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1.
Bioorg Med Chem ; 23(11): 2636-45, 2015 Jun 01.
Artículo en Inglés | MEDLINE | ID: mdl-25907365

RESUMEN

Scaffolds of natural products represent promising starting points for the development of focused compound libraries. Here, we describe the development of a synthetic route to a compound library based on the hexahydropyrrolo indole (HPI) scaffold, the denoting structural motif of the HPI natural product family. To this end, a two-step approach consisting of a batch synthesis of an advanced functionalizable HPI intermediate followed by the establishment of reaction conditions that allow derivatization of this scaffold at three different positions is described. Subsequently, the optimized methods were applied to the synthesis of a 276-member library.


Asunto(s)
Productos Biológicos/síntesis química , Descubrimiento de Drogas , Indoles/síntesis química , Bibliotecas de Moléculas Pequeñas/síntesis química , Reacción de Cicloadición , Estructura Molecular
2.
Bioorg Med Chem Lett ; 22(1): 689-95, 2012 Jan 01.
Artículo en Inglés | MEDLINE | ID: mdl-22079756

RESUMEN

Libraries of dibasic compounds designed around the molecular scaffold of the DA(2)/ß(2) dual agonist sibenadet (Viozan™) have yielded a number of promising starting points that have been further optimised into novel potent and selective target molecules with required pharmacokinetic properties. From a shortlist, 31 was discovered as a novel, high potency, and highly efficacious ß(2)-agonist with high selectivity and a duration of action commensurable with once daily dosing.


Asunto(s)
Agonistas Adrenérgicos beta/síntesis química , Agonistas Adrenérgicos beta/farmacología , Química Farmacéutica/métodos , Animales , Asma/tratamiento farmacológico , Broncodilatadores/farmacología , Línea Celular Tumoral , AMP Cíclico/metabolismo , Diseño de Fármacos , Cobayas , Humanos , Concentración 50 Inhibidora , Modelos Químicos , Unión Proteica , Enfermedad Pulmonar Obstructiva Crónica/tratamiento farmacológico , Tiazoles/farmacología , Factores de Tiempo
3.
Bioorg Med Chem Lett ; 18(2): 798-803, 2008 Jan 15.
Artículo en Inglés | MEDLINE | ID: mdl-18240390

RESUMEN

The CXCR2 SAR of a series of bicyclic antagonists such as the 2-aminothiazolo[4,5-d]pyrimidine 3b was investigated by systematic variation of the fused pyrimidine-based heterocyclic cores. Replacement of the aminothiazole ring with a 2-thiazolone alternative led to a series of thiazolo[4,5-d]pyrimidine-2(3H)-one antagonists with markedly improved biological and pharmacokinetic properties, which are suitable pharmacological tools to probe the in vivo effects of CXCR2 antagonism combined with the associated CCR2 activity.


Asunto(s)
Pirimidinas/química , Pirimidinas/farmacología , Receptores de Interleucina-8B/antagonistas & inhibidores , Administración Oral , Animales , Disponibilidad Biológica , Evaluación Preclínica de Medicamentos , Pirimidinas/administración & dosificación , Pirimidinas/farmacocinética , Ratas , Relación Estructura-Actividad
4.
Sci Total Environ ; 419: 250-64, 2012 Mar 01.
Artículo en Inglés | MEDLINE | ID: mdl-22297247

RESUMEN

A multifaceted instrumental approach was employed to determine the chemistry and mineralogy of pulverized-coal-combustion fly ashes from two Chinese power plants. Techniques included traditional optical microscopy, X-ray diffraction, and chemical analysis along with a variety of electron beam methods. The aim is to demonstrate and bring together the wide variety of procedures dealing with F as the key element of concern, and determining its location in the mineral nanoparticles. The Hg content of the Anwen (Songzao coalfield) fly ashes is higher than that of the Diandong (East Yunnan) fly ashes, possibly owing to the greater C and Cl in the Anwen fly ashes. Both fly ash sources contain a variety of amorphous and nano-crystalline trace-element-bearing particles, both associated with multi-walled carbon nanotubes and as particles independent of carbons.


Asunto(s)
Contaminantes Atmosféricos/análisis , Contaminantes Atmosféricos/química , Ceniza del Carbón/análisis , Ceniza del Carbón/química , Carbono/química , China , Espectrometría de Masas , Microscopía Electrónica , Nanopartículas/análisis , Nanopartículas/química , Centrales Eléctricas , Dispersión de Radiación , Análisis Espectral
5.
Bioorg Med Chem Lett ; 17(10): 2731-4, 2007 May 15.
Artículo en Inglés | MEDLINE | ID: mdl-17382543

RESUMEN

As part of a Lead Optimisation programme to identify small molecule antagonists of the human CXCR2 receptor, a series of substituted thiazolo[4,5-d]pyrimidines was prepared via the application of a novel tandem displacement reaction.


Asunto(s)
Receptores de Interleucina-8B/antagonistas & inhibidores , Tiazoles/farmacología , Animales , Humanos , Ratas , Receptores de Citocinas/antagonistas & inhibidores , Relación Estructura-Actividad , Tiazoles/química
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