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New Protocolin Analogues Modified in Position 2 or 3 of the Peptide Chain and Their Myotropic Effects in Insects

Identyfikatory
Warianty tytułu
Języki publikacji
EN
Abstrakty
EN
New analogues of insect neuromodulator proctolin (H-Arg-Tyr-Leu-Pro-Thr-OH) modified in position 2 and 3 of the peptide chain by natural or non-natural amino acid residues were synthesized. For modification of proctolin at position 2 a series of novel L-homophenylalanine derivatives H-Hpa(4-NO2)-OH (1), Boc-Hpa(4-NO2)-OH (2), Boc-Hpa(4-NH2)-OH (3), Boc-Hpa(4-NH-Z)-OH (4), Boc-Phg(4-Me2N)-OH (5) were obtained. The following two groups of proctolin analogues modified at positions 2 and 3such as: 1/ H-Arg-X2-Leu-Pro-Thr-OH, where X2 = Hpa (6), Hpa(4-NO2) (7), Hpa(4-NH2) (8), and Hpa(4-N-Me2) (9), and 2/ H-Arg-Tyr-X3-Pro-Thr-OH, where X3 = Ile (10), Phe (11), Arg (12), Sar (13), Nva (14), Nle (15), Asn (16), Asp (17), Gln (18), Glu (19), Lys (20), and _-Abu (21), were synthesized. Myotropic activity of proctolin analogues (6-21) was assayed in vitro on the semi-isolated heart of the yellow mealworm Tenebrio molitor. Analogues 10-12 and 20 retained more that 60% of proctolin activity. Other analogues showed a weak or none activity.
Rocznik
Strony
1425--1431
Opis fizyczny
Bibliogr. 13 poz., rys.
Twórcy
autor
  • Faculty of Chemistry, University of Wrocław, PL 50-383 Wrocław, Poland
autor
  • Department of Animal Physiology, A. Mickiewicz University, 60-225 Poznań, Poland
  • Faculty of Chemistry, University of Wrocław, PL 50-383 Wrocław, Poland
Bibliografia
  • 1. Konopińska D., J. Peptide Res., 49, 457 (1997).
  • 2. Konopińska D. and Rosiński G., J. Peptide Sei., 5, 533 (1999).
  • 3. Gray A.S., Osbome R.H. and Jewess P.J., J. Insect Physiol., 40, 595 (1994).
  • 4. Hinton J.M., Osbome R.H., Ode B., Hammond S.J. and Blagbbrough J.S., Bioorg. Med. Chem. Letters, 5, 3007 (1995).
  • 5. Hinton J.M., Osbome R.H., Bartosz-Bechowski H. and Konopińska D., J. Insect Physiol, 42, 449 (1996).
  • 6. Kuczer M., Rosiński G., Lisowski M., Picur B. and Konopińska D., Int. J. Peptide Protein Res., 48,286 (1996).
  • 7. Szeszel-Fedorowicz W., Lisowski M., Rosiński G., Issbemer J., Osbome R.H. and Konopińska D., Polish J. Chem., 75, 411 (2001).
  • 8. Konopińska D., Rosiński G. and Sobótka W., Pol. J. Pharmacol, and Pharm., 44, 505 (1992).
  • 9. Bertins J.R. and Nikiforovich G.V., Bioorg. Chimia, 5, 1581, (1979).
  • 10. Rosiński G. and Gäde G.,J. Insect Physiol, 33,451 (1988).
  • 11. Bergel F. and Stocka J.A., J. Chem. Soc., 238, 2409 (1954).
  • 12. Moroder L., Hallett A., Wünsch E., Keller O. and Wersin G., Hoppe-Seyler’s Z. Physiol Chem., 357, 1651 (1976).
  • 13. Konopińska D., Sobótka W., Lesicki A., Rosiński G. and Sujak P., Int. J, Peptide Protein Res., 27, 597 (1986).
Typ dokumentu
Bibliografia
Identyfikator YADDA
bwmeta1.element.baztech-article-BUJ1-0021-0007
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