| Literature DB >> 15177461 |
Jeffrey J Hale1, George Doherty, Leslie Toth, Sander G Mills, Richard Hajdu, Carol Ann Keohane, Mark Rosenbach, James Milligan, Gan-Ju Shei, Gary Chrebet, James Bergstrom, Deborah Card, Michael Forrest, Shu-Yu Sun, Sarah West, Huijuan Xie, Naomi Nomura, Hugh Rosen, Suzanne Mandala.
Abstract
Structurally modified 3-(N-benzylamino)propylphosphonic acid S1P receptor agonists that maintain affinity for S1P1, and have decreased affinity for S1P3 are efficacious, but exhibit decreased acute cardiovascular toxicity in rodents than do nonselective agonists.Entities:
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Year: 2004 PMID: 15177461 DOI: 10.1016/j.bmcl.2004.04.070
Source DB: PubMed Journal: Bioorg Med Chem Lett ISSN: 0960-894X Impact factor: 2.823