reference/1832897

http://rdf.ncbi.nlm.nih.gov/pubchem/reference/1832897

Outgoing Links

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contentType	Journal Article\|Research Support, N.I.H., Extramural
endingPage	4133
issn	1520-4804 0022-2623
issueIdentifier	10
pageRange	4111-4133
publicationName	Journal of Medicinal Chemistry
startingPage	4111
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bibliographicCitation	Abulwerdi FA, Liao C, Mady AS, Gavin J, Shen C, Cierpicki T, Stuckey JA, Showalter HD, Nikolovska-Coleska Z. 3-Substituted-N-(4-hydroxynaphthalen-1-yl)arylsulfonamides as a novel class of selective Mcl-1 inhibitors: structure-based design, synthesis, SAR, and biological evaluation. J Med Chem. 2014 May 22;57(10):4111–33. PMID: 24749893; PMCID: PMC4033665.
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date	2014-05-07-04:00^^<http://www.w3.org/2001/XMLSchema#date>
identifier	https://pubmed.ncbi.nlm.nih.gov/24749893 https://doi.org/10.1021/jm500010b https://pubmed.ncbi.nlm.nih.gov/PMC4033665
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language	English
source	https://pubmed.ncbi.nlm.nih.gov/ https://www.crossref.org/
title	3-Substituted-N-(4-Hydroxynaphthalen-1-yl)arylsulfonamides as a Novel Class of Selective Mcl-1 Inhibitors: Structure-Based Design, Synthesis, SAR, and Biological Evaluation
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Predicate

Subject

citesAsDataSource

isDiscussedBy

http://rdf.ncbi.nlm.nih.gov/pubchem/gene/GID597
http://rdf.ncbi.nlm.nih.gov/pubchem/gene/GID4170
http://rdf.ncbi.nlm.nih.gov/pubchem/gene/GID598
http://rdf.ncbi.nlm.nih.gov/pubchem/gene/GID599
http://rdf.ncbi.nlm.nih.gov/pubchem/gene/GID17210
http://rdf.ncbi.nlm.nih.gov/pubchem/gene/GID596

Total number of triples: 304.