Inventor
Deborah A. Mischke
Inventor
Defiance, MO, US
Overview
Patents· 57 as inventor
Public. Assignee & technology derived from the patent record. Each patent links to its LexDana page.
C07Dprimary
C07DHeterocyclic compounds27%
C07CAcyclic or carbocyclic compounds21%
C07BGeneral methods of organic chemistry17%
B01DSeparation12%
A61PSpecific therapeutic activity of chemical compounds or medicinal preparations10%
A61KPreparations for medical, dental or toiletry purposes9%
Y02ATechnologies for adaptation to climate change2%
Y02PClimate change mitigation technologies in the production or processing of goods2%
A01NPreservation of bodies of humans or animals or plants or parts thereof1%
C04BLime, magnesia1%
PatentTitleYear
7,700,658'(R)-chiral halogenated substituted fused heterocyclic amino compounds useful for inhibiting cholesterol ester transfer protein activity'20107,253,211'(R)-chiral halogenated substituted fused heterocyclic amino compounds useful for inhibiting cholesterol ester transfer protein activity'20077,122,536'(R)-chiral halogenated substituted fused heterocyclic amino compounds useful for inhibiting cholesterol ester transfer protein activity'20067,119,203'Piperidinyl- and piperazinyl-sulfonylmethyl hydroxamic acids and their use as protease inhibitors'20067,067,670'Sulfamato hydroxamic acid metalloprotease inhibitor'20066,924,313'Substituted tertiary-heteroalkylamines useful for inhibiting cholesteryl ester transfer protein activity'20056,890,928'Aromatic sulfone hydroxamic acids and their use as protease inhibitors'20056,890,937'Aromatic sulfone hydroxamic acid metalloprotease inhibitor'20056,861,561'Substituted aromatic policyclic tertiary-heteroalkylamines useful for inhibiting cholesteryl ester transfer protein activity'20056,803,388'(R)-Chiral halogenated substituted n,n-bis-phenyl aminoalcohol compounds useful for inhibiting cholesteryl ester transfer protein activity'20046,800,646'Sulfamato hydroxamic acid metalloprotease inhibitor'20046,787,570'Substituted N-cycloalkyl-N-benzyl aminoalcohol compounds useful for inhibiting cholesteryl ester transfer protein activity'20046,765,023'Use of substituted N, N-disubstituted reverse aminoalcohol compounds useful for inhibiting cholesteryl ester transfer protein activity'20046,750,228'Aromatic sulfone hydroxamic acid metalloprotease inhibitor'20046,750,233'Aromatic sulfone hydroxamic acid metalloprotease inhibitor'20046,723,752'(R)-chiral halogenated substituted n-benzyl-n-phenyl aminoalcohol compounds useful for inhibiting cholesteryl ester transfer protein activity'20046,723,753'Substituted n-benzyl-n-phenyl aminoalcohol compounds useful for inhibiting cholesteryl ester transfer protein activity'20046,710,089'Substituted N-fused-phenyl-N-benzyl aminoalcohol compounds useful for inhibiting cholesteryl ester transfer protein activity'20046,699,898'Substituted N,N-disubstituted non-fused heterocyclo amino compounds useful for inhibiting cholesteryl ester transfer protein activity'20046,696,435'Substituted N,N-disubstituted fused-heterocyclo amino compounds useful for inhibiting cholesteryl ester transfer protein activity'20046,696,472'Substituted N-phenoxy-N-phenyl aminoalcohol compounds useful for inhibiting cholesteryl ester transfer protein activity'20046,689,794'Aromatic sulfone hydroxamates and their use as protease inhibitors'20046,683,113'(R)-chiral halogenated substituted N,N-Bis-benzyl aminioalcohol compounds useful for inhibiting cholesteryl ester transfer protein activity'20046,683,093'Aromatic sulfone hydroxamic acids and their use as protease inhibitors'20046,683,099'Substituted N,N-disubstituted cycloalkyl aminoalcohol compounds useful for inhibiting cholesteryl ester transfer protein activity'20046,677,382'Substituted N,N-bis-phenyl aminoalcohol compounds useful for inhibiting cholesteryl ester transfer protein activity'20046,677,379'Substituted N,N-disubstituted diamino compounds useful for inhibiting cholesteryl ester transfer protein activity'20046,677,375'Substituted N,N-bis-benzyl aminoalcohol compounds useful for inhibiting cholesteryl ester transfer protein activity'20046,677,380'Substituted N, N-disubstituted mercapto amino compounds useful for inhibiting cholesteryl ester transfer protein activity'20046,677,353'Substituted N-phenyl-N-heteroaralkyl aminoalcohol compounds useful for inhibiting cholesteryl ester transfer protein activity'20046,677,341'(R)-Chiral halogenated substituted heteroaryl benzyl aminoalcohol compounds useful for inhibiting cholesteryl ester transfer protein activity'20046,586,433'Substituted N-heteroaryl-N-phenyl aminoalcohol compounds useful for inhibiting cholesteryl ester transfer protein activity'20036,583,183'Substituted n-phenyl-n-fused-benzyl aminoalcohol compounds useful for inhibiting cholesteryl ester transfer protein activity'20036,544,974'(R)-chiral halogenated substituted fused heterocyclic amino compounds useful for inhibiting cholesteryl ester transfer protein activity'20036,521,607'(R)-chiral halogenated substituted N-phenoxy N-phenyl aminoalcohol compounds useful for inhibiting cholesteryl ester transfer protein activity'20036,492,367'Sulfamato hydroxamic acid metalloprotease inhibitor'20026,482,862'Method of using substituted N-benzyl-N-phenyl aminoalcohols for inhibiting cholesteryl ester transfer protein activity'20026,479,552'Use of substituted N, N-disubstituted diamino compounds for inhibiting cholesteryl ester transfer protein activity'20026,476,057'Use of substituted N, N-disubstituted cycloalkyl aminoalcohol compounds for inhibiting cholesteryl ester transfer protein activity'20026,476,075'Use of substituted N, N-bis-benzyl aminoalcohol compounds inhibiting cholesteryl ester transfer protein activity'20026,462,092'Use of substituted N, N-disubstituted reverse aminoalcohol compounds for inhibiting cholesteryl ester transfer protein activity'20026,458,849'use of substituted N,N-disubstituted mercapto amino compounds for inhibiting cholesteryl ester transfer protein activity'20026,458,852'Use of substituted N, N-bis-phenyl aminoalcohol compounds for inhibiting cholesteryl ester transfer protein activity'20026,458,803'Substituted N-phenyl-N-heteroaralkyl aminoalcohol compounds for inhibiting cholesteryl ester transfer protein activity'20026,455,519'Use of substituted N, N-disubstituted fused-heterocyclo amino compounds for inhibiting cholesteryl ester transfer protein activity'20026,451,823'Use of substituted N-phenoxy-N-phenyl aminoalcohol compounds for inhibiting cholesteryl ester transfer protein activity'20026,451,830'Use of substituted N,N-disubstituted non-fused heterocyclo amino compounds for inhibiting cholesteryl ester transfer protein activity'20026,448,295'Use of substituted N-fused-phenyl-N-benzyl aminoalcohol compounds for inhibiting cholesteryl ester transfer protein activity'20026,448,250'Sulfamato hydroxamic acid metalloprotease inhibitor'20026,372,758'Sulfamato hydroxamic acid metalloprotease inhibitor'20025,536,700'Herbicidal compositions comprising aryl-5-haloalkylpyrazoles and glyphosate, it\'s salts, diquat or paraquat'19965,530,126'Process for the preparation of substituted 6-(pyrazol-3yl)-1,4-benzoxazin-3-ones'19965,498,624'Selected pyrazolyl derivatives'19965,496,956'Herbicidal substituted aryl-haloalkylpyrazoles'19965,489,571'Herbicidal substituted aryl-haloalkylpyrazoles'19965,281,571'Herbicidal benzoxazinone- and benzothiazinone-substituted pyrazoles'19944,601,744'Esters of N,N\'-methylene-bis-[N-[(diaryloxyphosphinyl)methyl]glycine] as herbicides'1986Career & activity timeline
Assembled from patent assignee/location history and declaration credentials.
1986–1996Patents assigned to MONSANTO CO (7)· patent assignee history
1986Based in Creve Coeur, MO, US· patent location history
1994–2010Based in Defiance, MO, US· patent location history
2002–2005Patents assigned to SEARLE & CO (17)· patent assignee history
2003–2006Patents assigned to PHARMACIA CORP (24)· patent assignee history
2004–2010Patents assigned to PFIZER (7)· patent assignee history
2004Patents assigned to PHARMACIA CORP GLOBAL PATENT D (1)· patent assignee history
2004Based in Ballwin, MO, US· patent location history
Inventor activity
Assignee and location history derived from the patent record.
Assignees
| Assignee | Patents | Span |
|---|---|---|
| PHARMACIA CORP | 24 | 2003–2006 |
| SEARLE & CO | 17 | 2002–2005 |
| MONSANTO CO | 7 | 1986–1996 |
| PFIZER | 7 | 2004–2010 |
| PHARMACIA CORP GLOBAL PATENT D | 1 | 2004 |
Locations
| Location | Patents | Span |
|---|---|---|
| Defiance, MO, US | 55 | 1994–2010 |
| Ballwin, MO, US | 1 | 2004 |
| Creve Coeur, MO, US | 1 | 1986 |