套细胞淋巴瘤
癌症研究
化学
流式细胞术
MMP9公司
细胞生长
分子生物学
生物
淋巴瘤
免疫学
生物化学
下调和上调
基因
作者
Wei Yan,Ying Yang,Wei Yang,Minjie Wei
标识
DOI:10.2174/1871520620666201013150312
摘要
We designed M3 through structure-based molecular docking, which can specifically bind to MMP9 and inhibit the activity of MMP9. M3 could be a potential antagonist in the treatment of MCL with MMP9 overexpression.
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