loadpatents
Patent applications and USPTO patent grants for MCINNES; Campbell.The latest application filed is for "3-amino-4-[4-[4 (dimethylcarbamoyl) phenyl]-1,4-diazepan-1-yl]thieno[2,3-b]pyridine-2-carboxamide for use in cancer therapy and formulations comprising the same".
Patent | Date |
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3-amino-4-[4-[4 (dimethylcarbamoyl) Phenyl]-1,4-diazepan-1-yl]thieno[2,3-b]pyridine-2-carboxamide For Use In Cancer Therapy And Formulations Comprising The Same App 20220226343 - RONINSON; Igor ;   et al. | 2022-07-21 |
Bicyclic Pyridine Compositions And Methods Of Using The Same For Cancer Therapy App 20220135583 - RONINSON; Igor B. ;   et al. | 2022-05-05 |
Design And Optimization Of Type Iv Braf Inhibitors For The Treatment Of Melanoma App 20220127585 - MCINNES; CAMPBELL ;   et al. | 2022-04-28 |
Peptide based inhibitors of Raf kinase protein dimerization and kinase activity Grant 11,162,083 - McInnes , et al. November 2, 2 | 2021-11-02 |
Quinoline-based Compounds And Methods Of Inhibiting Cdk8/19 App 20210276956 - Roninson; Igor ;   et al. | 2021-09-09 |
Quinoline-based compounds and methods of inhibiting CDK8/19 Grant 11,014,906 - Roninson , et al. May 25, 2 | 2021-05-25 |
Small Molecule Inhibitors Selective for Polo-Like Kinase Proteins App 20200399297 - MCINNES; CAMPBELL ;   et al. | 2020-12-24 |
Quinoline-based Compounds And Methods Of Inhibiting Cdk8/19 App 20200062728 - Roninson; Igor ;   et al. | 2020-02-27 |
Peptide Based Inhibitors of Raf Kinase Protein Dimerization and Kinase Activity App 20190382738 - MCINNES; CAMPBELL ;   et al. | 2019-12-19 |
Selective Inhibitors of the Polo-Like Kinase 1 Polo-Box Domain App 20190269784 - McInnes; Campbell | 2019-09-05 |
Fragment ligated inhibitors selective for the polo box domain of PLK1 Grant 10,067,131 - McInnes , et al. September 4, 2 | 2018-09-04 |
Cyclin based inhibitors of CDK2 and CDK4 Grant 9,982,015 - McInnes , et al. May 29, 2 | 2018-05-29 |
Small Molecule Inhibitors Selective For Polo-Like Kinase Proteins App 20170283445 - McInnes; Campbell ;   et al. | 2017-10-05 |
Cyclin Based Inhibitors Of Cdk2 And Cdk4 App 20170218018 - Mcinnes; Campbell ;   et al. | 2017-08-03 |
Cyclin based inhibitors of CDK2 and CDK4 Grant 9,376,465 - McInnes , et al. June 28, 2 | 2016-06-28 |
Cyclin based inhibitors of CDK2 and CDK4 Grant 9,328,139 - McInnes , et al. May 3, 2 | 2016-05-03 |
Method of Forming Fragment Ligated Inhibitors App 20160011195 - McInnes; Campbell ;   et al. | 2016-01-14 |
Fragment Ligated Inhibitors Selective for the Polo Box Domain of PLK1 App 20150315555 - McInnes; Campbell ;   et al. | 2015-11-05 |
Fragment ligated inhibitors selective for the polo box domain of PLK1 Grant 9,175,357 - McInnes , et al. November 3, 2 | 2015-11-03 |
Cyclin Based Inhibitors of CDK2 and CDK4 App 20150011730 - McInnes; Campbell ;   et al. | 2015-01-08 |
Cyclin Based Inhibitors Of Cdk2 And Cdk4 App 20140316107 - McInnes; Campbell ;   et al. | 2014-10-23 |
Cyclin Based Inhibitors of CDK2 and CDK4 App 20140296484 - McInnes; Campbell ;   et al. | 2014-10-02 |
Cyclin Based Inhibitors of CDK2 and CDK4 App 20130289240 - McInnes; Campbell ;   et al. | 2013-10-31 |
Cyclin based inhibitors of CDK2 and CDK4 Grant 8,566,072 - McInnes , et al. October 22, 2 | 2013-10-22 |
Fragment Ligated Inhibitors Selective for the Polo Box Domain of PLK1 App 20120202970 - McInnes; Campbell ;   et al. | 2012-08-09 |
Cyclin Based Inhibitors of CDK2 and CDK4 App 20110257365 - McInnes; Campbell ;   et al. | 2011-10-20 |
Pyrimidine compounds Grant 7,897,605 - Wang , et al. March 1, 2 | 2011-03-01 |
4-Heteroaryl Pyrimidine Derivatives and use thereof as Protein Kinase Inhibitors App 20090215805 - Wood; Gavin ;   et al. | 2009-08-27 |
Thiazolo-, oxazalo and imidazolo-quinazoline compounds capable of inhibiting protein kinases Grant 7,576,091 - McInnes , et al. August 18, 2 | 2009-08-18 |
Pyrimidine compounds App 20080287439 - Wang; Shudong ;   et al. | 2008-11-20 |
p21 peptides Grant 7,449,544 - Zheleva , et al. November 11, 2 | 2008-11-11 |
Pyrimidine compounds Grant 7,432,260 - Wang , et al. October 7, 2 | 2008-10-07 |
Crystal Structure of Human Proliferating Cell Nuclear Antigen (Pcna) and Uses Thereof App 20080167385 - Kontopidis; George ;   et al. | 2008-07-10 |
Method for Identifying Inhibitors Using a Homology Model of Polo-Like Kinase 1 App 20080132484 - McInnes; Campbell ;   et al. | 2008-06-05 |
P21 derived peptides and uses thereof App 20060293245 - Zheleva; Daniella I. ;   et al. | 2006-12-28 |
Cyclin groove inhibitors App 20060281687 - Andrews; Martin J.I. ;   et al. | 2006-12-14 |
Thiazolo-, oxazalo and imidazolo-quinazoline compounds capable of inhibiting protein kinases App 20060264628 - McInnes; Campbell ;   et al. | 2006-11-23 |
Benzthiazole-3 oxides useful for the treatment of proliferative disorders App 20060040997 - McInnes; Campbell ;   et al. | 2006-02-23 |
Pyrimidine compounds App 20050192300 - Wang, Shudong ;   et al. | 2005-09-01 |
p21 peptides App 20040176301 - Zheleva, Daniella I. ;   et al. | 2004-09-09 |
p21 peptides App 20030036628 - Zheleva, Daniella I. ;   et al. | 2003-02-20 |
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