中国科学院机构知识库网格
Chinese Academy of Sciences Institutional Repositories Grid
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CAS IR Grid
机构
上海药物研究所 [14]
金属研究所 [2]
合肥物质科学研究院 [2]
广州生物医药与健康研... [1]
采集方式
OAI收割 [19]
内容类型
期刊论文 [18]
学位论文 [1]
发表日期
2022 [2]
2020 [3]
2018 [6]
2017 [4]
2014 [1]
2013 [1]
更多
学科主题
药物化学 [1]
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浏览/检索结果:
共19条,第1-10条
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A Phase 2 Study of Befotertinib in Patients with EGFR T790M Mutated NSCLC after Prior EGFR TKIs
期刊论文
OAI收割
JOURNAL OF THORACIC ONCOLOGY, 2022, 卷号: 17
作者:
Lu, S.
;
Zhang, Y.
;
Zhang, G.
;
Zhou, J.
;
Cang, S.
  |  
收藏
  |  
浏览/下载:119/0
  |  
提交时间:2022/12/23
third-generation EGFR-TKI
befotertinib
T790M
Impact of clinical and molecular features on efficacy and outcome of patients with non-small cell lung cancer receiving second-line osimertinib
期刊论文
OAI收割
BMC CANCER, 2022, 卷号: 22
作者:
Jin, Ying
;
Lin, Chen
;
Shi, Xun
;
He, Qiong
;
Yan, Junrong
  |  
收藏
  |  
浏览/下载:85/0
  |  
提交时间:2022/12/23
Clinical and molecular features
Efficacy and outcome
EGFR T790M mutation
Non-small-cell lung cancer
Osimertinib
Safety, Clinical Activity, and Pharmacokinetics of Al flutinib (AST2818) in Patients With Advanced NSCLC With EGFR T790M Mutation
期刊论文
OAI收割
JOURNAL OF THORACIC ONCOLOGY, 2020, 卷号: 15, 期号: 6, 页码: 1015-1026
作者:
Shi, Yuankai
;
Zhang, Shucai
;
Hu, Xingsheng
;
Feng, Jifeng
;
Ma, Zhiyong
  |  
收藏
  |  
浏览/下载:103/0
  |  
提交时间:2020/12/24
Alflutinib
NSCLC
EGFR T790M mutation
Efficacy
Safety
Discovery of a novel third-generation EGFR inhibitor and identification of a potential combination strategy to overcome resistance
期刊论文
OAI收割
MOLECULAR CANCER, 2020, 卷号: 19, 期号: 1, 页码: 15
作者:
Zhang, Tao
;
Qu, Rong
;
Chan, Shingpan
;
Lai, Mengzhen
;
Tong, Linjiang
  |  
收藏
  |  
浏览/下载:92/0
  |  
提交时间:2020/07/01
Non-small cell lung cancer (NSCLC)
EGFR T790M
Small-molecule inhibitor
Drug resistance
Ack1
BBB-penetrating codelivery liposomes treat brain metastasis of non-small cell lung cancer with EGFR(T790M) mutation
期刊论文
OAI收割
THERANOSTICS, 2020, 卷号: 10, 期号: 14, 页码: 6122-6135
作者:
Yin, Weimin
;
Zhao, Yuge
;
Kang, Xuejia
;
Zhao, Pengfei
;
Zhao, Xuhong
  |  
收藏
  |  
浏览/下载:96/0
  |  
提交时间:2020/07/01
brain targeting delivery
tumor-associated macrophage
non-small cell lung cancer (NSCLC)
drug resistance
tyrosine kinase inhibitors (TKI)
EGFR T790M mutation
Remodeling Tumor-Associated Macrophages and Neovascularization Overcomes EGFR(T790M)-Associated Drug Resistance by PD-L1 Nanobody-Mediated Codelivery
期刊论文
OAI收割
SMALL, 2018, 卷号: 14, 期号: 47
作者:
Yin, Weimin
;
Yu, Xiaolu
;
Kang, Xuejia
;
Zhao, Yuge
;
Zhao, Pengfei
  |  
收藏
  |  
浏览/下载:115/0
  |  
提交时间:2019/01/08
antiangiogenesis
EGFR(T790M) mutation
PD-L1 nanobody
simvastatin
tumor-associated macrophage
Discovery of novel 2,4-diarylaminopyrimidine derivatives as potent and selective epidermal growth factor receptor (EGFR) inhibitors against L858R/T790M resistance mutation
期刊论文
OAI收割
EUROPEAN JOURNAL OF MEDICINAL CHEMISTRY, 2018, 卷号: 152, 页码: 298-306
作者:
Yan, Qi
;
Chen, Yuzhe
;
Tang, Baiyou
;
Xiao, Qiang
;
Qu, Rong
  |  
收藏
  |  
浏览/下载:84/0
  |  
提交时间:2019/01/08
EGFR inhibitors
Pyrimidine derivatives
Mutant selective inhibitors
AZD9291
T790M
YL143, a novel mutant selective irreversible EGFR inhibitor, overcomes EGFR(L858R, T790M)-mutant resistance in vitro and in vivo
期刊论文
OAI收割
CANCER MEDICINE, 2018, 卷号: 7, 期号: 4, 页码: 1430-1439
作者:
Zhang, Zhang
;
Zou, Jian
;
Yu, Lei
;
Luo, Jinfeng
;
Li, Yan
  |  
收藏
  |  
浏览/下载:79/0
  |  
提交时间:2019/01/08
EGFR inhibitor
lung cancer
pharmacokinetic
selectively
T790M mutation
Synthesis and Biological Activities of Novel 2-Aminobenzimidazoles EGFR~(T790M) Inhibitors
期刊论文
OAI收割
Chinese Journal of Synthetic Chemistry, 2018, 卷号: 26, 期号: 9, 页码: 637-646
作者:
Duan Jingyi
;
Zhang Yinyong
;
Qian Anran
;
Tong Linjiang
;
Xie Hua
  |  
收藏
  |  
浏览/下载:41/0
  |  
提交时间:2019/01/08
1-fluoro-2-nitroarene
trans-4-aminocyclohexanol hydrochloride
2-aminobenzimidazole
EGFR~(T790M) inhibitor
synthesis
biological activity
新型2-氨基苯并咪唑类EGFR~(T790M)抑制剂的合成及其生物活性
期刊论文
OAI收割
合成化学, 2018, 卷号: 026, 期号: 009, 页码: 637
作者:
段京义
;
张银勇
;
潜安然
;
童林江
;
谢华
  |  
收藏
  |  
浏览/下载:21/0
  |  
提交时间:2020/07/01
1-氟-2-硝基芳烃
反式-4-氨基环己醇盐酸盐
2-氨基苯并咪唑
EGFR^T790M
抑制剂
合成
抗肿瘤活性