1,369
Views
13
CrossRef citations to date
0
Altmetric
Research Article

Evaluation of Antiaris africana methanol extract and compounds for antioxidant and antitumor activities

, , , , &
Pages 1042-1049 | Received 23 Oct 2008, Accepted 02 Mar 2009, Published online: 19 Oct 2009

Figures & data

Figure 1. Chemical structures of compounds isolated from the stem bark of Antiaris africana.

Figure 1.  Chemical structures of compounds isolated from the stem bark of Antiaris africana.

Figure 2. Free radical scavenging activity of the methanol extract, compounds from Antiaris africana, and vitamin C: values with the same letter are not significantly different (ANOVA, p < 0.05). 1, betulinic acid; 2, 3β-acetoxy-1β,11α-dihydroxy-olean-12-ene; 3, ursolic acid; 4, oleanolic acid; 5, strophanthidol; 6, periplogenin; 7, convallatoxin; 8, strophanthidinic acid; 9, methylstrophanthinate; 10, 3,3′-dimethoxy-4′-O-β-d-xylopyronosylellagic acid.

Figure 2.  Free radical scavenging activity of the methanol extract, compounds from Antiaris africana, and vitamin C: values with the same letter are not significantly different (ANOVA, p < 0.05). 1, betulinic acid; 2, 3β-acetoxy-1β,11α-dihydroxy-olean-12-ene; 3, ursolic acid; 4, oleanolic acid; 5, strophanthidol; 6, periplogenin; 7, convallatoxin; 8, strophanthidinic acid; 9, methylstrophanthinate; 10, 3,3′-dimethoxy-4′-O-β-d-xylopyronosylellagic acid.

Figure 3. Antitumor activity of the methanol extract and compounds from Antiaris africana as obtained in Crown gall assay: values with the same letter are not significantly different (ANOVA, p < 0.05). 1, betulinic acid; 2, 3β-acetoxy-1β,11α-dihydroxy-olean-12-ene; 3, ursolic acid; 4, oleanolic acid; 5, strophanthidol; 6, periplogenin; 7, convallatoxin; 8, strophanthidinic acid; 9, methylstrophanthinate; 10, 3,3′-dimethoxy-4′-O-β-d-xylopyronosylellagic acid.

Figure 3.  Antitumor activity of the methanol extract and compounds from Antiaris africana as obtained in Crown gall assay: values with the same letter are not significantly different (ANOVA, p < 0.05). 1, betulinic acid; 2, 3β-acetoxy-1β,11α-dihydroxy-olean-12-ene; 3, ursolic acid; 4, oleanolic acid; 5, strophanthidol; 6, periplogenin; 7, convallatoxin; 8, strophanthidinic acid; 9, methylstrophanthinate; 10, 3,3′-dimethoxy-4′-O-β-d-xylopyronosylellagic acid.

Figure 4. Effects of the methanol extract and compounds from Antiaris africana on (A) DU-145 and (B) Hep G2 cell survivals: values with the same letter are not significantly different (ANOVA, p < 0.05). 1, betulinic acid; 2, 3β-acetoxy-1β,11α-dihydroxy-olean-12-ene; 7, convallatoxin; 8, strophanthidinic acid; 9, methylstrophanthinate; 10, 3,3′-dimethoxy-4′-O-β-d-xylopyronosylellagic acid.

Figure 4.  Effects of the methanol extract and compounds from Antiaris africana on (A) DU-145 and (B) Hep G2 cell survivals: values with the same letter are not significantly different (ANOVA, p < 0.05). 1, betulinic acid; 2, 3β-acetoxy-1β,11α-dihydroxy-olean-12-ene; 7, convallatoxin; 8, strophanthidinic acid; 9, methylstrophanthinate; 10, 3,3′-dimethoxy-4′-O-β-d-xylopyronosylellagic acid.

Table 1. Activity of the crude extract from A. africana, selected compounds, and doxorubicin on human cancer cell lines DU-145 and Hep G2.

Reprints and Corporate Permissions

Please note: Selecting permissions does not provide access to the full text of the article, please see our help page How do I view content?

To request a reprint or corporate permissions for this article, please click on the relevant link below:

Academic Permissions

Please note: Selecting permissions does not provide access to the full text of the article, please see our help page How do I view content?

Obtain permissions instantly via Rightslink by clicking on the button below:

If you are unable to obtain permissions via Rightslink, please complete and submit this Permissions form. For more information, please visit our Permissions help page.