“…Its bark is yellowish gray, and it is used in traditional medicine to relieve inflammation, skin tumors and warts [4]. The chemical study of B. fagaroides over the years has included the characterization of 19 lignans structures classified into four groups: eight are aryltetralins: podophyllotoxin (1), β-peltatin-A-methylether (2), 5 ′ -desmethoxy-βpeltatin-A-methylether (3), desoxypodophyllotoxin (4), acetyl podophyllotoxin (5), morelensine (6), burseranin (7) and acetylpicropodophyllotoxin (8); three are dibenzylbutyrolac-tone: desmethoxy-yatein (9), yatein (10) and hinoquinin (11); three are aryldihydronaphtalene: 7 ′ ,8 ′ -dehydropodophyllotoxin (12), 7 ′ ,8 ′ -dehydroacethyl podophyllotoxin (13) and 7 ′ ,8 ′ -dehydro trans-p-cumaroylpodophyllotoxin (14); and five are lignan dibenzylbutanes: 9-acetyl-9 ′ -pentadecanoyldihydroclusin (15), 2,3-desmethoxy-secoisolintetralin monoacetate (16), dihydroclusin diacetate (17), 2,3-demethoxy-secoisolintetralin diacetate (18) and dihydroclusin mono acetate (19) [5][6][7]. These compounds have been isolated from the bark using solvents with different polarities [5,6,[8][9][10], and these compounds present important cytotoxic activity with IC 50 values ranging from 12 µgmL −1 (burseranin, 7) to 4.43 × 10 −6 µgmL −1 (β-peltatin-A-methylether, 2).…”