These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.
155 related articles for article (PubMed ID: 38009481)
1. Novel bioactive 2-phenyl-4-aminopyrimidine derivatives as EGFR Xu S; Zhou Z; He J; Guo J; Huang X; An Y; Pan Q; Xu S; Zhu W Arch Pharm (Weinheim); 2024 Feb; 357(2):e2300460. PubMed ID: 38009481 [TBL] [Abstract][Full Text] [Related]
2. Insights into the Overcoming EGFR Zhang X; He J; Xu S; Fu L; Zheng P; Xu S; Pan Q; Zhu W ChemMedChem; 2024 May; 19(9):e202300634. PubMed ID: 38351876 [TBL] [Abstract][Full Text] [Related]
3. Identification of novel aminopyrimidine derivatives for the treatment of mutant NSCLC. Hu L; Shi S; Song X; Ma F; Ji O; Qi B Eur J Med Chem; 2024 Feb; 265():116074. PubMed ID: 38142512 [TBL] [Abstract][Full Text] [Related]
4. Novel EGFR inhibitors against resistant L858R/T790M/C797S mutant for intervention of non-small cell lung cancer. Wang X; Qin Z; Qiu W; Xu K; Bai Y; Zeng B; Ma Y; Yang S; Shi Y; Fan Y Eur J Med Chem; 2024 Nov; 277():116711. PubMed ID: 39094277 [TBL] [Abstract][Full Text] [Related]
5. LS-106, a novel EGFR inhibitor targeting C797S, exhibits antitumor activities both in vitro and in vivo. Liu Y; Lai M; Li S; Wang Y; Feng F; Zhang T; Tong L; Zhang M; Chen H; Chen Y; Song P; Li Y; Bai G; Ning Y; Tang H; Fang Y; Chen Y; Lu X; Geng M; Ding K; Yu K; Xie H; Ding J Cancer Sci; 2022 Feb; 113(2):709-720. PubMed ID: 34855271 [TBL] [Abstract][Full Text] [Related]
6. Design, synthesis and evaluation of the Brigatinib analogues as potent inhibitors against tertiary EGFR mutants (EGFR Fang H; Wu Y; Xiao Q; He D; Zhou T; Liu W; Yang CH; Xie Y Bioorg Med Chem Lett; 2022 Sep; 72():128729. PubMed ID: 35413415 [TBL] [Abstract][Full Text] [Related]
7. Design, synthesis and biological evaluation of phosphoroxy quinazoline derivatives as potential EGFR Guo Y; Gao B; Gao P; Wang Y; Gou S Bioorg Med Chem; 2023 Jul; 90():117338. PubMed ID: 37269687 [TBL] [Abstract][Full Text] [Related]
8. Response to Brigatinib Targeted Therapy in Non-Small Cell Lung Cancer Harboring Epidermal Growth Factor Receptor Exon 19 Deletion, T790M, and cis-C797S Triple Mutations: A Case Report. Chen ZW; Lin G; Shih HJ; Wu CE Int J Mol Sci; 2022 Dec; 24(1):. PubMed ID: 36614045 [TBL] [Abstract][Full Text] [Related]
9. Design, synthesis, and antitumor activity evaluation of potent fourth-generation EGFR inhibitors for treatment of Osimertinib resistant non-small cell lung cancer (NSCLC). Zhang Y; Tong L; Yan F; Huang P; Zhu CL; Pan C Bioorg Chem; 2024 Jun; 147():107394. PubMed ID: 38691906 [TBL] [Abstract][Full Text] [Related]
10. HJM-561, a Potent, Selective, and Orally Bioavailable EGFR PROTAC that Overcomes Osimertinib-Resistant EGFR Triple Mutations. Du Y; Chen Y; Wang Y; Chen J; Lu X; Zhang L; Li Y; Wang Z; Ye G; Zhang G Mol Cancer Ther; 2022 Jul; 21(7):1060-1066. PubMed ID: 35499406 [TBL] [Abstract][Full Text] [Related]
12. Conformational Constrained 4-(1-Sulfonyl-3-indol)yl-2-phenylaminopyrimidine Derivatives as New Fourth-Generation Epidermal Growth Factor Receptor Inhibitors Targeting T790M/C797S Mutations. Chen H; Lai M; Zhang T; Chen Y; Tong L; Zhu S; Zhou Y; Ren X; Ding J; Xie H; Lu X; Ding K J Med Chem; 2022 May; 65(9):6840-6858. PubMed ID: 35446588 [TBL] [Abstract][Full Text] [Related]
13. Design, Synthesis, and Biological Evaluation of Novel EGFR PROTACs Targeting C797S Mutation. Zhu Y; Ye X; Wu Y; Shen H; Cai Z; Xia F; Min W; Hou Y; Wang L; Wang X; Xiao Y; Yang P J Med Chem; 2024 May; 67(9):7283-7300. PubMed ID: 38676656 [TBL] [Abstract][Full Text] [Related]
14. Discovery of new cyclopropane sulfonamide derivatives as EGFR inhibitors to overcome C797S-mediated resistance and EGFR double mutation. Yao H; Ren Y; Wu F; Liu J; Li J; Cao L; Yan M; Li X Eur J Med Chem; 2024 Sep; 275():116590. PubMed ID: 38908104 [TBL] [Abstract][Full Text] [Related]
15. Discovery of Novel Fourth-Generation EGFR Inhibitors to Overcome C797S-Mediated Resistance. Zhu Y; Ye X; Shen H; Li J; Cai Z; Min W; Hou Y; Dong H; Wu Y; Wang L; Wang X; Xiao Y; Yang P J Med Chem; 2023 Nov; 66(21):14633-14652. PubMed ID: 37885208 [TBL] [Abstract][Full Text] [Related]
16. Discovery and structural optimization of potent epidermal growth factor receptor (EGFR) inhibitors against L858R/T790M/C797S resistance mutation for lung cancer treatment. Wang C; Wang X; Huang Z; Wang T; Nie Y; Yang S; Xiang R; Fan Y Eur J Med Chem; 2022 Jul; 237():114381. PubMed ID: 35447433 [TBL] [Abstract][Full Text] [Related]
17. Modification of osimertinib to discover new potent EGFR Xi XX; Zhao HY; Mao YZ; Xin M; Zhang SQ Eur J Med Chem; 2023 Dec; 261():115865. PubMed ID: 37839342 [TBL] [Abstract][Full Text] [Related]
18. Design, synthesis and antitumor activity of 4-arylamine substituted pyrimidine derivatives as noncovalent EGFR inhibitors overcoming C797S mutation. Zuo Y; Long Z; Li R; Le Y; Zhang S; He H; Yan L Eur J Med Chem; 2024 Feb; 265():116106. PubMed ID: 38169271 [TBL] [Abstract][Full Text] [Related]
19. Psorachromene induces apoptosis and suppresses tumor growth in NSCLC cells harboring EGFR L858R/T790M/C797S. Wang TH; Leu YL; Chen CC; Li HJ; Yang SC; Huang KY; Chen CY Phytother Res; 2022 May; 36(5):2116-2126. PubMed ID: 35229911 [TBL] [Abstract][Full Text] [Related]
20. BBT-176, a Novel Fourth-Generation Tyrosine Kinase Inhibitor for Osimertinib-Resistant EGFR Mutations in Non-Small Cell Lung Cancer. Lim SM; Fujino T; Kim C; Lee G; Lee YH; Kim DW; Ahn JS; Mitsudomi T; Jin T; Lee SY Clin Cancer Res; 2023 Aug; 29(16):3004-3016. PubMed ID: 37249619 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]