Orally available sphingosine 1-phosphate receptor agonists and antagonists

作者: Timothy L. MacDonald , Kevin R. Lynch

DOI:

关键词: ArylS1P receptor activityStereochemistryTautomerChemistryAlkylPhosphatePhosphonateSphingosine-1-phosphate receptor

摘要: The present invention relates to S1P analogs that have activity as receptor modulating agents and the use of such compounds treat diseases associated with inappropriate activity. general structure (I) wherein R 11 is C 5 -C 18 alkyl or alkenyl; Q selected from group consisting 3 6 optionally substituted cycloalkyl, heterocyclic, aryl heteroaryl and; 2 H, 1 4 alkyl, (C alkyl)OH alkyl)NH ; 23 H 15 a phosphonate ester phosphate pharmaceutically acceptable salt tautomer thereof.

参考文章(53)
Diana Peters, Tejal B. Vyas, Ashwani K. Gupta, Fatemeh Kooshesh, Rajender Kamboj, Donald G. Munroe, Identification of lysolipid receptors involved in inflammatory response ,(1998)
Hideo Ohta, Akihiro Ueno, Tomoko Watanabe, Mikio Yagi, Rika Nagao, Novel isoxazole and thiazole compounds and use thereof as drugs ,(2001)
Ghotas Evindar, Ashis K. Saha, Malcolm J. Kavarana, Barry Morgan, Alexander L. Satz, Methods and compositions for modulating sphingosine-1-phosphate (s1p) receptor activity ,(2005)
George A. Doherty, Edward M. Scolnick, Richard Hajdu, Jeffrey J. Hale, Zhen Li, Sander G. Mills, Michael J. Forrest, Suzanne M. Mandala, Hugh Rosen, Selective s1p1/edg1 receptor agonists ,(2003)
Mark D. Okusa, Timothy L. MacDonald, Christopher E. Heise, Webster L. Santos, Kevin R. Lynch, Novel lysophosphatidic acid receptor agonists and antagonists ,(2001)
Alexandre L'Heureux, Yong-Jin Wu, Li-Qiang Sun, Huan He, 1-aryl-2-hydroxyethyl amides as potassium channel openers ,(2003)
Peter Buehlmayer, Carsten Spanka, Klaus Hinterding, Frédéric Zecri, Amino-propanol derivatives ,(2003)