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7 results for “Anadenanthera”
Sequence-based microsatellite data of Anadenanthera colubrina (Leguminosae)
<p>The file contains SSRseq genotyping data of <em>Anadenanthera colubrina</em> populations. Individuals from two life stages were scored at 25 SSRseq loci. Goncalves AL, García MV, Chancerel E, Lepais O, Heuertz M. High-throughput sequence-based microsatellite genotyping for the non-model Neotropical tree species <em>Anadenanthera colubrina</em> (Leguminosae).</p> <p>The file contains</p> <p>- Two different data sets:</p> <p>GS: Genotypes based on sequence identity.<br>GL: Genotypes based on amplicon length.</p> <p>- Allele sequence information</p>
Figure 2 in Phytochemical characterization, and antioxidant and antibacterial activities of the hydroethanolic extract of Anadenanthera peregrina stem bark
Figure 2. HPLC-PDA chromatographic profiles (λ = 254 nm) of: (A) sample extract; (B) gallic acid standard; (C) catechin standard; and (D) epicatechin standard, followed by UV spectra (190-400 nm).
Figure 1 in Phytochemical characterization, and antioxidant and antibacterial activities of the hydroethanolic extract of Anadenanthera peregrina stem bark
Figure 1. Erythrocyte hemolysis in a 5% red blood cell suspension by the hydroethanolic extract of A. peregrina stem bark. (A) 5% suspension of red blood cells; (B) hemolysis after 1 min of reaction; (C) advanced hemolysis after 5 min; and (D) completely hemolyzed red blood cells within 10 min of reaction. Bars: At (A) 1.000×; (B) 500×; (C) 650×; and (D) 1.800×.
Figure 1 in Anadenanthera colubrina (Fabaceae) logs in the Atlantic Forest biome: first host plant for Thoracibidion lineatocolle (Col.: Cerambycidae) and a new host for Temnopis megacephala (Col.: Cerambycidae)
Figure 1. Temnopis megacephala (A) and Thoracibidion lineatocolle (B) (Coleoptera:Cerambycidae) adults emerged from Anadenanthera colubrina (Fabaceae) logs harvested in the Atlantic Forest biome.
Table 3 in Phytochemical characterization, and antioxidant and antibacterial activities of the hydroethanolic extract of Anadenanthera peregrina stem bark
<p><b>Table 3.</b> Diameter of the inhibitory zone of the hydroethanolic extract of <i>Anadenanthera peregrina</i> stem bark against <i>Staphylococcus aureus</i> (ATCC 25923) and <i>Escherichia coli</i> (ATCC 25922).</p><table><tbody><tr><th></th><th><b>A. peregrina extract concentration</b></th><th></th><th></th></tr></tbody><tbody><tr><th><b>Strain</b></th><td></td><td></td><td></td><td><b>C +</b></td><td><b>C -</b></td></tr><tr><th></th><td><b>50 µL</b></td><td><b>100 µL</b></td><td><b>200 µL</b></td><td></td><td></td></tr><tr><th><i>E. coli</i></th><td>-</td><td>-</td><td>-</td><td>29 mm</td><td>-</td></tr><tr><th><i>S. aureus</i></th><td>10 mm</td><td>16 mm</td><td>20 mm</td><td>35 mm</td><td>-</td></tr></tbody></table>
Table 2 in Phytochemical characterization, and antioxidant and antibacterial activities of the hydroethanolic extract of Anadenanthera peregrina stem bark
<p><b>Table 2.</b> Physicochemical properties,antioxidant activity,and total phenolic content of the hydroethanolic extract of <i>A.peregrina</i> stem bark.</p><table><tbody><tr><th>Sample</th><th>pH</th><th>Density (g cm 3)</th><th>DPPH (IC 50)</th><th><b>Total Phenolics (g GAE 100 g-</b> 1)</th></tr></tbody><tbody><tr><th><b>A. peregrina extract</b></th><td>5.21 ± 0.01</td><td>0.956</td><td>44.13 mg mL-1</td><td>6.40 ± 0.08</td></tr></tbody></table>
Table 1 in Phytochemical characterization, and antioxidant and antibacterial activities of the hydroethanolic extract of Anadenanthera peregrina stem bark
<p><b>Table 1.</b> Phytochemical prospecting of the main secondary metabolite groups of the hydroethanolic extract of <i>A. peregrina</i> stem bark.</p><table><tbody><tr><th><b>Secondary metabolite</b></th><th><b>Hydroethanolic extract of A. peregrina</b></th></tr><tr><th><b>Cardiac glycosides</b></th></tr></tbody><tbody><tr><th>Kedd reagent test</th><td>++</td></tr><tr><th>Keller–Kiliani reagent test</th><td>++</td></tr><tr><th>Baljet reagent test</th><td>-</td></tr><tr><th>Raymond–Marthoud reagent test</th><td>+++</td></tr><tr><th><b>Alkaloids</b></th></tr><tr><th>Libermann–Bouchardat reagent test</th><td>-</td></tr><tr><th>Wagner reagent test</th><td>-</td></tr><tr><th>Mayer’s reagent test</th><td>-</td></tr><tr><th><b>Organic acids</b></th></tr><tr><th>Pascová reagent test</th><td>++</td></tr><tr><th><b>Reducing sugars</b></th></tr><tr><th>Fehling reagent test</th><td>++</td></tr><tr><th><b>Non-reducing sugars</b></th></tr><tr><th>Fehling + HCl test</th><td>-</td></tr><tr><th><b>Coumarins</b></th></tr><tr><th>UV light 254 and 365 nm</th><td>+</td></tr><tr><th><b>Saponins</b></th></tr><tr><th>Foamy</th><td>-</td></tr><tr><th>Haemolytic</th><td>+++</td></tr><tr><th><b>Polysaccharides</b></th></tr><tr><th>Reactive lugol</th><td>-</td></tr><tr><th><b>Phenols</b></th></tr><tr><th>FeCl 3 <b>Tannins</b></th><td>+++</td></tr><tr><th>FeCl3 <b>Flavonoids</b></th><td>Gr</td></tr><tr><th>Pb(C2 H 3O2)2</th><td>++</td></tr><tr><th><b>Purines</b></th><td><b>-</b></td></tr><tr><th><b>Catechins</b></th><td>+++</td></tr><tr><th><b>Benzoquinone derivatives</b></th><td>+++</td></tr><tr><th><b>Depsids and depsidones</b></th><td>+++</td></tr><tr><th><b>Steroids and triterpenoids</b></th><td><b>-</b></td></tr><tr><th><b>Sesquiterpenolactones</b></th><td>-</td></tr></tbody></table>
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