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1.
Bioorg Med Chem Lett ; 20(13): 3936-40, 2010 Jul 01.
Artigo em Inglês | MEDLINE | ID: mdl-20570148

RESUMO

A novel pyrrole-2-carboxamide series of p38alpha inhibitors, discovered through the application of virtual screening, is presented. Following evaluation of activity, selectivity and developability properties of commercially available analogues, a synthesis program enabled rapid assessment of the series' suitability for further lead optimisation studies.


Assuntos
Amidas/farmacologia , Descoberta de Drogas , Inibidores de Proteínas Quinases/farmacologia , Pirróis/química , Proteínas Quinases p38 Ativadas por Mitógeno/antagonistas & inibidores , Amidas/síntese química , Amidas/química , Relação Dose-Resposta a Droga , Ensaios de Triagem em Larga Escala , Estrutura Molecular , Inibidores de Proteínas Quinases/síntese química , Inibidores de Proteínas Quinases/química , Estereoisomerismo , Relação Estrutura-Atividade
3.
J Med Chem ; 54(14): 5131-43, 2011 Jul 28.
Artigo em Inglês | MEDLINE | ID: mdl-21699136

RESUMO

A kinase-focused screening set of fragments has been assembled and has proved successful for the discovery of ligand-efficient hits against many targets. Here we present some of our general conclusions from this exercise. Notably, we present the first profiling results for literature fragments that have previously been used as starting points for optimization against individual kinases. We consider the importance of screening format and the extent to which selectivity is helpful in selecting fragments for progression. Results are also outlined for fragments targeting the DFG-out conformation and for atypical kinases such as PIM1 and lipid kinases.


Assuntos
Inibidores Enzimáticos/química , Modelos Moleculares , Fosfotransferases/antagonistas & inibidores , Fosfotransferases/química , Relação Quantitativa Estrutura-Atividade , Adenina/química , Trifosfato de Adenosina/química , Compostos de Anilina/química , Sítios de Ligação , Ensaios de Triagem em Larga Escala , Indazóis/química , Indóis/química , Isoenzimas/antagonistas & inibidores , Isoenzimas/química , Fosfatidilinositol 3-Quinases/química , Inibidores de Fosfoinositídeo-3 Quinase , Ligação Proteica , Inibidores de Proteínas Quinases/química , Proteínas Proto-Oncogênicas c-pim-1/antagonistas & inibidores , Proteínas Proto-Oncogênicas c-pim-1/química , Piridinas/química , Pirimidinas/química , Bibliotecas de Moléculas Pequenas
4.
J Pharmacol Exp Ther ; 312(1): 373-81, 2005 Jan.
Artigo em Inglês | MEDLINE | ID: mdl-15316093

RESUMO

Demonstration that IkappaB kinase 2 (IKK-2) plays a pivotal role in the nuclear factor-kappaB-regulated production of proinflammatory molecules by stimuli such as tumor necrosis factor (TNF)-alpha and interleukin (IL)-1 suggests that inhibition of IKK-2 may be beneficial in the treatment of rheumatoid arthritis. In the present study, we demonstrate that a novel, potent (IC(50) = 17.9 nM), and selective inhibitor of human IKK-2, 2-[(aminocarbonyl)amino]-5-(4-fluorophenyl)-3-thiophenecarboxamide (TPCA-1), inhibits lipopolysaccharide-induced human monocyte production of TNF-alpha, IL-6, and IL-8 with an IC(50) = 170 to 320 nM. Prophylactic administration of TPCA-1 at 3, 10, or 20 mg/kg, i.p., b.i.d., resulted in a dose-dependent reduction in the severity of murine collagen-induced arthritis (CIA). The significantly reduced disease severity and delay of disease onset resulting from administration of TPCA-1 at 10 mg/kg, i.p., b.i.d. were comparable to the effects of the antirheumatic drug, etanercept, when administered prophylactically at 4 mg/kg, i.p., every other day. Nuclear localization of p65, as well as levels of IL-1beta, IL-6, TNF-alpha, and interferon-gamma, were significantly reduced in the paw tissue of TPCA-1- and etanercept-treated mice. In addition, administration of TPCA-1 in vivo resulted in significantly decreased collagen-induced T cell proliferation ex vivo. Therapeutic administration of TPCA-1 at 20 mg/kg, but not at 3 or 10 mg/kg, i.p., b.i.d., significantly reduced the severity of CIA, as did etanercept administration at 12.5 mg/kg, i.p., every other day. These results suggest that reduction of proinflammatory mediators and inhibition of antigen-induced T cell proliferation are mechanisms underlying the attenuation of CIA by the IKK-2 inhibitor, TPCA-1.


Assuntos
Amidas/uso terapêutico , Antiasmáticos/uso terapêutico , Artrite Experimental/tratamento farmacológico , Citocinas/metabolismo , Proteínas Serina-Treonina Quinases/antagonistas & inibidores , Tiofenos/uso terapêutico , Trifosfato de Adenosina/metabolismo , Amidas/farmacologia , Animais , Antiasmáticos/farmacologia , Artrite Experimental/induzido quimicamente , Artrite Experimental/metabolismo , Artrite Experimental/prevenção & controle , Ligação Competitiva , Proliferação de Células/efeitos dos fármacos , Quimiocinas/metabolismo , Colágeno , Citocinas/efeitos dos fármacos , Modelos Animais de Doenças , Humanos , Quinase I-kappa B , Interleucina-6/metabolismo , Interleucina-8/metabolismo , Lipopolissacarídeos/farmacologia , Masculino , Camundongos , Camundongos Endogâmicos DBA , Monócitos/efeitos dos fármacos , Monócitos/metabolismo , NF-kappa B/metabolismo , Linfócitos T/citologia , Linfócitos T/efeitos dos fármacos , Tiofenos/farmacologia , Fator de Transcrição RelA , Fator de Necrose Tumoral alfa/metabolismo
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