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1.
J Nat Prod ; 82(12): 3242-3248, 2019 12 27.
Artículo en Inglés | MEDLINE | ID: mdl-31742403

RESUMEN

Melongenaterpenes A-L (1-12), 12 new sesquiterpenoids with rare spiro[4.5]decane skeletons, were isolated from the roots of Solanum melongena. Their 2D structures and relative configurations were determined based on NMR and HRESIMS data. The absolute configuration of melongenaterpene A (1) was defined by X-ray crystallographic analysis. The absolute configurations of the remaining compounds were determined by comparison of their NMR data with 1 and consideration of the biosynthetic pathway. This is the first report of the crystal structure of a vetispirane-type sesquiterpenoid. None of the compounds exhibited cytotoxic activity against the three human cancer cell lines HepG2, HeLa, and MCF-7.


Asunto(s)
Antineoplásicos Fitogénicos/aislamiento & purificación , Raíces de Plantas/química , Sesquiterpenos/aislamiento & purificación , Solanum melongena/química , Antineoplásicos Fitogénicos/química , Antineoplásicos Fitogénicos/farmacología , Cristalografía por Rayos X , Células HeLa , Células Hep G2 , Humanos , Células MCF-7 , Estructura Molecular , Sesquiterpenos/química , Sesquiterpenos/farmacología , Análisis Espectral/métodos
2.
Molecules ; 24(10)2019 May 17.
Artículo en Inglés | MEDLINE | ID: mdl-31109015

RESUMEN

Cardiovascular disease is one of the leading causes of morbidity and mortality worldwide. Mangiferin is a natural glucosylxanthone with antioxidant and anti-inflammatory properties, which has been confirmed to protect cardiac cells from myocardial infarction and myocardial ischemia reperfusion injury (MIRI); however, the underlying mechanism is still unclear. As oxidative stress is a major pathogenesis of MIRI, an H9C2 cell injury induced by hydrogen peroxide (H2O2) was established to simulate MIRI in vitro. Herein, the protective effect of mangiferin against MIRI was evaluated and the isobaric tags for relative and absolute quantitation (iTRAQ)-based proteomics was applied to explore the underlying molecular mechanism. In this research, mangiferin markedly ameliorated the oxidative imbalance by increasing the antioxidative capacity of the H9C2 cell. Moreover, proteomics analysis revealed that mangiferin pretreatment brought twenty differently-expressed proteins back to normal, most of which were related to glucose and fatty acid metabolism. Glycolysis, citrate cycle, and fatty acid degradation pathways were highlighted by Kyoto Encyclopedia of Gene and Genomes (KEGG) analysis. Western blot validation of six cardiac metabolism-related proteins were consistent with the proteomics analysis. Taken together, mangiferin protected the cardiomyocytes from MIRI by enhancing the antioxidant capacity and increasing the activities of glycolysis, citrate cycle, and fatty acid degradation pathways.


Asunto(s)
Cardiotónicos/farmacología , Peróxido de Hidrógeno/efectos adversos , Miocitos Cardíacos/citología , Proteómica/métodos , Xantonas/farmacología , Animales , Línea Celular , Ciclo del Ácido Cítrico/efectos de los fármacos , Regulación de la Expresión Génica/efectos de los fármacos , Glucólisis/efectos de los fármacos , Miocitos Cardíacos/efectos de los fármacos , Miocitos Cardíacos/metabolismo , Estrés Oxidativo/efectos de los fármacos , Ratas
3.
Nat Prod Res ; 36(15): 3979-3987, 2022 Aug.
Artículo en Inglés | MEDLINE | ID: mdl-33769155

RESUMEN

Three new sesquiterpenoid alkaloids, cangorin K (1), dimacroregelines C (2) and D (3), as well as two known sesquiterpenoids (4-5), were isolated from the roots of Tripterygium wilfordii Hook. f. The structures of new compounds were characterised by extensive 1D and 2D NMR spectroscopic analyses, as well as HRESIMS data, and the known compounds were established by 1 D NMR spectra referring to the literatures. Cytotoxicity evaluation of these compounds against two human tumour lines (SMMC7721, LN229) was investigated by CCK-8 assay and displayed that compounds 1-4 showed potent cytotoxicity against SMMC7721 cell with IC50 value in the range of 0.26-9.67 µΜ and compounds 1-5 showed potent cytotoxicity against LN-229 cell with IC50 values in the range of 0.50-7.38 µΜ.


Asunto(s)
Alcaloides , Sesquiterpenos , Alcaloides/química , Humanos , Estructura Molecular , Raíces de Plantas/química , Sesquiterpenos/química , Tripterygium/química
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