Abstract
Chemical investigation of the roots of Ligularia sagitta has resulted in the characterization of six eremophilenolides 6β,8β-dimethoxy-10β-hydroxyeremophil-7(11)-en-12,8α-olide
(1), 6β-angeloyloxy-10β-hydroxy-8β-methoxyeremophil-7(11)-en-12,8α-olide (2), 6β-(2′-methylbutanoyloxy)-10β-hydroxy-8β-methoxyeremophil-7(11)-en-12,8α-olide
(3), 6β-angeloyloxy-10β-hydroxy-8α-methoxyeremophil-7(11)-en-12,8β-olide (4), 6β-(2′-methylbutanoyloxy)-10β-hydroxy-8α-methoxyeremophil-7(11)-en-12,8β-olide
(5) and 8β,10β-dihydroxy-6β-methoxyeremophil-7(11)-en-12,8α-olide (6), together with one monoterpene (3R,4R,6S)-3,6-dihydroxy-1-menthene (7), two triterpenes lupeol (8) and ursolic acid (9), and β-sitosterol (10). The structures of five new constituents (1 - 5) were elucidated by spectroscopic methods including 2D-NMR experiments. The compounds
1, 5 and 7 showed antibacterial activity by being assayed against Staphylococcus aureus, Bacillus subtilis and Escherichia coli.
Key words
Ligularia sagitta
- Compositae - Eremophilenolides - Sesquiterpenes - antibacterial activity
References
- 1 Jiangsu College of New M edicine, A Dictionary of the Traditional Chinese M edicines.
Shanghai Science and Technology Press. Shanghai; 1977: pp. 1152, 2349
- 2
Chen H M, Cai M S, Jia Z J.
Sesquiterpenes from Ligularia intermedia
.
Phytochemistry.
1997;
45
1441-4
- 3
Chen H M, Jia Z J, Yang L.
Sesquiterpenes and a diterpene lactone with an unusual carbon skeleton from Ligularia sagitta
.
Phytochemistry.
1992;
31
2146-7
- 4
Jia Z J, Chen H M, Qiu J L. et al .
The structure of sagittolactone.
Chin Sci Bull.
1992;
37
773-4
- 5
Zhao Y, Jia Z J, Tan R X.
New eremophilane type lactones.
Planta Med.
1992;
58
365-7
- 6
Zhao Y, Peng H R, Jia Z J.
Six new eremophilane derivatives from two Ligularia species.
Journal of Natural Products.
1994;
57
1626-30
- 7
Zhang S M, Zhao G L, Li R, Lin G Q.
Eremophilane sesquiterpenes from Cacalia roborowskii
.
Phytochemistry.
1998;
48
519-24
- 8
Maria D, Cesar A.
Monoterpenes and lignans from Mikania saltensis
.
Journal of Natural Products.
1991;
54
1162-4
- 9
Delgado G, Rios M Y.
Monoterpenes from Chrysactinia mexicana
.
Phytochemistry.
1991;
30
3129-31
- 10 Xu S Y, Bian Q L, Chen X Y. In, Pharmacology Experimental Methods. People’s Health
Press Beijing; 1982: pp. 1340-7
- 11
Sugama K, Hayashi K, Mitsuhashi H.
Eremophilenolides from Petasites japonicus
.
Phytochemistry.
1985;
24
1531-5
- 12
Moriyama Y, Takahashi T.
New sesquiterpene lactones of eremophilane-type from Ligularia fauriei (F.) Koidz.
Bull Chem Soc Jpn.
1976;
49
3196-9
- 13
Naya K, Kanazawa R, Sawada M.
The photosensitized oxygenation of furanoeremophilanes I. The isomeric hydroperoxides
from petasalbin and their transformations to lactones.
Bull Chem Soc Jpn.
1975;
48
3220-6
- 14
Naya K, Matsumoto T, Makiyama M, Tsumura M.
The conversion of furanoeremophilanes to epieremophilenolides.
Heterocycles.
1978;
10
177-84
- 15
Ishizaki Y, Tanahashi Y, Takahashi T.
The structure of ligularenolide - a new sesquiterpene lactone of eremophilane type.
Tetrahedron.
1970;
26
5387-93
- 16
Aclinou P, Massiot G.
Absolute configuration of eremophilenolides from Hertia cheirifolia
.
Phytochemistry.
1993;
34
859-60
- 17
Mao M J, Jia Z J.
Eremophilane sesquiterpenes from Cacalia ainsliaeflora
.
Planta Med.
2002;
68
55-9
Prof. Dr. Zhong-Jian Jia and Dr. Kun Gao
College of Chemistry and Chemical Engineering
National Laboratory of Applied Organic Chemistry
Lanzhou University
Lanzhou 730000
People’s Republic of China
Fax: +86-0931-8912582
eMail: jiazj@lzu.edu.cn