β-methyl substitution of cyclohexylalanine in Dmt-Tic-Cha-Phe peptides results in highly potent δ opioid antagonists

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dc.contributor.authorToth, Gezaen
dc.contributor.authorIoja, Enikoen
dc.contributor.authorTomboly, Csabaen
dc.contributor.authorBallet, Stevenen
dc.contributor.authorTourwe, Dirken
dc.contributor.authorPeter, Antalen
dc.contributor.authorMartinek, Tamasen
dc.contributor.authorChung, Nga N.en
dc.contributor.authorSchiller, Peter W.en
dc.contributor.authorBenyhe, Sandoren
dc.contributor.authorBorsodi, Annaen
dc.contributor.schoolSchool of Chemistry and Physics : Chemistryen
dc.date.issued2006en
dc.descriptionCopyright © 2006 American Chemical Societyen
dc.identifier.citationJournal of Medicinal Chemistry, 2006; 50(2):328-333en
dc.identifier.doi10.1021/jm060721uen
dc.identifier.issn0022-2623en
dc.identifier.urihttp://hdl.handle.net/2440/47171
dc.publisherAmerican Chemical Societyen
dc.titleβ-methyl substitution of cyclohexylalanine in Dmt-Tic-Cha-Phe peptides results in highly potent δ opioid antagonistsen
dc.title.alternativebeta-methyl substitution of cyclohexylalanine in Dmt-Tic-Cha-Phe peptides results in highly potent delta opioid antagonistsen
dc.typeJournal articleen

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