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The synthesis of androstane brassinosteroid analogues with alpha-azido acid ester groups in position 17beta
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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, ORCIDNumber of authors 9 Source Title Steroids. - : Elsevier - ISSN 0039-128X
Roč. 75, č. 12 (2010), s. 1005-1010Number 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 ; Jana Procházková, Tel.: 220 183 418 Year of Publishing 2011
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