Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
1362190 | Bioorganic & Medicinal Chemistry Letters | 2011 | 4 Pages |
Abstract
Each stereoisomer of 3-[methyl(1,2,3,4-tetrahydro-2-naphthalenyl)amino]-1-indanone, 1a–d, was prepared and evaluated in vitro for its ability to prevent mediator release induced by different degranulating agents from rodent mast cells and also in vivo against passive cutaneous anaphylaxis. The manner in which the stereoisomers prevented direct membrane activation was found to be highly dependent on the stereochemistry of the individual isomers. Stereoisomer 1b was the most active isomer in vivo, exhibiting superior activity to disodium cromoglycate.
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Related Topics
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Authors
Adam J. Byrne, James W. Barlow, John J. Walsh,