中药HER2/HSP90蛋白的潜在双靶点抑制剂

Jhih-Ying Chen, Chia-Min Chen, Pei-Chun Chang, J. Tsai
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引用次数: 0

摘要

癌症是致命的疾病。值得注意的是,癌症的治疗仍然缺乏有效的抗癌药物。多靶点药物的开发是未来的一个重要方向。人表皮生长因子受体(EGFR和HER2)和热休克蛋白90 (HSP90)已被证明是多种癌细胞系的有用靶点。开发针对这两种蛋白的双靶点药物可能会更有效地治疗癌症。我们进行了基于配体的QSAR建模,以选择潜在的中药候选化合物来抑制HER2/HSP90。结果表明,环koreanine B、dehydropodophyllotoxin、alloimperatorine、wanpeinine A、zierin、n -去甲基去甲缩聚素、去乙酰亮氨酸、dianthramine、gnoscopine和formon柄花素可能具有抑制HER2/HSP90的潜力。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
The Potential Dual-Target Inhibitors for HER2/HSP90 Proteins from Traditional Chinese Medicine
Cancer is a fatal disease. It is worth noting that the treatment of cancer still lacks effective drugs for cancer resistance. The development of multi-target drugs is an important direction in the future. Human epidermal growth factor receptor (EGFR and HER2) and Heat shock protein 90 (HSP90) have been proven to be useful targets in various cancer cell lines. To develop dual-target drugs for these two proteins may be more effective in cancer treatment. We performed ligand-based QSAR modeling to select potential TCM candidate compounds for HER2/HSP90 inhibition. The results show that cyclokoreanine B, dehydropodophyllotoxin, alloimperatorine, wanpeinine A, zierin, N-demethylnoracronycine, desacetyleupaserrin, dianthramine, gnoscopine, and formononetin might have the potential for HER2/HSP90 inhibition.
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