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20条,第1-10条 帮助

条数/页: 排序方式:
Design, Synthesis, and Biological Evaluation of Potent and Selective PROTAC Degraders of Oncogenic KRASG12D 期刊论文  OAI收割
JOURNAL OF MEDICINAL CHEMISTRY, 2024, 卷号: 67, 期号: 2, 页码: 1147-1167
作者:  
Zhou, Chuan;  Fan, Zisheng;  Gu, Yuejiao;  Ge, Zhiming;  Tao, Zhaofan
  |  收藏  |  浏览/下载:10/0  |  提交时间:2024/02/27
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:8/0  |  提交时间:2023/12/08
Stimuli-activatable PROTACs for precise protein degradation and cancer therapy 期刊论文  OAI收割
SCIENCE BULLETIN, 2023, 卷号: 68, 期号: 10, 页码: 1069-1085
作者:  
Gao, Jing;  Yang, Lei;  Lei, Shumin;  Zhou, Feng;  Nie, Huijun
  |  收藏  |  浏览/下载:8/0  |  提交时间:2023/10/17
Discovery of a Potent, Cooperative, and Selective SOS1 PROTAC ZZ151 with In Vivo Antitumor Efficacy in KRAS-Mutant Cancers 期刊论文  OAI收割
JOURNAL OF MEDICINAL CHEMISTRY, 2023, 卷号: 66, 期号: 6, 页码: 4197-4214
作者:  
Zhou, Zehui;  Zhou, Guizhen;  Zhou, Chuan;  Fan, Zisheng;  Cui, Rongrong
  |  收藏  |  浏览/下载:2/0  |  提交时间:2024/03/27
Design, Synthesis, and Bioevaluation of Pyrido[2,3-d]pyrimidin-7-ones as Potent SOS1 Inhibitors 期刊论文  OAI收割
ACS MEDICINAL CHEMISTRY LETTERS, 2023, 页码: 183-190
作者:  
Liu, Meiying;  Zhou, Guizhen;  Su, Wenhong;  Gu, Yuejiao;  Gao, Mingshan
  |  收藏  |  浏览/下载:7/0  |  提交时间:2024/03/27
Engineered bioorthogonal POLY-PROTAC nanoparticles for tumour-specific protein degradation and precise cancer therapy 期刊论文  OAI收割
NATURE COMMUNICATIONS, 2022, 卷号: 13, 期号: 1, 页码: 14
作者:  
Gao, Jing;  Hou, Bo;  Zhu, Qiwen;  Yang, Lei;  Jiang, Xingyu
  |  收藏  |  浏览/下载:41/0  |  提交时间:2022/08/30

Design, synthesis and structure-activity relationship studies of pyrido [2,3-d]pyrimidin-7-ones as potent Janus Kinase 3 (JAK3) covalent inhibitors & nbsp;

期刊论文  OAI收割

BIOORGANIC & MEDICINAL CHEMISTRY LETTERS, 2022, 卷号: 64, 页码: 7
作者:  
Su, Wenhong;  Chen, Zhiwen;  Liu, Meiying;  He, Rui;  Liu, Chaoyi
  |  收藏  |  浏览/下载:33/0  |  提交时间:2022/08/16
Design, synthesis and structure-activity relationship studies of pyrido [2,3-d]pyrimidin-7-ones as potent Janus Kinase 3 (JAK3) covalent inhibitors 期刊论文  OAI收割
BIOORGANIC & MEDICINAL CHEMISTRY LETTERS, 2022, 卷号: 64, 页码: 128680
作者:  
Su, Wenhong;  Chen, Zhiwen;  Liu, Meiying;  He, Rui;  Liu, Chaoyi
  |  收藏  |  浏览/下载:11/0  |  提交时间:2024/03/21
Discovery of the First-in-Class Agonist-Based SOS1 PROTACs Effective in Human Cancer Cells Harboring Various KRAS Mutations 期刊论文  OAI收割
JOURNAL OF MEDICINAL CHEMISTRY, 2022, 卷号: 65, 期号: 5, 页码: 3923-3942
作者:  
Zhou, Chuan;  Fan, Zisheng;  Zhou, Zehui;  Li, Yupeng;  Cui, Rongrong
  |  收藏  |  浏览/下载:36/0  |  提交时间:2022/06/15
Design, Synthesis, and Biological Evaluation of Novel EGFR PROTACs Targeting Del19/T790M/C797S Mutation 期刊论文  OAI收割
ACS MEDICINAL CHEMISTRY LETTERS, 2022, 卷号: 13, 期号: 2, 页码: 278-283
作者:  
Zhang, Hualin;  Xie, Ruliang;  AI-furas, Hawaa;  Li, Yupeng;  Wu, Qingxia
  |  收藏  |  浏览/下载:26/0  |  提交时间:2022/06/15