1 Kinase and Histone Deacetylase Hybrid Inhibitors for Cancer Therapy
来源:J MED CHEM( P 0022-2623 E 1520-4804 ) 发表时间: 2019/04
类型:期刊论文 为本人加分:3631.700595
2 Small Molecular Gemcitabine Prodrugs for Cancer Therapy
来源:CURR MED CHEM( P 0929-8673 E 1875-533X ) 发表时间: 2020/01
类型:期刊论文 为本人加分:2196.810018
3 Anti-tumor activity evaluation of novel tubulin and HDAC dual-targeting inhibitors
来源:BIOORG MED CHEM LETT( P 0960-894X E 1464-3405 ) 发表时间: 2019/09
类型:期刊论文 为本人加分:1886.081770
4 The function of the selective inhibitors of cycloxygenase 2
来源:MINI-REV MED CHEM( P 1389-5575 E 1875-5607 ) 发表时间: 2006/12
类型:期刊论文 为本人加分:1745.151699
5 Tip60: Main Functions and Its Inhibitors
来源:MINI-REV MED CHEM( P 1389-5575 E 1875-5607 ) 发表时间: 2017/01
类型:期刊论文 为本人加分:1347.789756
6 Novel HDAC6 selective inhibitors with 4-aminopiperidine-1-carboxamide as the core structure enhanced..
来源:BIOSCI TRENDS( P 1881-7815 E 1881-7823 ) 发表时间: 2019/02
类型:期刊论文 为本人加分:1026.844661
7 Design, synthesis and biological evaluation of 4-piperidin-4-yl-triazole derivatives as novel histon..
来源:BIOSCI TRENDS( P 1881-7815 E 1881-7823 ) 发表时间: 2019/04
类型:期刊论文 为本人加分:1020.780617
8 The Synthesis and Activity Evaluation of a Bestatin Derivative (LYP) as an Aminopeptidase N Inhibito..
来源:LETT DRUG DES DISCOV( P 1570-1808 E 1875-628X ) 发表时间: 2009/09
类型:期刊论文 为本人加分:999.081084
贡献度:单独第一作者;共同通讯作者
9 Design, synthesis and antitumor activity evaluation of novel HDAC inhibitors with tetrahydrobenzothi..
来源:BIOORG CHEM( P 0045-2068 E 1090-2120 ) 发表时间: 2021/03
类型:期刊论文 为本人加分:981.510180
贡献度:单独通讯作者
10 Design and synthesis of novel histone deacetylase 6 inhibitors with benzyl-triazole as the core skel..
来源:BIOSCI TRENDS( P 1881-7815 E 1881-7823 ) 发表时间: 2019/06
类型:期刊论文 为本人加分:870.510151