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Similarity analysis, synthesis, and bioassay of antibacterial cyclic peptidomimetics

The chemical similarity of antibacterial cyclic peptides and peptidomimetics was studied in order to identify new promising cyclic scaffolds. A large descriptor space coupled with cluster analysis was employed to digitize known antibacterial structures and to gauge the potential of new peptidomimeti...

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Detalles Bibliográficos
Autores principales: Berhanu, Workalemahu M, Ibrahim, Mohamed A, Pillai, Girinath G, Oliferenko, Alexander A, Khelashvili, Levan, Jabeen, Farukh, Mirza, Bushra, Ansari, Farzana Latif, ul-Haq, Ihsan, El-Feky, Said A, Katritzky, Alan R
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Beilstein-Institut 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3458733/
https://www.ncbi.nlm.nih.gov/pubmed/23019443
http://dx.doi.org/10.3762/bjoc.8.128
Descripción
Sumario:The chemical similarity of antibacterial cyclic peptides and peptidomimetics was studied in order to identify new promising cyclic scaffolds. A large descriptor space coupled with cluster analysis was employed to digitize known antibacterial structures and to gauge the potential of new peptidomimetic macrocycles, which were conveniently synthesized by acylbenzotriazole methodology. Some of the synthesized compounds were tested against an array of microorganisms and showed antibacterial activity against Bordetella bronchistepica, Micrococcus luteus, and Salmonella typhimurium.