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Tripeptides as Efficient Asymmetric Catalysts for 1,4-Addition Reactions of Aldehydes to Nitroolefins-A Rational Approach

Angewandte Chemie (International ed.), 2008-02, Vol.47 (10), p.1871-1874

2008

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Development of an orally delivered GLP-1 receptor agonist through peptide engineering and drug delivery to treat chronic disease

Scientific reports, 2021-11, Vol.11 (1), p.22521-22521, Article 22521

2021

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Is more better? A comparison of tri- and tetrapeptidic catalysts

Organic & biomolecular chemistry, 2017-07, Vol.15 (28), p.5877-5881

2017

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Increased Structural Complexity Leads to Higher Activity: Peptides as Efficient and Versatile Catalysts for Asymmetric Aldol Reactions

Organic letters, 2005-03, Vol.7 (6), p.1101-1103

2005

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Potency optimization of Huwentoxin-IV on hNav1.7: A neurotoxin TTX-S sodium-channel antagonist from the venom of the Chinese bird-eating spider Selenocosmia huwena

Peptides (New York, N.Y. : 1980), 2013-06, Vol.44, p.40-46

2013

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Investigating Sequence Space: How Important is the Spatial Arrangement of Functional Groups in the Asymmetric Aldol Reaction Catalyst H-Pro-Pro-Asp-NH2?

Advanced synthesis & catalysis, 2008-05, Vol.350 (7-8), p.1046-1052

2008

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TREM2 shedding by cleavage at the H157‐S158 bond is accelerated for the Alzheimer's disease‐associated H157Y variant

EMBO molecular medicine, 2017-10, Vol.9 (10), p.1366-1378

2017

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Peptidic catalysts developed by combinatorial screening methods

Current opinion in chemical biology, 2007-06, Vol.11 (3), p.269-278

2007

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Recombinant expression and in vitro characterisation of active Huwentoxin-IV

PloS one, 2013-12, Vol.8 (12), p.e83202

2013

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Systems Biology and Peptide Engineering to Overcome Absorption Barriers for Oral Peptide Delivery: Dosage Form Optimization Case Study Preceding Clinical Translation

Pharmaceutics, 2023-10, Vol.15 (10), p.2436

2023

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New ionic liquid-modified silica gels as recyclable materials for l-proline- or H–Pro–Pro–Asp–NH2-catalyzed aldol reaction

Green chemistry : an international journal and green chemistry resource : GC, 2007-01, Vol.9 (12), p.1328-1334

2007

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Ionic Liquid Acceleration of Solid-Phase Suzuki−Miyaura Cross-Coupling Reactions

Organic letters, 2002-09, Vol.4 (18), p.3071-3073

2002

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Solid-supported and pegylated H-Pro-Pro-Asp-NHR as catalysts for asymmetric aldol reactions

Biopolymers, 2006, Vol.84 (1), p.105-113

2006

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A 'triflate-like' tetrafluoroarylsulfonate linker for multifunctional solid-phase organic synthesis

Chemical communications (Cambridge, England), 2004-09 (17), p.1916-1917

2004

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Stapled Vasoactive Intestinal Peptide (VIP) Derivatives Improve VPAC2 Agonism and Glucose-Dependent Insulin Secretion

ACS medicinal chemistry letters, 2013-12, Vol.4 (12), p.1163-1168

2013

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Peptide–polyethylene glycol conjugates: Synthesis and properties of peptides bearing a C-terminal polyethylene glycol chain

Bioorganic & medicinal chemistry, 2006-09, Vol.14 (18), p.6197-6201

2006

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Separating stereoisomers of di-, tri-, and tetrapeptides using capillary electrophoresis with contactless conductivity detection

Journal of separation science, 2008-02, Vol.31 (3), p.565-573

2008

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Targeted oral peptide delivery using multi-unit particulates: Drug and permeation enhancer layering approach

Journal of controlled release, 2021-10, Vol.338, p.784-791

2021

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PS-COD and PS-9-BBN: Polymer-Supported Reagents for Solution-Phase Parallel Synthesis

Organic letters, 2005-03, Vol.7 (5), p.831-833

2005

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Functional group requirements within the peptide H-Pro-Pro-Asp-NH2 as a catalyst for aldol reactions

Tetrahedron, 2007-08, Vol.63 (35), p.8420-8424

2007

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Affinity maturation of the RLIP76 Ral binding domain to inform the design of stapled peptides targeting the Ral GTPases

The Journal of biological chemistry, 2021-01, Vol.296, p.100101, Article 100101

2021

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The discovery and maturation of peptide biologics targeting the small G-protein Cdc42: A bioblockade for Ras-driven signaling

The Journal of biological chemistry, 2020-02, Vol.295 (9), p.2866-2884

2020

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Synthesis of Functionalized 1,5-Cyclooctadienes by LICKOR Metalation

Journal of organic chemistry, 2002-08, Vol.67 (17), p.6250-6252

2002

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Is more better? A comparison of tri- and tetrapeptidic catalystsElectronic supplementary information (ESI) available. See DOI: 10.1039/c7ob01039g

2017-07

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Affinity maturation of the RLIP76 Ral binding domain to inform the design of stapled peptides targeting the Ral GTPases

The Journal of biological chemistry, 2020-11, Vol.296, p.100101

2020

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Tripeptides as Efficient Asymmetric Catalysts for 1,4-Addition Reactions of Aldehydes to Nitroolefins-A Rational Approach

Development of an orally delivered GLP-1 receptor agonist through peptide engineering and drug delivery to treat chronic disease

Is more better? A comparison of tri- and tetrapeptidic catalysts

Increased Structural Complexity Leads to Higher Activity: Peptides as Efficient and Versatile Catalysts for Asymmetric Aldol Reactions

Potency optimization of Huwentoxin-IV on hNav1.7: A neurotoxin TTX-S sodium-channel antagonist from the venom of the Chinese bird-eating spider Selenocosmia huwena

Investigating Sequence Space: How Important is the Spatial Arrangement of Functional Groups in the Asymmetric Aldol Reaction Catalyst H-Pro-Pro-Asp-NH2?

TREM2 shedding by cleavage at the H157‐S158 bond is accelerated for the Alzheimer's disease‐associated H157Y variant

Peptidic catalysts developed by combinatorial screening methods

Recombinant expression and in vitro characterisation of active Huwentoxin-IV

Systems Biology and Peptide Engineering to Overcome Absorption Barriers for Oral Peptide Delivery: Dosage Form Optimization Case Study Preceding Clinical Translation

New ionic liquid-modified silica gels as recyclable materials for l-proline- or H–Pro–Pro–Asp–NH2-catalyzed aldol reaction

Ionic Liquid Acceleration of Solid-Phase Suzuki−Miyaura Cross-Coupling Reactions

Solid-supported and pegylated H-Pro-Pro-Asp-NHR as catalysts for asymmetric aldol reactions

A 'triflate-like' tetrafluoroarylsulfonate linker for multifunctional solid-phase organic synthesis

Stapled Vasoactive Intestinal Peptide (VIP) Derivatives Improve VPAC2 Agonism and Glucose-Dependent Insulin Secretion

Peptide–polyethylene glycol conjugates: Synthesis and properties of peptides bearing a C-terminal polyethylene glycol chain

Separating stereoisomers of di-, tri-, and tetrapeptides using capillary electrophoresis with contactless conductivity detection

Targeted oral peptide delivery using multi-unit particulates: Drug and permeation enhancer layering approach

PS-COD and PS-9-BBN: Polymer-Supported Reagents for Solution-Phase Parallel Synthesis

Functional group requirements within the peptide H-Pro-Pro-Asp-NH2 as a catalyst for aldol reactions

Affinity maturation of the RLIP76 Ral binding domain to inform the design of stapled peptides targeting the Ral GTPases

The discovery and maturation of peptide biologics targeting the small G-protein Cdc42: A bioblockade for Ras-driven signaling

Synthesis of Functionalized 1,5-Cyclooctadienes by LICKOR Metalation

Is more better? A comparison of tri- and tetrapeptidic catalystsElectronic supplementary information (ESI) available. See DOI: 10.1039/c7ob01039g

Affinity maturation of the RLIP76 Ral binding domain to inform the design of stapled peptides targeting the Ral GTPases

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