Planta Med 2001; 67(9): 811-814
DOI: 10.1055/s-2001-18854
Original Paper
Pharmacology
© Georg Thieme Verlag Stuttgart · New York

Anticomplement Activity of Terpenoids from the Spores of Ganoderma lucidum

Byung Sun Min1 , Jiang Jing Gao1 , Masao Hattori1 , Hyeong Kyu Lee2 , Young Ho Kim3
  • 1 Institute of Natural Medicine, Toyama Medical and Pharmaceutical University, Toyama, Japan
  • 2 Natural Product Biosynthesis Research Unit, Korea Research Institute of Bioscience and Biotechnology, Teajon, Korea
  • 3 College of Pharmacy, Chungnam National University, Taejon, Korea
Further Information

Publication History

November 10, 2000

March 31, 2001

Publication Date:
06 December 2001 (online)

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Abstract

A new lanostane-type terpenoid, lucidenic acid SP1 (1), was isolated from a CHCl3-soluble fraction of Ganoderma lucidum spores together with four other known compounds (2 - 5). The structure of lucidenic acid SP1 was determined to be 3β,7β-dihydroxy-4,4,14α-trimethyl-11,15-dioxo-5α-chol-8-en-24-oic acid by spectroscopic means including 2D-NMR. Twelve triterpenes (1 - 12) isolated from G. lucidum spores were investigated in vitro for their anticomplementary activity. Compounds 1 - 5 were inactive, whereas ganoderiol F (8), ganodermanondiol (9) and ganodermanontriol (10) showed a strong anticomplement activity against the classical pathway (CP) of the complement system with IC50 values of 4.8, 41.7, and 17.2 μM, respectively. The potency of these triterpene alcohols (8 - 10) in inhibiting CP activity was improved when the number of hydroxymethyl groups on the side chain moiety is increased. On the other hand, the ganoderic acids 1 - 7, which contain a carboxyl group in the side chain, and lucidumols A and B (11, 12) had little activity on this system.