Title of article
Delayed fibril formation of amylin(20–29) by incorporation of alkene dipeptidosulfonamide isosteres obtained by solid phase olefin cross metathesis
Author/Authors
Arwin J. Brouwer، نويسنده , , Ronald C. Elgersma، نويسنده , , Monika Jagodzinska، نويسنده , , Dirk T.S. Rijkers، نويسنده , , Rob M.J. Liskamp، نويسنده ,
Issue Information
روزنامه با شماره پیاپی سال 2008
Pages
7
From page
78
To page
84
Abstract
The synthesis of a new peptidomimetic structure, the alkene dipeptidosulfonamide isostere, is described. The synthesis is based on a cross metathesis reaction between two allylic building blocks, both in solution and on the solid phase. This method was also applicable to the solid phase synthesis of alkene dipeptide isosteres. Derivatives of amylin(20–29) containing the alkene dipeptidosulfonamide isostere as well as the alkene dipeptide isostere were successfully synthesized using the solid phase cross metathesis method. Investigation of relations between structure and fibril formation of these amylin(20–29) derivatives showed retardation of fibril formation and altered secondary structures, compared to native amylin(20–29).
Keywords
Alkenedipeptidosulfonamide isosteres , Alkenedipeptide isosteres , peptidomimetics , amyloid , Solid phase cross metathesis
Journal title
Bioorganic & Medicinal Chemistry Letters
Serial Year
2008
Journal title
Bioorganic & Medicinal Chemistry Letters
Record number
798923
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