Literature DB >> 15127936

Novel Gly building units for backbone cyclization: synthesis and incorporation into model peptides.

Sharon Gazal1, Gary Gellerman, Chaim Gilon.   

Abstract

We report the preparation of novel building units for backbone cyclization that have the general formula Fmoc-Nalpha[CH(R)CO2Al]Gly-OH. These building units were prepared by the reductive alkylation method using allyl esters of several amino acids as starting material and hence, respectively, contain the side chain of these amino acids. These N-alkylated Gly building units were incorporated in model backbone cyclic peptides. The resulting crude backbone cyclic peptides were obtained in high degree of purity according to HPLC and mass spectrometric analyses.

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Year:  2003        PMID: 15127936     DOI: 10.1016/j.peptides.2003.09.020

Source DB:  PubMed          Journal:  Peptides        ISSN: 0196-9781            Impact factor:   3.750


  3 in total

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Authors:  Nir Qvit; Opher S Kornfeld
Journal:  J Vis Exp       Date:  2016-01-26       Impact factor: 1.355

Review 2.  Recent Innovations in Peptide Based Targeted Drug Delivery to Cancer Cells.

Authors:  Yosi Gilad; Michael Firer; Gary Gellerman
Journal:  Biomedicines       Date:  2016-05-26

3.  Cyclizing Painkillers: Development of Backbone-Cyclic TAPS Analogs.

Authors:  Alaa Talhami; Avi Swed; Shmuel Hess; Oded Ovadia; Sarit Greenberg; Adi Schumacher-Klinger; David Rosenthal; Deborah E Shalev; Mattan Hurevich; Philip Lazarovici; Amnon Hoffman; Chaim Gilon
Journal:  Front Chem       Date:  2020-11-12       Impact factor: 5.221

  3 in total

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