Synthesis and biological evaluation of γ-aminophosphonates as potent, subtype-selective sphingosine 1-phosphate receptor agonists and antagonists
- 15 January 2007
- journal article
- Published by Elsevier BV in Bioorganic & Medicinal Chemistry
- Vol. 15 (2), 663-677
- https://doi.org/10.1016/j.bmc.2006.10.060
Abstract
No abstract availableKeywords
This publication has 41 references indexed in Scilit:
- Enhancement of capillary leakage and restoration of lymphocyte egress by a chiral S1P1 antagonist in vivoNature Chemical Biology, 2006
- Selective sphingosine 1-phosphate 1 receptor activation reduces ischemia-reperfusion injury in mouse kidneyAmerican Journal of Physiology-Renal Physiology, 2006
- Asymmetric synthesis and biological evaluation of the enantiomeric isomers of the immunosuppressive FTY720-phosphateBioorganic & Medicinal Chemistry, 2005
- Synthesis of benzimidazole based analogues of sphingosine-1-phosphate: discovery of potent, subtype-selective S1P4 receptor agonistsBioorganic & Medicinal Chemistry Letters, 2004
- Ligand-, Copper-, and Amine-Free Sonogashira Reaction of Aryl Iodides and Bromides with Terminal AlkynesThe Journal of Organic Chemistry, 2004
- Syntheses of sphingosine-1-phosphate analogues and their interaction with EDG/S1P receptorsBioorganic & Medicinal Chemistry Letters, 2004
- Identification of Edg1 Receptor Residues That Recognize Sphingosine 1-PhosphatePublished by Elsevier BV ,2000
- Mild, efficient cleavage of arenesulfonamides by magnesium reductionChemical Communications, 1997
- The Improved Synthesis of Boc-Abu(PO3Me2)-OH and Its Use for the Facile Synthesis of Glu-Abu(P)-LeuAustralian Journal of Chemistry, 1992
- A greatly improved procedure for ruthenium tetroxide catalyzed oxidations of organic compoundsThe Journal of Organic Chemistry, 1981