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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...

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Detalles Bibliográficos
Autores principales: 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
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Taylor & Francis 2022
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
Descripción
Sumario: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.