Design of new small molecules derived from indolin-2-one as potent TRKs inhibitors using a computer-aided drug design approach

Rachid Haloui, Khaoula Mkhayar, Ossama Daoui, Kaouakeb El Khattabi, Abdelmoula El abbouchi, Samir Chtita, Souad Elkhattabi
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Abstract

Tropomyosin receptor kinase (TRKs) enzymes are responsible for cancers associated with the neurotrophic tyrosine kinase receptor gene fusion and are identified as effective targets for anticancer d...
用计算机辅助药物设计方法设计出提取自吲哚啉-2-酮的新小分子,作为有效的 TRKs 抑制剂
肌球蛋白受体激酶(TRKs)是与神经营养性酪氨酸激酶受体基因融合相关的癌症的罪魁祸首,已被确定为抗癌药物的有效靶点。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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