000 | 01840 a2200529 4500 | ||
---|---|---|---|
005 | 20250518044927.0 | ||
264 | 0 | _c20191104 | |
008 | 201911s 0 0 eng d | ||
022 | _a1768-3254 | ||
024 | 7 |
_a10.1016/j.ejmech.2019.06.037 _2doi |
|
040 |
_aNLM _beng _cNLM |
||
100 | 1 | _aChen, Shulun | |
245 | 0 | 0 |
_aDesign, synthesis and antitumor study of a series of N-Cyclic sulfamoylaminoethyl substituted 1,2,5-oxadiazol-3-amines as new indoleamine 2, 3-dioxygenase 1 (IDO1) inhibitors. _h[electronic resource] |
260 |
_bEuropean journal of medicinal chemistry _cOct 2019 |
||
300 |
_a38-55 p. _bdigital |
||
500 | _aPublication Type: Journal Article | ||
650 | 0 | 4 |
_aAmines _xchemical synthesis |
650 | 0 | 4 | _aAnimals |
650 | 0 | 4 |
_aAntineoplastic Agents _xchemical synthesis |
650 | 0 | 4 | _aCell Line, Tumor |
650 | 0 | 4 |
_aCell Proliferation _xdrug effects |
650 | 0 | 4 | _aDose-Response Relationship, Drug |
650 | 0 | 4 | _aDrug Design |
650 | 0 | 4 | _aDrug Screening Assays, Antitumor |
650 | 0 | 4 |
_aEnzyme Inhibitors _xchemical synthesis |
650 | 0 | 4 | _aFemale |
650 | 0 | 4 | _aHEK293 Cells |
650 | 0 | 4 | _aHumans |
650 | 0 | 4 |
_aIndoleamine-Pyrrole 2,3,-Dioxygenase _xantagonists & inhibitors |
650 | 0 | 4 | _aMale |
650 | 0 | 4 | _aMice |
650 | 0 | 4 | _aMice, Inbred BALB C |
650 | 0 | 4 | _aMolecular Structure |
650 | 0 | 4 |
_aOxadiazoles _xchemical synthesis |
650 | 0 | 4 | _aRats |
650 | 0 | 4 | _aRats, Sprague-Dawley |
650 | 0 | 4 | _aStructure-Activity Relationship |
700 | 1 | _aGuo, Wei | |
700 | 1 | _aLiu, Xiaohua | |
700 | 1 | _aSun, Pu | |
700 | 1 | _aWang, Yi | |
700 | 1 | _aDing, Chunyong | |
700 | 1 | _aMeng, Linghua | |
700 | 1 | _aZhang, Ao | |
773 | 0 |
_tEuropean journal of medicinal chemistry _gvol. 179 _gp. 38-55 |
|
856 | 4 | 0 |
_uhttps://doi.org/10.1016/j.ejmech.2019.06.037 _zAvailable from publisher's website |
999 |
_c29830693 _d29830693 |