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Biologically active alkylated coumarins from Kayea assamica
Authors:Lee Kyung-Hee  Chai Hee-Byung  Tamez Pamela A  Pezzuto John M  Cordell Geoffrey A  Win Khin Khin  Tin-Wa Maung
Affiliation:Program for Collaborative Research in the Pharmaceutical Sciences, Department of Medicinal Chemistry and Pharmacognosy, College of Pharmacy, University of Illinois at Chicago, Chicago, IL 60612, USA.
Abstract:Four coumarin derivatives, theraphins A (1), B (2), C (3), and D (4), along with three known xanthones, 2-hydroxyxanthone, 1,7-dihydroxyxanthone, and 5-hydroxy-1-methoxyxanthone, were isolated from the bark of Kayea assamica (Clusiaceae) native to Myanmar. Their structures were determined using spectroscopic and chemical techniques. The absolute configuration of 1 was established by the modified Mosher ester method. Theraphins A (1), B (2), and C (3) exhibited good cytotoxicity against Col2, KB, and LNCaP human cancer cell lines. Theraphin D (4) showed mild activity only against the KB cell line. The coumarins also exhibited mild antimalarial activities.
Keywords:Kayea assamica   Clusiaceae   Alkylated coumarins   Xanthones   Cytotoxicity   Antimalarial activity
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