摘要：

The present invention relates to N-terminally modified derivatives of human glucagon-like peptide-1 (GLP-1) and analogues thereof having a protracted profile of action, as well as the use of such derivatives in pharmaceutical compositions for the treatment of obesity, insulin dependent or non-insulin dependent diabetes mellitus. The GLP-1 derivatives have a lipophilic substituent attached to at least one amino acid residue and are substituted at the N-terminal end with a substituent comprising an optionally substituted 5- or 6-membered ring system, e.g. an imidazole.

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