宋婷

个人信息Personal Information

副教授

硕士生导师

性别:女

毕业院校:大连理工大学

学位:博士

所在单位:医学部

学科:有机化学. 细胞生物学

办公地点:大连理工大学西部新校区化学综合楼C508

联系方式:Email: songting@dlut.edu.cn Tel: 18098885828

电子邮箱:songting@dlut.edu.cn

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Fragment-based design, synthesis, and biological evaluation of N-substituted-5-(4-isopropylthiophenol)-2-hydroxynicotinamide derivatives as novel Mcl-1 inhibitors

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论文类型:期刊论文

发表时间:2013-02-01

发表刊物:EUROPEAN JOURNAL OF MEDICINAL CHEMISTRY

收录刊物:SCIE、PubMed、Scopus

卷号:60

页面范围:410-420

ISSN号:0223-5234

关键字:Fragment-based; Apoptosis; Mcl-1; LE; FQ

摘要:We have previously reported a nanomolar inhibitor of antiapoptotic Mcl-1 protein, 3-thiomorpholin-8-oxo-8H-acenaphtho [1,2-b] pyrrole-9-carbonitrile (S1). S1 plays its function by binding to the BH3 groove of Mcl-1. Basing on this spacial structural characteristic, we developed a novel class of Mcl-1 inhibitor using fragment-based drug discovery approach. By dissecting S1, we identified the compound 4 with a 2-hydroxypyridine core as the starting fragment. In the following molecular growth, we used the ligand efficiency evaluation and fit quality score to assess the fragments. A novel potent compound, N-benzyl-5-(4-isopropylthiophenol)-2-hydroxyl nicotinamide (12c), which binds Mcl-1 with an IC50 value of 54 nM was obtained. Compound 12c demonstrated a better aqueous solubility than S1. (C) 2012 Elsevier Masson SAS. All rights reserved.