reference/8729293

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contentType	Journal Article\|Research Support, Non-U.S. Gov't
endingPage	56
issn	0223-5234
pageRange	39-56
publicationName	European Journal of Medicinal Chemistry
startingPage	39
hasFundingAgency	http://rdf.ncbi.nlm.nih.gov/pubchem/organization/MD5_ed775de13cd235d4c7e8efd57a7a2ed0 http://rdf.ncbi.nlm.nih.gov/pubchem/organization/MD5_8ffb2f66b6d0be00d02662616bbcc2a7 http://rdf.ncbi.nlm.nih.gov/pubchem/organization/MD5_a1a93ae58c37b3daa03047deb1683150
bibliographicCitation	Jiang X, Zhou J, Ai J, Song Z, Peng X, Xing L, Xi Y, Guo J, Yao Q, Ding J, Geng M, Zhang A. Novel tetracyclic benzo[b]carbazolones as highly potent and orally bioavailable ALK inhibitors: Design, synthesis, and structure—activity relationship study. European Journal of Medicinal Chemistry. 2015 Nov;105():39–56. doi: 10.1016/j.ejmech.2015.10.005.
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date	2015-11-13-04:00^^<http://www.w3.org/2001/XMLSchema#date>
identifier	https://doi.org/10.1016/j.ejmech.2015.10.005 https://pubmed.ncbi.nlm.nih.gov/26476749
isPartOf	https://portal.issn.org/resource/ISSN/0223-5234 http://rdf.ncbi.nlm.nih.gov/pubchem/journal/21651
language	English
source	https://pubmed.ncbi.nlm.nih.gov/ https://www.crossref.org/
title	Novel tetracyclic benzo[b]carbazolones as highly potent and orally bioavailable ALK inhibitors: Design, synthesis, and structure—activity relationship study
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