New ecdysteroids from Serratula tinctoria

Six new ecdysteroids have been isolated from Serratula tinctoria; these are: the 2,22- and 3,22-diacetates of 20-hydroxyecdysone, 5beta-hydroxyrubrosterone, 3-epi-poststerone, 3-epi-rubrosterone, and 22-oxo-20-hydroxyecdysone. These minor compounds were found together with the known ecdysteroids, 20...

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Published inPlanta medica Vol. 58; no. 4; p. 358
Main Authors Rudel, D. (Centre National de la Recherche Scientifique, Ecole Normale Superieure, Paris (France). Dept. de Biologie, Lab. de Biochimie et Physiologie du Developpement), Bathori, M, Gharbi, J, Girault, J.P, Racz, I, Melis, K, Szendrei, K, Lafont, R
Format Journal Article
LanguageEnglish
Published Germany 01.08.1992
Subjects
COMPOSICION QUIMICA
Compositae
COMPOSITION CHIMIQUE
Ecdysteroids
ESTRUCTURA QUIMICA
FITOALEXINA
INSECTICIDAS
INSECTICIDE
PHYTOALEXINE
PLANTAS MEDICINALES
PLANTE MEDICINALE
Serratula
SERRATULA TINCTORIA
STRUCTURE CHIMIQUE
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Abstract Six new ecdysteroids have been isolated from Serratula tinctoria; these are: the 2,22- and 3,22-diacetates of 20-hydroxyecdysone, 5beta-hydroxyrubrosterone, 3-epi-poststerone, 3-epi-rubrosterone, and 22-oxo-20-hydroxyecdysone. These minor compounds were found together with the known ecdysteroids, 20-hydroxyecdysone, its 2-, 3-, and 22-monoacetates, rubrosterone, poststerone, polypodine B (5beta,20-dihydroxyecdysone), pterosterone (25-deoxy-20,24- dihvdroxyecdysone), and makisterone C (24-ethyl-20-- hydroxvecdysone). All these ecdysteroids were isolated by a combination of several chromatographic techniques (liquid chromatography on alumina, DCCC, and HPLC), then identified using standard mass spectrometric and 2D(1)H-NMR techniques.
AbstractList Six new ecdysteroids have been isolated from SERRATULA TINCTORIA; these are: the 2,22- and 3,22-diacetates of 20-hydroxyecdysone, 5beta-hydroxyrubrosterone, 3-epi-poststerone, 3-epi-rubrosterone, and 22-oxo-20-hydroxyecdysone. These minor compounds were found together with the known ecdysteroids, 20-hydroxyecdysone, its 2-, 3-, and 22-monoacetates, rubrosterone, poststerone, polypodine B (5beta,20-dihydroxyecdysone), pterosterone (25-deoxy-20,24-dihydroxyecdysone), and makisterone C (24-ethyl-20-hydroxyecdysone). All these ecdysteroids were isolated by a combination of several chromatographic techniques (liquid chromatography on alumina, DCCC, and HPLC), then identified using standard mass spectrometric and 2D (1)H-NMR techniques.
Six new ecdysteroids have been isolated from Serratula tinctoria; these are: the 2,22- and 3,22-diacetates of 20-hydroxyecdysone, 5beta-hydroxyrubrosterone, 3-epi-poststerone, 3-epi-rubrosterone, and 22-oxo-20-hydroxyecdysone. These minor compounds were found together with the known ecdysteroids, 20-hydroxyecdysone, its 2-, 3-, and 22-monoacetates, rubrosterone, poststerone, polypodine B (5beta,20-dihydroxyecdysone), pterosterone (25-deoxy-20,24- dihvdroxyecdysone), and makisterone C (24-ethyl-20-- hydroxvecdysone). All these ecdysteroids were isolated by a combination of several chromatographic techniques (liquid chromatography on alumina, DCCC, and HPLC), then identified using standard mass spectrometric and 2D(1)H-NMR techniques.
Author Rudel, D. (Centre National de la Recherche Scientifique, Ecole Normale Superieure, Paris (France). Dept. de Biologie, Lab. de Biochimie et Physiologie du Developpement)
Girault, J.P
Lafont, R
Gharbi, J
Bathori, M
Szendrei, K
Melis, K
Racz, I
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Snippet Six new ecdysteroids have been isolated from Serratula tinctoria; these are: the 2,22- and 3,22-diacetates of 20-hydroxyecdysone, 5beta-hydroxyrubrosterone,...
Six new ecdysteroids have been isolated from SERRATULA TINCTORIA; these are: the 2,22- and 3,22-diacetates of 20-hydroxyecdysone, 5beta-hydroxyrubrosterone,...
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StartPage 358
SubjectTerms COMPOSICION QUIMICA
Compositae
COMPOSITION CHIMIQUE
Ecdysteroids
ESTRUCTURA QUIMICA
FITOALEXINA
INSECTICIDAS
INSECTICIDE
PHYTOALEXINE
PLANTAS MEDICINALES
PLANTE MEDICINALE
Serratula
SERRATULA TINCTORIA
STRUCTURE CHIMIQUE
Title New ecdysteroids from Serratula tinctoria
URI https://www.ncbi.nlm.nih.gov/pubmed/17226485
Volume 58
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