| 000 | 01835 a2200517 4500 | ||
|---|---|---|---|
| 005 | 20250516214329.0 | ||
| 264 | 0 | _c20150330 | |
| 008 | 201503s 0 0 eng d | ||
| 022 | _a1768-3254 | ||
| 024 | 7 |
_a10.1016/j.ejmech.2014.05.041 _2doi |
|
| 040 |
_aNLM _beng _cNLM |
||
| 100 | 1 | _aBian, Jinlei | |
| 245 | 0 | 0 |
_a2-Substituted 3-methylnaphtho[1,2-b]furan-4,5-diones as novel L-shaped ortho-quinone substrates for NAD(P)H:quinone oxidoreductase (NQO1). _h[electronic resource] |
| 260 |
_bEuropean journal of medicinal chemistry _cJul 2014 |
||
| 300 |
_a56-67 p. _bdigital |
||
| 500 | _aPublication Type: Journal Article; Research Support, Non-U.S. Gov't | ||
| 650 | 0 | 4 |
_aAntineoplastic Agents _xchemical synthesis |
| 650 | 0 | 4 | _aCell Line, Tumor |
| 650 | 0 | 4 |
_aCell Proliferation _xdrug effects |
| 650 | 0 | 4 |
_aCell Survival _xdrug effects |
| 650 | 0 | 4 | _aDose-Response Relationship, Drug |
| 650 | 0 | 4 | _aDrug Screening Assays, Antitumor |
| 650 | 0 | 4 |
_aEnzyme Inhibitors _xchemical synthesis |
| 650 | 0 | 4 |
_aFurans _xchemical synthesis |
| 650 | 0 | 4 | _aHumans |
| 650 | 0 | 4 | _aModels, Molecular |
| 650 | 0 | 4 | _aMolecular Structure |
| 650 | 0 | 4 |
_aNAD(P)H Dehydrogenase (Quinone) _xantagonists & inhibitors |
| 650 | 0 | 4 |
_aNaphthalenes _xchemical synthesis |
| 650 | 0 | 4 | _aStructure-Activity Relationship |
| 700 | 1 | _aDeng, Bang | |
| 700 | 1 | _aXu, Lili | |
| 700 | 1 | _aXu, Xiaoli | |
| 700 | 1 | _aWang, Nan | |
| 700 | 1 | _aHu, Tianhan | |
| 700 | 1 | _aYao, Zeyu | |
| 700 | 1 | _aDu, Jianyao | |
| 700 | 1 | _aYang, Li | |
| 700 | 1 | _aLei, Yonghua | |
| 700 | 1 | _aLi, Xiang | |
| 700 | 1 | _aSun, Haopeng | |
| 700 | 1 | _aZhang, Xiaojin | |
| 700 | 1 | _aYou, Qidong | |
| 773 | 0 |
_tEuropean journal of medicinal chemistry _gvol. 82 _gp. 56-67 |
|
| 856 | 4 | 0 |
_uhttps://doi.org/10.1016/j.ejmech.2014.05.041 _zAvailable from publisher's website |
| 999 |
_c23867589 _d23867589 |
||