Inventor
DELLARIA JOSEPH F
US45 patents
⚠️ This page may combine multiple inventors who share the name “DELLARIA JOSEPH F”. Patents are grouped by organization below to help distinguish them — per-person disambiguation is on the roadmap.
3M INNOVATIVE PROPERTIES CO
22 patentsUS6797718B2Sep 28, 2004
Ether substituted imidazopyridines
3M INNOVATIVE PROPERTIES CO212 citations99
US6720333B2Apr 13, 2004
Amide substituted imidazopyridines
3M INNOVATIVE PROPERTIES CO90 citations99
US6716988B2Apr 6, 2004
Urea substituted imidazopyridines
3M INNOVATIVE PROPERTIES CO91 citations99
US6667312B2Dec 23, 2003
Thioether substituted imidazoquinolines
3M INNOVATIVE PROPERTIES CO322 citations99
US6664264B2Dec 16, 2003
Thioether substituted imidazoquinolines
3M INNOVATIVE PROPERTIES CO346 citations99
US6545017B1Apr 8, 2003
Urea substituted imidazopyridines
3M INNOVATIVE PROPERTIES CO369 citations99
US6545016B1Apr 8, 2003
Amide substituted imidazopyridines
3M INNOVATIVE PROPERTIES CO368 citations99
US6525064B1Feb 25, 2003
Sulfonamido substituted imidazopyridines
3M INNOVATIVE PROPERTIES CO385 citations99
US7288550B2Oct 30, 2007
Thioether substituted imidazoquinolines
3M INNOVATIVE PROPERTIES CO68 citations98
US7220758B2May 22, 2007
Ether substituted imidazopyridines
3M INNOVATIVE PROPERTIES CO68 citations98
US6953804B2Oct 11, 2005
Aryl ether substituted imidazoquinolines
3M INNOVATIVE PROPERTIES CO70 citations98
US6949649B2Sep 27, 2005
Thioether substituted imidazoquinolines
3M INNOVATIVE PROPERTIES CO67 citations98
US6921826B2Jul 26, 2005
Thioether substituted imidazoquinolines
3M INNOVATIVE PROPERTIES CO71 citations98
US6720422B2Apr 13, 2004
Amide substituted imidazopyridines
3M INNOVATIVE PROPERTIES CO82 citations98
US6720334B2Apr 13, 2004
Urea substituted imidazopyridines
3M INNOVATIVE PROPERTIES CO95 citations98
US6696465B2Feb 24, 2004
Sulfonamido substituted imidazopyridines
3M INNOVATIVE PROPERTIES CO220 citations98
US6670372B2Dec 30, 2003
Aryl ether substituted imidazoquinolines
3M INNOVATIVE PROPERTIES CO296 citations98
US6664260B2Dec 16, 2003
Heterocyclic ether substituted imidazoquinolines
3M INNOVATIVE PROPERTIES CO292 citations98
US7125890B2Oct 24, 2006
Ether substituted imidazopyridines
3M INNOVATIVE PROPERTIES CO67 citations97
US6989389B2Jan 24, 2006
Aryl ether substituted imidazoquinolines
3M INNOVATIVE PROPERTIES CO102 citations97
US6677348B2Jan 13, 2004
Aryl ether substituted imidazoquinolines
3M INNOVATIVE PROPERTIES CO362 citations97
US7968563B2Jun 28, 2011
Oxime and hydroxylamine substituted imidazo[4,5-c] ring compounds and methods
3M INNOVATIVE PROPERTIES CO47 citations94
ABBOTT LAB
22 patentsUS5459150AOct 17, 1995
Indole derivatives which inhibit leukotriene biosynthesis
ABBOTT LAB49 citations95
US5095031AMar 10, 1992
Indole derivatives which inhibit leukotriene biosynthesis
ABBOTT LAB41 citations92
US4992464AFeb 12, 1991
Heteroaryl N-hydroxy amides and ureas with polar substituents as 5-lipoxygenase inhibitors
ABBOTT LAB26 citations92
US5776984AJul 7, 1998
Prostaglandin synthase-2 inhibitors
ABBOTT LAB17 citations89
US5681842AOct 28, 1997
Prostaglandin synthase-2 inhibitors
ABBOTT LAB31 citations89
US5164388ANov 17, 1992
Heterocyclic peptide renin inhibitors
ABBOTT LAB34 citations89
US4645759AFeb 24, 1987
Renin inhibiting compounds
ABBOTT LAB22 citations80
US5446062AAug 29, 1995
((4-alkoxypyran-4-yl) substituted) ether, arylalkyl-, arylalkenyl-, and arylalkynyl)urea inhibitors of 5-lipoxygenase
ABBOTT LAB7 citations73
US5426111AJun 20, 1995
[Alkoxy-, alkenyloxy-, alkynyloxy-, and phenylmethyloxyalkoxycycloalkyl or alkoxycycloheteroalkyl]naphtho[2,3-c]furan-1(3H)-one inhibitors of 5-lipoxygenase
ABBOTT LAB7 citations73
US5516795AMay 14, 1996
Heteroatom substituted propanyl derivatives having 5-lipoxygenase inhibitory activity
ABBOTT LAB16 citations72
US5354865AOct 11, 1994
Phenylmethyl derivatives having lipoxygenase inhibitory activity
ABBOTT LAB18 citations71
US5214204AMay 25, 1993
Arylamidoalkyl-n-hydroxyurea compounds having lipoxygenase inhibitory activity
ABBOTT LAB7 citations71
US4652551AMar 24, 1987
Renin inhibiting compounds
ABBOTT LAB17 citations71
US5484786AJan 16, 1996
Pyran-4-ylmethyl substituted arylalkylaryl-, arylalkenylylaryl-, and arylalkynylarylurea inhibitors of 5-lipoxygenase
ABBOTT LAB6 citations62
US5446055AAug 29, 1995
Polyether naphthalenic lignan lactones as inhibitors of 5-lipoxygenase
ABBOTT LAB2 citations62
US5432194AJul 11, 1995
(4-alkoxypyran-4-yl) substituted arylalkylaryl-, aryalkenylaryl-, and aryalkynylarylurea inhibitors of 5-lipoxygenase
ABBOTT LAB2 citations62
US5407959AApr 18, 1995
(Trans-1,4-dialkoxycyclohexyl) substituted arylalkylaryl-arylalkenylaryl-, and arylalkynylarylurea inhibitors of 5-lipoxygenase
ABBOTT LAB2 citations62
US5475009ADec 12, 1995
1, 2-dialkoxyethanes as 5-lipoxygenase inhibitors
ABBOTT LAB5 citations61
US5346914ASep 13, 1994
(4-alkoxypyran-4-yl) substituted arylalkylaryl-, arylalkenylaryl-, and arylalkynylarylurea inhibitors of 5-lipoxygenase
ABBOTT LAB2 citations61
US5514702AMay 7, 1996
Arylamidoalkyl-N-hydroxyurea compounds having lipoxygenase inhibitory activity
ABBOTT LAB3 citations60
US5350765ASep 27, 1994
Ether-containing inhibitors of 5-lipoxygenase
ABBOTT LAB0 citations52
US5268379ADec 7, 1993
Ether-containing inhibitors of 5-lipoxygenase
ABBOTT LAB1 citations52