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
|