Croatica Chemica Acta, Vol. 58 No. 4, 1985.
Izvorni znanstveni članak
Ecdysteroids. Selective Protections and Synthesis of Potential Tools for Biochemical Studies
Denis Guedin-Vuong
; Centre de Neurochimie CNRS, Universite Louis Pasteur, 5 rue Blaise Pascal, 67084,Strasbourg, France
Yoichi Nakatani
; Centre de Neurochimie CNRS, Universite Louis Pasteur, 5 rue Blaise Pascal, 67084,Strasbourg, France
Guy Ourisson
; Centre de Neurochimie CNRS, Universite Louis Pasteur, 5 rue Blaise Pascal, 67084,Strasbourg, France
Sažetak
B-Ecdysone and cyasterone bave been transformed into the ecdysterone analogue 4, wbich carries a [3-(p-hydroxyphenyl).-propoxylj- group at the end of the side chain. This derivative should be useful for various biochemical investigations (I-labelling, affinity chromatography), since it exhibits a marked ecdysterone-like activity in two independent biological tests. The synthetic scheme makes use of highly selective protections of the hydroxyl groups of phytoecdysteroids.
Ključne riječi
Hrčak ID:
178044
URI
Datum izdavanja:
6.3.1986.
Posjeta: 629 *