Literature DB >> 2437065

Cyclization of peptides on a solid support. Application to cyclic analogs of substance P.

O Ploux, G Chassaing, A Marquet.   

Abstract

The general conditions for cyclization of peptides on polymer matrix by disulfide bridge formation are reported. This procedure is based on attack of 3-nitro-2-pyridinesulfenyl group (Npys) by a thiol function. It has been used for synthesis of five cyclic analogs of Substance P.

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Year:  1987        PMID： 2437065     DOI： 10.1111/j.1399-3011.1987.tb02242.x

Source DB:  PubMed          Journal:  Int J Pept Protein Res        ISSN： 0367-8377


  2 in total

1.  Glycosylated cell-penetrating peptides and their conjugates to a proapoptotic peptide: preparation by click chemistry and cell viability studies.

Authors:  Laurence Dutot; Pascaline Lécorché; Fabienne Burlina; Rodrigue Marquant; Vanessa Point; Sandrine Sagan; Gérard Chassaing; Jean-Maurice Mallet; Solange Lavielle
Journal:  J Chem Biol       Date:  2009-11-10

2.  Interaction of tachykinins with their receptors studied with cyclic analogues of substance P and neurokinin B.

Authors:  O Ploux; S Lavielle; G Chassaing; S Julien; A Marquet; P d'Orléans-Juste; S Dion; D Regoli; J C Beaujouan; L Bergström
Journal:  Proc Natl Acad Sci U S A       Date:  1987-11       Impact factor: 11.205
  2 in total

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