Synthesis and Analgesic Activity of New Analogues of Tyr-MIF Including Pyrrole Moiety

Pain is one of many medical problems of modern society. Together with a number of other diseases such as heart attacks, strokes, tumors, etc. it ranks among the first in manifestation. There are a huge number of medical drugs more or less effective against pain in a practice. Globally, the searching...

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Bibliographic Details
Published in:International journal of peptide research and therapeutics 2016-06, Vol.22 (2), p.243-248
Main Authors: Danalev, Dancho L., Vladimirova, Stanislava P., Borisov, Borislav P., Nocheva, Hristina H., Bocheva, Adriana I., Marinkova, Dessislava A., Naydenova, Emilia D., Lozanov, Valentin S.
Format: Article
Language:English
Subjects:
Analgesics
Animal Anatomy
Biochemistry
Biomedical and Life Sciences
Chemical synthesis
Histology
Life Sciences
Molecular Medicine
Morphology
Peptides
Pharmaceutical sciences
Pharmaceutical Sciences/Technology
Pharmacology/Toxicology
Polymer Sciences
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Summary:Pain is one of many medical problems of modern society. Together with a number of other diseases such as heart attacks, strokes, tumors, etc. it ranks among the first in manifestation. There are a huge number of medical drugs more or less effective against pain in a practice. Globally, the searching of new molecules with analgesic activity and better selectivity or greater effect at lower doses continues. In addition, some groups trying to improve the properties of known molecules in medical practice as various heterocyclic compounds by modifying one or another of their part. Other groups work on the creation of new mimetics of natural molecules with well established physiological activity. In this global context, here we report the synthesis of two new compounds which are hybrid molecules between the specifically substituted pyrrole (Pyr) and analogues of Tyr-MIF-1 peptide. All investigations on the analgesic activity show better activity at the same dose than natural Tyr-MIF-1 peptide for the analogue Pyr-Tyr-Phe-Leu-Ala-OH. Compound Pyr-Ala-Leu-Phe-Tyr-OH has no better effect comparable to that of the parent peptide. The obtained results clearly show that it is essential that Tyr residue occupies N-terminal position of MIF-1 analogue. The lack of better activity of the analogue Pyr-Ala-Leu-Phe-Tyr-OH reveals that Pyr residue does not influence on the analgesic activity. In addition we found that C-terminal amide function generally presented in natural MIF-1 is not absolutely necessary for activity.
ISSN:1573-3149
1573-3904
DOI:10.1007/s10989-015-9502-8