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1.
Nat Prod Res ; 31(16): 1920-1929, 2017 Aug.
Artigo em Inglês | MEDLINE | ID: mdl-28032511

RESUMO

Two novel compounds bearing heterocyclic nitrogen, 2-pyridone alkaloid (1) and alloxazine derivative (2), along with the known pretenellin B (3), pyridovericin (4) and lumichrome (5) were isolated from a culture of the entomopathogenic fungal strain Beauveria bassiana. The chemical structures of 2-pyridone alkaloid and alloxazine derivative were established on the basis of the interpretation of spectroscopic data. The isolated compounds were evaluated in a panel of five cancer cell lines and pyridovericin exhibited cytotoxicity (IC50, µM) against cancer cell lines: HL-60 (25.9 ± 0.3), HCT8 (34.6 ± 3.6), MDA-MB435 (34.8 ± 3.8) and SF295 (31.1 ± 0.6). Considering that other pyridone compounds display good cytotoxic activity, it would be suggested to obtain new semi synthetic derivatives of pyridovericin, for the development of new cytotoxic chemical entities.


Assuntos
Alcaloides/química , Antineoplásicos/farmacologia , Beauveria/química , Alcaloides/isolamento & purificação , Alcaloides/farmacologia , Antineoplásicos/química , Beauveria/metabolismo , Linhagem Celular Tumoral , Ensaios de Seleção de Medicamentos Antitumorais , Flavinas/química , Flavinas/isolamento & purificação , Humanos , Estrutura Molecular , Monossacarídeos/química , Piridonas/química , Piridonas/isolamento & purificação , Piridonas/farmacologia , Metabolismo Secundário
2.
Nat Prod Res ; 26(23): 2168-75, 2012.
Artigo em Inglês | MEDLINE | ID: mdl-22239222

RESUMO

From cultures of thermophilic soil fungus Humicola grisea var thermoidea, a δ-lactam derivative (3-(2-(4-hydroxyphenyl)-2-oxoethyl)-5,6-dihydropyridin-2(1H)-one) that displayed anti-allergic activity was isolated, which was predicted by in silico computational chemistry approaches. The in vitro anti-allergic activity was investigated by ß-hexosaminidase release assay in rat basophilic leukaemia RBL-2H3 cells. The δ-lactam derivative exhibited similar anti-allergic activity (IC(50) = 18.7 ± 6.7 µM) in comparison with ketotifen fumarate (IC(50) = 15.0 ± 1.3 µM) and stronger anti-allergic activity than azelastine (IC(50) = 32.0 µM). Also, the MTT cytotoxicity assay with RBL-2H3 cells showed that δ-lactam does not display cytotoxicity at concentrations lower than 50 µM. This study suggests that the δ-lactam derivative has the potential to be used as a lead compound in the development of anti-allergic drugs for clinical use in humans.


Assuntos
Antialérgicos/química , Antialérgicos/farmacologia , Ascomicetos/química , Lactamas/química , Piridonas/química , Piridonas/farmacologia , Animais , Degranulação Celular/efeitos dos fármacos , Linhagem Celular Tumoral , Sobrevivência Celular/efeitos dos fármacos , Simulação por Computador , Relação Dose-Resposta a Droga , Avaliação Pré-Clínica de Medicamentos/métodos , Concentração Inibidora 50 , Cetotifeno/farmacologia , Espectroscopia de Ressonância Magnética , Estrutura Molecular , Ftalazinas/farmacologia , Ratos , Microbiologia do Solo , beta-N-Acetil-Hexosaminidases/metabolismo
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