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name:-0.015635967254639
name:-0.0061080455780029
MCINNES; Campbell Patent Filings

MCINNES; Campbell

Patent Applications and Registrations

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".

Company Profile
6.15.31
  • MCINNES; Campbell - Irmo SC
  • McInnes; Campbell - Dundee GB
  • McInnes, Campbell - Longforgan GB
*profile and listings may contain filings by different individuals or companies with the same name. Review application materials to confirm ownership/assignment.
Patent Activity
PatentDate
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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