Literature DB >> 18032035

Delayed fibril formation of amylin(20-29) by incorporation of alkene dipeptidosulfonamide isosteres obtained by solid phase olefin cross metathesis.

Arwin J Brouwer1, Ronald C Elgersma, Monika Jagodzinska, Dirk T S Rijkers, Rob M J Liskamp.   

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).

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Year:  2007        PMID: 18032035     DOI: 10.1016/j.bmcl.2007.11.009

Source DB:  PubMed          Journal:  Bioorg Med Chem Lett        ISSN: 0960-894X            Impact factor:   2.823


  2 in total

Review 1.  Amide Bond Bioisosteres: Strategies, Synthesis, and Successes.

Authors:  Shikha Kumari; Angelica V Carmona; Amit K Tiwari; Paul C Trippier
Journal:  J Med Chem       Date:  2020-08-04       Impact factor: 7.446

2.  Preparation of Functionalized α,β-Unsaturated Sulfonamides via Olefin Cross-Metathesis.

Authors:  Łukasz Woźniak; Adam A Rajkiewicz; Louis Monsigny; Anna Kajetanowicz; Karol Grela
Journal:  Org Lett       Date:  2020-06-17       Impact factor: 6.005

  2 in total

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