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Comprehensive Analysis for Histone Acetylation of Human Colon Cancer Cells Treated with a novel HDAC
ISSN号:1381-6128
期刊名称:Current Pharmaceutical Design
时间:2014.4
页码:1866-1873
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:
Ma, Zhenyi|Xu, Liyan|Li, Enmin|Zhang, Kai|
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
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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
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
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