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Structure-Activity Relationship of Propargylamine-Based HDAC Inhibitors.Largazole Analogues as Histone Deacetylase Inhibitors and Anticancer Agents: An Overview of Structure-Activity Relationships.Novel histone deacetylase 6 (HDAC6) selective inhibitors: a patent evaluation (WO2014181137).A Novel Dual HDAC6 and Tubulin Inhibitor, MPT0B451, Displays Anti-tumor Ability in Human Cancer Cells in Vitro and in Vivo.
P2860
description
2016 nî lūn-bûn
@nan
2016年の論文
@ja
2016年学术文章
@wuu
2016年学术文章
@zh-cn
2016年学术文章
@zh-hans
2016年学术文章
@zh-my
2016年学术文章
@zh-sg
2016年學術文章
@yue
2016年學術文章
@zh
2016年學術文章
@zh-hant
name
Structural biology: HDAC6 finally crystal clear.
@en
Structural biology: HDAC6 finally crystal clear.
@nl
type
label
Structural biology: HDAC6 finally crystal clear.
@en
Structural biology: HDAC6 finally crystal clear.
@nl
prefLabel
Structural biology: HDAC6 finally crystal clear.
@en
Structural biology: HDAC6 finally crystal clear.
@nl
P2860
P356
P1476
Structural biology: HDAC6 finally crystal clear.
@en
P2093
P2860
P2888
P304
P356
10.1038/NCHEMBIO.2158
P50
P577
2016-08-01T00:00:00Z
P6179
1015565107