Insulin-incretin conjugates comprising a peptide having agonist activity at the glucagon-like 1 (GLP-1) receptor, the glucagon (GCG) receptor, and/or the gastric inhibitory protein (GIP) receptor conjugated to an insulin molecule having agonist activity at the insulin receptor and use of the conjugates for treatment of metabolic diseases, for example, Type 2 diabetes, are described.
The invention relates to compounds of the formula
to a process for making same and to the use of the products in the solid phase peptide synthesis.
The compounds of formula I are versatile peptide intermediates for the solid phase peptide synthesis (SPPS) of peptide drugs which comprise a Glu-fatty alkyl side chain building block attached to a Lys-part of the peptide chain.
The invention relates to compounds of the formula
to a process for making same and to the use of the products in the solid phase peptide synthesis.
The compounds of formula I are versatile peptide intermediates for the solid phase peptide synthesis (SPPS) of peptide drugs which comprise a Glu-fatty alkyl side chain building block attached to a Lys-part of the peptide chain.
本发明涉及如下公式的化合物,其制备方法以及将所得产物用于固相肽合成的用途。公式 I 的化合物是用于固相肽合成(SPPS)的多功能肽中间体,用于合成具有Glu-脂肪烷基侧链构建块的肽药物,该构建块连接到肽链的Lys部分。
AMINO DIACIDS CONTAINING PEPTIDE MODIFIERS
申请人:CHEMICAL & BIOPHARMACEUTICAL LABORATORIES OF PATRAS S.A.
公开号:US20160207957A1
公开(公告)日:2016-07-21
The present invention relates to peptide modifier compounds of Formula (1), or a salt thereof, wherein: a is an integer from 1 to 10, more preferably from 1 to 3; b is an integer from 0 to 7; Z is a terminal group and Y is a bivalent group. Further aspects of the invention relate to intermediates in the preparation of compounds of Formula (1), and the use of compounds of Formula 1 in the synthesis of peptide derivatives.