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Identification of novel pyrrolopyrimidine and pyrrolopyridine derivatives as potent ENPP1 inhibitors

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dc.contributor.authorJeong, Hee Jin-
dc.contributor.authorLee, Hye Lim-
dc.contributor.authorKim, Sung Joon-
dc.contributor.authorJeong, Jeong Hyun-
dc.contributor.authorJi, Su Hyun-
dc.contributor.authorKim, Han Byeol-
dc.contributor.authorKang, Miso-
dc.contributor.authorChung, Hwan Won-
dc.contributor.authorPark, Chan Sun-
dc.contributor.authorChoo, Hyunah-
dc.contributor.authorYoon, Hyo Jae-
dc.contributor.authorKim, Nam-Jung-
dc.contributor.authorLee, Duck-Hyung-
dc.contributor.authorLee, Sang Hee-
dc.contributor.authorHan, Seo-Jung-
dc.date.accessioned2022-09-23T03:40:41Z-
dc.date.available2022-09-23T03:40:41Z-
dc.date.created2022-09-23-
dc.date.issued2022-12-31-
dc.identifier.issn1475-6366-
dc.identifier.urihttps://scholar.korea.ac.kr/handle/2021.sw.korea/143706-
dc.description.abstractIn 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.-
dc.languageEnglish-
dc.language.isoen-
dc.publisherTAYLOR & FRANCIS LTD-
dc.subjectPROTEIN-
dc.subjectNPP1-
dc.titleIdentification of novel pyrrolopyrimidine and pyrrolopyridine derivatives as potent ENPP1 inhibitors-
dc.typeArticle-
dc.contributor.affiliatedAuthorYoon, Hyo Jae-
dc.identifier.doi10.1080/14756366.2022.2119566-
dc.identifier.scopusid2-s2.0-85137311073-
dc.identifier.wosid000850701000001-
dc.identifier.bibliographicCitationJOURNAL OF ENZYME INHIBITION AND MEDICINAL CHEMISTRY, v.37, no.1, pp.2434 - 2451-
dc.relation.isPartOfJOURNAL OF ENZYME INHIBITION AND MEDICINAL CHEMISTRY-
dc.citation.titleJOURNAL OF ENZYME INHIBITION AND MEDICINAL CHEMISTRY-
dc.citation.volume37-
dc.citation.number1-
dc.citation.startPage2434-
dc.citation.endPage2451-
dc.type.rimsART-
dc.type.docTypeArticle-
dc.description.journalClass1-
dc.description.isOpenAccessY-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
dc.relation.journalResearchAreaBiochemistry & Molecular Biology-
dc.relation.journalResearchAreaPharmacology & Pharmacy-
dc.relation.journalWebOfScienceCategoryBiochemistry & Molecular Biology-
dc.relation.journalWebOfScienceCategoryChemistry, Medicinal-
dc.subject.keywordPlusNPP1-
dc.subject.keywordPlusPROTEIN-
dc.subject.keywordAuthorENPP1-
dc.subject.keywordAuthorSTING-
dc.subject.keywordAuthorcancer immunotherapy-
dc.subject.keywordAuthorinnate immunity-
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