货号 | 9000593-1mg |
描述 | A1-Phytoprostane-I is a cyclopentenone isoprostane produced by the action of reactive oxygen species on α-linolenic acid in plants.1,2,3 There are two A1-phytoprostanes, both having the single ketone group on the ring structure. This isoform results from cyclization between carbons 9 and 13 of linolenic acid, as opposed to carbons 3 and 7 in A1-phytoprostane-II. A1-Phytoprostanes induce the expression of glutathione-S-transferase, increase phytoalexin biosynthesis, and trigger the expression of several genes involved in primary and secondary metabolism in plants.1,4,3 |
别名 | 16-A1-Phytoprostane;Phytoprostane A1;PPA1; |
供应商 | Cayman |
应用文献 | |
1.Thoma, I.,Loeffler, C.,Sinha, A.K., et al. Cyclopentenone isoprostanes induced by reactive oxygen species trigger defense gene activation and phytoalexin accumulation in plants. Plant Journal 34(3), 363-375 (2003). 2.Jahn, U.,Galano, J.M., and Durand, T. Beyond prostaglandins--chemistry and biology of cyclic oxygenated metabolites formed by free-radical pathways from polyunsaturated fatty acids. Angewandte Chemie International Edition 47, 5894-5955 (2008). 3.Mueller, M.J., and Berger, S. Reactive electrophilic oxylipins: Pattern recognition and signalling. Phytochemistry 70, 1511-1521 (2009). 4.Dueckershoff, K.,Mueller, S.,Mueller, M.J., et al. Impact of cyclopentenone-oxylipins on the proteome of Arabidopsis thaliana. Biochim.Biophys.Acta. 1784, 1975-1985 (2008). | |
运输条件 | Wet ice in continental US; may vary elsewhere |
存放说明 | -20 |
纯度 | ≥90% (trans isomer mix) |
计算分子量 | 308.4 |
分子式 | C18H28O4 |
CAS号 | 1035557-09-5 |
稳定性 | ≥ 1 year |
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