Synthesis of Granuliberin-R and Various Fragment Peptides and Their Histamine-Releasing Activities
Granuliberin-R and various fragment peptides were synthesized and their histaminereleasing activities were examined. The relative potencies of granuliberin-R, H-Phe-Gly-Phe-Leu-Pro-Ile-Tyr-Arg-Arg-Pro-Ala-Ser-NH2, as liberators of histamine from mast cells are very similar to those of substance P an...
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Veröffentlicht in: | Chemical & pharmaceutical bulletin 1980/03/25, Vol.28(3), pp.887-892 |
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Hauptverfasser: | , , , , , , , , , |
Format: | Artikel |
Sprache: | eng |
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Zusammenfassung: | Granuliberin-R and various fragment peptides were synthesized and their histaminereleasing activities were examined. The relative potencies of granuliberin-R, H-Phe-Gly-Phe-Leu-Pro-Ile-Tyr-Arg-Arg-Pro-Ala-Ser-NH2, as liberators of histamine from mast cells are very similar to those of substance P and bradykinin. Studies on the histamine-releasing activity of various fragment peptides of granuliberin-R showed that a 4-amino acid central sequence, -Ile-Tyr-Arg-Arg-, is the minimum requirement for the releasing action of this frog skin peptide. |
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ISSN: | 0009-2363 1347-5223 |
DOI: | 10.1248/cpb.28.887 |