Ecdysteroid glycosides: Identification, chromatographic properties, and biological significance

被引:14
作者
Maria, A
Girault, JP
Saatov, Z
Harmatha, J
Dinan, L
Lafont, R
机构
[1] Univ Paris 06, Lab Endocrinol Mol & Evolut, EA 3501, F-75252 Paris, France
[2] Univ Paris 06, IFR83, F-75252 Paris, France
[3] Univ Paris 05, Chim & Biochim Pharmacol & Toxicol Lab, CNRS, UMR 8601, F-75270 Paris, France
[4] Inst Chem Plant Substances, Tashkent 700170, Uzbekistan
[5] Acad Sci Czech Republ, Inst Organ Chem & Biochem, CR-16610 Prague, Czech Republic
[6] Univ Exeter, Dept Biol Sci, Hatherly Labs, Exeter EX4 4PS, Devon, England
关键词
D O I
10.1093/chromsci/43.3.149
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Ecdysteroid glycosides are found in both animals and plants. The Chromatographic behavior of these molecules is characteristic, as they appear much more polar than their corresponding free aglycones when analyzed by normal-phase high-performance liquid chromatography (HPLC), whereas the presence of glycosidic moieties has a very limited (if any) impact on polarity when using reversed-phase HPLC. Biological activity is greatly reduced because the presence of this bulky substituent probably impairs the interaction with ecdysteroid receptor(s). 2-Deoxy-20-hydroxyecdysone 22-O-β-D- glucopyranoside, which has been isolated from the dried aerial parts of Silene nutans (Caryophyllaceae), is used as a model compound to describe the rationale of ecdysteroid glycoside purification and identification.
引用
收藏
页码:149 / 157
页数:9
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