Your browser doesn't support javascript.
loading
Mostrar: 20 | 50 | 100
Resultados 1 - 2 de 2
Filtrar
Más filtros

Banco de datos
Tipo del documento
Intervalo de año de publicación
1.
Chem Biodivers ; 21(5): e202400090, 2024 May.
Artículo en Inglés | MEDLINE | ID: mdl-38486477

RESUMEN

Streptomide (1), a new amide analogue, streptomynone (2), a new quinolinone, and ten known compounds including three aliphatic acids (3-5), two amides (6-7), four cyclic dipeptides (8-11), and an adenosine (12) were isolated from the fermentation broth of Streptomyces sp. YIM S01983 isolated from a sediment sample collected in Bendong Village, Huadong Town, Chuxiong, China. Their structures were determined by analysis of the 1D/2D-NMR and HR-ESI-MS spectra. Compound 12 presented weak antimicrobial activities against Candida albicans and Aligenes faecalis (MIC=64 µg/mL). Compounds 7 and 12 showed weak cytotoxic activity against MHCC97H.


Asunto(s)
Amidas , Candida albicans , Pruebas de Sensibilidad Microbiana , Quinolonas , Streptomyces , Streptomyces/química , Streptomyces/metabolismo , Amidas/química , Amidas/farmacología , Amidas/aislamiento & purificación , Candida albicans/efectos de los fármacos , Quinolonas/química , Quinolonas/farmacología , Quinolonas/aislamiento & purificación , Humanos , Línea Celular Tumoral , Antibacterianos/farmacología , Antibacterianos/química , Antibacterianos/aislamiento & purificación , Antifúngicos/farmacología , Antifúngicos/química , Antifúngicos/aislamiento & purificación , Antineoplásicos/farmacología , Antineoplásicos/química , Antineoplásicos/aislamiento & purificación , Enterococcus faecalis/efectos de los fármacos , Estructura Molecular , Relación Estructura-Actividad , Ensayos de Selección de Medicamentos Antitumorales
2.
Indian J Microbiol ; 61(4): 519-523, 2021 Dec.
Artículo en Inglés | MEDLINE | ID: mdl-34744207

RESUMEN

Ten compounds (1-10) were obtained from soil-derived Penicillium cremeogriseum W1-1 with the antimicrobial guided isolation procedure. Among them, 4 presented broad-spectrum antimicrobial activities and its preliminary mechanisms were evaluated. Compound 4 showed growth inhibition on drug-resistant pathogenic strains Escherichia coli and Candida albicans with post-contact effect (PCE), changed the morphology and membrane structure, killed cells with leakage, inhibited the growth of C. albicans by eradicating biofilms. Interestingly, the fraction containing 4 presented in vivo anti-pathogenic activities in mice, indicating this indole diterpenoid alkaloid could been used as potential antimicrobial agent.

SELECCIÓN DE REFERENCIAS
DETALLE DE LA BÚSQUEDA