Discovery of Novel Sphingosine-1-Phosphate-1 Receptor Agonists for the Treatment of Multiple Sclerosis

Authors
Park, Sun JunYeon, Seul KiYoowon KimKim, Hyeon JeongKIm Si WonKIM, JU SHINChoi, Ji WonByung, Eun KimElijah, Hwejin LeeKim Ri-umSEO, SEON HEELee, Jae IckJun Woo KimHa-Yeon LeeHayoung HwangYong-Sun BahnEunji CheongPark, Jong HyunPark, Ki Duk
Issue Date
2022-02
Publisher
American Chemical Society
Citation
Journal of Medicinal Chemistry, v.65, no.4, pp.3539 - 3562
Abstract
The 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.
Keywords
LYMPHOCYTE EGRESS; S1P(1); POTENT; MODULATOR; OZANIMOD; IDENTIFICATION; OPTIMIZATION; DISEASE; FTY720; ASSAY
ISSN
0022-2623
URI
https://pubs.kist.re.kr/handle/201004/76794
DOI
10.1021/acs.jmedchem.1c01979
Appears in Collections:
KIST Article > 2022
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