Results 311 to 320 of about 211,010 (331)
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Synthesis of Cyclic Endiamino Peptides

Journal of the American Chemical Society, 2005
Several building blocks for endiamino peptides, as well as several cyclic endiamino peptides themselves, and pyrazin-6-one, which embodies the endiamino group, were prepared. The variety of synthesized compounds shows the potential of this synthesis in the preparation of many different groups of compounds.
Doron, Pappo   +3 more
openaire   +2 more sources

All-cis Cyclic Peptides

Journal of the American Chemical Society, 2005
Amide bonds -NH-CO- preferentially exist in trans conformations, the cis conformation being thermodynamically unfavored with respect to the trans by about 2 kcal/mol. Yet, the main reason most proteins or peptides cannot be made from cis-peptide plaques only lies in that connecting them into open chains appears to be sterically impracticable.
Romuald, Poteau, Georges, Trinquier
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Synthesis of cyclic tryptathionine peptides

International Journal of Peptide and Protein Research, 1987
The helicity of the tryptathionine moiety of the phallotoxins has been recognized by comparison with cyclic tryptathionine tripeptides. In order to investigate the influence of the configuration of the component amino acids on the conformation of the cyclic peptides, six analogue thioether tripeptides containing L‐ and D‐alanine and L‐ and D‐cysteine ...
Zanotti, G., Beijer, B., Wieland, T.
openaire   +3 more sources

Cyclic peptides revisited

Biopolymers, 1985
AbstractA multistep computational scheme was used to deduce possible conformations for a cyclic antagonist analog of somatostatin that has been reported by Coy and coworkers. An algebraic algorithm was used to find dihedral angles that give cyclic structures, the energy was computed for these structures, the lower‐energy structures were classified into
openaire   +1 more source

Cyclic Peptide Synthesis with Thioacids

Organic Letters, 2010
C-Terminal amino acid 9-fluorenylmethylthioesters may be carried through Boc chemistry solution phase peptide synthesis sequences. After insertion of the final residue in the form of an Fmoc carbamate, treatment with piperidine releases a seco-peptide as a C-terminal thioacid that on treatment with Sanger's reagent undergoes cyclization to a cyclic ...
Sasaki, Kaname, Crich, David
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New cyclic peptide proteasome inhibitors

Bioorganic & Medicinal Chemistry Letters, 2009
Here we report the study of a new series of vinyl ester cyclopeptide analogues synthesized on the basis of our previous development of a class of cyclopeptides derived from our linear prototype inhibitors. In these compounds, the exocyclic pharmacophoric unit Leu-VE was linked to the gamma-carboxyl group of the glutamic acid residue at the C-terminal ...
BALDISSEROTTO, Anna   +3 more
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Synthesis of Cyclic Peptides and Cyclic Proteins via Ligation of Peptide Hydrazides

ChemBioChem, 2012
Intramolecular ligation of peptide hydrazides is reported to occur readily, causing the lactamization of fully unprotected peptides in an epimerization-free manner. This method relies on the routine procedures of Fmoc solid-phase peptide synthesis. It can be used to prepare cyclic peptides and cyclic proteins under simpler, mild conditions at lower ...
Ji-Shen, Zheng   +4 more
openaire   +2 more sources

Cyclic, Modified and Conjugated Peptides

ChemInform, 2003
AbstractFor Abstract see ChemInform Abstract in Full Text.
openaire   +1 more source

Cyclic peptides. Amino acid-cyclic peptides complexes

Journal of the American Chemical Society, 1974
Charles M. Deber, Elkan R. Blout
openaire   +1 more source

Cyclic Peptides

2008
Juan Granja, Roberto Brea
openaire   +1 more source

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