Studies on peptides. LII. Application of the trifluoromethanesulphonic acid procedure to the synthesis of a peptide with somatostatin activity
- PMID: 171088
- DOI: 10.1248/cpb.23.1596
Studies on peptides. LII. Application of the trifluoromethanesulphonic acid procedure to the synthesis of a peptide with somatostatin activity
Similar articles
-
The use of picric acid as a simple monitoring procedure for automated peptide synthesis.Anal Biochem. 1975 Dec;69(2):497-503. doi: 10.1016/0003-2697(75)90152-9. Anal Biochem. 1975. PMID: 1217716 No abstract available.
-
Peptide-chelating agent conjugate for selective targeting of somatostatin receptor type 1: synthesis and characterization.Biopolymers. 2004;76(6):527-34. doi: 10.1002/bip.20169. Biopolymers. 2004. PMID: 15526334
-
The investigation of Fmoc-cysteine derivatives in solid phase peptide synthesis.Pept Res. 1989 Jan-Feb;2(1):147-52. Pept Res. 1989. PMID: 2577698
-
[Synthesis of peptides using an organosulfonic acid deprotecting procedure].Yakugaku Zasshi. 1983 Aug;103(8):805-18. Yakugaku Zasshi. 1983. PMID: 6319661 Review. Japanese. No abstract available.
-
Radiometal-labeled somatostatin analogs for applications in cancer imaging and therapy.Methods Mol Biol. 2007;386:227-40. doi: 10.1007/978-1-59745-430-8_8. Methods Mol Biol. 2007. PMID: 18604948 Review.
Cited by
-
Cytophilic gamma-globulin and tuftsin.Surv Immunol Res. 1982;1(1):9-16. doi: 10.1007/BF02918236. Surv Immunol Res. 1982. PMID: 6195710 Review. No abstract available.
-
The characteristics of purified HL60 tuftsin receptors.Mol Cell Biochem. 1990 Jan 18;92(1):77-84. doi: 10.1007/BF00220722. Mol Cell Biochem. 1990. PMID: 2308578
MeSH terms
Substances
LinkOut - more resources
Other Literature Sources