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Identification of novel pyrrolopyrimidine and pyrrolopyridine derivatives as potent ENPP1 inhibitors
In an effort to discover novel scaffolds of non-nucleotide-derived Ectonucleotide pyrophosphatase/phosphodiesterase 1 (ENPP1) inhibitors to stimulate the Stimulator of Interferon Genes (STING) pathway, we designed and synthesised pyrrolopyrimidine and pyrrolopyridine derivatives and performed struct...
Autores principales: | , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Taylor & Francis
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9467556/ https://www.ncbi.nlm.nih.gov/pubmed/36069240 http://dx.doi.org/10.1080/14756366.2022.2119566 |
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author | Jeong, Hee Jin Lee, Hye Lim Kim, Sung Joon Jeong, Jeong Hyun Ji, Su Hyun Kim, Han Byeol Kang, Miso Chung, Hwan Won Park, Chan Sun Choo, Hyunah Yoon, Hyo Jae Kim, Nam-Jung Lee, Duck-Hyung Lee, Sang Hee Han, Seo-Jung |
author_facet | Jeong, Hee Jin Lee, Hye Lim Kim, Sung Joon Jeong, Jeong Hyun Ji, Su Hyun Kim, Han Byeol Kang, Miso Chung, Hwan Won Park, Chan Sun Choo, Hyunah Yoon, Hyo Jae Kim, Nam-Jung Lee, Duck-Hyung Lee, Sang Hee Han, Seo-Jung |
author_sort | Jeong, Hee Jin |
collection | PubMed |
description | In an effort to discover novel scaffolds of non-nucleotide-derived Ectonucleotide pyrophosphatase/phosphodiesterase 1 (ENPP1) inhibitors to stimulate the Stimulator of Interferon Genes (STING) pathway, we designed and synthesised pyrrolopyrimidine and pyrrolopyridine derivatives and performed structure-activity relationship (SAR) study. We found 18p possessed high potency (IC(50) = 25.0 nM) against ENPP1, and activated STING pathway in a concentration dependent manner. Also, in response to STING pathway activation, cytokines such as IFN-β and IP-10 were induced by 18p in a concentration dependent manner. Finally, we discovered that 18p causes inhibition of tumour growth in 4T1 syngeneic mouse model. This study provides new insight into the designing of novel ENPP1 inhibitors and warrants further development of small molecule immune modulators for cancer immunotherapy. |
format | Online Article Text |
id | pubmed-9467556 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Taylor & Francis |
record_format | MEDLINE/PubMed |
spelling | pubmed-94675562022-09-13 Identification of novel pyrrolopyrimidine and pyrrolopyridine derivatives as potent ENPP1 inhibitors Jeong, Hee Jin Lee, Hye Lim Kim, Sung Joon Jeong, Jeong Hyun Ji, Su Hyun Kim, Han Byeol Kang, Miso Chung, Hwan Won Park, Chan Sun Choo, Hyunah Yoon, Hyo Jae Kim, Nam-Jung Lee, Duck-Hyung Lee, Sang Hee Han, Seo-Jung J Enzyme Inhib Med Chem Research Paper In an effort to discover novel scaffolds of non-nucleotide-derived Ectonucleotide pyrophosphatase/phosphodiesterase 1 (ENPP1) inhibitors to stimulate the Stimulator of Interferon Genes (STING) pathway, we designed and synthesised pyrrolopyrimidine and pyrrolopyridine derivatives and performed structure-activity relationship (SAR) study. We found 18p possessed high potency (IC(50) = 25.0 nM) against ENPP1, and activated STING pathway in a concentration dependent manner. Also, in response to STING pathway activation, cytokines such as IFN-β and IP-10 were induced by 18p in a concentration dependent manner. Finally, we discovered that 18p causes inhibition of tumour growth in 4T1 syngeneic mouse model. This study provides new insight into the designing of novel ENPP1 inhibitors and warrants further development of small molecule immune modulators for cancer immunotherapy. Taylor & Francis 2022-09-07 /pmc/articles/PMC9467556/ /pubmed/36069240 http://dx.doi.org/10.1080/14756366.2022.2119566 Text en © 2022 The Author(s). Published by Informa UK Limited, trading as Taylor & Francis Group. https://creativecommons.org/licenses/by/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) ), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Research Paper Jeong, Hee Jin Lee, Hye Lim Kim, Sung Joon Jeong, Jeong Hyun Ji, Su Hyun Kim, Han Byeol Kang, Miso Chung, Hwan Won Park, Chan Sun Choo, Hyunah Yoon, Hyo Jae Kim, Nam-Jung Lee, Duck-Hyung Lee, Sang Hee Han, Seo-Jung Identification of novel pyrrolopyrimidine and pyrrolopyridine derivatives as potent ENPP1 inhibitors |
title | Identification of novel pyrrolopyrimidine and pyrrolopyridine derivatives as potent ENPP1 inhibitors |
title_full | Identification of novel pyrrolopyrimidine and pyrrolopyridine derivatives as potent ENPP1 inhibitors |
title_fullStr | Identification of novel pyrrolopyrimidine and pyrrolopyridine derivatives as potent ENPP1 inhibitors |
title_full_unstemmed | Identification of novel pyrrolopyrimidine and pyrrolopyridine derivatives as potent ENPP1 inhibitors |
title_short | Identification of novel pyrrolopyrimidine and pyrrolopyridine derivatives as potent ENPP1 inhibitors |
title_sort | identification of novel pyrrolopyrimidine and pyrrolopyridine derivatives as potent enpp1 inhibitors |
topic | Research Paper |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9467556/ https://www.ncbi.nlm.nih.gov/pubmed/36069240 http://dx.doi.org/10.1080/14756366.2022.2119566 |
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