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Natural proteinaceous inhibitors of serine proteases

Current pharmaceutical design, 2013, Vol.19 (6), p.1068

Debowski, Dawid

2013

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Design, Synthesis, and Antitumor Evaluation of an Opioid Growth Factor Bioconjugate Targeting Pancreatic Ductal Adenocarcinoma

Pharmaceutics, 2024-02, Vol.16 (2), p.283

2024

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Bowman-Birk Inhibitors: Insights into Family of Multifunctional Proteins and Peptides with Potential Therapeutical Applications

Pharmaceuticals (Basel, Switzerland), 2020-11, Vol.13 (12), p.421

2020

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Vasopressin and Its Analogues: From Natural Hormones to Multitasking Peptides

International journal of molecular sciences, 2022-03, Vol.23 (6), p.3068

2022

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Conjugates of Ciprofloxacin and Levofloxacin with Cell-Penetrating Peptide Exhibit Antifungal Activity and Mammalian Cytotoxicity

International journal of molecular sciences, 2020-06, Vol.21 (13), p.4696

2020

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Antibiotic-Based Conjugates Containing Antimicrobial HLopt2 Peptide: Design, Synthesis, Antimicrobial and Cytotoxic Activities

ACS chemical biology, 2019-10, Vol.14 (10), p.2233-2242, Article acschembio.9b00538

2019

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Lactoferricin B Combined with Antibiotics Exhibits Leukemic Selectivity and Antimicrobial Activity

Molecules (Basel, Switzerland), 2024-02, Vol.29 (3), p.678

2024

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Synthesis of Novel Arginine Building Blocks with Increased Lipophilicity Compatible with Solid-Phase Peptide Synthesis

Molecules (Basel, Switzerland), 2023-11, Vol.28 (23), p.7780

2023

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Autophagy of Candida albicans cells after the action of earthworm Venetin-1 nanoparticle with protease inhibitor activity

Scientific reports, 2023-08, Vol.13 (1), p.14228-14228, Article 14228

2023

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Antimicrobial Activity of Chimera Peptides Composed of Human Neutrophil Peptide 1 (HNP-1) Truncated Analogues and Bovine Lactoferrampin

Bioconjugate chemistry, 2018-09, Vol.29 (9), p.3060-3071

2018

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Cyclic Peptidic Furin Inhibitors Developed by Combinatorial Chemistry

ACS medicinal chemistry letters, 2023-04, Vol.14 (4), p.458-465

2023

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Natural Proteinaceous Inhibitors of Serine Proteases

Current pharmaceutical design, 2012-12, Vol.19 (6), p.1068-1084

Debowski, Dawid

2012

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Natural Proteinaceous Inhibitors of Serine Proteases

Current pharmaceutical design, 2012-12, Vol.19 (6), p.1068-1084

Debowski, Dawid

2012

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Analogues of trypsin inhibitor SFTI-1 modified in the conserved P1′ position by synthetic or non-proteinogenic amino acids retain their inhibitory activity

Journal of peptide science, 2011-04, Vol.17 (4), p.281-287

2011

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Inhibitors of Matriptase-2 Based on the Trypsin Inhibitor SFTI-1

Chembiochem : a European journal of chemical biology, 2015-07, Vol.16 (11), p.1601-1607

2015

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Peptide conjugates of lactoferricin analogues and antimicrobials—Design, chemical synthesis, and evaluation of antimicrobial activity and mammalian cytotoxicity

Peptides (New York, N.Y. : 1980), 2019-07, Vol.117, p.170079-170079, Article 170079

2019

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Matriptase-2: monitoring and inhibiting its proteolytic activity

Future medicinal chemistry, 2018-12, Vol.10 (23), p.2745-2761

2018

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Interactions between trypsin and its peptidic inhibitors studied by isothermal titration calorimetry (ITC)

Journal of thermal analysis and calorimetry, 2016-01, Vol.123 (1), p.807-812

2016

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Truncation of Huia versabilis Bowman-Birk inhibitor increases its selectivity, matriptase-1 inhibitory activity and proteolytic stability

Biochimie, 2020-04, Vol.171-172, p.178-186

2020

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Inhibition of human and yeast 20S proteasome by analogues of trypsin inhibitor SFTI-1

PloS one, 2014-02, Vol.9 (2), p.e89465-e89465

2014

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Design and chemical syntheses of potent matriptase‐2 inhibitors based on trypsin inhibitor SFTI‐1 isolated from sunflower seeds

Biopolymers, 2017-11, Vol.108 (6), p.n/a

2017

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Bladder cancer detection using a peptide substrate of the 20S proteasome

The FEBS journal, 2016-08, Vol.283 (15), p.2929-2948

2016

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Investigation of peptide splicing using two‐peptide‐chain analogs of trypsin inhibitor SFTI‐1

The FEBS journal, 2013-12, Vol.280 (23), p.6213-6222

2013

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Spliced analogues of trypsin inhibitor SFTI‐1 and their application for tracing proteolysis and delivery of cargos inside the cells

Biopolymers, 2017-03, Vol.108 (2), p.np-n/a

2017

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Introduction of non-natural amino acid residues into the substrate-specific P1 position of trypsin inhibitor SFTI-1 yields potent chymotrypsin and cathepsin G inhibitors

Bioorganic & medicinal chemistry, 2009-05, Vol.17 (9), p.3302-3307

2009

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Natural proteinaceous inhibitors of serine proteases

Design, Synthesis, and Antitumor Evaluation of an Opioid Growth Factor Bioconjugate Targeting Pancreatic Ductal Adenocarcinoma

Bowman-Birk Inhibitors: Insights into Family of Multifunctional Proteins and Peptides with Potential Therapeutical Applications

Vasopressin and Its Analogues: From Natural Hormones to Multitasking Peptides

Conjugates of Ciprofloxacin and Levofloxacin with Cell-Penetrating Peptide Exhibit Antifungal Activity and Mammalian Cytotoxicity

Antibiotic-Based Conjugates Containing Antimicrobial HLopt2 Peptide: Design, Synthesis, Antimicrobial and Cytotoxic Activities

Lactoferricin B Combined with Antibiotics Exhibits Leukemic Selectivity and Antimicrobial Activity

Synthesis of Novel Arginine Building Blocks with Increased Lipophilicity Compatible with Solid-Phase Peptide Synthesis

Autophagy of Candida albicans cells after the action of earthworm Venetin-1 nanoparticle with protease inhibitor activity

Antimicrobial Activity of Chimera Peptides Composed of Human Neutrophil Peptide 1 (HNP-1) Truncated Analogues and Bovine Lactoferrampin

Cyclic Peptidic Furin Inhibitors Developed by Combinatorial Chemistry

Natural Proteinaceous Inhibitors of Serine Proteases

Natural Proteinaceous Inhibitors of Serine Proteases

Analogues of trypsin inhibitor SFTI-1 modified in the conserved P1′ position by synthetic or non-proteinogenic amino acids retain their inhibitory activity

Inhibitors of Matriptase-2 Based on the Trypsin Inhibitor SFTI-1

Peptide conjugates of lactoferricin analogues and antimicrobials—Design, chemical synthesis, and evaluation of antimicrobial activity and mammalian cytotoxicity

Matriptase-2: monitoring and inhibiting its proteolytic activity

Interactions between trypsin and its peptidic inhibitors studied by isothermal titration calorimetry (ITC)

Truncation of Huia versabilis Bowman-Birk inhibitor increases its selectivity, matriptase-1 inhibitory activity and proteolytic stability

Inhibition of human and yeast 20S proteasome by analogues of trypsin inhibitor SFTI-1

Design and chemical syntheses of potent matriptase‐2 inhibitors based on trypsin inhibitor SFTI‐1 isolated from sunflower seeds

Bladder cancer detection using a peptide substrate of the 20S proteasome

Investigation of peptide splicing using two‐peptide‐chain analogs of trypsin inhibitor SFTI‐1

Spliced analogues of trypsin inhibitor SFTI‐1 and their application for tracing proteolysis and delivery of cargos inside the cells

Introduction of non-natural amino acid residues into the substrate-specific P1 position of trypsin inhibitor SFTI-1 yields potent chymotrypsin and cathepsin G inhibitors

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