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1.
Chem Biodivers ; 21(4): e202400029, 2024 Apr.
Artigo em Inglês | MEDLINE | ID: mdl-38270294

RESUMO

Two new alpiniamide-type polyketides, alpiniamides H-I (1-2), in addition to four recognized compounds, were discovered in Streptomyces sp. ZSA65 derived from the marine sediments. The planar structure and absolute configuration of alpiniamides H-I were elucidated using a combination of 1D, 2D NMR, HRESIMS data analysis, Mosher's method and ECD calculations. The antibiofilm and antibacterial activities against P. aeruginosa were evaluated using the microdilution method. Notably, Compound 2 exhibited strong antibiofilm property.


Assuntos
Policetídeos , Streptomyces , Policetídeos/farmacologia , Policetídeos/química , Streptomyces/química , Antibacterianos/farmacologia , Espectroscopia de Ressonância Magnética , Biofilmes , Estrutura Molecular
2.
Chem Biodivers ; 21(2): e202301712, 2024 Feb.
Artigo em Inglês | MEDLINE | ID: mdl-38031386

RESUMO

A novel staurosporine derivate, streptomholyrine A (1), along with 6 known compounds were identified from the rice-based solid fermentation of marine-derived Streptomyces sp. ZS-A121. The planar structure and absolute configuration of streptomholyrine A were elucidated using a combination of 1D, 2D NMR, HRESIMS data analysis, chemical transformation, ECD and NMR calculations. Screening of all these compounds revealed their cytotoxic activity against HCT-116 cell lines, with IC50 values ranging from 0.012 to 11.67 µM, except for the known 1H-indole-3-hydroxyacetyl, which showed no inhibition activity. Furthermore, streptomholyrine A, along with two known staurosporine derivatives, k252d and staurosporine, exhibited activities against Candida albicans, with MICs of 12.5, 25.0 and 50.0 µg/ml, respectively.


Assuntos
Actinobacteria , Antineoplásicos , Streptomyces , Humanos , Estaurosporina/farmacologia , Estaurosporina/metabolismo , Antifúngicos/farmacologia , Antifúngicos/metabolismo , Streptomyces/química , Antineoplásicos/química , Estrutura Molecular
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