PMID-sentid Pub_year Sent_text comp_official_name comp_offsetprotein_name organism prot_offset 28853575-4 2017 The pyrazolopyrimidine-based core differs structurally from that of aminopyrimidine-based third-generation EGFR inhibitors and therefore constitutes a new set of inhibitors that target this mechanism of drug resistance. 2-aminopyrimidine 68-83 epidermal growth factor receptor Homo sapiens 107-111 34534838-0 2021 Design, synthesis and biological evaluation of aminopyrimidine derivatives bearing a 4,5,6,7-tetrahydrothieno (3,2-c)pyridine as potent EGFR inhibitors. 2-aminopyrimidine 47-62 epidermal growth factor receptor Homo sapiens 136-140 34534838-1 2021 To resolve the problem of drug resistance caused by epidermal growth factor receptor (EGFR) mutations in non-small cell lung cancer, we used the principle of collocation to design and synthesize a series of aminopyrimidine derivatives with 4,5,6,7-tetrahydrothieno (3,2-c)pyridine side chains (according to the binding mode of AZD9291 to EGFRT790M) for use as EGFRL858R/T790M kinase inhibitors. 2-aminopyrimidine 207-222 epidermal growth factor receptor Homo sapiens 52-84 34534838-1 2021 To resolve the problem of drug resistance caused by epidermal growth factor receptor (EGFR) mutations in non-small cell lung cancer, we used the principle of collocation to design and synthesize a series of aminopyrimidine derivatives with 4,5,6,7-tetrahydrothieno (3,2-c)pyridine side chains (according to the binding mode of AZD9291 to EGFRT790M) for use as EGFRL858R/T790M kinase inhibitors. 2-aminopyrimidine 207-222 epidermal growth factor receptor Homo sapiens 86-90 34819010-4 2022 Based on our previous studies, we assumed that a hybrid of aminopyrimidine derivatives as EGFR inhibitors and benzocheromen derivatives as cytotoxic agents can induce apoptosis in EGFR positive cancer cells. 2-aminopyrimidine 59-74 epidermal growth factor receptor Homo sapiens 90-94 34819010-4 2022 Based on our previous studies, we assumed that a hybrid of aminopyrimidine derivatives as EGFR inhibitors and benzocheromen derivatives as cytotoxic agents can induce apoptosis in EGFR positive cancer cells. 2-aminopyrimidine 59-74 epidermal growth factor receptor Homo sapiens 180-184 30204041-0 2018 Unraveling structural requirements of amino-pyrimidine T790M/L858R double mutant EGFR inhibitors: 2D and 3D QSAR study. 2-aminopyrimidine 38-54 epidermal growth factor receptor Homo sapiens 81-85 26451770-0 2015 Novel hydrazone moiety-bearing aminopyrimidines as selective inhibitors of epidermal growth factor receptor T790M mutant. 2-aminopyrimidine 31-47 epidermal growth factor receptor Homo sapiens 75-107 26451770-2 2015 Here, a series of novel aminopyrimidines bearing a hydrazone moiety were identified as potent and selective EGFR inhibitors. 2-aminopyrimidine 24-40 epidermal growth factor receptor Homo sapiens 108-112