Literature DB >> 22429468

Indole-propionic acid derivatives as potent, S1P3-sparing and EAE efficacious sphingosine-1-phosphate 1 (S1P1) receptor agonists.

Qinghua Meng1, Baowei Zhao, Qiongfeng Xu, Xuesong Xu, Guanghui Deng, Chengyong Li, Linbo Luan, Feng Ren, Hailong Wang, Heng Xu, Yan Xu, Haibo Zhang, Jia-Ning Xiang, John D Elliott, Taylor B Guo, Yonggang Zhao, Wei Zhang, Hongtao Lu, Xichen Lin.   

Abstract

Novel indole-propionic acid derivatives were developed as sphingosine-1-phosphate (S1P) receptor agonists through a systematic SAR study. The optimized and S1P(3) selective S1P(1) agonist 9f induced peripheral blood lymphocyte reduction in vivo and has an excellent efficacy in mouse experimental autoimmune encephalomyelitis (EAE).
Copyright © 2012 Elsevier Ltd. All rights reserved.

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Year:  2012        PMID: 22429468     DOI: 10.1016/j.bmcl.2012.02.083

Source DB:  PubMed          Journal:  Bioorg Med Chem Lett        ISSN: 0960-894X            Impact factor:   2.823


  3 in total

Review 1.  Modulators of the Sphingosine 1-phosphate receptor 1.

Authors:  Mariangela Urbano; Miguel Guerrero; Hugh Rosen; Edward Roberts
Journal:  Bioorg Med Chem Lett       Date:  2013-09-29       Impact factor: 2.823

Review 2.  Fatty acids role in multiple sclerosis as "metabokines".

Authors:  Haojun Yu; Shuwei Bai; Yong Hao; Yangtai Guan
Journal:  J Neuroinflammation       Date:  2022-06-17       Impact factor: 9.587

Review 3.  Chemical and genetic tools to explore S1P biology.

Authors:  Stuart M Cahalan
Journal:  Curr Top Microbiol Immunol       Date:  2014       Impact factor: 4.291

  3 in total

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