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1.
Nat Prod Res ; 34(11): 1521-1527, 2020 Jun.
Artículo en Inglés | MEDLINE | ID: mdl-30445866

RESUMEN

A new ester (1) and a terpenoid (2) were isolated from the dried whole plant of Disporopsis aspersa (HUA) ENGL. ex DIELS for the first time and their structures were elucidated, as well as their biological activities are described. The two compounds all showed good antifungal activities, especially furanone (2) exhibited better antifungal activity against Pseudoperonospora cubensis and Phytophthora infestans with EC50 value of 22.82, 18.90 µg/mL, respectively. Compound 1 exhibited a significant promotion on the neurite outgrowth in NGF-induced PC-12 cells, and moderate inhibition on the NO production induced by lipopolysaccharide (LPS) in BV-2 microglial cells.


Asunto(s)
Antiinflamatorios/aislamiento & purificación , Antifúngicos/aislamiento & purificación , Asparagaceae/química , Proyección Neuronal/efectos de los fármacos , Extractos Vegetales/farmacología , Animales , Antiinflamatorios/farmacología , Antifúngicos/farmacología , Ésteres/aislamiento & purificación , Ésteres/farmacología , Microglía/efectos de los fármacos , Óxido Nítrico/antagonistas & inhibidores , Células PC12/efectos de los fármacos , Células PC12/ultraestructura , Phytophthora infestans/efectos de los fármacos , Extractos Vegetales/química , Ratas , Terpenos/aislamiento & purificación , Terpenos/farmacología
2.
Bioorg Med Chem ; 26(16): 4644-4649, 2018 09 01.
Artículo en Inglés | MEDLINE | ID: mdl-30119995

RESUMEN

A series of l-pyroglutamic acid analogues from natural product lead were designed and synthesized, as well as their antifungal activities against Phytophthora infestans, neuritogenic activities, antibacterial activities and anti-inflammatory activities are described. The bioassays and SAR study showed that the majority of l-pyroglutamic acid esters have a significant antifungal activity against P. infestans, especially 2d and 2j demonstrated the best activities with EC50 values of 1.44 and 1.21 µg mL-1, which were about seven times that of commercial azoxystrobin (7.85 µg mL-1). Moreover, compounds 2e, 2g and 4d displayed anti-inflammatory activity against LPS-induced NO production in BV-2 microglial cells; neuritogenic activity in NGF-induced PC-12 cells is the same activity. This study demonstrates that compounds 2d and 2j are potential drugs to control P. infestans.


Asunto(s)
Antifúngicos/síntesis química , Productos Biológicos/química , Ácido Pirrolidona Carboxílico/análogos & derivados , Animales , Antiinflamatorios/síntesis química , Antiinflamatorios/química , Antiinflamatorios/farmacología , Antifúngicos/química , Antifúngicos/farmacología , Línea Celular , Lipopolisacáridos/farmacología , Ratones , Microglía/citología , Microglía/efectos de los fármacos , Microglía/metabolismo , Óxido Nítrico/metabolismo , Células PC12 , Phytophthora infestans/efectos de los fármacos , Ácido Pirrolidona Carboxílico/síntesis química , Ácido Pirrolidona Carboxílico/farmacología , Ratas , Relación Estructura-Actividad
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