reference/18854580

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endingPage	7124
issn	1520-4804 0022-2623
issueIdentifier	15
pageRange	7111-7124
publicationName	Journal of Medicinal Chemistry
startingPage	7111
hasFundingAgency	http://rdf.ncbi.nlm.nih.gov/pubchem/organization/MD5_04f794624302b6a485aa08655acfd4b8 http://rdf.ncbi.nlm.nih.gov/pubchem/organization/MD5_6e6a1576e1dd63880dbb1cc636c5850b http://rdf.ncbi.nlm.nih.gov/pubchem/organization/MD5_51316612a5e325aa65098699ad4567ce http://rdf.ncbi.nlm.nih.gov/pubchem/organization/MD5_691206896ab09f902180db0d50bc601e http://rdf.ncbi.nlm.nih.gov/pubchem/organization/MD5_487baf6554eb36bb22c6138d90a7c50f http://rdf.ncbi.nlm.nih.gov/pubchem/organization/MD5_d8bf1b8a20fd2206046febe5b38ecb1a
bibliographicCitation	Hao Y, Wang X, Zhang T, Sun D, Tong Y, Xu Y, Chen H, Tong L, Zhu L, Zhao Z, Chen Z, Ding J, Xie H, Xu Y, Li H. Discovery and Structural Optimization of N5-Substituted 6,7-Dioxo-6,7-dihydropteridines as Potent and Selective Epidermal Growth Factor Receptor (EGFR) Inhibitors against L858R/T790M Resistance Mutation. J Med Chem. 2016 Aug 11;59(15):7111–24. doi: 10.1021/acs.jmedchem.6b00403. PMID: 27396610.
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date	2016-07-21-04:00^^<http://www.w3.org/2001/XMLSchema#date>
identifier	https://pubmed.ncbi.nlm.nih.gov/27396610 https://doi.org/10.1021/acs.jmedchem.6b00403
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language	English
source	https://www.crossref.org/ https://pubmed.ncbi.nlm.nih.gov/
title	Discovery and Structural Optimization of N5-Substituted 6,7-Dioxo-6,7-dihydropteridines as Potent and Selective Epidermal Growth Factor Receptor (EGFR) Inhibitors against L858R/T790M Resistance Mutation
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