Synthesis of New Brassinosteroid 24-Norcholane Type Analogs Conjugated in C-3 with Benzoate Groups
The metabolism of brassinosteroid leads to structural modifications in the ring skeleton or the side alkyl chain. The esterification and glycosylation at C-3 are the most common metabolic pathways, and it has been suggested that conjugate brassinosteroids are less active or inactive. In this way, pl...
Main Authors: | Karoll Ferrer, Katy Díaz, Miroslav Kvasnica, Andrés F. Olea, Mauricio Cuellar, Luis Espinoza |
---|---|
Format: | Article |
Language: | English |
Published: |
MDPI AG
2021-02-01
|
Series: | Molecules |
Subjects: | |
Online Access: | https://www.mdpi.com/1420-3049/26/4/1173 |
Similar Items
-
Synthesis and Biological Activity of New Brassinosteroid Analogs of Type 24-Nor-5β-Cholane and 23-Benzoate Function in the Side Chain
by: Nitza Soto, et al.
Published: (2021-05-01) -
Epimeric Mixtures of Brassinosteroid Analogs: Synthesis, Plant Growth, and Germination Effects in Tomato (<i>Lycopersicum esculentum</i> Mill.)
by: Nitza Soto, et al.
Published: (2020-06-01) -
Exogenous Application of Brassinosteroid 24-Norcholane 22(<i>S</i>)-23-Dihydroxy Type Analogs to Enhance Water Deficit Stress Tolerance in <i>Arabidopsis thaliana</i>
by: Katy Díaz, et al.
Published: (2021-01-01) -
New Brassinosteroid Analogs with 23,24-Dinorcholan Side Chain, and Benzoate Function at C-22: Synthesis, Assessment of Bioactivity on Plant Growth, and Molecular Docking Study
by: Vanessa Aitken, et al.
Published: (2023-12-01) -
Synthesis of New Steroidal Carbamates with Plant-Growth-Promoting Activity: Theoretical and Experimental Evidence
by: Daylin Fernández Pacheco, et al.
Published: (2021-02-01)