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用机械化学解决具有空间位阻 NHC 配体的高细胞毒性银配合物的挑战性合成。

Solving the challenging synthesis of highly cytotoxic silver complexes bearing sterically hindered NHC ligands with mechanochemistry.

机构信息

IBMM, Univ Montpellier, CNRS, ENSCM, Montpellier, France.

Normandie University, LCMT, ENSICAEN, UNICAEN, CNRS, 14000, Caen, France.

出版信息

Dalton Trans. 2020 Sep 22;49(36):12592-12598. doi: 10.1039/d0dt00410c.

Abstract

The use of ball-mills enabled the straightforward synthesis of a variety of silver(i) complexes featuring challenging NHC ligands. Sterically hindered including electron-poor or with very low solubility imidazolium salts were ground with silver(i) oxide to furnish heteroleptic or homoleptic complexes in high yields and short reaction times. The synthesis of heteroleptic bis-NHC silver(i) complexes was also performed for the first time in a ball mill. The efficiency and rapidity of the mechanochemical approach enabled the generation of a library of unprecedented NHC silver complexes, whose cytotoxicity on the HCT116 colorectal cancer cell line was evaluated providing a rare example of medicinal mechanochemistry. The cationic silver complexes were found to be more potent than the neutral analogues, with IC50 values down to 21 nM and 256 times more potent than cisplatin.

摘要

球磨机的使用使得合成具有挑战性的 NHC 配体的各种银(I)配合物变得简单。空间位阻大的包括电子缺电子或溶解度非常低的咪唑鎓盐与氧化银一起研磨,以高产率和短反应时间得到杂配或同配配合物。杂配双 NHC 银(I)配合物的合成也是首次在球磨机中进行。机械化学方法的效率和快速性使得能够生成前所未有的 NHC 银配合物库,评估其对 HCT116 结直肠癌细胞系的细胞毒性,提供了药物机械化学的罕见实例。发现阳离子银配合物比中性类似物更有效,IC50 值低至 21 nM,比顺铂强 256 倍。

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