Planta Med. 2003 Mar; 69(3): 258-64.

New dihydrobenzofurans and triterpenoids from roots of Microglossa pyrifolia.

Schmidt TJ, Hildebrand MR, Willuhn G.

Institut f�r Pharmazeutische Biologie der Heinrich-Heine-Universit�t D�sseldorf, D�sseldorf, Germany. [email protected]

From the roots of Microglossa pyrifolia (Lam.) Kuntze (Asteraceae, tribe Astereae), used in East African traditional Medicine to treat a variety of ailments, seven dihydrobenzofurans and seven triterpenoids (five dammaranes and two 28- nor-oleanenes) were isolated. Their structures were elucidated by spectroscopic (UV, MS and NMR) means. With the exception of the tremetone derivative 1, all of the dihydrobenzofurans found in this drug possess the rare 6-acetyl-5-hydroxy substitution pattern. Dihydrobenzofurans 1 [methyl 2-(5-acetyl-2,3-dihydrobenzo[beta]furan-2-yl)propenoate], 3 (methyl2-(6-acetyl-5-hydroxy-2,3-dihydrobenzofuran-2-yl)propenoate] and 7 (6-acetyl-5-hydroxy-2-(1-hydroxy-2-propenyl)-3-methoxy-2,3-dihydrobenzofuran) as well as the triterpenes 3beta-acetoxy-25-hydroxydammara-20,23-diene ( 9), 3beta-acetoxy-24-oxo-dammara-20,25-diene ( 11), 17beta-hydroxy-3,16-dioxo-28-norolean-12-ene ( 12) and 17beta-hydroxy-3,11,16-trioxo-28-norolean-12-ene ( 13) are new natural products, to the best of our knowledge.