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Solid phase peptide synthesis on hydrophilic supports
Authors:DARREN R. ENGLEBRETSEN  DAVID R.K. HARDING
Abstract:Beaded cellulose (Perloza) was modified with acrylonitrile followed by reduction with diborane to give a functionalised support containing aminopropyl groups. This spacer arm was then further extended with a glycolamido or an Fmoc-amino acid-4-oxymethylphenoxyacetyl moiety. A number of peptides, including the Merrifield test peptide leucyl-alanyl-glycyl-valine, leucine-enkephalin, Acyl Carrier Protein (65–74). angiotensin I and II, ACTH(4-11) and LHRH were synthesised on the aminopropyl beaded cellulose support using modified t-butyloxycarbonyl (Boc) or fluorenylmethoxycarbonyl (Fmoc) synthesis protocols. The peptides were cleaved from the support and further purified.
Keywords:acid and base labile linkers  boron trifluoride cleavage  t-butyloxycarbonyl  hydrophilic aminopropyl beaded cellulose  9-fluorenylmethyloxycarbonyl  solid phase peptide synthesis
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