Methyl esters of 23,24-Dinor-5α-cholan-22-oic acids as brassinosteroid Analogues. Synthesis, evaluation of plant growth promoting activity and Molecular docking

[1]  Reed M. Stein,et al.  A practical guide to large-scale docking , 2021, Nature Protocols.

[2]  A. Olea,et al.  Synthesis of New Steroidal Carbamates with Plant-Growth-Promoting Activity: Theoretical and Experimental Evidence , 2021, International journal of molecular sciences.

[3]  A. Olea,et al.  Exogenous Application of Brassinosteroid 24-Norcholane 22(S)-23-Dihydroxy Type Analogs to Enhance Water Deficit Stress Tolerance in Arabidopsis thaliana , 2021, International journal of molecular sciences.

[4]  J. Oklestkova,et al.  Synthesis and Biological Activity of Brassinosteroid Analogues with a Nitrogen-Containing Side Chain , 2020, International journal of molecular sciences.

[5]  Yuehui He,et al.  Roles of Brassinosteroids in Plant Reproduction , 2020, International journal of molecular sciences.

[6]  Trevor M. Nolan,et al.  Brassinosteroids: Multidimensional Regulators of Plant Growth, Development, and Stress Responses[OPEN] , 2019, Plant Cell.

[7]  A. Bajguz.  Brassinosteroids in Microalgae: Application for Growth Improvement and Protection Against Abiotic Stresses , 2019, Brassinosteroids: Plant Growth and Development.

[8]  M. A. Iglesias-Arteaga,et al.  Synthesis of dimeric spirostanols linked through a 1,4-dimethylidenebenzene moiety by double BF3·Et2O-catalyzed aldol condensation of steroid sapogenins and terephtalaldehyde , 2018, Steroids.

[9]  P. Ahmad,et al.  Brassinosteroids Regulate Growth in Plants Under Stressful Environments and Crosstalk with Other Potential Phytohormones , 2018, Journal of Plant Growth Regulation.

[10]  H. Siddiqui,et al.  Regulation of photosynthesis by brassinosteroids in plants , 2018, Acta Physiologiae Plantarum.

[11]  M. Strnad,et al.  Synthesis of novel aryl brassinosteroids through alkene cross-metathesis and preliminary biological study , 2017, Steroids.

[12]  S. Jang,et al.  Rice Lamina Joint Inclination Assay. , 2017, Bio-protocol.

[13]  T. Kohchi,et al.  Occurrence of brassinosteroids in non-flowering land plants, liverwort, moss, lycophyte and fern. , 2017, Phytochemistry.

[14]  S. Wendeborn,et al.  Biological activity of brassinosteroids - direct comparison of known and new analogs in planta. , 2017 .

[15]  E. Fedina,et al.  Brassinosteroid-induced changes of lipid composition in leaves of Pisum sativum L. during senescence , 2017, Steroids.

[16]  K. Berka,et al.  Design, synthesis and biological activities of new brassinosteroid analogues with a phenyl group in the side chain. , 2016, Organic & biomolecular chemistry.

[17]  Jia Li,et al.  Brassinosteroids Regulate Root Growth, Development, and Symbiosis. , 2016, Molecular plant.

[18]  K. Berka,et al.  Biological activities of new monohydroxylated brassinosteroid analogues with a carboxylic group in the side chain , 2014, Steroids.

[19]  M. A. Iglesias-Arteaga,et al.  Synthesis and plant growth promoting activity of dinorcholanic lactones bearing the 5α-hydroxy-6-oxo moiety , 2013, The Journal of Steroid Biochemistry and Molecular Biology.

[20]  J. O. Cáceres,et al.  Studies in Natural Products Chemistry , 2013 .

[21]  M. A. Iglesias-Arteaga,et al.  Synthesis and plant growth promoting activity of polyhydroxylated ketones bearing the 5α-hydroxy-6-oxo moiety and cholestane side chain , 2012, Steroids.

[22]  M. Romero-Ávila,et al.  A rapid and simple one-pot procedure for the synthesis of 3β-acetoxy-5α-hydroxy-6-oxo steroids , 2010 .

[23]  M. Dračínský,et al.  Synthesis of fluorinated brassinosteroids based on alkene cross-metathesis and preliminary biological assessment. , 2009, Journal of medicinal chemistry.

[24]  S. Hayat,et al.  Effects of brassinosteroids on the plant responses to environmental stresses. , 2009, Plant physiology and biochemistry : PPB.

[25]  M. Romero-Ávila,et al.  Synthesis and biological activity of furostanic analogues of brassinosteroids bearing the 5α-hydroxy-6-oxo moiety , 2007, Steroids.

[26]  A. Bajguz,et al.  Metabolism of brassinosteroids in plants. , 2007, Plant physiology and biochemistry : PPB.

[27]  Matthew P. Repasky,et al.  Extra precision glide: docking and scoring incorporating a model of hydrophobic enclosure for protein-ligand complexes. , 2006, Journal of medicinal chemistry.

[28]  A. Hunter,et al.  An efficient one-pot synthesis generating 4-ene-3,6-dione functionalised steroids from steroidal 5-en-3β-ols using a modified Jones oxidation methodology , 2006, Steroids.

[29]  Woody Sherman,et al.  Use of an Induced Fit Receptor Structure in Virtual Screening , 2006, Chemical biology & drug design.

[30]  Daniel G. Rivera,et al.  Synthesis and preliminary bioactivity evaluation of new pregnane brassinosteroid-like compounds , 2005 .

[31]  S. Ananich,et al.  Advances in the chemical synthesis of brassinosteroids , 1997, Chemistry of Natural Compounds.

[32]  B. Schneider,et al.  Synthesis of [26,27-2H6]brassinosteroids from 23,24-bisnorcholenic acid methyl ester , 2004, Steroids.

[33]  Daniel G. Rivera,et al.  Synthesis of pregnane ketols as metabolic precurs ors of analogues of plant growth regulators , 2004 .

[34]  Matthew P. Repasky,et al.  Glide: a new approach for rapid, accurate docking and scoring. 1. Method and assessment of docking accuracy. , 2004, Journal of medicinal chemistry.

[35]  M. Zullo,et al.  Synthesis and biological activity of three new 5a-hydroxy spirostanic brassinosteroid analogues , 2003 .

[36]  A. Tretyn,et al.  The chemical characteristic and distribution of brassinosteroids in plants. , 2003, Phytochemistry.

[37]  A. Cian,et al.  Toward a total synthesis of brassinosteroids; structure assessment of the Ireland–Claisen products of geranyl and neryl esters , 2002 .

[38]  T. Zoller,et al.  Toward a total synthesis of brassinosteroids; stereoselective generation of the hydrindane ring system , 2002 .

[39]  M. A. Iglesias-Arteaga,et al.  Spirostanic analogues of teasterone. Synthesis, characterisation and biological activity of laxogenin, (23S)-hydroxylaxogenin and 23-ketolaxogenin (23-oxolaxogenin) , 2001 .

[40]  J. Ramirez.  Effects on Bioactivity due to C-5 Heteroatom Substituents on Synthetic 28-Homobrassinosteroid Analogs , 2000 .

[41]  L. Kohout,et al.  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 , 2000 .

[42]  J. Ferrer,et al.  New synthetic brassinosteroids: a 5α-hydroxy-6-ketone analog with strong plant growth promoting activity , 1998 .

[43]  G. Punte,et al.  (25R)-5β-Hydroxyspirost-2-en-6-one , 1997 .

[44]  M. Strnad,et al.  Preparation of 2α,3α-dihydroxy-7-oxa-6-oxo-23,24-dinor-B-homo-5α-cholanic acid, its esters and amides as brassinolide analogues , 1986 .

[45]  L. Fieser,et al.  Selective Oxidation with N-Bromosuccinimide. I. Cholic Acid , 1949 .

[46]  D. Turner,et al.  Sterols. CII. Chlorogenin , 1940 .