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US Patent 8367658 Pyrazin-2-yl-pyridin-2-yl-amine and pyrazin-2-yl-pyrimidin-4-yl-amine compounds and their use

Patent 8367658 was granted and assigned to Cancer Research Technology Limited on February, 2013 by the United States Patent and Trademark Office.

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Patent
Patent

Patent attributes

Current Assignee
‌
Cancer Research Technology Limited
Patent Jurisdiction
United States Patent and Trademark Office
United States Patent and Trademark Office
Patent Number
8367658
Patent Inventor Names
David Hugh Williams0
Ian Collins0
Jane Elizabeth Scanlon0
John Charles Reader0
Kwai Ming Cheung0
Michael Cherry0
Nelly Piton0
Nicolas Proisy0
...
Date of Patent
February 5, 2013
Patent Application Number
13241887
Date Filed
September 23, 2011
Patent Citations Received
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US Patent 12006332 Aminopyrimidine derivatives as phosphatidylinositol phosphate kinase inhibitors
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US Patent 11667651 Aminopyridine derivatives as phosphatidylinositol phosphate kinase inhibitors
0
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US Patent 11787792 5-[[4-[[morpholin-2-yl]methylamino]-5-(trifluoromethyl)-2 Pyridyl]Amino]Pyrazine-2-carbonitrile and therapeutic uses thereof
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US Patent 11945798 Substituted aminopyridine compounds as EGFR inhibitors
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US Patent 11981658 Substituted aminopyridine compounds as EGFR inhibitors
0
Patent Primary Examiner
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Kristin Bianchi
Patent abstract

The present invention pertains generally to the field of therapeutic compounds, and more specifically to certain biarylamine compounds (referred to herein as BAA compounds), and especially certain pyrazin-2-yl-pyridin-2-yl-amine and pyrazine-2-yl-pyrimidin-4-yl-amine compounds, which, inter alia, inhibit Checkpoint Kinase 1 (CHK1) kinase function. The present invention also pertains to pharmaceutical compositions comprising such compounds, and the use of such compounds and compositions, both in vitro and in vivo, to inhibit CHK1 kinase function, and in the treatment of diseases and conditions that are mediated by CHK1, that are ameliorated by the inhibition of CHK1 kinase function, etc., including proliferative conditions such as cancer, etc., optionally in combination with another agent, for example, (a) a DNA topoisomerase I or II inhibitor; (b) a DNA damaging agent; (c) an antimetabolite or TS inhibitor; (d) a microtubule targeted agent; and (e) ionising radiation.

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