| Literature DB >> 3410635 |
J L Torres1, F Reig, G Valencia, R E Rodríguez, J M García-Antón.
Abstract
Different synthetic strategies have been attempted for the synthesis of a glycosylpeptide resulting from the covalent bonding of a sugar residue to the C-terminal carboxyl group of an enkephalin related pentapeptide. The final structure is: Tyr-D-Met-Gly-Phe-Pro [N1.5-beta-D-glucopyranosyl] amide. The in vitro potency on the GPI test of this analogue was IC50 = 64.0 nM. However, its antinociceptive activity by tail immersion tests, after intraperitoneal administration, was 2000 and 200 times higher than morphine in rats and mice, respectively.Entities:
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Year: 1988 PMID: 3410635 DOI: 10.1111/j.1399-3011.1988.tb00906.x
Source DB: PubMed Journal: Int J Pept Protein Res ISSN: 0367-8377