Search Results - "Bain, Jenny"
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The selectivity of protein kinase inhibitors: a further update
Published in Biochemical journal (15-12-2007)“…The specificities of 65 compounds reported to be relatively specific inhibitors of protein kinases have been profiled against a panel of 70-80 protein kinases…”
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2
The specificities of protein kinase inhibitors: an update
Published in Biochemical journal (01-04-2003)“…We have previously examined the specificities of 28 commercially available compounds, reported to be relatively selective inhibitors of particular…”
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The selectivity of inhibitors of protein kinase CK2: an update
Published in Biochemical journal (01-11-2008)“…CK2 (casein kinase 2) is a very pleiotropic serine/threonine protein kinase whose abnormally high constitutive activity has often been correlated to…”
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4
BIRB796 Inhibits All p38 MAPK Isoforms in Vitro and in Vivo
Published in The Journal of biological chemistry (20-05-2005)“…The compound BIRB796 inhibits the stress-activated protein kinases p38α and p38β and is undergoing clinical trials for the treatment of inflammatory diseases…”
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5
Quinalizarin as a potent, selective and cell-permeable inhibitor of protein kinase CK2
Published in Biochemical journal (15-07-2009)“…Emodin (1,3,8-trihydroxy-6-methyl-anthraquinone) is a moderately potent and poorly selective inhibitor of protein kinase CK2, one of the most pleiotropic…”
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6
D4476, a cell-permeant inhibitor of CK1, suppresses the site-specific phosphorylation and nuclear exclusion of FOXO1a
Published in EMBO reports (01-01-2004)“…The protein kinase CK1 phosphorylates serine residues that are located close to another phosphoserine in the consensus pSer‐Xaa‐Xaa‐Ser. This specificity…”
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Synthesis, Kinase Inhibitory Potencies, and in Vitro Antiproliferative Evaluation of New Pim Kinase Inhibitors
Published in Journal of medicinal chemistry (22-10-2009)“…Members of the Pim kinase family have been identified as promising targets for the development of antitumor agents. After a screening of pyrrolo[2,3-a]- and…”
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8
Exploitation of KESTREL to identify NDRG family members as physiological substrates for SGK1 and GSK3
Published in Biochemical journal (15-12-2004)“…We detected a protein in rabbit skeletal muscle extracts that was phosphorylated rapidly by SGK1 (serum- and glucocorticoid-induced kinase 1), but not by…”
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9
Optimization of Protein Kinase CK2 Inhibitors Derived from 4,5,6,7-Tetrabromobenzimidazole
Published in Journal of medicinal chemistry (02-12-2004)“…Casein kinase 2 (CK2) is a ubiquitous, essential, and highly pleiotropic protein kinase whose abnormally high constitutive activity is suspected to underlie…”
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10
Tetrabromocinnamic Acid (TBCA) and Related Compounds Represent a New Class of Specific Protein Kinase CK2 Inhibitors
Published in Chembiochem : a European journal of chemical biology (02-01-2007)“…Abnormally high constitutive activity of protein kinase CK2, levels of which are elevated in a variety of tumours, is suspected to underlie its pathogenic…”
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Biochemical and three-dimensional-structural study of the specific inhibition of protein kinase CK2 by [5-oxo-5,6-dihydroindolo-(1,2-a)quinazolin-7-yl]acetic acid (IQA)
Published in Biochemical journal (15-09-2003)“…IQA [[5-oxo-5,6-dihydro-indolo(1,2-a)quinazolin-7-yl]acetic acid] is a novel ATP/GTP site-directed inhibitor of CK2 ('casein kinase 2'), a pleiotropic and…”
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12
Inhibition of Protein Kinase CK2 by Condensed Polyphenolic Derivatives. An in Vitro and in Vivo Study
Published in Biochemistry (Easton) (12-10-2004)“…ATP site-directed inhibitors that can target individual kinases are powerful tools for use in signal transduction research, all the more so in the case of a…”
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13
Inhibition of RET tyrosine kinase by SU5416
Published in Journal of molecular endocrinology (01-10-2006)“…Thyroid neoplasia is frequently associated with rearranged during transfection (RET) proto-oncogene mutations that cause hyperactivation of RET kinase…”
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14
New 2-bromomethyl-8-substituted-benzo[ c]chromen-6-ones. Synthesis and biological properties
Published in Bioorganic & medicinal chemistry letters (03-01-2005)“…[Display omitted] New 2-bromomethyl-8-substituted-benzo[ c]chromen-6-ones have been synthesized and their bioactive properties have been evaluated on different…”
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15
Calmodulin-dependent protein kinase kinase-β is an alternative upstream kinase for AMP-activated protein kinase
Published in Cell metabolism (01-07-2005)“…The AMP-activated protein kinase (AMPK) is a critical regulator of energy balance at both the cellular and whole-body levels. Two upstream kinases have been…”
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16
The Mnks Are Novel Components in the Control of TNFα Biosynthesis and Phosphorylate and Regulate hnRNP A1
Published in Immunity (Cambridge, Mass.) (01-08-2005)“…Posttranscriptional regulatory mechanisms control TNFα expression through AU-rich elements in the 3′UTR of its mRNA. This is mediated through Erk and p38 MAP…”
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Synthesis, Pim kinase inhibitory potencies and in vitro antiproliferative activities of diversely substituted pyrrolo[2,3-a]carbazoles
Published in Bioorganic & medicinal chemistry (15-09-2010)“…The synthesis of new pyrrolo[2,3-a]carbazole derivatives diversely substituted at the C-6 to C-9 positions is described. These compounds were tested for their…”
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Solenopsin, the alkaloidal component of the fire ant (Solenopsis invicta), is a naturally occurring inhibitor of phosphatidylinositol-3-kinase signaling and angiogenesis
Published in Blood (15-01-2007)“…Phosphatidylinositol-3-kinase (PI3K), and its downstream effector Akt, or protein kinase Bα (PKBα), play a major regulatory role in control of apoptosis,…”
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The Mnks Are Novel Components in the Control of TNF[alpha] Biosynthesis and Phosphorylate and Regulate hnRNP A1
Published in Immunity (Cambridge, Mass.) (01-08-2005)“…Posttranscriptional regulatory mechanisms control TNFα expression through AU-rich elements in the 3'UTR of its mRNA. This is mediated through Erk and p38 MAP…”
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20
New 2-bromomethyl-8-substituted-benzo[c]chromen-6-ones. Synthesis and biological properties
Published in Bioorganic & medicinal chemistry letters (01-01-2005)Get full text
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