Synthesis of a silk-inspired peptide–oligothiophene conjugate

Autor:	Elena Mena-Osteritz, Peter Bäuerle, Annette Rösler, Günther Götz, Harm-Anton Klok
Rok vydání:	2004
Předmět:	Magnetic Resonance Spectroscopy Polymers Stereochemistry Carboxylic acid Carboxylic Acids Silk Peptide Sequence (biology) Thiophenes Biochemistry Acylation chemistry.chemical_compound Microscopy Scanning Tunneling Spectroscopy Fourier Transform Infrared Physical and Theoretical Chemistry chemistry.chemical_classification Oligopeptide Molecular Structure biology Organic Chemistry technology industry and agriculture biology.organism_classification chemistry Tetra lipids (amino acids peptides and proteins) Peptides Derivative (chemistry) Conjugate
Zdroj:	Org. Biomol. Chem.. 2:3541-3544
ISSN:	1477-0539 1477-0520
DOI:	10.1039/b415454a
Popis:	The first example of an oligothiophene-peptide conjugate, which was obtained by solid-phase acylation of a resin-bound silk-inspired oligopeptide sequence with a carboxylic acid functionalized regioregular tetra(3-hexylthiophene) derivative, is reported.
Databáze:	OpenAIRE
Externí odkaz:	https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7337f540dff2869cd60a2c75c54b719b https://doi.org/10.1039/b415454a Zobrazit plný text záznamu