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Chemical Constituents from the Leaf and Twig of Acer okamotoanum Nakai and their Cytotoxicity  

Jin, Wen-Yi (College of Pharmacy, Chungnam National University)
Min, Byung-Sun (College of Pharmacy, Catholic University of Daegu)
Youn, Ui-Jung (College of Pharmacy, Chungnam National University)
Hung, Tran-Manh (College of Pharmacy, Chungnam National University)
Song, Kyung-Sik (College of Agriculture and life Science, Kyungpook National University)
Seong, Yeon-Hee (College of Veterinary Medicine, Chungbuk National University)
Bae, Ki-Hwan (College of Pharmacy, Chungnam National University)
Publication Information
Korean Journal of Medicinal Crop Science / v.14, no.2, 2006 , pp. 77-81 More about this Journal
Abstract
As a result of cytotoxic compounds against cancer cell lines from natural sources, senven compounds were isolated from the leaf and twig of Acer okamotoanum Nakai. The compounds (1-7) were identified as ethyl gallate (1), methyl gallate (2), gallic acid (3), trans $resveratrol-3-O-{\beta}-D-glucopyranoside$ (4), acertannin (5), nikoenoside (6), and fraxin (7) by physicochemical and spectroscopic data (including mp, UV, IR, MS, $^1H-NMR,\;^{13}C-NMR$, DEPT, and HMBC) in comparison with those of published papers. All the compounds were tested for their cytotoxic activity against L1210, HL-60, K562, and B16F10 cancer cell lines in vitro by MTT assay method. Compounds 1-3 and 5 showed cytotoxic activity against all tested cell lines with $IC_{50}$ values ranged from 12.5 to $72.2\;{\mu}M$. Of the compounds, methyl gallate (2) exhibited the most potent cytotoxic activity against L1210, HL-60, K562, and B16F10 tumor cells with $IC_{50}$ values of 12.5, 48.3, 22.8, and $22.8\;{\mu}M$, respectively. Other compounds did not show any cytotoxic activity against four cancer cell lines.
Keywords
Acer okamotoanum; Aceraceae; chemical constituent; MTT; cytotoxicity;
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Times Cited By KSCI : 1  (Citation Analysis)
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1 Charles JP (1993) The Aldrich Library of $^{13}C$ and $^1H$ FT NMR Spectra. 2:1147 C
2 Choi YH, Han SS, Lee HO, Baek SH (2005) Biological activity of bioactive components from Acer ginnala Max. Bulletin of the Korean Chemical Society 26: 1450-1452   DOI
3 Du YH, Cui CB, Li WX, Cai B, Han B, Yao X S (2003) Studies on the anticancer constituents of Canarium bengalense Roxb. - polyphenolic cell cycle inhibitors. Zhongguo Yaowu Huaxue Zazhi 13:320-323
4 Kim HJ, Woo ER, Shin CG, Park HK (1998b) A new flavonol glycoside gallate ester from Acer okamotoanum and its inhibitory activity against human immunodeficiency virus-1 (HIV1) integrase. J. Nat. Prod. 61:145-148   DOI   ScienceOn
5 Klaus B, Niels FL, Soren RJ, Bent JN (1980) The structure of acertannin. Phytochemistry 19:2033   DOI   ScienceOn
6 Mosmann T (1983) Rapid colorimetric assay for cellular growth and survival: application to proliferation and cytotoxicity assays. J. Immunol. Methods 65:55-63   DOI   ScienceOn
7 Hata K, Kozawa M, Baba K (1975) New stilbene glucose Chinese crude drug Heshouwu root of Polygonum multiflorum, Yakugaku Zasshi 95:211-213   DOI
8 Yaki A, Koizumi Y, Nishioka I (1971) Studies on Rhubarb (Rhei rhizoma). 1. Stilbene derivatives from 'Dodaioo', Syoyakugaku Zasshi 25:52-54
9 Kim CM, Shin MK, An DK, Lee KS (1998a) Dictionary of Traditional Medicines. Jung-Dam Publishing House. Seoul. pp.3915-3916
10 Liu RM, Sun QH, Sun AL, Cui JC (2005) Isolation and purification of coumarin compounds from Cortex fraxinus by highspeed counter-current chromatography. Journal of chromatography A 1072:195-199   DOI   ScienceOn
11 Redwane A, Lazrek HB, Bouallam S, Markouk M, Ama rouch H, Jana M (2002) Larvicidal activity of extracts from Quercus lustitania var. infectoria galls (Oliv.). Journal of Ethnopharmacology 79:261-263   DOI   ScienceOn
12 Nakagawa Y, Tayama S (1995) Cytotoxicity of propyl gallate and related compounds in isolated rat hepatocytes. Tokyotoritsu Eisei Kenkyusho Kenkyu Nenpo 46:254-257
13 Morikawa T, Tao J, Veda K, Matsuda H, Yoshikawa M (2003) Medicinal Foodstuffs. XXXI. Structures of new aromatic constituents and inhibitors of degranulation in RBL-2H3 cells from a Japanese folk medicine, the stem bark of Acer nikoense. Chem. Pharm. Bull. 51:62-67   DOI   ScienceOn
14 Pierre WT, Bernard FG, Francois H, Joseph V, Jean-Michel M (1998) Isolation, identification, and antioxidant activity of three stilbene glucosides newly extracted from Vitis vinifera cell cultures. J. Nat. Prod. 61:655-657   DOI   ScienceOn