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Journal of medicinal chemistry · 2016

Potent and Selective Agonists of Sphingosine 1-Phosphate 1 (S1P1): Discovery and SAR of a Novel Isoxazole Based Series.

СтатьяНазвание и аннотация: Перевод в очереди
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Watterson Scott H, Guo Junqing, Spergel Steve H, Langevine Charles M, Moquin Robert V, Shen Ding Ren, Yarde Melissa, Cvijic Mary Ellen, Banas Dana, Liu Richard, Suchard Suzanne J, Gillooly Kathleen, Taylor Tracy, Rex-Rabe Sandra, Shuster David J, McIntyre Kim W, Cornelius Georgia, D'Arienzo Celia, Marino Anthony, Balimane Praveen, Warrack Bethanne, Salter-Cid Luisa, McKinnon Murray, Barrish Joel C, Carter Percy H, Pitts William J, Xie Jenny, Dyckman Alaric J

Аннотация

Sphingosine 1-phosphate (S1P) is the endogenous ligand for the sphingosine 1-phosphate receptors (S1P1-5) and evokes a variety of cellular responses through their stimulation. The interaction of S1P with the S1P receptors plays a fundamental physiological role in a number of processes including vascular development and stabilization, lymphocyte migration, and proliferation. Agonism of S1P1, in particular, has been shown to play a significant role in lymphocyte trafficking from the thymus and secondary lymphoid organs, resulting in immunosuppression. This article will detail the discovery and SAR of a potent and selective series of isoxazole based full agonists of S1P1. Isoxazole 6d demonstrated impressive efficacy when administered orally in a rat model of arthritis and in a mouse experimental autoimmune encephalomyelitis (EAE) model of multiple sclerosis.

Предметные рубрики MeSH

ИП Урсолов Владлен Сергеевич

ИНН 500118482352 · ОГРНИП 314500117700049

Реквизиты и контакты