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Wojciech Czestkowski

Lodz University of Technology

11

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16

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Discovery of OATD-01, a First-in-Class Chitinase Inhibitor as Potential New Therapeutics for Idiopathic Pulmonary Fibrosis.

2020 Journal of Medicinal Chemistry
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Benzoxazepine-Derived, Selective, Orally Bioavailable Inhibitor of Human Acidic Mammalian Chitinase

2020 ACS Medicinal Chemistry Letters
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Development of Dual Chitinase Inhibitors as PotentialNew Treatment for Respiratory System Diseases

2019 Journal of Medicinal Chemistry
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Crystal structure of human chitotriosidase-1 (hCHIT) catalytic domain in complex with compound 7a

2018
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The first structurally analysed nucleic acid building block containing the Reese protecting group: 2'-O-[1-(2-fluorophenyl)-4-methoxypiperidin-4-yl]-β-D-(1'R,2'R,3'R,4'R)-uridine.

2015 Acta Crystallographica Section C-crystal Structure Communications
- Rafal Kruszynski
- Wojciech Czestkowski
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Crystal structure of human Arginase-2 complexed with inhibitor 11d: {(5R)-5-amino-5-carboxy-5-[(3-endo)-8-(3,4-dichlorobenzyl)-8-azabicyclo[3.2.1]oct-3-yl]pentyl}(trihydroxy)borate(1-)

2013
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1‐Bromo‐2,4‐dinitrobenzene

2002 Acta Crystallographica Section E: Crystallographic Communications
- Rafal Kruszynski
- Wojciech Czestkowski
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(3‐Methylbut‐2‐enyl)ammonium chloride

2001 Acta Crystallographica Section E-structure Reports Online
- Rafal Kruszynski
- Wojciech Czestkowski
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Citations (1)