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Synthesis and peptide binding properties of methoxypyrrole amino acids (MOPAS).

Bonauer, C. and Zabel, M. and König, B. (2004) Synthesis and peptide binding properties of methoxypyrrole amino acids (MOPAS). Org. Lett. 6, 1349 - 1352.

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Methoxypyrrole amino acids (MOPAS) have been prepared and were introduced into small peptides with hairpin structures. The intra- and intermolecular binding properties of this heterocyclic amino acid mimicking a dipeptido beta-strand was investigated by NMR titration and X-ray crystal structure analysis. The data reveal a hydrogen bonding pattern that is complementary to a peptide beta-sheet.

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Item Type:Article
Institutions:Chemistry and Pharmacy > Institut für Organische Chemie > Lehrstuhl Prof. Dr. Burkhard König
Chemistry and Pharmacy > Institut für Anorganische Chemie > Arbeitskreis Prof. Dr. Nikolaus Korber
Projects:GRK 760, Graduiertenkolleg Medizinische Chemie
Identification Number:
15101739PubMed ID
Dewey Decimal Classification:500 Science > 540 Chemistry & allied sciences
Refereed:Yes, this version has been refereed
Created at the University of Regensburg:Yes
Deposited On:05 Mar 2009 10:54
Last Modified:09 Nov 2010 14:51
Item ID:6242
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