Zobrazeno 1 - 10
of 18
pro vyhledávání: '"Robert M. Valerio"'
Publikováno v:
International Journal of Peptide and Protein Research. 33:428-438
A general method for the synthesis of O-phosphonotyrosyl peptides using solid phase methodology is described. Protected O-phosphonotyrosine derivatives with the general structure Boc-Tyr(R2PO3)-OH (R = methyl, ethyl or benzyl) were prepared as potent
Publikováno v:
Tetrahedron Letters. 37:3019-3022
Formation of ether derivatives of phenolic containing structures using solid phase Mitsunob functionalized polyethylene pins was investigated. Using the Multipin approach, a range of reaction parameters were systematically varied in parallel experime
Publikováno v:
Tetrahedron Letters. 35:9079-9082
High-power sonication enables hydrophobic peptides, that would otherwise cleave with poor efficiency, to cleave and elute from the solid support in good yield. The method is demonstrated in conjunction with the multipin method of multiple synthesis u
Publikováno v:
Reactive Polymers. 22:203-212
Radiation grafting of a range of monomers allows a diversity of surface characteristics to be generated on a common plastic support. Taken together with the modular 8-column, 12-row format used with the multipin method of peptide synthesis, many thou
Publikováno v:
The Journal of Organic Chemistry. 59:2197-2203
A method for simultaneously preparing large numbers of peptide amides is described. Side-chain deprotected, support-bound peptide esters (1) and (2) are incubated with ammonia/tetrahydrofuran vapor. The cleaved peptide amides (3) are then eluted from
Publikováno v:
Tetrahedron Letters. 34:4411-4414
Peptides prepared on Pepsyn KB resin were cleaved with ammonia/tetrahydrofuran vapour and then eluted from the resin in a two step process. The method is a general one, applicable to simultaneous multiple peptide synthesis on resin supports.
Publikováno v:
Bioorganic & Medicinal Chemistry Letters. 3:1253-1256
All possible single and multiple L- to D- amino acid replacements of a potent hexapeptide endothelin receptor ligand were synthesized and tested. While most of these 64 analogues were inactive on the ETRA receptor, three showed submicromolar activity
Publikováno v:
Bioorganic & Medicinal Chemistry Letters. 3:519-524
We determined the SAR of the potent hexapeptide endothelin ligand Ac-Dphe-Orn-Asp-Ile-Ile-Trp-OH1 (1) through the systematic replacement of each residue with 50 amino acid substitutes. Multipin peptide synthesis methods allowed us to rapidly synthesi
Publikováno v:
The Journal of Organic Chemistry. 56:6659-6666
Autor:
Nicolas Ede, N. Joe Maeji, Debra S. Chiefari, Ian W. James, Tom J. Mason, Andrew M. Bray, K. H. Ang, Robert M. Valerio, Liana M. Lagniton
Publikováno v:
Chinese Peptide Symposia ISBN: 0792349636
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::eeecacac33d1e6036df2b1fab333d626
https://doi.org/10.1007/0-306-46859-x_22
https://doi.org/10.1007/0-306-46859-x_22