Planta Med 2001; 67(1): 87-89
DOI: 10.1055/s-2001-10621
Letter

© Georg Thieme Verlag Stuttgart · New York

Antifungal Chalcones from Maclura tinctoria

H. N. ElSohly1,*, A. S. Joshi1 , A. C. Nimrod1 , L. A. Walker1, 2 , A. M. Clark1, 3
  • 1 National Center for Natural Products Research, Research Institute of Pharmaceutical Sciences, University of Mississippi, University, Mississippi, U.S.A.
  • 2 Department of Pharmacology, University of Mississippi, University, Mississippi, U.S.A.
  • 3 Department of Pharmacognosy, School of Pharmacy, Thad Cochran Research Center, University of Mississippi, University, Mississippi, U.S.A.
Further Information

Publication History

February 11, 2000

May 13, 2000

Publication Date:
31 December 2001 (online)

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Abstract

Five prenylated flavonoids, including one new natural product, were isolated from an ethanol extract of the leaves of Maclura tinctoria (L.) Gaud. The new compound has been characterized as 2′,4′,4,2″-tetrahydroxy-3′-[3″-methylbut-3″-enyl]chalcone (1). The known compounds were identified as 2′,4′,4-trihydroxy-3′-[3″-methylbut-3″-enyl]chalcone (isobavachalcone) (2), 4,2′-dihydroxy-2″-[1-hydroxy-1-methylethyl]-2″,3″-dihydrofurano[4″,5″:3′,4′]chalcone (bakuchalcone) (3), 4,4′,5″-trihydroxy-6″,6″-dimethyldihydropyrano[2″,3″:5′,6″]chalcone (bavachromanol) (4), and 5,7,3′,4′-tetrahydroxy-6,8-diprenylisoflavone (6,8-diprenylorobol) (5). All the isolated compounds were evaluated against the AIDS-related opportunistic fungal pathogens, Candida albicans and Cryptococcus neoformans. Compound 2 was active against both yeasts.

References

Dr. Hala N. ElSohly

National Center for Natural Products Research

School of Pharmacy

University of Mississippi

University

MS 38677

USA

Email: helsohly@olemiss.edu

Fax: +1 662-915-7062