Crossref Cited-by Linking logo

Collect. Czech. Chem. Commun. 1998, 63, 1635-1645
https://doi.org/10.1135/cccc19981635

The Effect of Electrostatic Properties and Abibility to Form Hydrogen-Bonds on the Activity of Brassinosteroid Side-Chain Analogs

Carme Brosaa, Ismael Zamoraa, Emma Terricabrasa and Ladislav Kohoutb

a Institut Quimic de Sarria, CETS, Universität Ramon Llull, Via Augusta 390, 08024 Barcelona, Spain
b Institute of Organic Chemistry and Biochemistry, Academy of Sciences of the Czech Republic, 166 10 Prague 6, Czech Republic

Crossref Cited-by Linking

  • Ferrer-Pertuz Karoll, Espinoza Luis, Mella Jaime: Insights into the Structural Requirements of Potent Brassinosteroids as Vegetable Growth Promoters Using Second-Internode Elongation as Biological Activity: CoMFA and CoMSIA Studies. IJMS 2017, 18, 2734. <https://doi.org/10.3390/ijms18122734>
  • Hnilickova Jaroslava, Kohout Ladislav, Capdevila Enric, Esteve Ana, Vilaplana Marc, Molist Meritxell, Brosa Carme, Swaczynova-Oklestkova Jana, Slavikova Barbora: The synthesis of androstane brassinosteroid analogues with α-azido acid ester groups in position 17β. Steroids 2010, 75, 1005. <https://doi.org/10.1016/j.steroids.2010.06.012>
  • Morera-Boado Cercis, Alonso-Becerra Esther, González-Jonte Raúl, Montero-Cabrera Luis Alberto, García-de-la-Vega José Manuel: A theoretical approach to the solvation of brassinosteroids. Journal of Molecular Graphics and Modelling 2009, 27, 600. <https://doi.org/10.1016/j.jmgm.2008.09.013>
  • Suardíaz Reynier, Maestre Mitcheell, Suárez Ernesto, Bernardo Yamilet, Alonso-Becerra Esther, Pérez Carlos: Molecular Dynamics and NMR Analysis of the Configurational 13C Assignment of Epimeric 22,23-Epoxides of Stigmasterol. J. Phys. Chem. A 2008, 112, 8333. <https://doi.org/10.1021/jp804570g>
  • Šíša Miroslav, Vilaplana-Polo Marc, Ballesteros Carme Brosa, Kohout Ladislav: Brassinolide activities of 2α,3α-diols versus 3α,4α-diols in the bean second internode bioassay: Explanation by molecular modeling methods. Steroids 2007, 72, 740. <https://doi.org/10.1016/j.steroids.2007.06.009>
  • Morera-Boado Cercis, Alonso-Becerra Esther, Montero-Cabrera Luis A., González-Jonte Raul: Validation of performances of some semiempirical Hamiltonians for predicting molecular structure calculation of natural brassinosteroids: Towards understanding their biological activity by electron exchange effects. Journal of Molecular Structure: THEOCHEM 2007, 819, 109. <https://doi.org/10.1016/j.theochem.2007.05.034>
  • Rivera Daniel G, Coll Francisco: Synthesis and preliminary bioactivity evaluation of new pregnane brassinosteroid-like compounds. Can. J. Chem. 2005, 83, 1084. <https://doi.org/10.1139/v05-051>
  • Šíša Miroslav, Buděšínský Miloš, Kohout Ladislav: Synthesis and Biological Activity of 7a-Homo- and 7a,7b-Dihomo-5α-cholestane Analogues of Brassinolide. Collect. Czech. Chem. Commun. 2003, 68, 2171. <https://doi.org/10.1135/cccc20032171>
  • Kohout Ladislav, Chodounská Hana, Macek Tomáš, Strnad Miroslav: Synthesis of (20S)-2α,3α-Dihydroxy-6-oxo-7-oxa-7a-homo-5α-pregnane-20-carboxylic Acid as a Brassinosteroid Part of Ligands for Binding to Affinity Chromatography Carriers. Collect. Czech. Chem. Commun. 2000, 65, 1754. <https://doi.org/10.1135/cccc20001754>