Cargando…
Improved Synthesis of the Selected Serine Protease uPA Inhibitor UAMC-00050, a Lead Compound for the Treatment of Dry Eye Disease
[Image: see text] The α-aminophosphonate UAMC-00050, a newly developed trypsin-like serine protease inhibitor, is a lead compound for the treatment of dry eye syndrome and ocular inflammation. The medicinal chemistry route developed at the University of Antwerp possessed several problems hampering t...
Autores principales: | , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Chemical Society
2022
|
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9594321/ https://www.ncbi.nlm.nih.gov/pubmed/36311379 http://dx.doi.org/10.1021/acs.oprd.2c00244 |
_version_ | 1784815385907822592 |
---|---|
author | Ceradini, Davide Cacivkins, Pavel Ramos-Llorca, Alba Shubin, Kirill |
author_facet | Ceradini, Davide Cacivkins, Pavel Ramos-Llorca, Alba Shubin, Kirill |
author_sort | Ceradini, Davide |
collection | PubMed |
description | [Image: see text] The α-aminophosphonate UAMC-00050, a newly developed trypsin-like serine protease inhibitor, is a lead compound for the treatment of dry eye syndrome and ocular inflammation. The medicinal chemistry route developed at the University of Antwerp possessed several problems hampering the scale-up such as poor yields for some of the steps, hazardous reagents, and environmental footprint. Herein, we report an optimized route for the UAMC-00050, in which environmental unfriendly solvents were excluded, hazardous reagents were replaced with safer alternatives, and are more efficient in terms of atom economy. Every reaction step was optimized to reach a higher yield, and design of experiment was used to find the optimum conditions in the last step. Furthermore, all the flash chromatography purifications of intermediates were replaced with plug filtration, slurry purifications, or crystallization. The overall yield was increased from 3% in the medicinal chemistry route to 22% in the process development route. |
format | Online Article Text |
id | pubmed-9594321 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | American Chemical Society |
record_format | MEDLINE/PubMed |
spelling | pubmed-95943212022-10-26 Improved Synthesis of the Selected Serine Protease uPA Inhibitor UAMC-00050, a Lead Compound for the Treatment of Dry Eye Disease Ceradini, Davide Cacivkins, Pavel Ramos-Llorca, Alba Shubin, Kirill Org Process Res Dev [Image: see text] The α-aminophosphonate UAMC-00050, a newly developed trypsin-like serine protease inhibitor, is a lead compound for the treatment of dry eye syndrome and ocular inflammation. The medicinal chemistry route developed at the University of Antwerp possessed several problems hampering the scale-up such as poor yields for some of the steps, hazardous reagents, and environmental footprint. Herein, we report an optimized route for the UAMC-00050, in which environmental unfriendly solvents were excluded, hazardous reagents were replaced with safer alternatives, and are more efficient in terms of atom economy. Every reaction step was optimized to reach a higher yield, and design of experiment was used to find the optimum conditions in the last step. Furthermore, all the flash chromatography purifications of intermediates were replaced with plug filtration, slurry purifications, or crystallization. The overall yield was increased from 3% in the medicinal chemistry route to 22% in the process development route. American Chemical Society 2022-09-30 2022-10-21 /pmc/articles/PMC9594321/ /pubmed/36311379 http://dx.doi.org/10.1021/acs.oprd.2c00244 Text en © 2022 The Authors. Published by American Chemical Society https://creativecommons.org/licenses/by-nc-nd/4.0/Permits non-commercial access and re-use, provided that author attribution and integrity are maintained; but does not permit creation of adaptations or other derivative works (https://creativecommons.org/licenses/by-nc-nd/4.0/). |
spellingShingle | Ceradini, Davide Cacivkins, Pavel Ramos-Llorca, Alba Shubin, Kirill Improved Synthesis of the Selected Serine Protease uPA Inhibitor UAMC-00050, a Lead Compound for the Treatment of Dry Eye Disease |
title | Improved Synthesis
of the Selected Serine Protease
uPA Inhibitor UAMC-00050, a Lead Compound for the Treatment of Dry
Eye Disease |
title_full | Improved Synthesis
of the Selected Serine Protease
uPA Inhibitor UAMC-00050, a Lead Compound for the Treatment of Dry
Eye Disease |
title_fullStr | Improved Synthesis
of the Selected Serine Protease
uPA Inhibitor UAMC-00050, a Lead Compound for the Treatment of Dry
Eye Disease |
title_full_unstemmed | Improved Synthesis
of the Selected Serine Protease
uPA Inhibitor UAMC-00050, a Lead Compound for the Treatment of Dry
Eye Disease |
title_short | Improved Synthesis
of the Selected Serine Protease
uPA Inhibitor UAMC-00050, a Lead Compound for the Treatment of Dry
Eye Disease |
title_sort | improved synthesis
of the selected serine protease
upa inhibitor uamc-00050, a lead compound for the treatment of dry
eye disease |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9594321/ https://www.ncbi.nlm.nih.gov/pubmed/36311379 http://dx.doi.org/10.1021/acs.oprd.2c00244 |
work_keys_str_mv | AT ceradinidavide improvedsynthesisoftheselectedserineproteaseupainhibitoruamc00050aleadcompoundforthetreatmentofdryeyedisease AT cacivkinspavel improvedsynthesisoftheselectedserineproteaseupainhibitoruamc00050aleadcompoundforthetreatmentofdryeyedisease AT ramosllorcaalba improvedsynthesisoftheselectedserineproteaseupainhibitoruamc00050aleadcompoundforthetreatmentofdryeyedisease AT shubinkirill improvedsynthesisoftheselectedserineproteaseupainhibitoruamc00050aleadcompoundforthetreatmentofdryeyedisease |