Cancer Drug Research Laboratory, Department of Medicine, Division of Medical Oncology, The Research Institute of the McGill University Health Center/Glen Hospital, Montreal, QC, H4A 3J1, Canada.
Scientific Support, Chemical Computing Group Inc., Montreal, QC, H3A 2R7, Canada.
Eur J Med Chem. 2020 Apr 15;192:112185. doi: 10.1016/j.ejmech.2020.112185. Epub 2020 Feb 26.
Over the past decade, we described a novel tumour targeted approach that sought to design "combi-molecules" to hit two distinct targets in tumour cells. Here, to generate small combi-molecules with strong DNA damaging potential while retaining EGFR inhibitory potency, we developed the first synthetic strategy to access the 6-N, N-disubstituted quinazoline scaffold and designed JS61 to possess a nitrogen mustard function directly attached to the 6-position of the quinazoline ring. We compared its biological activity with that of structures containing either a hemi mustard or a non-alkylating substituent. Surprisingly, the results showed that JS61, while capable of inducing strong DNA damage, exhibited moderate EGFR inhibitory potency. In contrast, "combi-molecules" with no bulky substituent at the N-6 position (e.g. ZR2002 and JS84) showed stronger EGFR and growth inhibitory potency than JS61 in a panel of lung cancer cells. To rationalize these results, X-ray crystallography and molecular modeling studies were undertaken, and the data obtained indicated that bulkiness of the 6-N,N-disubstituted moieties hinder its binding to the ATP site and affects binding reversibility.
在过去的十年中,我们描述了一种新的肿瘤靶向方法,旨在设计“组合分子”来靶向肿瘤细胞中的两个不同靶点。在这里,为了产生具有强 DNA 损伤潜力同时保留 EGFR 抑制活性的小分子组合分子,我们开发了第一种合成策略来获得 6-N,N-取代的喹唑啉骨架,并设计了 JS61 使其具有直接连接到喹唑啉环 6 位的氮芥功能。我们将其与含有半氮芥或非烷基取代基的结构的生物活性进行了比较。令人惊讶的是,结果表明,JS61 虽然能够诱导强烈的 DNA 损伤,但对 EGFR 的抑制活性适中。相比之下,在一组肺癌细胞中,没有在 N-6 位置带有大体积取代基的“组合分子”(例如 ZR2002 和 JS84)显示出比 JS61 更强的 EGFR 和生长抑制活性。为了合理化这些结果,进行了 X 射线晶体学和分子建模研究,获得的数据表明,6-N,N-取代基的体积会阻碍其与 ATP 结合位点的结合,并影响结合的可逆性。