TY - JOUR
T1 - Antiplasmodial activity of lignans and extracts from Pycnanthus angolensis
AU - Abrantes, Marta
AU - Mil-Homens, Tânia
AU - Duarte, Noélia
AU - Lopes, Dinora
AU - Cravo, Pedro
AU - Do Céu Madureira, Maria
AU - Ferreira, Maria José U.
PY - 2008/9/1
Y1 - 2008/9/1
N2 - The dichloromethane, methanol and aqueous ethanol extracts of the stem bark of Pycnanthus angolensis were evaluated for their in vitro activity against the 3D7 Plasmodium falciparum strain. The CH2C12 extract was the most active showing an 1C50= 1.6 μg/ mL. From this extract, a new dibenzylbutane lignan, threo-4,4′-dihydroxy-3-methoxylignan (1) named pycnantolol, together with the known lignans (-)-dihydroguaiaretic acid (2), helio-buphthalmin (3), talaumidin (4), hinokinin (5), the labdane-type diterpene ozic acid (6), and the steroids stigmast-4-en-6β-ol-3-one (7), β3-sitosterol (8) and stigmasterol (9) were isolated. Their structures were established on the basis of physical and spectroscopic methods, including 2 D NMR experiments (COSY, HMQC, HMBC and NOESY). The antimalarial activity of compounds 1-7 was evaluated against 3D7 and Dd2 P. falciparum strains. Despite the significant activity displayed by the crude CH2C12 extract, the isolated compounds showed weaker antiplasmodial activity. The lowest IC50 value was obtained for talaumidin (4) (IC50 = 20.7μg/mL against the Dd2-chloroquine resistant P. falciparum strain).
AB - The dichloromethane, methanol and aqueous ethanol extracts of the stem bark of Pycnanthus angolensis were evaluated for their in vitro activity against the 3D7 Plasmodium falciparum strain. The CH2C12 extract was the most active showing an 1C50= 1.6 μg/ mL. From this extract, a new dibenzylbutane lignan, threo-4,4′-dihydroxy-3-methoxylignan (1) named pycnantolol, together with the known lignans (-)-dihydroguaiaretic acid (2), helio-buphthalmin (3), talaumidin (4), hinokinin (5), the labdane-type diterpene ozic acid (6), and the steroids stigmast-4-en-6β-ol-3-one (7), β3-sitosterol (8) and stigmasterol (9) were isolated. Their structures were established on the basis of physical and spectroscopic methods, including 2 D NMR experiments (COSY, HMQC, HMBC and NOESY). The antimalarial activity of compounds 1-7 was evaluated against 3D7 and Dd2 P. falciparum strains. Despite the significant activity displayed by the crude CH2C12 extract, the isolated compounds showed weaker antiplasmodial activity. The lowest IC50 value was obtained for talaumidin (4) (IC50 = 20.7μg/mL against the Dd2-chloroquine resistant P. falciparum strain).
KW - Antimalarial activity
KW - Lignans
KW - Myristicaceae
KW - Plasmodium falciparum
KW - Pycnanthus angolensis
UR - http://www.scopus.com/inward/record.url?scp=52949122155&partnerID=8YFLogxK
UR - https://www.thieme-connect.com/products/ejournals/abstract/10.1055/s-2008-1081317
U2 - 10.1055/s-2008-1081317
DO - 10.1055/s-2008-1081317
M3 - Article
C2 - 18671202
AN - SCOPUS:52949122155
SN - 0032-0943
VL - Vol. 74
SP - 1408
EP - 1412
JO - Planta Medica
JF - Planta Medica
IS - n.º 11
ER -