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dc.contributor.authorPark, Sun Jun-
dc.contributor.authorYeon, Seul Ki-
dc.contributor.authorYoowon Kim-
dc.contributor.authorKim, Hyeon Jeong-
dc.contributor.authorKIm Si Won-
dc.contributor.authorKIM, JU SHIN-
dc.contributor.authorChoi, Ji Won-
dc.contributor.authorByung, Eun Kim-
dc.contributor.authorElijah, Hwejin Lee-
dc.contributor.authorKim Ri-um-
dc.contributor.authorSEO, SEON HEE-
dc.contributor.authorLee, Jae Ick-
dc.contributor.authorJun Woo Kim-
dc.contributor.authorHa-Yeon Lee-
dc.contributor.authorHayoung Hwang-
dc.contributor.authorYong-Sun Bahn-
dc.contributor.authorEunji Cheong-
dc.contributor.authorPark, Jong Hyun-
dc.contributor.authorPark, Ki Duk-
dc.date.accessioned2024-01-12T03:32:29Z-
dc.date.available2024-01-12T03:32:29Z-
dc.date.created2022-03-16-
dc.date.issued2022-02-
dc.identifier.issn0022-2623-
dc.identifier.urihttps://pubs.kist.re.kr/handle/201004/76794-
dc.description.abstractThe sphingosine-1-phosphate-1 (S1P1) receptor agonists have great potential for the treatment of multiple sclerosis (MS) because they can inhibit lymphocyte egress through receptor internalization. We designed and synthesized triazole and isoxazoline derivatives to discover a novel S1P1agonist for MS treatment. Of the two scaffolds, the isoxazoline derivative was determined to have excellent in vitro efficacy and drug-like properties. Among them, compound 21l was found to have superior drug-like properties as well as excellent in vitro efficacies (EC50= 7.03 nM in β-arrestin recruitment and EC50= 11.8 nM in internalization). We also confirmed that 21l effectively inhibited lymphocyte egress in the peripheral lymphocyte count test and significantly improved the clinical score in the experimental autoimmune encephalitis MS mouse model. ? 2022 American Chemical Society. All rights reserved.-
dc.languageEnglish-
dc.publisherAmerican Chemical Society-
dc.titleDiscovery of Novel Sphingosine-1-Phosphate-1 Receptor Agonists for the Treatment of Multiple Sclerosis-
dc.typeArticle-
dc.identifier.doi10.1021/acs.jmedchem.1c01979-
dc.description.journalClass1-
dc.identifier.bibliographicCitationJournal of Medicinal Chemistry, v.65, no.4, pp.3539 - 3562-
dc.citation.titleJournal of Medicinal Chemistry-
dc.citation.volume65-
dc.citation.number4-
dc.citation.startPage3539-
dc.citation.endPage3562-
dc.description.isOpenAccessN-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
dc.identifier.wosid000797940600048-
dc.identifier.scopusid2-s2.0-85124131577-
dc.relation.journalWebOfScienceCategoryChemistry, Medicinal-
dc.relation.journalResearchAreaPharmacology & Pharmacy-
dc.type.docTypeArticle-
dc.subject.keywordPlusLYMPHOCYTE EGRESS-
dc.subject.keywordPlusS1P(1)-
dc.subject.keywordPlusPOTENT-
dc.subject.keywordPlusMODULATOR-
dc.subject.keywordPlusOZANIMOD-
dc.subject.keywordPlusIDENTIFICATION-
dc.subject.keywordPlusOPTIMIZATION-
dc.subject.keywordPlusDISEASE-
dc.subject.keywordPlusFTY720-
dc.subject.keywordPlusASSAY-
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