000 | 01657 a2200445 4500 | ||
---|---|---|---|
005 | 20250517200349.0 | ||
264 | 0 | _c20180322 | |
008 | 201803s 0 0 eng d | ||
022 | _a1768-3254 | ||
024 | 7 |
_a10.1016/j.ejmech.2018.01.021 _2doi |
|
040 |
_aNLM _beng _cNLM |
||
100 | 1 | _aAboeldahab, Alshimaa M A | |
245 | 0 | 0 |
_aSpirohydantoins and 1,2,4-triazole-3-carboxamide derivatives as inhibitors of histone deacetylase: Design, synthesis, and biological evaluation. _h[electronic resource] |
260 |
_bEuropean journal of medicinal chemistry _cFeb 2018 |
||
300 |
_a79-92 p. _bdigital |
||
500 | _aPublication Type: Journal Article | ||
650 | 0 | 4 |
_aAntineoplastic Agents _xchemical synthesis |
650 | 0 | 4 |
_aCell Proliferation _xdrug effects |
650 | 0 | 4 | _aCrystallography, X-Ray |
650 | 0 | 4 | _aDose-Response Relationship, Drug |
650 | 0 | 4 | _aDrug Design |
650 | 0 | 4 | _aDrug Screening Assays, Antitumor |
650 | 0 | 4 | _aHep G2 Cells |
650 | 0 | 4 |
_aHistone Deacetylase Inhibitors _xchemical synthesis |
650 | 0 | 4 |
_aHistone Deacetylases _xmetabolism |
650 | 0 | 4 | _aHumans |
650 | 0 | 4 | _aMCF-7 Cells |
650 | 0 | 4 | _aModels, Molecular |
650 | 0 | 4 | _aMolecular Structure |
650 | 0 | 4 |
_aPolymerization _xdrug effects |
650 | 0 | 4 | _aStructure-Activity Relationship |
650 | 0 | 4 |
_aTriazoles _xchemical synthesis |
650 | 0 | 4 |
_aTubulin _xmetabolism |
700 | 1 | _aBeshr, Eman A M | |
700 | 1 | _aShoman, Mai E | |
700 | 1 | _aRabea, Safwat M | |
700 | 1 | _aAly, Omar M | |
773 | 0 |
_tEuropean journal of medicinal chemistry _gvol. 146 _gp. 79-92 |
|
856 | 4 | 0 |
_uhttps://doi.org/10.1016/j.ejmech.2018.01.021 _zAvailable from publisher's website |
999 |
_c28039968 _d28039968 |