Planta Med 2007; 73(12): 1298-1303
DOI: 10.1055/s-2007-981618
Natural Product Chemistry
Original Paper
© Georg Thieme Verlag KG Stuttgart · New York

Minor Limonoids from Melia toosendan and their Antibacterial Activity

Qiong Zhang1 , Yao Shi1 , Xue-Ting Liu1 , Jing-Yu Liang1 , Nancy Y. Ip2 , Zhi-Da Min1
  • 1Department of Natural Medicinal Chemistry, China Pharmaceutical University, Nanjing, P. R. China
  • 2Department of Biochemistry and Biotechnology Research Institute, The Hong Kong University of Science and Technology, Hong Kong, P. R. China
Weitere Informationen

Publikationsverlauf

Received: March 22, 2007 Revised: July 4, 2007

Accepted: August 21, 2007

Publikationsdatum:
24. September 2007 (online)

Abstract

In this study five new limonoids, toosendone [24,25,26,27-tetra-nor-6α-acetoxy-21,22-epoxy-7α-tigloyl-1α,3α,28-trihydroxyapotirucalla-(apoeupha)-14,20,22-trien-12-one, 1] and 12-ethoxynimbolinins A - D (2 - 5), together with five known limonoids, 1-acetyltrichilinin (6), 1-cinnamoyltrichilinin (7), trichilinin B (8), 1,7-di-O-acetyl-14,15-deoxyhavanensin (9) and 12-O-methylnimbolinin B (10),were isolated from the fruits of Melia toosendan. Their structures and relative configurations were established based on spectroscopic analysis. Compound 4 exhibited significant antibacterial activity against the oral pathogen, Porphyromonas gingivalis ATCC 33 277, with an MIC value of 15.6 μg/mL. Compounds 7 and 8 were also active against P. gingivalis ATCC 33 277, with MIC values of 31.3 and 31.5 μg/mL respectively.

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Prof. Zhi-Da Min

Department of Natural Medicinal Chemistry

China Pharmaceutical University

Nanjing 210009

People’s Republic of China

Telefon: +86-25-8322-0992

Fax: +86-25-8327-1335

eMail: zhdmin32@hotmail.com