Abstract
They are attempts to correlate the topography of the bioactive structures of DPDPE and deltorphins, two delta active peptide families. One of the methods utilized by us is the hybridization of necesary elements for bioactivity of these opioid peptide groups. We have found that a major point determining high activity of hybrid analogues is also the chirality of the amino acid residue in position 5. Replacing D-Pen(5) with L-Pen(5) resulted in dramatic increases in affinity for opioid delta receptors
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