Anticancer and Antioxidant Activity of Allergen-Removed Extract in Rhus verniciflua Stokes |
Kim, Myong-Jo
(College of Agricultural and Life Science, Kangwon National University)
Choi, Won-Cheol (Kwanghyeowon Medical Foundation Cancer Center) Barshinikov, A. M. (Russian N. N., Blockhin Cancer Center) Kobayashi, A. (Osaka National University) |
1 | Onishi N (1995) In Urushi: Elegant Asia. NEC Creative, Japan |
2 | Packer L, Glazer AN (1993) In Oxygen Radicals in Biological Systems : Oxygen Radicals and Antioxidants. Academic Press, Inc., San Diego, U. S. A |
3 | Yamauchi Y, Oshima R, Kumanotani J (1982) Configuration of the olefinic bonds in the heteroolefinic side-chains of Japanese lacquer urushiol. J. Chromatog. 243 : 71-84 DOI ScienceOn |
4 | Majima R (1922) Ber den Hauptbestandteil des Japan lacks, VIII. Mitteilung : Stellung der Doppelbindungen in der Seitenkette des Urushiols und Beweisf hrung, da das Urushiol eine Mischungist. Chem. Ber. 55B : 172-191 DOI |
5 | Kim MJ, Kim CJ, Kwak SS (1997) Antifungal activity of urushiol components in the sap of lacquer tree(Rhus verniciflua). KJPR Korean J. Plant. Res. 10(3) : 231-234 |
6 | Markiewitz KH, Dawson CR (1965) On the isolation of the allergenically active components of the toxic principle of poisonivy. J. Org. Chem. 30 : 1610-1613 DOI PUBMED |
7 | Kim WG, Kim JP, Kim CJ, Lee KH, Yoo ID (1996) Benzastatins A, B, C, and D : New free radical scavengers from Streptomyces nitrosporeus 30643. I. Taxonomy, fermentation, isolation, Physico-chemical properties and biological activities. J. Antibiotics 49 : 20-25 DOI ScienceOn |
8 | Hong DH, Han SB, Lee CW, Park SH, Jeon YJ, Kim MJ, . Kwak SS, Khn HM (1999) Cytotoxicity of urushiols isolated from sap of korean lacquer tree(Rhus verniciflua). Arch Pharm Res. 22 : 638-641 DOI ScienceOn |
9 | Xiong Q, Kadota S, Tadata T, Namba T (1996) Antioxidative effects of phenylethanoids from Cistanche deserticola. Biol. Pharm. Bull. 19 : 1580-1585 DOI ScienceOn |
10 | Hill GA, Mattacotti V, Graham WD (1934) The toxic principle of the poison ivy. Am. Chem. Soc. 56 : 2736-2738 DOI |
11 | James C, Murphy E, Watson S, Ernest C (1983) Toxicological evaluation of poison oak urushiol and its esterified derivative. Toxicology. 26 : 135-142 DOI ScienceOn |
12 | Du Y, Oshima R, Kumanotani J (1984) Reversed-phase liquid chromatographic separation and identification of constituents of urushiol in the sap of the lac tree, Rhus vernicifera. J. Chromatog. 284 : 463-473 DOI ScienceOn |
13 | Kim MJ, Choi YH, Kim WG, Kwak SS (1997) Antioxidative activity of urushiol derivatives from the sap of lacquer tree (Rhus vemciflua). KJPR Korean J. Plant. Res. 10(3) : 227-230 |
14 | Ohkawa H, Ohishi N, Ygi K (1979) Assay for lipid peroxides in animal tissues by thiobarbituric acid reaction. Anal. Biochem. 95 : 351-358 DOI ScienceOn |
15 | Tyman J H P (1979) Non-isoprenoid pong chain phenols. Chem. Soc. Rev. 8 : 499-537 DOI |
16 | Kenneth H, Chailes M, Dawson R (1964) On the isolation of the allergenically active components of the toxic principle of poison ivy. J. Org. Chem. 30 : 1610-1613 |
17 | Adawadkar PD, Elsohly MA (1983) An urushiol derivative from poison sumac. Phytochemistiy. 22 : 1280-1281 DOI ScienceOn |
18 | EISohly M, Adawadkai APD, Ma CY, Tumer CE (1982) Separation and characterization of poison ivy and poison oak urushiol components. J. Nat. Prod. 45 : 532-538 DOI |
19 | Jung DK, Song HK, Kim H (1990) the characteristics of allegic materials from Korean lacquer tree sap : Preperative analysis of lacquer tree sap. Res. Rept. RDA 33 : 675-682 |