Abstract
The synthesis of hybrid analogues of alkaloid nalindol acid and C-terminal fragments of opioid peptides aims to provide the final proof of the proposed topographical relation between opioid peptides and benzomorphan skeleton-containing alkaloids during interaction with receptors. The biological data indicate that the topographical requirements for Tyr1 and Phe4 in opioid peptides are similar for interactions with both δ and κ receptor types.
| Original language | English (US) |
|---|---|
| Pages (from-to) | 177-181 |
| Number of pages | 5 |
| Journal | Letters in Peptide Science |
| Volume | 2 |
| Issue number | 3-4 |
| DOIs | |
| State | Published - Nov 1995 |
Keywords
- Benzomorphan
- Computer-assisted intuitional analysis
- Dynorphin
- Enkephalin
- Morphinan
- Opioid
- Structure-activity relationships
ASJC Scopus subject areas
- Biochemistry