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1.
Eur J Med Chem ; 188: 112031, 2020 Feb 15.
Artículo en Inglés | MEDLINE | ID: mdl-31923861

RESUMEN

Hepatitis C virus (HCV) is a major cause of end-stage liver diseases. Direct-acting antivirals (DAAs), including inhibitors of nonstructural proteins (NS3/4A protease, NS5A, and NS5B polymerase), represent key components of anti-HCV treatment. However, some DAAs are associated with increased drug resistance and undesired side effects. Previous reports have shown that bisamides could be a novel class of cyclophilin A (CypA) inhibitors for treating HCV as a member of combinational therapies. To fully elucidate structure-activity relationships of bisamide derivatives and find a better hit compound with diverse binding modes, 16 biamides were designed with the help of docking program. They were then synthesized using one-pot four-component Ugi reaction. 7e with selectivity index of more than 18.9 (50% effective concentration of 5.3 µM, but no cytotoxicity at 100 µM) and unique binding mode that could be dived into gatekeeper pocket was selected as a new hit compound. Surface plasmon resonance experiments revealed that 7e is able to bind to CypA with a KD of 3.66 µM. Taken together, these results suggest that 7e as a CypA inhibitor could be used as an alternative anti-HCV agent in combinational therapy in the future.


Asunto(s)
Amidas/farmacología , Antivirales/farmacología , Ciclofilina A/antagonistas & inhibidores , Diseño de Fármacos , Hepacivirus/efectos de los fármacos , Hepatitis C/tratamiento farmacológico , Amidas/síntesis química , Amidas/química , Antivirales/síntesis química , Antivirales/química , Supervivencia Celular/efectos de los fármacos , Ciclofilina A/metabolismo , Relación Dosis-Respuesta a Droga , Hepacivirus/metabolismo , Hepatitis C/metabolismo , Humanos , Pruebas de Sensibilidad Microbiana , Simulación del Acoplamiento Molecular , Estructura Molecular , Relación Estructura-Actividad , Resonancia por Plasmón de Superficie , Células Tumorales Cultivadas
2.
Expert Opin Ther Pat ; 26(2): 229-43, 2016.
Artículo en Inglés | MEDLINE | ID: mdl-26610159

RESUMEN

INTRODUCTION: A number of plant-derived agents are used in many therapeutic areas. Berberine, an important protoberberine alkaloid, is present in a number of medicinal plants that have been widely used in traditional Chinese medicine for hundreds of years. Modern research has shown that berberine and its derivatives display several pharmacological effects through various mechanisms. AREAS COVERED: This review discusses recent and mostly Chinese patents that report the synthesis of berberine, berberine derivatives and berberine salts, and methods of preparation for formulations (traditional Chinese medicine) containing herbal components rich in berberine, along with their applications. The review covers several therapeutic effects of berberine, its derivatives and pharmaceutical formulations against cancer, obesity, diabetes, inflammation, atherosclerosis, Alzheimer's disease, rheumatoid arthritis and cardiovascular diseases. In addition, the mechanisms underlying the pharmacological effects are discussed. EXPERT OPINION: Modification of the functional groups of berberine has a significant effect on the pharmacological activity. However, studies on altering the atoms and size of the berberine skeleton are rare. Thus, it may be beneficial to initiate a drug development program focused on inserting heterocyclic rings of different sizes into berberine. Furthermore, structural modification to improve the safety, efficacy and selectivity is necessary to promote the use of berberine-based drugs in clinical settings.


Asunto(s)
Berberina/farmacología , Diseño de Fármacos , Medicina Tradicional China , Animales , Berberina/análogos & derivados , Berberina/química , Química Farmacéutica/métodos , Humanos , Patentes como Asunto , Plantas Medicinales/química
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