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1.
Pakistan Journal of Pharmaceutical Sciences. 2017; 30 (4): 1335-1339
em Inglês | IMEMR | ID: emr-189702

RESUMO

A new naturally occurring dibenzylbutyrolactone lignan named isocubebinic ether has been isolated from Knema patentinervia. The structure was established by spectroscopic methods, which include Ultraviolet, Infrared, Nuclear Magnetic Resonance and Mass Spectrometry. The compound showed activity in the stimulation of glucose uptake by 3T3-L1 adipocytes


Assuntos
Adipócitos , Lignanas , Éteres , Células 3T3-L1 , Glucose , Espectroscopia de Ressonância Magnética , Extratos Vegetais , Espectrometria de Massas , Caules de Planta
2.
Pakistan Journal of Pharmaceutical Sciences. 2014; 27 (1): 179-181
em Inglês | IMEMR | ID: emr-142998

RESUMO

An alkaloid from Maclurodendron porteri has been isolated and characterized. Extraction process was conducted by acid-base extraction method followed by column chromatography. The structure was established by nuclear magnetic resonance spectroscopy and mass spectrometry. The compound was identified as haplophytin B which occurs commonly in the Rutaceae family. However, this is the first time this alkaloid was isolated and reported from the species. The compound showed no inhibition against Staphylococus aureus, Pseudomonas aeruginosa, Bacillus cereus and Escherichia coli and no cytotoxic activity against H199 and A549 cell lines.


Assuntos
Compostos Heterocíclicos com 3 Anéis/isolamento & purificação , Alcaloides/química , Alcaloides/isolamento & purificação , Espectroscopia de Ressonância Magnética
3.
University of Aden Journal of Natural and Applied Sciences. 2010; 14 (2): 325-247
em Inglês | IMEMR | ID: emr-122767

RESUMO

The reaction of 0-vanillin 1 with phenylenediamine isomers 2-4 in dichloromethane formed three diaminobenzene derivatives: N,N'-bis [2-hydroxy-3-methoxybenzylidene]-1,2-diaminobenzene 5, N,N'-bis [2-hydroxy-3-methoxybenzylid-ene]-l,3-diaminobenzene 6 and N,N'-bis [2-hydroxy-3-methoxybenzylidene]-l,4-di-aminobenzene 7, respectively, All compounds were obtained as single crystals and the structures were determined by X-ray crystallography. All compounds were confirmed by FTIR, HRMS, ID and 2D NMR spectroscopy. The complete assignments of these compounds, using ID and 2D NMR including APT, DEPT-135, COSY, HMQC and HMBC in CDC1[3], will be discussed


Assuntos
Derivados de Benzeno/síntese química , Diaminas/química , Diaminas/síntese química , Análise Espectral
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