Inventor
Barry L. Parnas
Inventor
University City, MO, US
Overview
Patents· 31 as inventor
Public. Assignee & technology derived from the patent record. Each patent links to its LexDana page.
C07Cprimary
C07CAcyclic or carbocyclic compounds26%
C07DHeterocyclic compounds24%
C07BGeneral methods of organic chemistry23%
B01DSeparation22%
A61KPreparations for medical, dental or toiletry purposes3%
C08GMacromolecular compounds obtained otherwise than by reactions only involving unsaturated carbon-to-carbon bonds2%
PatentTitleYear
6,924,313'Substituted tertiary-heteroalkylamines useful for inhibiting cholesteryl ester transfer protein activity'20056,861,561'Substituted aromatic policyclic tertiary-heteroalkylamines useful for inhibiting cholesteryl ester transfer protein activity'20056,787,570'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'20046,723,753'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'20046,683,099'Substituted N,N-disubstituted cycloalkyl 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'20046,677,380'Substituted N, N-disubstituted mercapto amino 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'20046,677,382'Substituted N,N-bis-phenyl aminoalcohol 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'20046,586,433'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'20036,482,862'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'20026,476,075'Use of substituted N, N-bis-benzyl aminoalcohol compounds 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'20026,462,092'Use of substituted N, N-disubstituted reverse 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'20026,458,849'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'20026,455,519'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'20025,344,934'Preparation of urethane and caronate products'19945,223,638'Preparation of urethane and carbonate products'1993Career & activity timeline
Assembled from patent assignee/location history and declaration credentials.
1993–1994Patents assigned to MONSANTO CO (2)· patent assignee history
1993Based in St. Louis, MO, US· patent location history
1994–2005Based in University City, MO, US· patent location history
2002–2005Patents assigned to SEARLE & CO (13)· patent assignee history
2003–2004Patents assigned to PHARMACIA CORP (12)· patent assignee history
2004–2005Patents assigned to PFIZER (3)· patent assignee history
2004Patents assigned to PHARMACIA CORP GLOBAL PATENT D (1)· patent assignee history
Inventor activity
Assignee and location history derived from the patent record.
Assignees
| Assignee | Patents | Span |
|---|---|---|
| SEARLE & CO | 13 | 2002–2005 |
| PHARMACIA CORP | 12 | 2003–2004 |
| PFIZER | 3 | 2004–2005 |
| MONSANTO CO | 2 | 1993–1994 |
| PHARMACIA CORP GLOBAL PATENT D | 1 | 2004 |
Locations
| Location | Patents | Span |
|---|---|---|
| University City, MO, US | 30 | 1994–2005 |
| St. Louis, MO, US | 1 | 1993 |