Role of guanidine group at the N-terminal proctolin chain in cardioexcitatory effects in insects
- 12 January 2009
- journal article
- research article
- Published by Wiley in International Journal of Peptide and Protein Research
- Vol. 35 (1) , 12-16
- https://doi.org/10.1111/j.1399-3011.1990.tb00715.x
Abstract
Six proctolin analogues (I-VI) modified in position 1 of the peptide chain by the following amino acids: homo-Arg, Gac, Gav, Gap, Phe (p-guanidino) and Orn, were synthesized by conventional liquid phase method. The myotropic activity of the obtained peptides was investigated in cardioexcitatory test on two insect species, cockroach, Periplaneta americana L., and yellow mealworm, Tenebrio molitor.Keywords
This publication has 7 references indexed in Scilit:
- New N‐terminal modified proctolin analoguesInternational Journal of Peptide and Protein Research, 1988
- Synthesis of proctolin analogues and their cardioexcitatory effect on cockroach, Periplaneta americana L., and yellow mealworm, Tenebrio molitor L.International Journal of Peptide and Protein Research, 1986
- Analogs of the insect myotropic peptide proctolin: Synthesis and structure-activity studiesBiochemical and Biophysical Research Communications, 1979
- Synthesis of analogues of bradykinin with replacement of the arginine residues by 4-guanidinophenyl-L-alanineJournal of the Chemical Society, Perkin Transactions 1, 1977
- Peptide. XVII. Über die Synthese von Homoarginin‐BradykininenJournal für Praktische Chemie, 1970
- The use of sequestering agents in the preparation of ε-Acyl-L-lysine and δ-Acyl-L-ornithine derivativesAustralian Journal of Chemistry, 1965
- Über Peptidsynthesen, II. Herstellung und Verwendung der Dicyclohexylammoniumsalze von Acylaminosäuren und AcylpeptidenEuropean Journal of Organic Chemistry, 1961