Planta Med 2007; 73(7): 679-682
DOI: 10.1055/s-2007-981526
Pharmacology
Letter
© Georg Thieme Verlag KG Stuttgart · New York

Inhibition of Chitin Synthase 2 and Antifungal Activity of Lignans from the Stem Bark of Lindera erythrocarpa

Eui Il Hwang1 , Yun Mi Lee2 , Sang Myung Lee1 , Woon Hyung Yeo1 , Jae Sun Moon2 , Tae Hoon Kang2 , Ki Duk Park2 , Sung Uk Kim2
  • 1KT&G Central Research Institute, Daejeon, Korea
  • 2Division of Biomaterials Science, KRIBB, Daejeon, Korea
Further Information

Publication History

Received: August 28, 2006 Revised: April 23, 2007

Accepted: April 23, 2007

Publication Date:
31 May 2007 (online)

Abstract

Potent chitin synthase 2 inhibitors, methyllinderone (1), linderone (2) and kanakugiol (3) were isolated from the stem bark of L. erythrocarpa Makino (Lauraceae). These compounds inhibited chitin synthase 2 with IC50 values of 23.3, 21.4 and 23.8 μg/mL, respectively. Methyllinderone (1) and linderone (2) exhibited no inhibitory activities for chitin synthases 1 and 3 from S. cerevisiae, and chitin synthase 1 from Candida albicans up to the concentration of 280 μg/mL, while kanakugiol (3) exhibited very weak activity against chitin synthase 1 of C. albicans with an IC50 of 160 μg/mL. All of the compounds showed moderate to weak antifungal activities against various pathogenic fungi (MIC: 8 - >128 μg/mL) including Cryptococcus neoformans, Aspergillus fumigatus, and Colletotrichum lagenarium. The results indicate that these compounds are specific inhibitors of chitin synthase 2 and can potentially serve as antifungal agents.

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Dr. Sung Uk Kim

Division of Biomaterials Science

Korea Research Institute of Bioscience and Biotechnology

Daejon 305-806

Korea

Phone: +82-42-860-4554

Fax: +82-42-861-2675

Email: kimsu@kribb.re.kr

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