| 000 | 01480 a2200397 4500 | ||
|---|---|---|---|
| 005 | 20250516220053.0 | ||
| 264 | 0 | _c20150330 | |
| 008 | 201503s 0 0 eng d | ||
| 022 | _a1768-3254 | ||
| 024 | 7 |
_a10.1016/j.ejmech.2014.05.074 _2doi |
|
| 040 |
_aNLM _beng _cNLM |
||
| 100 | 1 | _aAbdelsamie, Ahmed S | |
| 245 | 0 | 0 |
_aInhibition of 17β-HSD1: SAR of bicyclic substituted hydroxyphenylmethanones and discovery of new potent inhibitors with thioether linker. _h[electronic resource] |
| 260 |
_bEuropean journal of medicinal chemistry _cJul 2014 |
||
| 300 |
_a394-406 p. _bdigital |
||
| 500 | _aPublication Type: Journal Article; Research Support, Non-U.S. Gov't | ||
| 650 | 0 | 4 |
_a17-Hydroxysteroid Dehydrogenases _xantagonists & inhibitors |
| 650 | 0 | 4 | _aAnimals |
| 650 | 0 | 4 | _aDose-Response Relationship, Drug |
| 650 | 0 | 4 | _aDrug Discovery |
| 650 | 0 | 4 |
_aEnzyme Inhibitors _xchemical synthesis |
| 650 | 0 | 4 | _aHumans |
| 650 | 0 | 4 | _aMice |
| 650 | 0 | 4 | _aModels, Molecular |
| 650 | 0 | 4 | _aMolecular Structure |
| 650 | 0 | 4 |
_aPhenols _xchemical synthesis |
| 650 | 0 | 4 | _aStructure-Activity Relationship |
| 650 | 0 | 4 |
_aSulfides _xchemistry |
| 700 | 1 | _aBey, Emmanuel | |
| 700 | 1 | _aHanke, Nina | |
| 700 | 1 | _aEmpting, Martin | |
| 700 | 1 | _aHartmann, Rolf W | |
| 700 | 1 | _aFrotscher, Martin | |
| 773 | 0 |
_tEuropean journal of medicinal chemistry _gvol. 82 _gp. 394-406 |
|
| 856 | 4 | 0 |
_uhttps://doi.org/10.1016/j.ejmech.2014.05.074 _zAvailable from publisher's website |
| 999 |
_c23918689 _d23918689 |
||