Three new flavonoids, quercetin-3-O-6-[methyl-(S)-3-hydroxy-3-methylglutaroyl(1→6]-β-d-glucopyranoside (1), kaempferol-3-O-[methyl-(S)-3-hydroxy-3-methylglutaroyl(1→6)]-β-d-glucopyranoside (2), and quercetin-3-O-6-[(E)-4-methoxy-5-methylhexa-2,4-dienoatyl(1→6)]-β-d-glucopyranoside (3), and two new alkaloids, 5-dehydroxymethyl-pyrrolemarumine 4″-O-α-l-rhamnopyranoside (4) and N 1-methyl-N 2-((4-O-α-l-rhamnopyranoside)benzyl) oxalamide (5), together with 45 known compounds (6–50) were isolated from the leaves of Moringa oleifera Lam. Among those compounds, 1-octacosanol (50), a straight-chain 28-carbon alcohol, exhibited good activity against diphenoxylate-induced constipation in mice, which is obtained as a laxative constituent from the plant for the first time. In order to have an accurate understanding of the content of compound 50, a quantification with gas chromatography–tandem mass spectrometry (GC–MS/MS) was carried out. The anti-inflammatory and α-glucosidase inhibitory activity of some compounds also was assessed.
Phytochemical study on the 95% ethyl alcohol extract of stems of Chenopodium ambrosioides resulted in the isolation of two new polyol monoterpenes, 4-hydroxy-4(α or β)-isopropyl-2-methyl-2-cyclohexen-1-one (1) and 1-methyl-4β- isopropyl-1-cyclohexene-4α,5α,6α-triol (2), together with five known compounds, (1S,2S,3R,4S)-1-methyl-4-(propan-2-yl)cyclohexane-1,2,3,4-tetrol (3), (1R,2S,3S,4S)- 1,2,3,4-tetrahydroxy-p-menthane (4), (1R,2S)-3-p-menthen-1,2-diol (5), (1R,4S)-p- menth-2-en-1-ol (6) and 1,4-dihydroxy-p-menth-2-ene (7). The structures of the new compounds were established on the basis of detailed spectroscopic evidence including extensive 1D and 2D NMR techniques. Compounds 1-7 were evaluated for their anti-inflammatory activity, and compound 1 showed moderate ability to inhibit NO production of LPS-stimulated RAW 264.7 macrophages with an IC value of 16.83 μM.
Objective: to investigate glass infiltrating rates (depth/time) within dental CAD/CAM alumina at different temperatures. Methods: micron α-alumina powder was prepared with cold isostastic pressure at 250 MPa and sintered at 1450°C. The presintered alumina specimens were then infiltrated with special glass at 1150°C, 1200°C and 1250 °C. The infiltrating depths and time to form the infiltrate at the different temperatures were evaluated. Results: As the infiltrating temperature increased, the viscosity of the infiltrating glass decreased, and the infiltrating depth increased. A 1 mm infiltration depth into the presintered alumina at 1150°C, 1200°C and 1250°C required 95 min, 22 min and 8 min, respectively. Conclusion: An optimal infiltrating time required to reach a suitable infiltration depth into the presintered alumina was observed at 1200°C, an important finding for clinical applications at this commonly used furnace temperature.
Objective: To test specimens of soak-colored Vita In-Ceram YZ zirconia ceramics and the colorimetric data of staining solution colorimetric plate. Methods: five sets of specimens were prepared, soaking and coloring them with LL1 to LL5 staining solution for 2 min respectively. Specimens were sintered for 2 h at 1530°C, and grinded one side of the specimens to 1.5 mm in thickness. The colors of the specimens and staining solution colorimetric plate were tested by spectrophotometer in black background. The chromatic aberration between the specimens and colorimetric plate were calculated as well as measured the lightness difference, hue angle difference, and saturation difference. Results: the colorimetric data of the dyed specimens are L: 59.81 ~ 78.93; a: 0.36 ~ 9.36; b: 19.62 ~ 26.91. The color space of the specimens and staining solution colorimetric plate was similar and the chromatic aberration was 4.02-6.96 NBS units. The biggest difference between them was the hue angle difference, mean 7.38, followed by the saturation difference, mean 2.31; minimum lightness difference, mean 2.29. Conclusion: staining solution colorimetric plate was suitable to be colorimetric reference for the color-matching of the basic layer of the ceramic. Proper chromatic aberration leaves color revision space for the translucent porcelain veneer.
Objective: To evaluate the biological safety of a colored zirconia ceramic regarding its hemolytic activity and short-term systemic toxicity. Methods: Fresh anti-coagulating rabbit blood was mixed with test materials and the hemolytic activities detected spectrophotometrically. Suspensions of the ceramic were fed to rats for one week while monitoring food consumption and relative growth rate and with subsequent pathology examinations of vital organs and tissues. Results: The hemolytic activity of the ceramics was <5%, and rats in all groups showed weekly relative growth rates of food utilization and body weight with no statistically significant differences. There were also no pathological changes observed among the various examined organs between the experimental and control groups. Conclusions: This colored ceramic showed good biocompatibility in terms of hemolytic activity and short-term systemic toxicity.
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