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- W2326420717 abstract "ADVERTISEMENT RETURN TO ISSUEPREVAddition/CorrectionNEXTORIGINAL ARTICLEThis notice is a correctionCorrections to Design, Synthesis, and Biological Evaluation of 6α- and 6β-N-Heterocyclic Substituted Naltrexamine Derivatives as μ Opioid Receptor Selective AntagonistsGuo Li, Lindsey C. Aschenbach, Jianyang Chen, Michael P. Cassidy, David L. Stevens, Bichoy H. Gabra, Dana E. Selley, William L. Dewey, Richard B. Westkaemper, and Yan Zhang*Cite this: J. Med. Chem. 2009, 52, 24, 8057Publication Date (Web):November 10, 2009Publication History Published online10 November 2009Published inissue 24 December 2009https://doi.org/10.1021/jm9016224Copyright © 2009 American Chemical SocietyRIGHTS & PERMISSIONSArticle Views802Altmetric-Citations1LEARN ABOUT THESE METRICSArticle Views are the COUNTER-compliant sum of full text article downloads since November 2008 (both PDF and HTML) across all institutions and individuals. These metrics are regularly updated to reflect usage leading up to the last few days.Citations are the number of other articles citing this article, calculated by Crossref and updated daily. Find more information about Crossref citation counts.The Altmetric Attention Score is a quantitative measure of the attention that a research article has received online. Clicking on the donut icon will load a page at altmetric.com with additional details about the score and the social media presence for the given article. Find more information on the Altmetric Attention Score and how the score is calculated. Share Add toView InAdd Full Text with ReferenceAdd Description ExportRISCitationCitation and abstractCitation and referencesMore Options Share onFacebookTwitterWechatLinked InReddit PDF (563 KB) Get e-AlertsSUBJECTS:Antagonists,Ligands,Molecular design,Reaction products,Receptors Get e-Alerts" @default.
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- W2326420717 date "2009-11-10" @default.
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- W2326420717 title "Corrections to Design, Synthesis, and Biological Evaluation of 6α- and 6β-<i>N</i>-Heterocyclic Substituted Naltrexamine Derivatives as μ Opioid Receptor Selective Antagonists" @default.
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