Location: Natural Products Utilization Research
Title: Flavan-3-ol-phenylpropanoid Conjugates from Anemopaegma arvense and Their Antioxident Activites Authors
|Pawar, Rahul - UNIVERSITY OF MISSISSIPPI|
|Ferreira, Daneel - UNIVERSITY OF MISSISSIPPI|
|Marais, Jannie P. - UNIVERSITY OF MISSISSIPPI|
|Khan, Shabana - UNIVERSITY OF MISSISSIPPI|
|Khan, Ikhlas - UNIVERSITY OF MISSISSIPPI|
Submitted to: Planta Medica
Publication Type: Peer Reviewed Journal
Publication Acceptance Date: June 8, 2007
Publication Date: July 1, 2007
Citation: Tabanca, N., Pawar, R.S., Ferreira, D., Marais, J.J., Khan, S.I., Wedge, D.E., Khan, I.A. 2007. Flavan-3-ol-phenylpropanoid Conjugates from Anemopaegma arvense and Their Antioxident Activites. Planta Medica. 73:1107-1111. Interpretive Summary: Erythroxylum catuaba is a vigorous-growing, small tree that produces yellow and orange flowers and small, dark yellow, oval-shaped, inedible fruit. It grows in the northern part of Brazil in Amazonas. "Catuaba" is the name given to a popular herbal medicine from Brazil and it has been attributed with analgesic, central nervous system stimulant, tonic and aphrodisiac properties. A new and three known flavan-3-ol type phenylpropanoids were isolated from the stem bark of Erythroxylum catuaba. Compounds 1-4 were subsequently evaluated for their antioxidant, anti-inflammatory, cytotoxicity, antimalarial and antimicrobial activities.
Technical Abstract: A new (1, catuabin A) and three known flavan-3-ol type phenylpropanoids, cinchonain Ia (2), cinchonain IIa (3), and kandelin A1 (4) were isolated from the stem bark of Erythroxylum catuaba. The structures of the compounds were determined by a combination of spectroscopic techniques. Isolated compounds were subsequently evaluated for their antioxidant, anti-inflammatory, cytotoxicity, antimalarial and antimicrobial activities. Compounds 1 and 3 exhibited stronger antioxidant activity than 2 and 4. However, anti-inflammatory, cytotoxic, antimalarial and antimicrobial activities were not observed for any of these compounds.