Planta Med 2007; 73(6): 572-577
DOI: 10.1055/s-2007-967196
Natural Product Chemistry
Original Paper
© Georg Thieme Verlag KG Stuttgart · New York

New Dihydrochalcones and Anti-Platelet Aggregation Constituents from the Leaves of Muntingia calabura

Jih-Jung Chen1 , Hsinn-Hsing Lee1 , Cheng-Dean Shih1 , Chang-Hui Liao2 , Ih-Sheng Chen3 , Tsung-Hsien Chou1 , 3
  • 1Graduate Institute of Pharmaceutical Technology, Tajen University, Pingtung, Taiwan
  • 2Graduate Institute of Natural Products, Chang Gung University, Taoyuan, Taiwan
  • 3Graduate Institute of Pharmaceutical Sciences, Kaohsiung Medical University, Kaohsiung, Taiwan
Further Information

Publication History

Received: November 1, 2006 Revised: January 8, 2007

Accepted: April 10, 2007

Publication Date:
22 May 2007 (online)

Preview

Abstract

Two new dihydrochalcones, 2,3-dihydroxy-4,3′,4′,5′-tetramethoxydihydrochalcone (1) and 4,2′,4′-trihydroxy-3′-methoxydihydrochalcone (2), and a new flavanone, (2R,3R)-(-)-3,5-dihydroxy-6,7-dimethoxyflavanone (3), together with nineteen known compounds have been isolated from the leaves of Muntingia calabura. The structures of three new compounds were determined through spectral analyses including extensive 2D-NMR data. Among the isolates, 2,3-dihydroxy-4,3′,4′,5′-tetramethoxydihydrochalcone, 5,7-dihydroxy-3-methoxyflavone, 5,7-dihydroxy-6-methoxyflavone, 5,4′-dihydroxy-3,7-dimethoxyflavone, (2S)-7,8,3′,4′,5′-pentamethoxyflavan, (2S)-5′-hydroxy-7,8,3′,4′-tetramethoxyflavan, and methyl gallate exhibited significant anti-platelet aggregation activity in vitro.

References

Dr. J. J. Chen

Department of Pharmacy

Tajen University

Pingtung 907

Taiwan

Phone: +886-8-762-4002 ext. 332

Fax: +886-8-7625308

Email: jjchen@mail.tajen.edu.tw