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DOI: 10.1055/s-2005-837818
© Georg Thieme Verlag KG Stuttgart · New York
Cytotoxic Activity of Lupane-Type Triterpenes from Glochidion sphaerogynum and Glochidion eriocarpum Two of which Induce Apoptosis
Publikationsverlauf
Received: May 4, 2004
Accepted: October 8, 2004
Publikationsdatum:
15. März 2005 (online)
Abstract
Six known lupanes lupenone (1), 3-epi-lupeol (2), glochidone (4), glochidonol (5), glochidiol (6) and lup-20(29)-ene-1β,3β-diol (7) were isolated from the roots and stem wood of Glochidion eriocarpum and three, 5, 6 and lup-20(29)ene-3α,23-diol (3), were isolated from the roots and stem wood of Glochidion sphaerogynum. Compounds were identified by 1H- and 13C-NMR techniques. Triterpenes 2 - 7 were tested against the growth of three human tumor cell lines, MCF-7, NCI-H-460 and SF-268. Lupanes 3, 5, and 6 exhibited strong inhibitory effects against all three; thus GI50 values for 3 were 12.7 ± 3.7, 17.9 ± 1.1 and 17.9 ± 0.5, for 5 9.0 ± 3.7, 4.9 ± 0.2 and 9.8 ± 0.5, and for 6 6.63 ± 0.7, 7.5 ± 0.5 and 9.7 ± 0.3.3. Epilupeol was less active, with GI50 values of 75.6 ± 11.7, 86.1 ± 12.4 and 80.9 ± 2.6 while 7 was moderately active only against MCF-7 (GI50 = 79.2 ± 2.4). Additional studies indicated that triterpenes 5 and 6 exerted their antiproliferative activity through the involvement of apoptosis while triterpene 3 did not.
Key words
Glochidion sphaerogynum - Glochidion eriocarpum - Euphorbiaceae - lupane triterpenes - Cytotoxic activity - apoptosis
References
- 1 Ganguly A K, Govindachari T R, Mohamed P A, Rahimtulla A D, Viswanathan N. Chemical constituents of Glochidion hohenackeri . Tetrahedron. 1966; 22 1513-9
- 2 Johns S R, Lamberton J A. New histamine alkaloids from a Glochidion species. Chem Commun 1966: 312-3
- 3 Johns S R, Lamberton J A. New imidazole alkaloids from a Glochidion species. Aust J Chem. 1967; 20 550-60
- 4 Hui W -H, Fung M -L. An examination of the Euphorbiaceae of Hong, Kong. Part VI. Isolation and structure of glochidonol, a new triterpene ketol from Glochidion wrightii . J Chem Soc C 1969: 1710-2
- 5 Hui W -H, Lee W -K, Ng K K, Chan C -K. An examination of the Euphorbiaeceae of Hong Kong. Part VII. Occurrence of triterpeonoids and steroids in three Glochidion species. Phytochemistry. 1970; 9 1099-102
- 6 Hui W -H, Lee W K. An examination of the Euphorbiaceae of Hong Kong. Part VIII. Lup-20(29)-ene-3α,23-diol, a new triterpene from Glochidion macrophyllum Benth. J Chem Soc C 1971: 1004-6
- 7 Ahmad A, Zaman A. Chemical constituents of Glochidion venulatum, Maesa indica and Rhamnus triquetra . Phytochemistry. 1973; 12 1826
- 8 Talapatra S K, Bhattacharyya S, Maiti B C, Talapatra B. Structure of glochicudiol - New triterpenoid from Glochidon multiloculare. Natural occurrence of dimedone. Chemistry and Industry (London) 1973: 1033-1034
- 9 Talapatra B, Dutta S, Maiti B C, Pradhan D K, Talapatra S K. Terpenoids and related compounds. XII. Terpenoid constituents of Indian Glochidion species, Glochidion acuminatum and Glochidion thomsonii. Partial synthesis of glochidone. Aust J Chem. 1974; 27 2711-4
- 10 Hui W -H, Li M -M. An examination of the Euphorbiaceae of Hong Kong. Part 11. Lupene triterpenoids from Glochidion eriocarpum . Phytochemistry. 1976; 15 561-2
- 11 Hui W -H, Li M -M. An examination of the Euphorbiaceae of Hong Kong. Part 16. Triterpenoids from Glochidion macrophyllum and G. puberum . Phytochemistry. 1978; 17 156-7
- 12 Lin C -H. Studies on the constituents of the stem of Glochidion rubrum Blume and Glochidion hongkongense Mull.-Arg. Kuo Li Chung-kuo I Yao Yen Chiu Su Yen Pao Kao 1978; 30 : 93; Chem Abstr. 1979; 91 2514y
- 13 Lin J -H, Chou C J, Liu K -C. Studies on the constituents of the stem of Glochidion rubrum Blume II. Kuo Li Chung-kuo I Yao Yen Chiu So Yen Chiu Pao Kao 1980; 118 - 121; Chem Abstr. 1980; 93 201020a
- 14 Sristava R, Kulshreshtha D H. Glochidioside, a triterpene glycoside from Glochidion heyneanum. Phytochemistry 1986; 25 : 2672 - 4. In a footnote these authors refer to an article by Dhawan BN, Rastogi RP, Singh KK, Tandon JS. Indian J Exptl Biol. 1977; 15 208, which reported that an alcoholic extract of the aerial parts of G. heyneanum showed anticancer activity in the PS system. This article has not been cited in Biological Abstracts
- 15 Sristava R, Kulshreshtha D H. Triterpenoids from Glochidion heyneanum . Phytochemistry. 1988; 27 3575-8
- 16 Takeda Y, Mima C, Masuda T, Hirata E, Takushi A, Otsuka H. Glochidiobioside, a glucoside of (7S,8R)-dihydro-dehydrodiconiferyl alcohol from leaves of Glochidion obovatum . Phytochemistry. 1988; 49 2137-9
- 17 Otsuka H, Hirata E, Takushi A, Shinzato T, Takeda Y, Bando M, Kido M. Glochidiono lactones A - F: Butenolide glucosides from leaves of Glochidion zeylanicum (Gaertn.) A. Juss. Chem Pharm Bull. 2000; 48 547-51
- 18 Otsuka H, Hirata E, Shinzato T, Takeda Y. Isolation of lignan glycosides and neolignan sulphate from the leaves of Glochidion zeylanicum (Gaertn.) A. Juss. Chem Pharm Bull. 2000; 48 1084-9
- 19 Reynolds W F, McLean S, Poplawski J, Enriquez R G, Escobar L I, Leon I. Total assignment of 13C and 1H spectra of three isomeric triterpenoid derivatives by 2D NMR: an investigation of the potential utility of 1H chemical shifts in structural investigations of complex natural products. Tetrahedron. 1986; 42 3419-28
- 20 Savona G, Bruno M, Rodríguez B, Marco J L. Triterpenoids from Salvia deserta . Phytochemistry. 1987; 26 3305-8
- 21 Monks A, Scudiero D, Skehan P, Shoemaker R, Paull K, Vistica D, Hose C, Langley J, Cronise P, Vaigro-Wolff A, Gray-Goodrich M, Campbell H, Mayo J, Boyd M. Feasibility of a high-flux anticancer drug screen using a diverse panel of cultured human tumor cell lines. Journal of the National Cancer Institute. 1991; 83 757-65
- 22 Skehan P, Storeng R, Scudiero D, Monks A, McMahon J, Vistica D, Warren J T, Bokesch H, Kenney S, Boyd M. New colorimetric cytotoxicity assay for anticancer-drug screening. Journal of the National Cancer Institute. 1990; 82 1107-12
Werner Herz
Department of Chemistry and Biochemistry
The Florida State University
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USA
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