Inventor
Robert McDowell
Inventor
San Francisco, CA, US
Overview
Patents· 65 as inventor
Public. Assignee & technology derived from the patent record. Each patent links to its LexDana page.
C07Dprimary
C07DHeterocyclic compounds30%
A61PSpecific therapeutic activity of chemical compounds or medicinal preparations25%
A61KPreparations for medical, dental or toiletry purposes19%
C07KPeptides11%
C07CAcyclic or carbocyclic compounds4%
G01NInvestigating or analysing materials by determining their chemical or physical properties3%
C12NMicroorganisms or enzymes3%
Y02ATechnologies for adaptation to climate change2%
Y10STechnical subjects covered by former uspc cross-reference art collections [xracs] and digests1%
C07BGeneral methods of organic chemistry1%
PatentTitleYear
11,123,3374-methylsulfonyl-substituted piperidine urea compounds202111,034,690Heterocyclic modulators of lipid synthesis202110,758,5254-methylsulfonyl-substituted piperidine urea compounds202010,226,449Heterocyclic modulators of lipid synthesis and combinations thereof201910,189,822Heterocyclic modulators of lipid synthesis201910,118,913Heterocyclic modulators of lipid synthesis201810,053,450Heterocyclic modulators of lipid synthesis20189,925,177'4-methylsulfonyl-substituted piperidine urea compounds'20189,809,591'Heterocyclic modulators of lipid synthesis'20179,663,516'Bicyclic-pyrimidinedione compounds'20179,624,173'Heterocyclic modulators of lipid synthesis'20179,585,883'Pyrimidinedione compounds'20179,428,502'Heterocyclic modulators of lipid synthesis'20169,199,945'Cycloalkyl-substituted pyrimidinedione compounds'20159,181,200'Pyrimidinedione compounds'20159,149,463'Methods and compositions of treating a Flaviviridae family viral infection'20159,101,628'Methods and composition of treating a flaviviridae family viral infection'20159,061,010'Methods of treating a Flaviviridae family viral infection and compositions for treating a Flaviviridae family viral infection'20158,895,598'Methods of treating a flaviviridae family viral infection, compositions for treating a flaviviridae family viral infection, and screening assays for identifying compositions for treating a flaviviridae family viral infection'20148,871,790'Heterocyclic modulators of lipid synthesis'20147,348,333'Cycloalkyl derivatives as inhibitors of bone resorption and vitronectin receptor antagonists'20087,259,159'Guanidino derivatives as inhibitors of cell adhesion'20077,214,487'Methods for identifying compounds that modulate enzymatic activities by employing covalently bonded target-extender complexes with ligand candidates'20077,094,869'Low molecular weight peptidomimetic growth hormone secretagogues'20066,919,178'Extended tethering approach for rapid identification of ligands'20056,867,208'Vitronectin receptor antagonists, their preparation and their use'20056,867,213'(2S)-2-(adamantan-1-ylmethoxycarbonylamino)-3-(4-(2-(1,4,5,6-tetrhydropyrimidin-2-ylcarbamoyl)ethyl)benzoylamino)propionic acid isopropyl ester, its preparation and its use'20056,806,279'Small-molecule inhibitors of interleukin-2'20046,747,148'Sulfonamide derivatives as inhibitors of bone resorption and as inhibitors of cell adhesion'20046,660,728'Thienyl substituted acylguanidines as inhibitors of bone resorption and vitronectin receptor antagonists'20036,620,820'Inhibitors of bone reabsorption and antagonists of vitronectin receptors'20036,566,366'Thienyl substituted acylguanidines as inhibitors of bone resorption and vitronectin receptor antagonists'20036,525,022'Receptor specific atrial natriuretic peptides'20036,492,356'Acylguanidine derivatives as inhibitors of bone resorption and as vitronectin receptor antagonists'20026,482,821'Vitronectin receptor antagonists, their preparation and their use'20026,459,001'Tricyclic compounds, their preparation process and the intermediates of this process, their use as medicaments and the pharmaceutical compositions containing them'20026,399,620'Cycloalkyl derivatives as inhibitors of bone resporption and vitronectin receptor antagonists'20026,387,895'Vitronectin receptor antagonists, their preparation and their use'20026,344,439'Agents for promoting bone formation'20026,339,082'Tricyclic compounds, preparation method and said method intermediates, application as medicines and pharmaceutical compositions containing same'20026,313,119'Sulfonamide derivatives as inhibitors of bone resorption and as inhibitors of cell adhesion'20016,277,845'Hydrazono-benzazulene derivatives, pharmaceutical compositions and intermediates'20016,271,198'Constrained helical peptides and methods of making same'20016,221,907'Tricyclic compounds having activity specific for integrins, particularly alphanubeta3 integrins, method for preparing same, intermediates therefor, use of said compounds as drugs, and pharmaceutical compositions containing same'20016,218,415'Inhibitors or bone reabsorption and antagonists of vitronectin receptors'20016,218,387'Vitronectin receptor anatagonists, their preparation and their use'20016,207,663'Vitronectin receptor antagonists, their preparation and use'20016,194,380'Agents for promoting bone formation'20016,034,216'Low molecular weight peptidomimetic growth hormone secretagogues'20006,011,045'Vitronectin receptor antagonists, their preparation and their use'20006,005,117'Imino compounds, process for their preparation and their use as victronectin antagonists'19995,990,145'Vitronectin receptor antagonists, their preparation and their use'19995,846,932'Receptor specific atrial natriuretic peptides'19985,843,941'Ras farnesyl transferase inhibitors'19985,798,337'Low molecular weight peptidomimetic growth hormone secretagogues'19985,756,452'Platelet aggregation inhibitors having high specificity for GP II.sub.b III.sub.a'19985,674,865'Nonpeptidyl integrin inhibitors having specificity for the GPII.sub.b III.sub.a'19975,674,863'Nonpeptidyl integrin inhibitors having specificity for the GPII.sub.b III.sub.a receptor'19975,665,704'Receptor specific atrial natriuretic peptides'19975,663,166'Nonpeptidyl integrin inhibitors having specificity for the GPII.sub.b III.sub.a receptor'19975,565,449'Nonpeptidyl integrin inhibitors having specificity for the GPII.sub.b III.sub.a receptor'19965,532,359'Ras farnesyl transferase inhibitors'19965,493,007'Platelet aggregation inhibitors having high specificity for GPIIBIIIA'19965,403,836'Benzazepine platelet aggregation inhibitors having specificity for the GPII.sub.b III.sub.a receptor'19955,250,679'Nonpeptidyl platelet aggregation inhibitors having specificity for the GPII.sub.b III.sub. receptor'1993Career & activity timeline
Assembled from patent assignee/location history and declaration credentials.
1993–2007Patents assigned to GENENTECH INC (36)· patent assignee history
1993–2021Based in San Francisco, CA, US· patent location history
1999–2005Patents assigned to HOECHST AG (10)· patent assignee history
2001–2005Patents assigned to AVENTIS PHARMA GMBH (5)· patent assignee history
2003Based in San Bernardino, CA, US· patent location history
2014–2019Patents assigned to 3 V BIOSCIENCES INC (5)· patent assignee history
2015–2021Patents assigned to MYOKARDIA INC (7)· patent assignee history
2019Based in Menlo Park, CA, US· patent location history
Inventor activity
Assignee and location history derived from the patent record.
Assignees
| Assignee | Patents | Span |
|---|---|---|
| GENENTECH INC | 36 | 1993–2007 |
| HOECHST AG | 10 | 1999–2005 |
| MYOKARDIA INC | 7 | 2015–2021 |
| 3 V BIOSCIENCES INC | 5 | 2014–2019 |
| AVENTIS PHARMA GMBH | 5 | 2001–2005 |
Locations
| Location | Patents | Span |
|---|---|---|
| San Francisco, California, US | 61 | 1993–2021 |
| Menlo Park, California, US | 2 | 2019 |
| San Bernardino, California, US | 2 | 2003 |