000 01722 a2200481 4500
005 20250516155947.0
264 0 _c20140318
008 201403s 0 0 eng d
022 _a1464-3391
024 7 _a10.1016/j.bmc.2013.06.009
_2doi
040 _aNLM
_beng
_cNLM
100 1 _aFeng, Taotao
245 0 0 _aNovel N-hydroxyfurylacrylamide-based histone deacetylase (HDAC) inhibitors with branched CAP group (Part 2).
_h[electronic resource]
260 _bBioorganic & medicinal chemistry
_cSep 2013
300 _a5339-54 p.
_bdigital
500 _aPublication Type: Journal Article; Research Support, Non-U.S. Gov't
650 0 4 _aAcrylamide
_xchemical synthesis
650 0 4 _aBinding Sites
650 0 4 _aCatalytic Domain
650 0 4 _aCell Line, Tumor
650 0 4 _aCell Proliferation
_xdrug effects
650 0 4 _aCrystallography, X-Ray
650 0 4 _aHCT116 Cells
650 0 4 _aHep G2 Cells
650 0 4 _aHistone Deacetylase 1
_xantagonists & inhibitors
650 0 4 _aHistone Deacetylase 6
650 0 4 _aHistone Deacetylase Inhibitors
_xchemical synthesis
650 0 4 _aHistone Deacetylases
_xchemistry
650 0 4 _aHumans
650 0 4 _aMolecular Docking Simulation
650 0 4 _aRecombinant Proteins
_xbiosynthesis
650 0 4 _aRepressor Proteins
_xantagonists & inhibitors
650 0 4 _aStructure-Activity Relationship
700 1 _aWang, Hai
700 1 _aSu, Hong
700 1 _aLu, Hui
700 1 _aYu, Liqin
700 1 _aZhang, Xiaojin
700 1 _aSun, Haopeng
700 1 _aYou, Qidong
773 0 _tBioorganic & medicinal chemistry
_gvol. 21
_gno. 17
_gp. 5339-54
856 4 0 _uhttps://doi.org/10.1016/j.bmc.2013.06.009
_zAvailable from publisher's website
999 _c22885783
_d22885783