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Biphenyl amide p38 kinase inhibitors 3: Improvement of cellular and in vivo activity

Autor
ANGELL, Richard1 ; ASTON, Nicola M1 ; PATEL, Shila1 ; SMEE, Penny A1 ; SMITH, Kathryn J1 ; SOMERS, Don O1 ; WALKER, Ann L1 ; BAMBOROUGH, Paul1 ; BUCKTON, Jacky B1 ; COCKERILL, Stuart1 ; DEBOECK, Suzanne J1 ; EDWARDS, Chris D1 ; HOLMES, Duncan S1 ; JONES, Katherine L1 ; LAINE, Dramane I1
[1] GlaxoSmithKline R&D, Medicines Research Centre, Gunnels Wood Road, Stevenage, Hertfordshire SG1 2NY, United Kingdom
Fuente

Bioorganic & medicinal chemistry letters (Print). 2008, Vol 18, Num 15, pp 4428-4432, 5 p

ISSN
0960-894X
Campo Científico
Biochemistry, molecular biology, biophysics; Pharmacology drugs
Editor
Elsevier, Oxford
País de la publicación
United Kingdom
Tipo de documento
Article
Idioma
English
Palabra clave de autor
p38 Kinase;p38 Alpha;p38;CSBP;MAP kinase;Inhibitors;Biphenyl amide;BPA;Biphenyl amides;BPAs;Protein kinase X-ray structure;Binding mode;Structure-based drug design;Kinase selectivity;Structure-activity relationships;PG-PS model;CIA model
Palabra clave (fr)
Animal Carboxamide Diffraction RX Dérivé du biphényle Dérivé du cyclopropane In vivo Inhibiteur Mitogen-activated protein kinase Mode liaison Modèle moléculaire Modélisation Pharmacocinétique Rat Relation structure activité Structure cristalline Structure moléculaire Voie intraveineuse Voie orale Biphényle-3,4p-dicarboxamide(N,N-bis[cyclopropylméthyl]-6-méthyl) Enzyme Mammalia Rodentia Transferases Vertebrata
Palabra clave (in)
Animal Carboxamide X ray diffraction Biphenyl derivatives Cyclopropane derivatives In vivo Inhibitor Mitogen-activated protein kinase Binding mode Molecular model Modeling Pharmacokinetics Rat Structure activity relation Crystalline structure Molecular structure Intravenous administration Oral administration Enzyme Mammalia Rodentia Transferases Vertebrata
Palabra clave (es)
Animal Carboxamida Difracción RX Bifenilo derivado Ciclopropano derivado In vivo Inhibidor Mitogen-activated protein kinase Modo de enlace Modelo molecular Modelización Farmacocinética Rata Relación estructura actividad Estructura cristalina Estructura molecular Vía intravenosa Vía oral Enzima Mammalia Rodentia Transferases Vertebrata
Clasificación
Pascal
002 Biological and medical sciences / 002B Medical sciences / 002B02 Pharmacology. Drug treatments / 002B02W Miscellaneous

Disciplina
General pharmacology
Procedencia
Inist-CNRS
Base de datos
PASCAL
Identificador INIST
20581897

Sauf mention contraire ci-dessus, le contenu de cette notice bibliographique peut être utilisé dans le cadre d’une licence CC BY 4.0 Inist-CNRS / Unless otherwise stated above, the content of this bibliographic record may be used under a CC BY 4.0 licence by Inist-CNRS / A menos que se haya señalado antes, el contenido de este registro bibliográfico puede ser utilizado al amparo de una licencia CC BY 4.0 Inist-CNRS

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