Bridged bicyclic peptides as potential drug scaffolds

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Location: Deutsche Nationalbibliothek Frankfurt am Main

Extent: Online-Ressource

Language: Englisch

Bibliographic citation: In: Chem. Sci., 2015, 6, 5473-5490 - DOI: 10.1039/c5sc01699a
Postprints der Universität Potsdam : Mathematisch-Naturwissenschaftliche Reihe ; 197

Event: Veröffentlichung

(where): Potsdam

(who): Universität Potsdam

(when): 2015

Creator: Bartoloni, Marco
Jin, Xian
Marcaida, Maria José
Banha, Joao
Dibonaventura, Ivan
Bongoni, Swathi
Bartho, Kathrin
Gräbner, Olivia
Sefkow, Michael
Darbre, Tamis
Reymond, Jean-Louis

URN: urn:nbn:de:kobv:517-opus4-81239

Rights: Der Zugriff auf das Objekt ist unbeschränkt möglich.

Last update: 14.08.2025, 10:58 AM CEST

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Associated

Bartoloni, Marco
Jin, Xian
Marcaida, Maria José
Banha, Joao
Dibonaventura, Ivan
Bongoni, Swathi
Bartho, Kathrin
Gräbner, Olivia
Sefkow, Michael
Darbre, Tamis
Reymond, Jean-Louis
Universität Potsdam

Time of origin

2015

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Trying to escape from flatland : generation and biological profiling of bridged bicyclic compounds

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Structure‐Based Design of Bicyclic Helical Peptides That Target the Oncogene β‐Catenin

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Chemical and chemoenzymatic routes to bridged homoarabinofuranosylpyrimidines: Bicyclic AZT analogues

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Trying to escape from flatland : generation and biological profiling of bridged bicyclic compounds

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Trying to Escape from Flatland: Generation and Biological Profiling of Bridged Bicyclic Compounds

Chemoenzymatic tandem cyclization for the facile synthesis of bicyclic peptides

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Structure‐Based Design of Bicyclic Helical Peptides That Target the Oncogene β‐Catenin

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Biaryl ether formation on peptides to access bridged cyclopeptide natural product scaffolds

Synthesis of Cyclic and Bicyclic Peptides

Biocompatible and Selective Generation of Bicyclic Peptides **

Synthetic Strategies and Applications of Fluorine‐Containing Bridged Bicyclic Compounds

Chemical and chemoenzymatic routes to bridged homoarabinofuranosylpyrimidines: Bicyclic AZT analogues

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Trying to escape from flatland : generation and biological profiling of bridged bicyclic compounds

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Trying to Escape from Flatland: Generation and Biological Profiling of Bridged Bicyclic Compounds

Chemoenzymatic tandem cyclization for the facile synthesis of bicyclic peptides

Bicyclic RGD peptides enhance nerve growth in synthetic PEG-based Anisogels

Structure‐Based Design of Bicyclic Helical Peptides That Target the Oncogene β‐Catenin

Chemoselective conjugation of biological active peptides to functional scaffolds

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Bridged bicyclic peptides as potential drug scaffolds

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Other Objects (12)

Biaryl ether formation on peptides to access bridged cyclopeptide natural product scaffolds

Synthesis of Cyclic and Bicyclic Peptides

Biocompatible and Selective Generation of Bicyclic Peptides **

Synthetic Strategies and Applications of Fluorine‐Containing Bridged Bicyclic Compounds

Chemical and chemoenzymatic routes to bridged homoarabinofuranosylpyrimidines: Bicyclic AZT analogues

Trying to escape from flatland : generation and biological profiling of bridged bicyclic compounds

Trying to Escape from Flatland: Generation and Biological Profiling of Bridged Bicyclic Compounds

Chemoenzymatic tandem cyclization for the facile synthesis of bicyclic peptides

Bicyclic RGD peptides enhance nerve growth in synthetic PEG-based Anisogels

Structure‐Based Design of Bicyclic Helical Peptides That Target the Oncogene β‐Catenin

Structure‐Based Design of Bicyclic Helical Peptides That Target the Oncogene β‐Catenin

Chemoselective conjugation of biological active peptides to functional scaffolds

Biaryl ether formation on peptides to access bridged cyclopeptide natural product scaffolds

Synthesis of Cyclic and Bicyclic Peptides

Biocompatible and Selective Generation of Bicyclic Peptides **

Synthetic Strategies and Applications of Fluorine‐Containing Bridged Bicyclic Compounds

Chemical and chemoenzymatic routes to bridged homoarabinofuranosylpyrimidines: Bicyclic AZT analogues

Trying to escape from flatland : generation and biological profiling of bridged bicyclic compounds

Trying to Escape from Flatland: Generation and Biological Profiling of Bridged Bicyclic Compounds

Chemoenzymatic tandem cyclization for the facile synthesis of bicyclic peptides

Bicyclic RGD peptides enhance nerve growth in synthetic PEG-based Anisogels

Structure‐Based Design of Bicyclic Helical Peptides That Target the Oncogene β‐Catenin

Structure‐Based Design of Bicyclic Helical Peptides That Target the Oncogene β‐Catenin

Chemoselective conjugation of biological active peptides to functional scaffolds

Biaryl ether formation on peptides to access bridged cyclopeptide natural product scaffolds

Synthesis of Cyclic and Bicyclic Peptides

Biocompatible and Selective Generation of Bicyclic Peptides **

Synthetic Strategies and Applications of Fluorine‐Containing Bridged Bicyclic Compounds

Chemical and chemoenzymatic routes to bridged homoarabinofuranosylpyrimidines: Bicyclic AZT analogues

Trying to escape from flatland : generation and biological profiling of bridged bicyclic compounds

Trying to Escape from Flatland: Generation and Biological Profiling of Bridged Bicyclic Compounds

Chemoenzymatic tandem cyclization for the facile synthesis of bicyclic peptides

Bicyclic RGD peptides enhance nerve growth in synthetic PEG-based Anisogels

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Chemoselective conjugation of biological active peptides to functional scaffolds

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