以微管蛋白和PARP-1为双靶点的新型抗肿瘤化合物的设计、合成及生物活性评价
序号 | 标题 | 类型 | 作者 |
---|---|---|---|
1 | Discovery of a Potent PLK1-PBD Small-Molecule Inhibitor as an Anticancer Drug Candidate through Structure-Based Design | 期刊论文 | Zhou Y;Yan F;Huo X;Niu M. M. |
2 | Structure-Based Virtual Screening and Biological Evaluation of Peptide Inhibitors for Polo-Box Domain | 期刊论文 | Yan F;Liu G;Chen T;Fu X;Niu M. M. |
3 | A Redox-Triggered Bispecific Supramolecular Nanomedicine Based on Peptide Self-Assembly for High-Efficacy and Low-Toxic Cancer Therapy | 期刊论文 | Yang Da Song;Yang Yin He;Zhou Yunjiang;Yu Li Li;Wang Rui Han;Di Bin;Niu Miao Miao |
4 | Structure-Based Pharmacophore Modeling, Virtual Screening, Molecular Docking and Biological Evaluation for Identification of Potential Poly (ADP-Ribose) Polymerase-1 (PARP-1) Inhibitors | 期刊论文 | Zhou Y;Tang S;Chen T;Niu M. M. |
5 | Structure-Based Pharmacophore Design and Virtual Screening for Novel Tubulin Inhibitors with Potential Anticancer Activity | 期刊论文 | Zhou Y;Di B;Niu M. M. |