中国科学院机构知识库网格
Chinese Academy of Sciences Institutional Repositories Grid
机构
采集方式
内容类型
发表日期
学科主题
筛选

浏览/检索结果: 共13条,第1-10条 帮助

条数/页: 排序方式:
Discovery of ARD-1676 as a Highly Potent and Orally Efficacious AR PROTAC Degrader with a Broad Activity against AR Mutants for the Treatment of AR plus Human Prostate Cancer 期刊论文  OAI收割
JOURNAL OF MEDICINAL CHEMISTRY, 2023, 卷号: 66, 期号: 18, 页码: 13280-13303
作者:  
Xiang, Weiguo;  Zhao, Lijie;  Han, Xin;  Xu, Tianfeng;  Kregel, Steven
  |  收藏  |  浏览/下载:23/0  |  提交时间:2023/12/08
Epigenetics 2.0: Special Issue on Epigenetics-Call for Papers 期刊论文  OAI收割
JOURNAL OF MEDICINAL CHEMISTRY, 2020, 卷号: 63, 期号: 21, 页码: 12129-12130
作者:  
Conway, Stuart J.;  Arimondo, Paola;  Arrowsmith, Cheryl;  Jin, Jian;  Luo, Cheng
  |  收藏  |  浏览/下载:12/0  |  提交时间:2021/05/24
Women in Medicinal Chemistry: Ad Maiora! 期刊论文  OAI收割
JOURNAL OF MEDICINAL CHEMISTRY, 2020, 卷号: 63, 期号: 5, 页码: 1777-1778
作者:  
Bolognesi, Maria Laura;  Ganamet, Kelly L.;  Liu, Hong;  Poulsen, Sally-Ann;  Georg, Gunda I.
  |  收藏  |  浏览/下载:12/0  |  提交时间:2020/07/01
Women in Medicinal Chemistry Special Issue Call for Papers 期刊论文  OAI收割
JOURNAL OF MEDICINAL CHEMISTRY, 2019, 卷号: 62, 期号: 8, 页码: 3783-3783
作者:  
Bolognesi, Maria Laura;  Ganamet, Kelly L.;  Liu, Hong;  Poulsen, Sally-Ann;  Georg, Gunda I.
  |  收藏  |  浏览/下载:11/0  |  提交时间:2020/07/01
Discovery of QCA570 as an Exceptionally Potent and Efficacious Proteolysis Targeting Chimera (PROTAC) Degrader of the Bromodomain and Extra-Terminal (BET) Proteins Capable of Inducing Complete and Durable Tumor Regression 期刊论文  OAI收割
JOURNAL OF MEDICINAL CHEMISTRY, 2018, 卷号: 61, 期号: 15, 页码: 6685-6704
作者:  
Qin, Chong;  Hu, Yang;  Zhou, Bing;  Fernandez-Salas, Ester;  Yang, Chao-Yie
  |  收藏  |  浏览/下载:54/0  |  提交时间:2019/01/08
Structure-Based Discovery of CF53 as a Potent and Orally Bioavailable Bromodomain and Extra-Terminal (BET) Bromodomain Inhibitor 期刊论文  OAI收割
JOURNAL OF MEDICINAL CHEMISTRY, 2018, 卷号: 61, 期号: 14, 页码: 6110-6120
作者:  
Zhao, Yujun;  Zhou, Bing;  Bai, Longchuan;  Liu, Liu;  Yang, Chao-Yie
  |  收藏  |  浏览/下载:58/0  |  提交时间:2019/01/08
Structure-Based Discovery of 4-(6-Methoxy-2-methyl-4-(quinolin-4-yl)-9H-pyrimido[4,5-b]indol-7-yl)-3,5-dimethylisoxazole (CD161) as a Potent and Orally Bioavailable BET Bromodomain Inhibitor 期刊论文  OAI收割
JOURNAL OF MEDICINAL CHEMISTRY, 2017, 卷号: 60, 期号: 9, 页码: 3887-3901
作者:  
Zhao, Yujun;  Bai, Longchuan;  Liu, Liu;  McEachern, Donna;  Stuckey, Jeanne A.
  |  收藏  |  浏览/下载:40/0  |  提交时间:2019/01/08
Discovery of a new class of highly potent small-molecule degraders of BET bromodomain proteins 会议论文  OAI收割
作者:  
Xu, Fuming;  Hu, Jiantao;  Zhou, Bing;  Chen, Zhuo;  Lin, Mei
  |  收藏  |  浏览/下载:30/0  |  提交时间:2019/01/08
Epigenetics: Novel Therapeutics Targeting Epigenetics 期刊论文  OAI收割
JOURNAL OF MEDICINAL CHEMISTRY, 2015, 卷号: 58, 期号: 2, 页码: 523-524
作者:  
Conway, Stuart J.;  Woster, Patrick M.;  Shen, Jing-Kang;  Georg, Gunda;  Wang, Shaomeng
  |  收藏  |  浏览/下载:15/0  |  提交时间:2019/01/08
Pyrimido[4,5-d]pyrimidin-4(1H)-one Derivatives as Selective Inhibitors of EGFR Threonine(790) to Methionine(790) (T790M) Mutants 期刊论文  OAI收割
ANGEWANDTE CHEMIE-INTERNATIONAL EDITION, 2013, 卷号: 52, 期号: 32
作者:  
Zhang, Lianwen;  Ding, Ke;  Wang, Shaomeng;  Ren, Xiaomei;  Li, Honglin
  |  收藏  |  浏览/下载:41/0  |  提交时间:2018/12/13