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68 results for “Vernonia”
Vernonia baldwinii (Asteraceae) - leaf - on upper stem
Image of Vernonia baldwinii (Asteraceae) - leaf - on upper stem
Vernonia arkansana (Asteraceae) - inflorescence - lateral view of flower
Image of Vernonia arkansana (Asteraceae) - inflorescence - lateral view of flower
Effect of Vernonia Cinerea Lozenges as a Smoking Cessation Aid in Patients With Non-communicable Diseases
ClinicalTrials.gov study NCT06268002. IPD Sharing: NO. Countries: 1. Publications: 0.
Fig. 7 in Phytoconstituents from Vernonia glaberrima Welw. Ex O. Hoffm. leaves and their cytotoxic activities on a panel of human cancer cell lines
Fig. 7. Surface structure of CDK2 (PDB ID 2DUV) showing the binding pose of lupeol (black). Blue colour depicts polar surface while brown colour indicates hydrophobic surfaces. (For interpretation of the references to colour in this figure legend, the reader is referred to the web version of this article.)
Fig. 5 in Phytoconstituents from Vernonia glaberrima Welw. Ex O. Hoffm. leaves and their cytotoxic activities on a panel of human cancer cell lines
Fig. 5. Effects of V. glaberrima compounds on the viability of HT-29 cell lines as determined by MTS assay.
Table 4 in Phytoconstituents from Vernonia glaberrima Welw. Ex O. Hoffm. leaves and their cytotoxic activities on a panel of human cancer cell lines
<p><b>Table 4</b> Docking scores of 5-methylcoumarin-4-β- glucoside and 4-hydroxy-5-methylcoumarin on carbonic anhydrase IX (CAIX) (PDB ID 3IAI).</p><table><tbody><tr><th></th><th>Name</th><th>Free binding energy (kcal/mol)</th><th>Estimated inhibition constant (Ki)</th></tr></tbody><tbody><tr><th>1</th><td>5-Methylcoumarin-4-β- glucoside</td><td><i>−</i> 6.97</td><td>7.78 μM</td></tr><tr><th>2</th><td>4-Hydroxy-5-methylcoumarin</td><td><i>−</i> 5.70</td><td>66.17 μM</td></tr><tr><th>3</th><td>Co-crystallized ligand</td><td><i>−</i> 6.01</td><td>39.32 μM</td></tr></tbody></table>
Table 3 in Phytoconstituents from Vernonia glaberrima Welw. Ex O. Hoffm. leaves and their cytotoxic activities on a panel of human cancer cell lines
<p><b>Table 3</b> Docking result for lupeol on CDK2 (PDB ID 2DUV).</p><table><tbody><tr><th></th><th>Name</th><th>Free binding energy (kcal/mol)</th><th>Estimated inhibition constant (Ki)</th></tr></tbody><tbody><tr><th>1</th><td>Lupeol</td><td><i>−</i> 11.06</td><td>7.82 nM</td></tr><tr><th>2</th><td>Co-crystallized</td><td><i>−</i> 11.08</td><td>7.57 nM</td></tr></tbody></table>
Fig. 1 in Bisabolane-type sesquiterpenes from Vernonia amygdalina: Absolute configuration and anti-inflammatory activity
Fig. 1. Chemical constitutents of 1–8 isolated from Vernonia amygdalina.
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