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Folding and self-assembly of aromatic and aliphatic urea oligomers: Towards connecting structure and function

Organic & biomolecular chemistry, 2010-07, Vol.8 (14), p.311-3117

2010

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Peptide-oligourea hybrids analogue of GLP-1 with improved action in vivo

Nature communications, 2019-02, Vol.10 (1), p.924-924, Article 924

2019

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Anion Recognition by Aliphatic Helical Oligoureas

Chemistry : a European journal, 2016-10, Vol.22 (44), p.15684-15692

2016

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Delivery of siRNA by tailored cell-penetrating urea-based foldamers

Chemical communications (Cambridge, England), 2021-02, Vol.57 (12), p.1458-1461

2021

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Helical Oligourea Foldamers as Powerful Hydrogen Bonding Catalysts for Enantioselective C–C Bond-Forming Reactions

Journal of the American Chemical Society, 2017-09, Vol.139 (36), p.12524-12532

2017

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Shaping quaternary assemblies of water-soluble non-peptide helical foldamers by sequence manipulation

Nature chemistry, 2015-11, Vol.7 (11), p.871-878

2015

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Synthetic foldamers

Chemical communications (Cambridge, England), 2011-01, Vol.47 (21), p.5933-5941

2011

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N-glycosylation of mouse TRAIL-R and human TRAIL-R1 enhances TRAIL-induced death

Cell death and differentiation, 2017-03, Vol.24 (3), p.500-510

2017

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Iterative Structure-Based Optimization of Short Peptides Targeting the Bacterial Sliding Clamp

Journal of medicinal chemistry, 2021-12, Vol.64 (23), p.17063-17078

2021

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Design of Oligourea-Based Foldamers with Antibacterial and Antifungal Activities

Molecules (Basel, Switzerland), 2022-03, Vol.27 (5), p.1749

2022

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Consequences of Isostructural Main-Chain Modifications for the Design of Antimicrobial Foldamers: Helical Mimics of Host-Defense Peptides Based on a Heterogeneous Amide/Urea Backbone

Angewandte Chemie (International ed.), 2010-01, Vol.49 (2), p.333-336

2010

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Multivalent DR5 Peptides Activate the TRAIL Death Pathway and Exert Tumoricidal Activity

Cancer research (Chicago, Ill.), 2010-02, Vol.70 (3), p.1101-1110

2010

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Suppression of tumor growth and angiogenesis by a specific antagonist of the cell-surface expressed nucleolin

PloS one, 2008-06, Vol.3 (6), p.e2518-e2518

2008

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Structural characterization of short hybrid urea/carbamate (U/C) foldamers: A case of partial helix unwinding

Biopolymers, 2013-11, Vol.100 (6), p.687-697

2013

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Innovative Self‐Assembly of 15‐Mer Chimeric α‐Peptide–Oligourea Foldamers toward Cl−‐Selective Ion Channels

Small science, 2024-08, Vol.4 (8), p.n/a

2024

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Peptide-Based Covalent Inhibitors Bearing Mild Electrophiles to Target a Conserved His Residue of the Bacterial Sliding Clamp

JACS Au, 2024-02, Vol.4 (2), p.432-440

2024

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Multimerization of an Apoptogenic TRAIL-Mimicking Peptide by Using Adamantane-Based Dendrons

Chemistry : a European journal, 2013-01, Vol.19 (5), p.1762-1768

2013

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Structural Effect of Organic Catalytic Pairs Based on Chiral Amino(thio)ureas and Phosphazene Bases for the Isoselective Ring-Opening Polymerization of Racemic Lactide

Macromolecules, 2023-05, Vol.56 (10), p.3607-3616

2023

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Optimal anchoring of a foldamer inhibitor of ASF1 histone chaperone through backbone plasticity

Science advances, 2021-03, Vol.7 (12)

2021

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Cell-free synthesis of amyloid fibrils with infectious properties and amenable to sub-milligram magic-angle spinning NMR analysis

Communications biology, 2022-11, Vol.5 (1), p.1202-1202, Article 1202

2022

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Block Copolymer Synthesis by a Sequential Addition Strategy from the Organocatalytic Group Transfer Polymerization of Methyl Methacrylate to the Ring‐Opening Polymerization of Lactide

Macromolecular rapid communications., 2022-10, Vol.43 (20), p.e2200395-n/a

2022

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In Silico-Guided Target Identification of a Scaffold-Focused Library: 1,3,5-Triazepan-2,6-diones as Novel Phospholipase A2 Inhibitors

Journal of medicinal chemistry, 2006-11, Vol.49 (23), p.6768-6778

2006

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Small Multivalent Architectures Mimicking Homotrimers of the TNF Superfamily Member CD40L: Delineating the Relationship between Structure and Effector Function

Journal of the American Chemical Society, 2007-11, Vol.129 (44), p.13480-13492

2007

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In Situ Generated DBU⋅HF Acts as a Fluorinating Agent in a Hexafluoroisobutylation Tandem Reaction: An Effective Route to 5,5,5,5’,5’,5’‐Hexafluoroleucine

European journal of organic chemistry, 2023-03, Vol.26 (10), p.n/a

2023

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Front Cover: In Situ Generated DBU⋅HF Acts as a Fluorinating Agent in a Hexafluoroisobutylation Tandem Reaction: An Effective Route to 5,5,5,5’,5’,5’‐Hexafluoroleucine (Eur. J. Org. Chem. 10/2023)

European journal of organic chemistry, 2023-03, Vol.26 (10), p.n/a

2023

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Folding and self-assembly of aromatic and aliphatic urea oligomers: Towards connecting structure and function

Peptide-oligourea hybrids analogue of GLP-1 with improved action in vivo

Anion Recognition by Aliphatic Helical Oligoureas

Delivery of siRNA by tailored cell-penetrating urea-based foldamers

Helical Oligourea Foldamers as Powerful Hydrogen Bonding Catalysts for Enantioselective C–C Bond-Forming Reactions

Shaping quaternary assemblies of water-soluble non-peptide helical foldamers by sequence manipulation

Synthetic foldamers

N-glycosylation of mouse TRAIL-R and human TRAIL-R1 enhances TRAIL-induced death

Iterative Structure-Based Optimization of Short Peptides Targeting the Bacterial Sliding Clamp

Design of Oligourea-Based Foldamers with Antibacterial and Antifungal Activities

Consequences of Isostructural Main-Chain Modifications for the Design of Antimicrobial Foldamers: Helical Mimics of Host-Defense Peptides Based on a Heterogeneous Amide/Urea Backbone

Multivalent DR5 Peptides Activate the TRAIL Death Pathway and Exert Tumoricidal Activity

Suppression of tumor growth and angiogenesis by a specific antagonist of the cell-surface expressed nucleolin

Structural characterization of short hybrid urea/carbamate (U/C) foldamers: A case of partial helix unwinding

Innovative Self‐Assembly of 15‐Mer Chimeric α‐Peptide–Oligourea Foldamers toward Cl−‐Selective Ion Channels

Peptide-Based Covalent Inhibitors Bearing Mild Electrophiles to Target a Conserved His Residue of the Bacterial Sliding Clamp

Multimerization of an Apoptogenic TRAIL-Mimicking Peptide by Using Adamantane-Based Dendrons

Structural Effect of Organic Catalytic Pairs Based on Chiral Amino(thio)ureas and Phosphazene Bases for the Isoselective Ring-Opening Polymerization of Racemic Lactide

Optimal anchoring of a foldamer inhibitor of ASF1 histone chaperone through backbone plasticity

Cell-free synthesis of amyloid fibrils with infectious properties and amenable to sub-milligram magic-angle spinning NMR analysis

Block Copolymer Synthesis by a Sequential Addition Strategy from the Organocatalytic Group Transfer Polymerization of Methyl Methacrylate to the Ring‐Opening Polymerization of Lactide

In Silico-Guided Target Identification of a Scaffold-Focused Library: 1,3,5-Triazepan-2,6-diones as Novel Phospholipase A2 Inhibitors

Small Multivalent Architectures Mimicking Homotrimers of the TNF Superfamily Member CD40L: Delineating the Relationship between Structure and Effector Function

In Situ Generated DBU⋅HF Acts as a Fluorinating Agent in a Hexafluoroisobutylation Tandem Reaction: An Effective Route to 5,5,5,5’,5’,5’‐Hexafluoroleucine

Front Cover: In Situ Generated DBU⋅HF Acts as a Fluorinating Agent in a Hexafluoroisobutylation Tandem Reaction: An Effective Route to 5,5,5,5’,5’,5’‐Hexafluoroleucine (Eur. J. Org. Chem. 10/2023)

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