Design and Synthesis of Novel MEK Inhibitors for the Treatment of Solid Tumors.

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Tác giả: Na Li, Fanglan Liu, Zhenshuo Luo, Lailiang Qu, Cheng Wang, Chunhua Xia, Jingting Zeng, Tiansheng Zhao

Ngôn ngữ: eng

Ký hiệu phân loại:

Thông tin xuất bản: England : Chemical biology & drug design , 2025

Mô tả vật lý:

Bộ sưu tập: NCBI

ID: 213767

Aberrant activation of the RAS/RAF/MEK/ERK pathway occurs in more than 30% of human cancers. As part of this pathway, MEK1/2 has crucial roles in tumorigenesis, cell proliferation, and inhibition of apoptosis. At present, a number of MEK1/2 inhibitors are approved for the treatment of melanoma. However, MEK1/2 inhibitors have poor single-drug efficacy in the treatment of solid tumors and are prone to drug resistance. A series of compounds containing a diarylamine skeleton and phenylacrylamide (acrylamide) have been designed and synthesized in this paper. The most promising compound M15 showed good inhibitory activity of MEK1 (IC
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