Identification of novel pyrrolopyrimidine and pyrrolopyridine derivatives as potent ENPP1 inhibitors

Authors
Jeong, Hee JinLee, Hye LimKim, Sung JoonJeong, Jeong HyunJi, Su HyunKim, Han ByeolKang, MisoChung, Hwan WonPark, Chan SunChoo, HyunahYoon, Hyo JaeKim, Nam-JungLee, Duck-HyungLee, Sang HeeHan, Seo-Jung
Issue Date
2022-12
Publisher
Taylor & Francis
Citation
Journal of Enzyme Inhibition and Medicinal Chemistry, v.37, no.1, pp.2434 - 2451
Abstract
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 (IC50 = 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-beta 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.
Keywords
PROTEIN; NPP1; ENPP1; STING; innate immunity; cancer immunotherapy
ISSN
1475-6366
URI
https://pubs.kist.re.kr/handle/201004/114270
DOI
10.1080/14756366.2022.2119566
Appears in Collections:
KIST Article > 2022
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