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Advanced Glycation End-Products (AGEs): Formation, Chemistry, Classification, Receptors, and Diseases Related to AGEs

Cells (Basel, Switzerland), 2022-04, Vol.11 (8), p.1312

2022

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Ice Binding Proteins: Diverse Biological Roles and Applications in Different Types of Industry

Biomolecules (Basel, Switzerland), 2020-02, Vol.10 (2), p.274

2020

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A fluorinated indole‐based MDM2 antagonist selectively inhibits the growth of p53wt osteosarcoma cells

The FEBS journal, 2019-04, Vol.286 (7), p.1360-1374

2019

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Optimized Inhibitors of MDM2 via an Attempted Protein‐Templated Reductive Amination

ChemMedChem, 2020-02, Vol.15 (4), p.370-375

2020

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Novel Cold-Adapted Recombinant Laccase KbLcc1 from Kabatiella bupleuri G3 IBMiP as a Green Catalyst in Biotransformation

International journal of molecular sciences, 2021-09, Vol.22 (17), p.9593

2021

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Green Oxidation of Amines by a Novel Cold-Adapted Monoamine Oxidase MAO P3 from Psychrophilic Fungi Pseudogymnoascus sp. P3

Molecules (Basel, Switzerland), 2021-10, Vol.26 (20), p.6237

2021

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Screening of Novel Laccase Producers—Isolation and Characterization of Cold-Adapted Laccase from Kabatiella bupleuri G3 Capable of Synthetic Dye Decolorization

Biomolecules (Basel, Switzerland), 2021-06, Vol.11 (6), p.828

2021

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Two‐Step Synthesis of Complex Artificial Macrocyclic Compounds

Angewandte Chemie International Edition, 2017-08, Vol.56 (36), p.10725-10729

International ed. in English, 2017

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An update patent review of MDM2-p53 interaction inhibitors (2019-2023)

Expert opinion on therapeutic patents, 2024-10

Twarda-Clapa, Aleksandra

2024

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2,3′-Bis(1′H-indole) heterocycles: New p53/MDM2/MDMX antagonists

Bioorganic & medicinal chemistry letters, 2015-12, Vol.25 (24), p.5661-5666

2015

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Epitope specificity and IgG subclass distribution of autoantibodies to cardiac troponin

Clinical chemistry (Baltimore, Md.), 2013-03, Vol.59 (3), p.512-518

2013

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Two‐Step Synthesis of Complex Artificial Macrocyclic Compounds

Angewandte Chemie, 2017-08, Vol.129 (36), p.10865-10869

2017

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Systematic ‘foldamerization’ of peptide inhibiting p53-MDM2/X interactions by the incorporation of trans- or cis-2-aminocyclopentanecarboxylic acid residues

European journal of medicinal chemistry, 2020-12, Vol.208, p.112814, Article 112814

2020

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Discovery of Highly Potent p53-MDM2 Antagonists and Structural Basis for Anti-Acute Myeloid Leukemia Activities

ACS chemical biology, 2014-03, Vol.9 (3), p.802-811

2014

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Structural Characterization of Human Coronavirus NL63 N Protein

Journal of virology, 2017-06, Vol.91 (11)

2017

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1,4,5-Trisubstituted Imidazole-Based p53–MDM2/MDMX Antagonists with Aliphatic Linkers for Conjugation with Biological Carriers

Journal of medicinal chemistry, 2017-05, Vol.60 (10), p.4234-4244

2017

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Crystal structure of the FAS1 domain of the hyaluronic acid receptor stabilin‐2

Acta crystallographica. Section D, Biological crystallography., 2018-07, Vol.74 (7), p.695-701

2018

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Rational design and synthesis of 1,5-disubstituted tetrazoles as potent inhibitors of the MDM2-p53 interaction

European journal of medicinal chemistry, 2017-01, Vol.126, p.384-407

2017

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Artificial Macrocycles as Potent p53–MDM2 Inhibitors

ACS medicinal chemistry letters, 2017-10, Vol.8 (10), p.1025-1030

2017

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The synthesis and characterization of tetramic acid derivatives as Mdm2-p53 inhibitors

Journal of molecular structure, 2019-08, Vol.1189, p.161-174

2019

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Hitting on the move: Targeting intrinsically disordered protein states of the MDM2-p53 interaction

European journal of medicinal chemistry, 2019-11, Vol.182, p.111588-111588, Article 111588

2019

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A fluorinated indole‐based MDM 2 antagonist selectively inhibits the growth of p53 wt osteosarcoma cells

The FEBS journal, 2019-04, Vol.286 (7), p.1360-1374

2019

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A Unique Mdm2-Binding Mode of the 3‑Pyrrolin-2-one- and 2‑Furanone-Based Antagonists of the p53-Mdm2 Interaction

ACS chemical biology, 2016-12, Vol.11 (12), p.3310-3318

2016

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2,30-Bis(10H-indole) heterocycles: New p53/MDM2/MDMX antagonists

Bioorganic & medicinal chemistry letters, 2015-12, Vol.25 (24), p.5661-5666

2015

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NMR fragment-based screening for development of the CD44-binding small molecules

Bioorganic chemistry, 2019-02, Vol.82, p.284-289

2019

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Advanced Glycation End-Products (AGEs): Formation, Chemistry, Classification, Receptors, and Diseases Related to AGEs

Ice Binding Proteins: Diverse Biological Roles and Applications in Different Types of Industry

A fluorinated indole‐based MDM2 antagonist selectively inhibits the growth of p53wt osteosarcoma cells

Optimized Inhibitors of MDM2 via an Attempted Protein‐Templated Reductive Amination

Novel Cold-Adapted Recombinant Laccase KbLcc1 from Kabatiella bupleuri G3 IBMiP as a Green Catalyst in Biotransformation

Green Oxidation of Amines by a Novel Cold-Adapted Monoamine Oxidase MAO P3 from Psychrophilic Fungi Pseudogymnoascus sp. P3

Screening of Novel Laccase Producers—Isolation and Characterization of Cold-Adapted Laccase from Kabatiella bupleuri G3 Capable of Synthetic Dye Decolorization

Two‐Step Synthesis of Complex Artificial Macrocyclic Compounds

An update patent review of MDM2-p53 interaction inhibitors (2019-2023)

2,3′-Bis(1′H-indole) heterocycles: New p53/MDM2/MDMX antagonists

Epitope specificity and IgG subclass distribution of autoantibodies to cardiac troponin

Two‐Step Synthesis of Complex Artificial Macrocyclic Compounds

Systematic ‘foldamerization’ of peptide inhibiting p53-MDM2/X interactions by the incorporation of trans- or cis-2-aminocyclopentanecarboxylic acid residues

Discovery of Highly Potent p53-MDM2 Antagonists and Structural Basis for Anti-Acute Myeloid Leukemia Activities

Structural Characterization of Human Coronavirus NL63 N Protein

1,4,5-Trisubstituted Imidazole-Based p53–MDM2/MDMX Antagonists with Aliphatic Linkers for Conjugation with Biological Carriers

Crystal structure of the FAS1 domain of the hyaluronic acid receptor stabilin‐2

Rational design and synthesis of 1,5-disubstituted tetrazoles as potent inhibitors of the MDM2-p53 interaction

Artificial Macrocycles as Potent p53–MDM2 Inhibitors

The synthesis and characterization of tetramic acid derivatives as Mdm2-p53 inhibitors

Hitting on the move: Targeting intrinsically disordered protein states of the MDM2-p53 interaction

A fluorinated indole‐based MDM 2 antagonist selectively inhibits the growth of p53 wt osteosarcoma cells

A Unique Mdm2-Binding Mode of the 3‑Pyrrolin-2-one- and 2‑Furanone-Based Antagonists of the p53-Mdm2 Interaction

2,30-Bis(10H-indole) heterocycles: New p53/MDM2/MDMX antagonists

NMR fragment-based screening for development of the CD44-binding small molecules

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