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1.
Fitoterapia ; 125: 49-54, 2018 Mar.
Artigo em Inglês | MEDLINE | ID: mdl-29269234

RESUMO

Seven new compounds, including four new chlorinated diphenyl ethers, namely chrysines A-D (1-4), one new dichlorinated xanthone, chrysoxanthone (5), dichloroorcinol (6), and one new benzeneacetic acid derivative, 3-isopentyl-4-hydroxy phenylacetic acid methyl ester (7), along with fourteen known compounds (8-21), were isolated from a deep-sea-derived fungus Penicillium chrysogenum SCSIO 41001. Their structures were determined by extensive spectroscopic methods and X-ray single-crystal diffraction analysis. All of the isolated compounds (1-21) were evaluated for their α-glucosidase inhibitory activity using PNPG method. Among them, nine compounds (2, 3, 5, 6, 8, 9, 13, 17, and 18) exhibited inhibitory activity against α-glucosidase with IC50 values of 0.35, 0.20, 0.04, 0.16, 0.15, 0.09, 0.14, 0.14, and 0.12mM, respectively (IC50 0.28mM for the positive control acarbose).


Assuntos
Inibidores de Glicosídeo Hidrolases/isolamento & purificação , Éteres Difenil Halogenados/isolamento & purificação , Penicillium chrysogenum/química , Xantonas/isolamento & purificação , Estrutura Molecular , Água do Mar/microbiologia , alfa-Glucosidases
2.
Fitoterapia ; 117: 71-78, 2017 Mar.
Artigo em Inglês | MEDLINE | ID: mdl-28108327

RESUMO

Five new compounds, including a cytotoxic dimeric isocoumarin, bipenicilisorin (1), a merosesquiterpenoid, yaminterritrem C (2), a citrinin dimer, penicitrinone F (3), a alkaloid, terremide D (4), and a δ-valerolacton, (E)-4-(propen-1-yl)-5,6-dihydro-2H-pyran-2-one (5), along with ten known compounds (6-15) were isolated from a deep-sea-derived fungus Penicillium chrysogenum SCSIO 41001. Their structures and absolute configurations were elucidated by NMR spectra, MS, CD, optical rotation, X-ray crystallography, and compared with literature data. Biological evaluation results revealed that 1 exhibited significant cytotoxic activities against K562, A549, and Huh-7 cell lines with IC50 values of 6.78, 6.94, and 2.59µM, respectively. Compound 3 exhibited moderate inhibitory activity against EV71 with IC50 value of 14.50µM. In addition, 13 and 14 showed specific COX-2 inhibitory activities with IC50 values of 1.09 and 1.97µM, respectively.


Assuntos
Citrinina/química , Penicillium chrysogenum/química , Alcaloides/química , Alcaloides/isolamento & purificação , Antineoplásicos/química , Antineoplásicos/isolamento & purificação , Linhagem Celular Tumoral , Citrinina/análogos & derivados , Citrinina/isolamento & purificação , Cristalografia por Raios X , Inibidores de Ciclo-Oxigenase/química , Inibidores de Ciclo-Oxigenase/isolamento & purificação , Humanos , Concentração Inibidora 50 , Isocumarinas/química , Isocumarinas/isolamento & purificação , Estrutura Molecular , Água do Mar/microbiologia , Sesquiterpenos/química , Sesquiterpenos/isolamento & purificação
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