Mondal Rajdeep, Keerthana Muthukumar, Pandurangan Nanjan, Shanmugaraju Sankarasekaran
Department of Chemistry, Indian Institute of Technology Palakkad, Palakkad, Kerala, 678557, India.
Department of Chemistry, Amrita School of Physical Sciences, Amrita Vishwa Vidyapeetham, Coimbatore, Tamil Nadu, 641112, India.
ChemMedChem. 2024 Dec 2;19(23):e202400558. doi: 10.1002/cmdc.202400558. Epub 2024 Oct 29.
There is a great deal of research interest in the design of alternative metallodrugs to Pt(II)-derivatives for cancer treatment. The low solubility of such drugs in biological mediums leading to poor bioavailability is the major hurdle of several metal-based anticancer agents. These issues have recently been addressed by designing bio-active ligands based on metal-containing anticancer agents. Conjugating with bioactive ligands has significantly improved the bioavailability of the metallodrugs and their cancer cell targeting ability. One such naturally available bioactive ligand is curcumin. Until recently, several curcumin-based anticancer metallodrugs have been developed and successfully demonstrated for their anticancer studies. In this article, we aim to highlight, the synthesis, structure, and anticancer properties of various Zn(II)-curcumin-based coordination complexes. The effect of introducing different functional groups, targeting ligands, and photo-active ligands on the anticancer potential of such complexes has been mentioned in detail. The current status and future perspective on curcumin-based metallodrugs for cancer treatment have also been stated.
对于设计用于癌症治疗的铂(II)衍生物替代金属药物,存在大量的研究兴趣。这类药物在生物介质中的低溶解度导致生物利用度差,这是几种金属基抗癌剂的主要障碍。最近,通过设计基于含金属抗癌剂的生物活性配体,这些问题得到了解决。与生物活性配体共轭显著提高了金属药物的生物利用度及其癌细胞靶向能力。姜黄素就是这样一种天然存在的生物活性配体。直到最近,已经开发了几种基于姜黄素的抗癌金属药物,并在抗癌研究中成功得到证实。在本文中,我们旨在突出各种基于锌(II)-姜黄素的配位络合物的合成、结构和抗癌特性。详细介绍了引入不同官能团、靶向配体和光活性配体对这类络合物抗癌潜力的影响。还阐述了基于姜黄素的金属药物用于癌症治疗的现状和未来前景。