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The synthesis of androstane brassinosteroid analogues with alpha-azido acid ester groups in position 17beta

SYSNO ASEP	0347182
Document Type	J - Journal Article
R&D Document Type	Journal Article
Subsidiary J	Článek ve WOS
Title	The synthesis of androstane brassinosteroid analogues with alpha-azido acid ester groups in position 17beta
Author(s)	Hniličková, Jaroslava (UOCHB-X) Kohout, Ladislav (UOCHB-X) Capdevila, E. (ES) Esteve, A. (ES) Vilaplana, M. (ES) Molist, M. (ES) Brosa, C. (ES) Swaczynová, Jana (UEB-Q) Slavíková, Barbora (UOCHB-X)_{RID, ORCID}
Number of authors	9
Source Title	Steroids. - : Elsevier - ISSN 0039-128X Roč. 75, č. 12 (2010), s. 1005-1010
Number of pages	6 s.
Language	eng - English
Country	US - United States
Keywords	brassinosteroids ; androstane analogues ; plant growth regulators
Subject RIV	CC - Organic Chemistry
R&D Projects	1QS510680561 GA AV ČR - Academy of Sciences of the Czech Republic (AV ČR)
	1M06030 GA MŠMT - Ministry of Education, Youth and Sports (MEYS)
CEZ	AV0Z40550506 - UOCHB-X (2005-2011)
	AV0Z50380511 - UEB-Q (2005-2011)
UT WOS	000281932500028
DOI	10.1016/j.steroids.2010.06.012
Annotation	Six new castasterone analogues with alpha-azido acid ester groups in position 17beta; were synthesized. The biological activities were evaluated in two bioassays: a rice lamina inclination test and bean second internode bioassays. The activities of the new analogues differ in these two bioassays.
Workplace	Institute of Organic Chemistry and Biochemistry
Contact	asep@uochb.cas.cz ; Kateřina Šperková, Tel.: 232 002 584 ; Viktorie Chládková, Tel.: 232 002 434
Year of Publishing	2011

Number of the records: 1