Abstract: The invention provides compounds of formula (I) wherein R is —CH3 or —CH2CH3 and pharmaceutically acceptable salts thereof. The compounds of formula (I) are useful in the treatment of diseases or disorders mediated by IKKE, TBK1 and/or SIK2 mechanisms in a subject, for example cancer and inflammatory and tissue repair disorders. The invention also provides uses of the compounds of formula (I) and compositions containing them.
Abstract: The invention provides compounds of formula (I) wherein R is —CH3 or —CH2CH3 and pharmaceutically acceptable salts thereof. The compounds of formula (I) are useful in the treatment of diseases or disorders mediated by IKKE, TBK1 and/or SIK2 mechanisms in a subject, for example cancer and inflammatory and tissue repair disorders. The invention also provides uses of the compounds of formula (I) and compositions containing them.
Abstract: Compounds of the general formula (I) and salts thereof are useful in the treatment of diseases associated with aberrant activity of the protein kinases IKK? and/or TBK-1 in which one of V and W is N, and the other of V and W is C—H; and R1, R2, R3 and R4 are as defined in the specification. The invention also provides uses of the compounds and compositions containing them.
Type:
Application
Filed:
February 21, 2014
Publication date:
January 7, 2016
Applicant:
DOMAINEX LIMITED
Inventors:
Gary Karl Newton, Mark Richard Stewart, Trevor Robert Perrior, Stuart Richard Crosby, Anna Hopkins, Gabriel Nefoita-Giras, Kerry Jenkins
Abstract: C Compounds of the general formula (I) and salts thereof are useful in the treatment of diseases associated with aberrant activity of the protein kinases IKK? and/or TBK-1: in which: R1 represents an aliphatic heterocyclyl group having 4, 5, 6 or 7 ring atoms, bonded to the phenyl group shown in formula I through a ring nitrogen atom, and optionally substituted by one or more substituents defined in the Specification; R2 represents a phenyl or heteroaryl group which is optionally substituted by one or more substituents defined in the Specification; and each of R3 and R4 independently represents a hydrogen atom or a C1-4 alkyl group.
Type:
Grant
Filed:
July 18, 2011
Date of Patent:
February 24, 2015
Assignee:
Domainex Limited
Inventors:
Trevor Robert Perrior, Gary Karl Newton, Mark Richard Stewart, Rehan Aqil
Abstract: Methods for producing and identifying fragments of proteins, and more particularly to methods for generating and identifying soluble protein domains are disclosed based on a method for generating a library of nucleic acid fragments from nucleic acid encoding a desired polypeptide, and more especially a library of essentially, randomly sampled fragments of coding DNA sequence predominantly of defined size range and a method for selecting cloned gene fragments from the library that encode soluble protein domains.
Type:
Grant
Filed:
November 8, 2002
Date of Patent:
October 7, 2014
Assignee:
Domainex Limited
Inventors:
Mark McAlister, Renos Savva, Laurence Pearl, Chrisostomos Prodromou, Paul C Driscoll
Abstract: C Compounds of the general formula (I) and salts thereof are useful in the treatment of diseases associated with aberrant activity of the protein kinases IKK? and/or TBK-1: in which: R1 represents an aliphatic heterocyclyl group having 4, 5, 6 or 7 ring atoms, bonded to the phenyl group shown in formula I through a ring nitrogen atom, and optionally substituted by one or more substituents defined in the Specification; R2 represents a phenyl or heteroaryl group which is optionally substituted by one or more substituents defined in the Specification; and each of R3 and R4 independently represents a hydrogen atom or a C1-4 alkyl group.
Type:
Application
Filed:
July 18, 2011
Publication date:
October 10, 2013
Applicant:
DOMAINEX LIMITED
Inventors:
Trevor Robert Perrior, Gary Karl Newton, Mark Richard Stewart, Rehan Aqil