Synthesis of the dodecapeptide amide corresponding to the entire amino acid sequence of granuliberin-R, a new frog skin peptide from Rana rugosa.
- 1 January 1978
- journal article
- research article
- Published by Pharmaceutical Society of Japan in CHEMICAL & PHARMACEUTICAL BULLETIN
- Vol. 26 (4) , 1222-1230
- https://doi.org/10.1248/cpb.26.1222
Abstract
Amino acid sequence of a new frog skin peptide named granuliberin-R [with potent mast cell degranulating activity], H-Phe-Gly-Phe-Leu-Pro-Ile-Tyr-Arg-Arg-Pro-Ala-Ser-NH2, was assessed by 2 conventional ways of synthesis: one by the methanesulfonic acid procedure and the other by the catalytic hydrogenation procedure at the final deprotection steps.This publication has 4 references indexed in Scilit:
- A new mast cell degranulating peptide, granuliberin-R, in the frog (Rana rugosa) skin.CHEMICAL & PHARMACEUTICAL BULLETIN, 1977
- A convenient synthesis of N-tert-butyloxycarbonyl-O-benzyl-L-serineThe Journal of Organic Chemistry, 1976
- Studies on peptides. 62. Synthesis of the protected octadecapeptide corresponding to positions 26 through 43 of porcine gastic inhibitory polypeptide (GIP).CHEMICAL & PHARMACEUTICAL BULLETIN, 1976
- Une nouvelle méthode de synthèse peptidiqueHelvetica Chimica Acta, 1951