| Literature DB >> 16789756 |
Steven Ballet1, Severo Salvadori, Claudio Trapella, Sharon D Bryant, Yunden Jinsmaa, Lawrence H Lazarus, Lucia Negri, Elisa Giannini, Roberta Lattanzi, Dirk Tourwé, Gianfranco Balboni.
Abstract
The Aba-Gly scaffold, incorporated into Dmt-Tic ligands (H-Dmt-Tic-Gly-NH-CH2-Ph, H-Dmt-Tic-Gly-NH-Ph, H-Dmt-Tic-NH-CH2-Bid), exhibited mixed micro/delta or delta opioid receptor activities with micro agonism. Substitution of Tic by Aba-Gly coupled to -NH-CH2-Ph (1), -NH-Ph (2), or -Bid (Bid=1H-benzimidazole-2-yl) (3) shifted affinity (Ki(micro)=0.46, 1.48, and 19.9 nM, respectively), selectivity, and bioactivity to micro-opioid receptors. These compounds represent templates for a new class of lead opioid agonists that are easily synthesized and suitable for therapeutic pain relief.Entities:
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Year: 2006 PMID: 16789756 PMCID: PMC2983084 DOI: 10.1021/jm0603264
Source DB: PubMed Journal: J Med Chem ISSN: 0022-2623 Impact factor: 7.446