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US 5,514,702 AGranted
Arylamidoalkyl-N-hydroxyurea compounds having lipoxygenase inhibitory activity
AssigneeAbbott Laboratories
InventorsJoseph F. Dellaria, Dee W. Brooks, Jimmie L. Moore, Kevin J. Sallin
Life of this patent
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Abstract
The present invention provides certain (substituted carbocyclic aryl)amidoalkyl- and (substituted heterocyclic aryl)amidoalkyl-N-Hydroxy urea compounds which inhibit lipoxygenase enzyme activity and are thus useful in the treatment of allergic and inflammatory disease states.
Claims7
A compound having the structure ##STR18## or a pharmaceutically acceptable salt thereof wherein R.sup.1 is NR.sup.2 R.sup.3 where R.sup.2 and R.sup.3 are independently selected from hydrogen and alkyl of from one to six carbon atoms;
- A is ##STR19## wherein R.sup.4 is selected from (a) phenoxy, optionally substituted with one, two, or three halogen atoms, alkyl of from one to six carbon atoms, haloalkyl of from one to six carbon atoms, phenylalkoxy in which the alkoxy portion is of from one to six carbon atoms, and
- (b) thiophenoxy, optionally substituted with one, two, or three halogen atoms, alkyl of from one to six carbon atoms, haloalkyl of from one to six carbon atoms;
- Y is a valence bond or is selected from
- alkylene of from one to six carbon atoms,
- alkenylene of from two to six carbon atoms, and
- oxyalkylene of from one to six carbon atoms;
- Z is oxygen or sulfur;
- B is ##STR20## wherein R.sup.9 is selected from hydrogen,
- alkyl of from one to six carbon atoms, and
- D is straight or branched chain alkylene of from one to six carbon atoms;
- and
- M is hydrogen or a pharmaceutically acceptable cation.
9 more elements
Dependencies are inferred from the claim text.