位置：成果数据库 > 期刊 > 期刊详情页
全新的Largazole类似物的生物活性评价:通过点击化学改变大环的构想
  • ISSN号：1948-5875
  • 期刊名称：ACS Medicinal Chemistry Letters
  • 时间：2012.12.7
  • 页码：11-13
  • 相关项目：组蛋白去乙酰化酶抑制剂Lar-7的构效关系及其抗肿瘤活性的研究
作者： 蒋晟|
同期刊论文项目
组蛋白去乙酰化酶抑制剂Lar-7的构效关系及其抗肿瘤活性的研究
期刊论文 30
同项目期刊论文
Discovery of Novel Class I Histone DeacetylaseInhibitors with Promising in Vitro Selectivity for Can
Design, synthesis, and biological evaluation of 1, 3-disubstituted-pyrazole derivatives as new class
Suberoylanilide hydroxamic acid suppresses inflammation-induced neovascularization
 Total synthesis of securinega alkaloids (-)-norsecurinine, (-)-niruroidine and (-)-flueggi
组蛋白去乙酰化酶抑制剂抗肿瘤临床研究进展
Biological Evaluation of New Largazole Analogues: Alteration of Macrocyclic Scaffold with Click Chem
Comprehensive Analysis for Histone Acetylation of Human Colon Cancer Cells Treated with a novel HDAC
Identification of novel bivalent mimetics of annonaceous acetogenins via a scaffold-hopping strategy
Biological evaluation of new mimetics of annonaceous acetogenins: Alteration of right scaffold by cl
Biological evaluation of 2-methylpyrimidine derivatives as active pan Bcr-Abl inhibitors
Design, synthesis, and biological evaluation of 1, 3-disubstitutedpyrazolederivatives as new class I
Design, synthesis, and biological evaluation of largazole derivatives:alteration of the zinc-binding
The application of click chemistry in thesynthesis of agents with anticancer activity
Design, synthesis, and biological evaluation of largazole derivatives: alteration of the zinc-bindin
New Ligands for Copper-Catalyzed C-N Coupling Reactions at Gentle Temperature
Total synthesis of securinega alkaloids (-)-norsecurinine, (-)-niruroidine and (-)-flueggine A
Design, synthesis, and biological evaluation of novel histone deacetylase 1 inhibitors through click
Synthesis of 3-[(Z)-Pentadec-8-enyl]catechol and Its Anti-angiogenesis Activity
Largazole, an inhibitor of class I histone deacetylases, attenuates inflammatory corneal neovascular