reference/5086661

http://rdf.ncbi.nlm.nih.gov/pubchem/reference/5086661

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Predicate	Object
contentType	Journal Article
endingPage	383
issn	0960-894X
issueIdentifier	2
pageRange	379-383
publicationName	Bioorganic & Medicinal Chemistry Letters
startingPage	379
bibliographicCitation	Cole DC, Ellingboe JW, Lennox WJ, Mazandarani H, Smith DL, Stock JR, Zhang G, Zhou P, Schechter LE. N1-arylsulfonyl-3-(1,2,3,6-tetrahydropyridin-4-yl)-1H-indole derivatives are potent and selective 5-HT6 receptor antagonists. Bioorganic & Medicinal Chemistry Letters. 2005 Jan;15(2):379–83. doi: 10.1016/j.bmcl.2004.10.064.
creator	http://rdf.ncbi.nlm.nih.gov/pubchem/author/MD5_d38c3b60111c6235039680f0b5ed4a4f http://rdf.ncbi.nlm.nih.gov/pubchem/author/MD5_a40c44e34736cc2c870778c41b3c0355 http://rdf.ncbi.nlm.nih.gov/pubchem/author/MD5_0c4ca03babd7cdb0a43b5e13ca016a99 http://rdf.ncbi.nlm.nih.gov/pubchem/author/MD5_656c117e28c24b4c6195397e7772653c http://rdf.ncbi.nlm.nih.gov/pubchem/author/MD5_40d90a7002fa12d3abb1dd1849d463db http://rdf.ncbi.nlm.nih.gov/pubchem/author/MD5_659233d6efebcbd45293b5ef2ab7250a http://rdf.ncbi.nlm.nih.gov/pubchem/author/MD5_6feb699c61ceb7e77422151b26308294 http://rdf.ncbi.nlm.nih.gov/pubchem/author/MD5_42ac25b41dfe35c423604374c2f628d1 http://rdf.ncbi.nlm.nih.gov/pubchem/author/MD5_1467f5d1294bf009ba5ec34ab1122189
date	2005-01-17-04:00^^<http://www.w3.org/2001/XMLSchema#date>
identifier	https://pubmed.ncbi.nlm.nih.gov/15603958 https://doi.org/10.1016/j.bmcl.2004.10.064
isPartOf	https://portal.issn.org/resource/ISSN/0960-894X http://rdf.ncbi.nlm.nih.gov/pubchem/journal/20409
language	English
source	https://pubmed.ncbi.nlm.nih.gov/ https://www.crossref.org/
title	N1-arylsulfonyl-3-(1,2,3,6-tetrahydropyridin-4-yl)-1H-indole derivatives are potent and selective 5-HT6 receptor antagonists
discusses	http://id.nlm.nih.gov/mesh/M0011238 http://id.nlm.nih.gov/mesh/M0018620 http://id.nlm.nih.gov/mesh/M0255580 http://id.nlm.nih.gov/mesh/M0000412 http://id.nlm.nih.gov/mesh/M0019685
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