N-Cyclic sulfamoylaminoethyl substituted 1,2,5-oxadiazol-3-amines as new indoleamine 2, 3-dioxygenase 1 (IDO1) inhibitors.
文献类型:期刊论文
作者 | Chen, Shulun; Guo, Wei; Sun, Pu; Meng, Linghua![]() ![]() |
刊名 | CANCER IMMUNOLOGY RESEARCH
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出版日期 | 2020-03-01 |
卷号 | 8期号:3页码:51-51 |
ISSN号 | 2326-6066 |
WOS研究方向 | Oncology ; Immunology |
语种 | 英语 |
WOS记录号 | WOS:000518188200074 |
出版者 | AMER ASSOC CANCER RESEARCH |
源URL | [http://119.78.100.183/handle/2S10ELR8/281340] ![]() |
专题 | 中国科学院上海药物研究所 |
作者单位 | Chinese Acad Sci, SIMM, Shanghai, Peoples R China |
推荐引用方式 GB/T 7714 | Chen, Shulun,Guo, Wei,Sun, Pu,et al. N-Cyclic sulfamoylaminoethyl substituted 1,2,5-oxadiazol-3-amines as new indoleamine 2, 3-dioxygenase 1 (IDO1) inhibitors.[J]. CANCER IMMUNOLOGY RESEARCH,2020,8(3):51-51. |
APA | Chen, Shulun,Guo, Wei,Sun, Pu,Meng, Linghua,&Zhang, Ao.(2020).N-Cyclic sulfamoylaminoethyl substituted 1,2,5-oxadiazol-3-amines as new indoleamine 2, 3-dioxygenase 1 (IDO1) inhibitors..CANCER IMMUNOLOGY RESEARCH,8(3),51-51. |
MLA | Chen, Shulun,et al."N-Cyclic sulfamoylaminoethyl substituted 1,2,5-oxadiazol-3-amines as new indoleamine 2, 3-dioxygenase 1 (IDO1) inhibitors.".CANCER IMMUNOLOGY RESEARCH 8.3(2020):51-51. |
入库方式: OAI收割
来源:上海药物研究所
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