1994
DOI: 10.1016/s0040-4020(01)89696-4
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Gel-phase peptide synthesis on a new high-capacity tetraethyleneglycol diacrylate-crosslinked polystyrene support: Synthesis of pardaxin 16–33.

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Cited by 54 publications
(40 citation statements)
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“…In addition to PS-DVB resin a number of polymers are used in the development of polymer 14,15 , Janda gel 16 , Tenta gel 17 and polyacrylamides 18 . Various organic polymer supports used were extensively reviewed 19,20 .…”
Section: The Selection Of Polymer Supportmentioning
confidence: 99%
“…In addition to PS-DVB resin a number of polymers are used in the development of polymer 14,15 , Janda gel 16 , Tenta gel 17 and polyacrylamides 18 . Various organic polymer supports used were extensively reviewed 19,20 .…”
Section: The Selection Of Polymer Supportmentioning
confidence: 99%
“…3. hER-NLS peptide Sepharose: The hER NLS sequence published by Chambon's group [Ylikomi et al, 1992] was used in the synthesis of hER NLS peptide. The hER amino acids 256 -303 (RKRDRGGRMLKHKRQR-DDGEGRGEVGSAGDMR AANL WPSPL-MIKRSKK) was synthesized on hydroxymethyl tetraethyleneglycol diacrylate crosslinked polystyrene support using standard Fmoc solid-phase peptide synthesis protocol [Renil et al, 1994].The coupling reactions were carried out using dicyclohexyl carbodiimide coupling procedure and threefold excess of Fmoc protected amino acid derivatives. The stepwise deprotection was carried out using 20% piperidine in N,NЈ dimethyl formamide.…”
Section: Preparation Of Affinity Matricesmentioning
confidence: 99%
“…[5][6][7][8][9] Another approach to this problem is to use PEG chains as crosslinking units within the resins. [10][11][12][13] Apart from modifications of PS-DVB, copolymerization of hydrophilic monomers has also been performed to prepare alternative materials for solid phase synthesis. [14][15][16][17][18][19][20][21][22] In a solid-phase reaction, the swollen polymer is the equivalent of the solvent in the corresponding solution-phase reaction.…”
Section: Introductionmentioning
confidence: 99%