Efficient route to C2 symmetric heterocyclic backbone modified cyclic peptides
about
Click chemistry in peptide-based drug designGeneration of Candidate Ligands for Nicotinic Acetylcholine Receptors via in situ Click Chemistry with a Soluble Acetylcholine Binding Protein TemplateConformationally homogeneous heterocyclic pseudotetrapeptides as three-dimensional scaffolds for rational drug design: receptor-selective somatostatin analogues.Synthesis of chemically modified bioactive peptides: recent advances, challenges and developments for medicinal chemistry.Solid-phase peptide head-to-side chain cyclodimerization: discovery of C(2)-symmetric cyclic lactam hybrid α-melanocyte-stimulating hormone (MSH)/agouti-signaling protein (ASIP) analogues with potent activities at the human melanocortin receptorsProbing the bioactive conformation of an archetypal natural product HDAC inhibitor with conformationally homogeneous triazole-modified cyclic tetrapeptides.Peptide cyclization and cyclodimerization by Cu(I)-mediated azide-alkyne cycloaddition.Enzymatic glycosylation of triazole-linked GlcNAc/Glc-peptides: synthesis, stability and anti-HIV activity of triazole-linked HIV-1 gp41 glycopeptide C34 analogues.Contemporary strategies for peptide macrocyclization.Click to join peptides/proteins together.Design and properties of functional nanotubes from the self-assembly of cyclic peptide templates.Peptide nanotubes.An eco-compatible strategy for the diversity-oriented synthesis of macrocycles exploiting carbohydrate-derived building blocksPeptide Macrocyclization Inspired by Non-Ribosomal Imine Natural Products.Peptide tertiary structure nucleation by side-chain crosslinking with metal complexation and double "click" cycloaddition.Self-assembly of a double calix[6]arene pseudorotaxane in oriented channels.Tandem deprotection-dimerization-macrocyclization route to C(2) symmetric cyclo-tetrapeptides.A combined molecular dynamic and quantum mechanic study of the solvent and guest molecule effect on the stability and length of heterocyclic peptide nanotubes
P2860
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P2860
Efficient route to C2 symmetric heterocyclic backbone modified cyclic peptides
description
2005 nî lūn-bûn
@nan
2005年の論文
@ja
2005年論文
@yue
2005年論文
@zh-hant
2005年論文
@zh-hk
2005年論文
@zh-mo
2005年論文
@zh-tw
2005年论文
@wuu
2005年论文
@zh
2005年论文
@zh-cn
name
Efficient route to C2 symmetric heterocyclic backbone modified cyclic peptides
@ast
Efficient route to C2 symmetric heterocyclic backbone modified cyclic peptides
@en
type
label
Efficient route to C2 symmetric heterocyclic backbone modified cyclic peptides
@ast
Efficient route to C2 symmetric heterocyclic backbone modified cyclic peptides
@en
prefLabel
Efficient route to C2 symmetric heterocyclic backbone modified cyclic peptides
@ast
Efficient route to C2 symmetric heterocyclic backbone modified cyclic peptides
@en
P2093
P2860
P356
P1433
P1476
Efficient route to C2 symmetric heterocyclic backbone modified cyclic peptides
@en
P2093
Jan H van Maarseveen
M Reza Ghadiri
W Seth Horne
P2860
P304
P356
10.1021/OL0518028
P407
P577
2005-09-01T00:00:00Z