Your browser doesn't support javascript.
loading
Mostrar: 20 | 50 | 100
Resultados 1 - 3 de 3
Filtrar
Más filtros













Base de datos
Intervalo de año de publicación
1.
Bioorg Med Chem Lett ; 28(20): 3372-3375, 2018 11 01.
Artículo en Inglés | MEDLINE | ID: mdl-30201291

RESUMEN

We report here the design and synthesis of a novel series of benzylamines that are potent and selective inhibitors of uPA with promising oral availability in rat. Further evaluation of one representative (ZK824859) of the new structural class showed that this compound lowered clinical scores when dosed in either acute or chronic mouse EAE models, suggesting that uPA inhibitors of this type could be useful for the treatment of multiple sclerosis.


Asunto(s)
Bencilaminas/uso terapéutico , Esclerosis Múltiple/tratamiento farmacológico , Inhibidores de Serina Proteinasa/uso terapéutico , Activador de Plasminógeno de Tipo Uroquinasa/antagonistas & inhibidores , Animales , Bencilaminas/síntesis química , Bencilaminas/química , Bencilaminas/farmacocinética , Sitios de Unión , Femenino , Humanos , Ratones , Modelos Moleculares , Estructura Molecular , Ratas , Inhibidores de Serina Proteinasa/síntesis química , Inhibidores de Serina Proteinasa/química , Inhibidores de Serina Proteinasa/farmacocinética , Relación Estructura-Actividad , Activador de Plasminógeno de Tipo Uroquinasa/química
2.
Bioorg Med Chem Lett ; 19(19): 5712-5, 2009 Oct 01.
Artículo en Inglés | MEDLINE | ID: mdl-19703768

RESUMEN

In this Letter we report the synthesis and evaluation of a series of non-amidine inhibitors of Urokinase Plasminogen Activator (uPA). Starting from compound 1, a significant change provided compounds in which the amidine, binding in the S1 pocket, was replaced with a primary amine. Further modifications led to the identification of potent, selective, and orally bioavailable uPA inhibitors.


Asunto(s)
Bencilaminas/química , Inhibidores de Serina Proteinasa/química , Activador de Plasminógeno de Tipo Uroquinasa/antagonistas & inhibidores , Administración Oral , Amidinas/química , Animales , Sitios de Unión , Cristalografía por Rayos X , Humanos , Ratas , Inhibidores de Serina Proteinasa/administración & dosificación , Inhibidores de Serina Proteinasa/síntesis química , Relación Estructura-Actividad , Activador de Plasminógeno de Tipo Uroquinasa/metabolismo
3.
Acta Crystallogr D Biol Crystallogr ; 64(Pt 2): 149-57, 2008 Feb.
Artículo en Inglés | MEDLINE | ID: mdl-18219114

RESUMEN

This article reports the crystal structures of inhibitors of the functional form of thrombin-activatable fibrinolysis inhibitor (TAFIa). In vivo experiments indicate that selective inhibitors of TAFIa would be useful in the treatment of heart attacks. Since TAFIa rapidly degrades in solution, the homologous protein porcine pancreatic carboxypeptidase B (pp-CpB) was used in these crystallography studies. Both TAFIa and pp-CpB are zinc-based exopeptidases that are specific for basic residues. The final development candidate, BX 528, is a potent inhibitor of TAFIa (2 nM) and has almost no measurable effect on the major selectivity target, carboxypeptidase N. BX 528 was designed to mimic the tripeptide Phe-Val-Lys. A sulfonamide replaces the Phe-Val amide bond and a phosphinate connects the Val and Lys groups. The phosphinate also chelates the active-site zinc. The electrostatic interactions with the protein mimic those of the natural substrate. The primary amine in BX 528 forms a salt bridge to Asp255 at the base of the S1' pocket. The carboxylic acid interacts with Arg145 and the sulfonamide is hydrogen bonded to Arg71. Isopropyl and phenyl groups replace the side chains of Val and Phe, respectively. A series of structures are presented here that illustrate the evolution of BX 528 from thiol-based inhibitors that mimic a free C-terminal arginine. The first step in development was the replacement of the thiol with a phosphinate. This caused a precipitous drop in binding affinity. Potency was reclaimed by extending the inhibitors into the downstream binding sites for the natural substrate.


Asunto(s)
Carboxipeptidasa B/metabolismo , Péptidos/química , Péptidos/metabolismo , Sitios de Unión , Carboxipeptidasa B/química , Carboxipeptidasa B2/química , Cristalografía por Rayos X/métodos , Humanos , Enlace de Hidrógeno , Modelos Moleculares , Estructura Molecular
SELECCIÓN DE REFERENCIAS
DETALLE DE LA BÚSQUEDA