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1.
J Med Chem ; 63(21): 12978-12991, 2020 11 12.
Artículo en Inglés | MEDLINE | ID: mdl-33100009

RESUMEN

Protein kinases C (PKCs) are a family of serine/threonine kinases involved in various cellular processes, including proliferation, differentiation, cell survival, and apoptosis. Here, we report the identification, structure-activity relationship (SAR), and 3D-QSAR studies of 69 natural indolocarbazoles, including 15 new compounds, from marine streptomyces strains. Interestingly, we found that the chair conformational isomer of 7-oxo-staurosporine (compound 15) inhibited PKCθ more potently than the corresponding boat isomer. An evaluation of kinase selectivity and antitumor efficacy revealed that 15 was a potent dual PKCθ/δ inhibitor and that it could efficiently inhibit tumor growth in pancreatic cancer (PC) by inducing cellular apoptosis and suppressing the NF-κB/p-P65 pathway. In addition, we demonstrated that overexpression of p-PKCδ and p-P65 was associated with poor survival rates in patients with PC, and p-PKCθ expression also showed significant positive correlations with p-PKCδ and p-P65 levels. Finally, the PC patient-derived xenograft model further confirmed the potential anti-PC efficacy of 15.


Asunto(s)
Carbazoles/química , Proteína Quinasa C-delta/antagonistas & inhibidores , Proteína Quinasa C-theta/antagonistas & inhibidores , Inhibidores de Proteínas Quinasas/química , Animales , Apoptosis/efectos de los fármacos , Sitios de Unión , Carbazoles/metabolismo , Carbazoles/farmacología , Carbazoles/uso terapéutico , Línea Celular Tumoral , Cristalografía por Rayos X , Humanos , Ratones , Ratones Endogámicos BALB C , Simulación del Acoplamiento Molecular , FN-kappa B/metabolismo , Neoplasias Pancreáticas/metabolismo , Neoplasias Pancreáticas/patología , Proteína Quinasa C-delta/metabolismo , Proteína Quinasa C-theta/metabolismo , Inhibidores de Proteínas Quinasas/metabolismo , Inhibidores de Proteínas Quinasas/farmacología , Inhibidores de Proteínas Quinasas/uso terapéutico , Agua de Mar/microbiología , Transducción de Señal/efectos de los fármacos , Streptomyces/química , Streptomyces/metabolismo , Relación Estructura-Actividad , Ensayos Antitumor por Modelo de Xenoinjerto
2.
Nat Prod Res ; 30(22): 2551-2558, 2016 Nov.
Artículo en Inglés | MEDLINE | ID: mdl-26728112

RESUMEN

Vineomycin A1 (1) and B2 (2) were isolated from the culture broth of marine actinomycete Streptomyces sp. A6H. Five hydrolysis products were obtained by rational hydrolysis and methanolysis of the fermentation extract. Their structures were characterised as aquayamycin (3), vineomycinone B2 (4), 9-C-D-olivosyltetrangulol (5), 7-O-methylgaltamycinone (6) and vineomycinone B2 methyl ester (7). In addition to these compounds, two ester derivatives, vineolactone A (8) and vineomycinone B2 benzyl ester (9) of compound 4 were generated semisynthetically. Compound 6 is a new analogue of galtamycinone, while compounds 8 and 9 are new members of vineomycins. Cytotoxic activities and antimicrobial activities were determined for all compounds. The results indicate that only compound 1 showed significant activities with IC50 value of 0.34 µM against H1975 and MIC value of 4 µg/mL against Staphylococcus aureus.

3.
Nat Prod Res ; 30(20): 2311-5, 2016 Oct.
Artículo en Inglés | MEDLINE | ID: mdl-27067647

RESUMEN

Four new analogues of brefeldin A named 7, 7-dimethoxybrefeldin C (3), 6ß-hydroxybrefeldin C (4), 4-epi-15-epi-brefeldin A (5), 4-epi-8α-hydroxy-15-epi-brefeldin C (6), together with four known analogues (1, 7-9) were isolated from a fermentation of the sediment-derived fungus Penicillium sp. DT-F29. The structures of these compounds were elucidated on the basis of extensive spectroscopic and chemical methods. In the bioactivity assays, only compounds 1 and 8 showed significant inhibitory activities against human lung adenocarcinoma cell. In addition, compound 1 was first reported for the potent ability to reactivate latent HIV with EC50 value of 0.03 µM.


Asunto(s)
Fármacos Anti-VIH/farmacología , Antineoplásicos/farmacología , Brefeldino A/análogos & derivados , Penicillium/química , Fármacos Anti-VIH/química , Antineoplásicos/química , Línea Celular Tumoral , Evaluación Preclínica de Medicamentos , Sedimentos Geológicos/microbiología , Humanos , Estructura Molecular
4.
Chemosphere ; 146: 442-9, 2016 Mar.
Artículo en Inglés | MEDLINE | ID: mdl-26741550

RESUMEN

Removal of the refractory organic matters in leachate brines generated from nanofiltration unit in two full-scale municipal solid waste landfill leachate treatment plants was investigated by Fenton oxidative-coagulation and ultraviolet photo - Fenton processes in this study. Fenton oxidative-coagulation was performed under the condition of an initial pH of 5.0 and low H2O2/Fe(2+) ratios. After precipitate separation, the remaining organic constituents were further oxidized by photo - Fenton process. For both leachate brines with varying pollution strength, more than 90% COD and TOC reductions were achieved at H2O2/Fe(2+) dosages of 35 mM/8 mM and 90 mM/10 mM, respectively. The effluent COD ranged 120-160 mg/L under the optimal operating conditions, and the biodegradability was increased significantly. Fenton oxidative-coagulation was demonstrated to contribute nearly 70% overall removal of organic matters. In the combined processes, the efficiency of hydrogen peroxide varied from 216 to 228%, which may significantly reduce the operating cost of conventional Fenton method. Six phthalic acid esters and thirteen polycyclic aromatic hydrocarbons were found in leachate brines, and, on the average, around 80% phthalic acid esters and 90% polycyclic aromatic hydrocarbons were removed by the combined treatments.


Asunto(s)
Peróxido de Hidrógeno/química , Hierro/química , Residuos Sólidos/análisis , Rayos Ultravioleta , Contaminantes Químicos del Agua/análisis , Purificación del Agua/métodos , Biodegradación Ambiental , Análisis de la Demanda Biológica de Oxígeno , Filtración , Floculación , Membranas Artificiales , Oxidación-Reducción , Contaminantes Químicos del Agua/efectos de la radiación
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