Conformational features responsible for the binding of cyclic analogues of enkephalin to opioid receptors III. Probable binding conformations of μ-agonists with phenylalanine in position 3
Author:
Publisher
Wiley
Subject
Biochemistry
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1399-3011.1991.tb00736.x/fullpdf
Reference22 articles.
1. Conformational features responsible for the binding of cyclic analogues of enkephalin to opioid receptors
2. A novel cyclic opioid peptide analog showing high preference for μ-receptors
3. Structure-activity relationships of cyclic opioid peptide analogs containing a phenylalanine residue in the 3-position
4. Dermorphin analogs carrying an increased positive net charge in their "message" domain display extremely high .mu.-opioid receptor selectivity
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4. 14-Membered cyclic opioids related to dermorphin and their partially retro-inverso modified analogues II. Preferred conformations in solution as studied by 1H-NMR spectroscopy;International Journal of Peptide and Protein Research;2009-01-12
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