reference/30289009

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contentType	Journal Article
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pageRange	3895-3899
publicationName	Bioorganic & Medicinal Chemistry Letters
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bibliographicCitation	Cumming JG, Bower JF, Waterson D, Faull A, Poyser PJ, Turner P, McDermott B, Campbell AD, Hudson J, James M, Winter J, Wood C. The design and synthesis of novel, potent and orally bioavailable N-aryl piperazine-1-carboxamide CCR2 antagonists with very high hERG selectivity. Bioorganic & Medicinal Chemistry Letters. 2012 Jun;22(12):3895–9. doi: 10.1016/j.bmcl.2012.04.118.
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date	2012-06-15-04:00^^<http://www.w3.org/2001/XMLSchema#date>
identifier	https://pubmed.ncbi.nlm.nih.gov/22608963 https://doi.org/10.1016/j.bmcl.2012.04.118
isPartOf	https://portal.issn.org/resource/ISSN/0960-894X http://rdf.ncbi.nlm.nih.gov/pubchem/journal/20409
language	English
source	https://www.crossref.org/ https://pubmed.ncbi.nlm.nih.gov/
title	The design and synthesis of novel, potent and orally bioavailable N-aryl piperazine-1-carboxamide CCR2 antagonists with very high hERG selectivity
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