Cargando…
Novel Small Molecule Inhibitors Targeting the IL-6/STAT3 Pathway or IL-1β
Development of small molecules that inhibit inflammatory cytokines is a desirable strategy for the treatment of inflammatory diseases such as rheumatoid arthritis (RA). Following up a previous study, we synthesized 10 novel compounds with a 2,5-diaminobenzoxazole moiety and evaluated their biologica...
Autores principales: | , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2022
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9101866/ https://www.ncbi.nlm.nih.gov/pubmed/35566047 http://dx.doi.org/10.3390/molecules27092696 |
_version_ | 1784707191683416064 |
---|---|
author | Yoo, Jihye Kim, Darong Park, Jiyoung Kim, Young-Kook Park Choo, Hea-Young Woo, Hyun Ae |
author_facet | Yoo, Jihye Kim, Darong Park, Jiyoung Kim, Young-Kook Park Choo, Hea-Young Woo, Hyun Ae |
author_sort | Yoo, Jihye |
collection | PubMed |
description | Development of small molecules that inhibit inflammatory cytokines is a desirable strategy for the treatment of inflammatory diseases such as rheumatoid arthritis (RA). Following up a previous study, we synthesized 10 novel compounds with a 2,5-diaminobenzoxazole moiety and evaluated their biological activities. Among them, compound 3e showed potent inhibitory activity on Interleukin 6 (IL-6)/Signal Transducer and Activator of Transcription 3 (STAT3) signaling inhibition (71.5%), and 3a showed excellent inhibitory activity on Interleukin 1 (IL-1β) (92.1%). To test in vivo anti-inflammatory activity, compounds 3a and 3e were administered by intraperitoneal (IP) injection after subcutaneous (SC) injection of zymosan A into the right footpad of mice. Inflammation on the footpad was reduced after administration of compounds 3a and 3e. Especially, compound 3a showed a significant ameliorative effect on zymosan-induced inflammation. From the in vivo and in vitro test results, we confirmed that our synthesized compounds are effective on the RA animal model through inhibition of the IL-6/STAT3 signaling pathway. Since drugs developed with small molecule inhibitors have several advantages over biological drugs, further study on these compounds is needed for the development of potent SMI drugs on RA. |
format | Online Article Text |
id | pubmed-9101866 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-91018662022-05-14 Novel Small Molecule Inhibitors Targeting the IL-6/STAT3 Pathway or IL-1β Yoo, Jihye Kim, Darong Park, Jiyoung Kim, Young-Kook Park Choo, Hea-Young Woo, Hyun Ae Molecules Article Development of small molecules that inhibit inflammatory cytokines is a desirable strategy for the treatment of inflammatory diseases such as rheumatoid arthritis (RA). Following up a previous study, we synthesized 10 novel compounds with a 2,5-diaminobenzoxazole moiety and evaluated their biological activities. Among them, compound 3e showed potent inhibitory activity on Interleukin 6 (IL-6)/Signal Transducer and Activator of Transcription 3 (STAT3) signaling inhibition (71.5%), and 3a showed excellent inhibitory activity on Interleukin 1 (IL-1β) (92.1%). To test in vivo anti-inflammatory activity, compounds 3a and 3e were administered by intraperitoneal (IP) injection after subcutaneous (SC) injection of zymosan A into the right footpad of mice. Inflammation on the footpad was reduced after administration of compounds 3a and 3e. Especially, compound 3a showed a significant ameliorative effect on zymosan-induced inflammation. From the in vivo and in vitro test results, we confirmed that our synthesized compounds are effective on the RA animal model through inhibition of the IL-6/STAT3 signaling pathway. Since drugs developed with small molecule inhibitors have several advantages over biological drugs, further study on these compounds is needed for the development of potent SMI drugs on RA. MDPI 2022-04-22 /pmc/articles/PMC9101866/ /pubmed/35566047 http://dx.doi.org/10.3390/molecules27092696 Text en © 2022 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Article Yoo, Jihye Kim, Darong Park, Jiyoung Kim, Young-Kook Park Choo, Hea-Young Woo, Hyun Ae Novel Small Molecule Inhibitors Targeting the IL-6/STAT3 Pathway or IL-1β |
title | Novel Small Molecule Inhibitors Targeting the IL-6/STAT3 Pathway or IL-1β |
title_full | Novel Small Molecule Inhibitors Targeting the IL-6/STAT3 Pathway or IL-1β |
title_fullStr | Novel Small Molecule Inhibitors Targeting the IL-6/STAT3 Pathway or IL-1β |
title_full_unstemmed | Novel Small Molecule Inhibitors Targeting the IL-6/STAT3 Pathway or IL-1β |
title_short | Novel Small Molecule Inhibitors Targeting the IL-6/STAT3 Pathway or IL-1β |
title_sort | novel small molecule inhibitors targeting the il-6/stat3 pathway or il-1β |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9101866/ https://www.ncbi.nlm.nih.gov/pubmed/35566047 http://dx.doi.org/10.3390/molecules27092696 |
work_keys_str_mv | AT yoojihye novelsmallmoleculeinhibitorstargetingtheil6stat3pathwayoril1b AT kimdarong novelsmallmoleculeinhibitorstargetingtheil6stat3pathwayoril1b AT parkjiyoung novelsmallmoleculeinhibitorstargetingtheil6stat3pathwayoril1b AT kimyoungkook novelsmallmoleculeinhibitorstargetingtheil6stat3pathwayoril1b AT parkchooheayoung novelsmallmoleculeinhibitorstargetingtheil6stat3pathwayoril1b AT woohyunae novelsmallmoleculeinhibitorstargetingtheil6stat3pathwayoril1b |