Literature DB >> 23512744

A multiple multicomponent approach to chimeric peptide-peptoid podands.

Daniel G Rivera1, Fredy León, Odette Concepción, Fidel E Morales, Ludger A Wessjohann.   

Abstract

The success of multi-armed, peptide-based receptors in supramolecular chemistry traditionally is not only based on the sequence but equally on an appropriate positioning of various peptidic chains to create a multivalent array of binding elements. As a faster, more versatile and alternative access toward (pseudo)peptidic receptors, a new approach based on multiple Ugi four-component reactions (Ugi-4CR) is proposed as a means of simultaneously incorporating several binding and catalytic elements into organizing scaffolds. By employing α-amino acids either as the amino or acid components of the Ugi-4CRs, this multiple multicomponent process allows for the one-pot assembly of podands bearing chimeric peptide-peptoid chains as appended arms. Tripodal, bowl-shaped, and concave polyfunctional skeletons are employed as topologically varied platforms for positioning the multiple peptidic chains formed by Ugi-4CRs. In a similar approach, steroidal building blocks with several axially-oriented isocyano groups are synthesized and utilized to align the chimeric chains with conformational constrains, thus providing an alternative to the classical peptido-steroidal receptors. The branched and hybrid peptide-peptoid appendages allow new possibilities for both rational design and combinatorial production of synthetic receptors. The concept is also expandable to other multicomponent reactions.
Copyright © 2013 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim.

Entities:  

Mesh:

Substances:

Year:  2013        PMID: 23512744     DOI: 10.1002/chem.201201591

Source DB:  PubMed          Journal:  Chemistry        ISSN: 0947-6539            Impact factor:   5.236


  5 in total

Review 1.  On-resin multicomponent protocols for biopolymer assembly and derivatization.

Authors:  Daniel G Rivera; Manuel G Ricardo; Aldrin V Vasco; Ludger A Wessjohann; Erik V Van der Eycken
Journal:  Nat Protoc       Date:  2021-01-20       Impact factor: 13.491

Review 2.  Chemical Conjugation in Drug Delivery Systems.

Authors:  Alexis Eras; Danna Castillo; Margarita Suárez; Nelson Santiago Vispo; Fernando Albericio; Hortensia Rodriguez
Journal:  Front Chem       Date:  2022-05-26       Impact factor: 5.545

Review 3.  Isocyanide-based multicomponent reactions towards cyclic constrained peptidomimetics.

Authors:  Gijs Koopmanschap; Eelco Ruijter; Romano Va Orru
Journal:  Beilstein J Org Chem       Date:  2014-03-04       Impact factor: 2.883

Review 4.  Selectivity in multiple multicomponent reactions: types and synthetic applications.

Authors:  Ouldouz Ghashghaei; Francesca Seghetti; Rodolfo Lavilla
Journal:  Beilstein J Org Chem       Date:  2019-02-21       Impact factor: 2.883

5.  Consecutive isocyanide-based multicomponent reactions: synthesis of cyclic pentadepsipeptoids.

Authors:  Angélica de Fátima S Barreto; Otilie E Vercillo; Ludger A Wessjohann; Carlos Kleber Z Andrade
Journal:  Beilstein J Org Chem       Date:  2014-05-05       Impact factor: 2.883

  5 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.