epub 2018 Dec 12.

Abstract

A series of tailored novobiocin-ferrocene conjugates was prepared in moderate yields and investigated for in vitro anticancer and antiplasmodial activity against the MDA-MB-231 breast cancer line and Plasmodium falciparum 3D7 strain, respectively. While the target compounds displayed moderate anticancer activity against the breast cancer cell line with IC values in the mid-micromolar range, compounds 10a-c displayed promising antiplasmodial activity as low as 0.889 µM. Furthermore, the most promising compounds were tested for inhibitory effects against a postulated target, heat shock protein 90 (Hsp90). A selection of tailored novobiocin derivatives bearing the organometallic ferrocene unit were synthesized and characterized by common spectroscopic techniques. The target compounds were investigated for in vitro anticancer and antimalarial activity against the MDA-MB-231 breast cancer cell line and Plasmodium falciparum 3D7 strain, respectively.

摘要

一系列定制的诺氟沙星-二茂铁缀合物以中等产率制备,并分别研究了它们对 MDA-MB-231 乳腺癌细胞系和恶性疟原虫 3D7 株的体外抗癌和抗疟活性。虽然目标化合物对乳腺癌细胞系显示出中等的抗癌活性,IC 值在中微摩尔范围内,但化合物 10a-c 表现出有希望的抗疟活性,低至 0.889µM。此外,最有前途的化合物被测试了对假定的靶点,热休克蛋白 90(Hsp90)的抑制作用。选择了一系列带有有机金属二茂铁单元的定制诺氟沙星衍生物,并通过常见的光谱技术进行了表征。目标化合物分别研究了它们对 MDA-MB-231 乳腺癌细胞系和恶性疟原虫 3D7 株的体外抗癌和抗疟活性。

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