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Anti-inflammatory compounds derived from Pseudopterogorgia elisabethae

Invented by: Robert S. Jacobs
Santa Barbara, CA

Russell G. Kerr
Boca Raton, FL

Originally Assigned to: The Regents of the University of California
Oakland, CA Florida Atlantic University Board of Trustees
[Now assigned to . . .]

Issued:2006-06-13
Filed:2004-08-02
Application No:10903261
Examined by:Badio; Barbara P.

Methods for treating, preventing, or inhibiting diseases and disorders associated with inflammation, cell-proliferation, and pain comprising the administration of a compound having the structural formula ##STR00001## wherein R.sub.1 is a hydrogen, alkyl, aryl, hydroxyalkyl, cycloalkyl, cycloalkenyl, carboxylic acid, alkylamino or amide group having from 2 to 20 carbon atoms, R.sub.2, R.sub.3, and R.sub.4 are each independently hydrogen or an acyl residue having from 1 to 6 carbon atoms, R.sub.5 is hydrogen, CH.sub.3, or CH.sub.2OH, and R.sub.6 is an organo group such as a hydrocarbon having from 1 to 10 carbon atoms are disclosed. Other seco-pseudopterosins and compounds related to pseudopterosins are disclosed.

[pdf] U.S. Pat. No. 7,060,686

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