Synthesis, Characterization and Catalytic Activity of NiO-CoO-MgO Nano-Composite Catalyst

The ternary NiO-CoO-MgO catalyst in three ratios 20:20:60, 25:25:50, and 30:30:40 for these component oxides respectively, were synthesized by co-precipitation method of their carbonates by addition of a precipitate agent in basic media, and then calcinated these carbonate to obtain of mixed oxides. The prepared catalysts were characterized by using Powder X-Ray Diffraction (PXRD), Fourier Infrared spectroscopy (FT-IR), and Atomic Force Microscopy techniques (AFM) were used for identification of the prepared catalysts. The result showed that the particle size of these catalyst ratios, were in the nano range and the smallest size was 25:25:50. The investigation of catalytic activity of prepared catalysts was done by photo decolorization of Celestine blue B dye from simulated industrial wastewaters in aqueous solution. The decolorization efficiency of dye reached 99.9% after irradiation time for 1 h. Study the effect of different reaction conditions such as the pH of the medium, the weight of semiconductor and temperature of mixture reaction were shown that the maximum degradation was observed in conditions at pH = 4, catalyst dosage = 0.08 g, and temperature = 303 K

Cytotoxic and xanthine oxidase inhibitory activities of chemical constituents of alphonsea cylindrica king

This study aimed to investigate the chemical constituents from Alphonsea cylindrica as well as their cytotoxic and xanthine oxidase inhibitory activities. The chemical compounds were isolated and purified by various chromatographic techniques and their structures were elucidated via modern spectroscopic techniques including NMR, MS, IR, UV and comparison with literature. A study on the barks of A. cylindrica has found eleven known compounds were identified as stigmasterol (1), isoursuline (2), cyathocaline (3), kinabaline (4), muniranine (5), isooncodine (6), iraqiine (7), O-methylmoschatoline (8), kareemine (9), atherospermidine (10) and N-methylouregidione (11). The cytotoxic effect of hexane, DCM and methanol of bark of A. cylindrica as well as the isolated compounds; 1, 2, 3, 4, 5, 7, 8, 9 and 10 were estimated on MCF-7 human breast cancer cells and isoursuline possessed the most potent inhibitory activity with IC50 value of 33 µg/ml. Eight compounds 1, 3, 4, 5, 6, 8, 10 and 11 displayed moderate inhibitory activity effect with IC50 < 100 μM against xanthine oxidase. As a conclusion, eleven compounds have been isolated from the bark of A. cylindrica King. Some of the compounds also showed potential against cytotoxicity and xanthine oxidase inhibitory activities. The findings of this study can enhance the understanding of the chemotaxonomy aspect of the A. cylindrica as well as its potential in traditional and modern medicin

Alkaloids from alphonsea elliptica barks and their biological activities

This study was carried out to investigate the phytochemicals from the barks of Alphonsea elliptica. The barks were harvested from Hutan Simpan Sembarong, Kluang, Johor; and extracted using dichloromethane (DCM), hexane and methanol successively. Isolation of dichloromethane crude extract was then performed using silica gel column chromatography and preparative thin layer chromatography (PTLC) techniques. Structural identification were carried out via 1D and 2D NMR, UV, IR, MS and comparison with reported data. Phytochemical study of the barks led to the isolation of five alkaloid in which two were oxoaporphines; atherospermidine (1) and liriodenine (2),two were dioxoaporphines;cepharadione A (3) and N-methylouregidione (4), and an azafluorenone alkaloid; kinabaline (5). The hexane, DCM, and methanol crude extracts, together with five isolated alkaloids, were tested for their radical scavenging activity, inhibition of xanthine oxidase activities and cytotoxicity. Atherospermidine and liriodenine possessed antioxidative activities with IC50 value of 20.17 and 10.73, respectively. Atherospermidine, liriodenine, N-methylouregidione and kinabaline showed xanthine oxidase inhibitiory activityof 46.29, 7.66, 42.10 and 50.72 μM,respectively. Meanwhile, atherospermidine, liriodenine, cepharadione A and kinabaline showed cytotoxicity against breast cancer cell line with IC50 89, 86, 79.85 and 62 μg/mL respectively. All the alkaloids tested in this study were isolated for the first time from this species while cepharadione A is reported for the first time in a species belongs to Alphonsea genus

Alkaloids from Alphonsea elliptica barks and their biological activities

This study was carried out to investigate the phytochemicals from the barks of Alphonsea elliptica. The barks were harvested from Hutan Simpan Sembarong, Kluang, Johor; and extracted using dichloromethane (DCM), hexane and methanol successively. Isolation of dichloromethane crude extract was then performed using silica gel column chromatography and preparative thin layer chromatography (PTLC)techniques. Structural identification were carried out via 1D and 2D NMR, UV, IR, MS and comparison with reported data. Phytochemical study of the barks led tothe isolation of five alkaloid in which two were oxoaporphines; atherospermidine (1) and liriodenine (2),two were dioxoaporphines;cepharadione A (3) and N- methylouregidione (4), and an azafluorenone alkaloid;kinabaline (5). The hexane, DCM, and methanol crude extracts, together with five isolated alkaloids, were tested for theirradical scavenging activity,inhibition of xanthine oxidase activities and cytotoxicity. Atherospermidine and liriodenine possessed antioxidative activities with IC50 value of 20.17 and 10.73, respectively. Atherospermidine, liriodenine, N-methylouregidione and kinabaline showed xanthine oxidase inhibitiory activityof 46.29, 7.66, 42.10 and 50.72 μM,respectively. Meanwhile, atherospermidine, liriodenine, cepharadione A and kinabaline showed cytotoxicity against breast cancer cell line with IC50 89, 86, 79.85 and 62 µg/mL respectively. All the alkaloids tested in this study were isolated for the first time from this species while Cepharadione A is reported for the first time in a species belongs to Alphonsea genus