The chemical and biological potential of C ring modified triterpenoids

• C ring modified oleanolic, ursolic and maslinic acid derivatives were synthesized.
• The compounds showed antitumor activity using different human cancer cell lines.
• Many of the compounds are cytotoxic even in a low μmol concentration.
• The compounds act by apoptosis.
• Small changes in constitution cause tremendous effects in their mode of action.

A convenient and elegant route has been developed to separate the natural regioisomers triterpenoids ursolic acid (UA) and oleanolic acid (OA) as well as derivatives thereof. Eleven unknown derivatives of OA were designed, synthesized, and their cytotoxicity was investigated. Further sixteen compounds were prepared to correlate all compounds in a SAR study. It could be shown that C-ring modifications of OA and UA have only a moderate influence onto the cytotoxic activity of the compounds but a significant impact onto the ability to trigger apoptosis in ovarian cancer cells (cell line A2780).

C-ring modifications of oleanolic and ursolic acid have only a moderate influence onto the cytotoxic activity of the compounds but the intact presence of this structural element has a significant impact onto the ability to trigger apoptosis in ovarian cancer cells (cell line A2780).Figure optionsDownload as PowerPoint slide