Lucie Borková

ORCID: 0000-0003-3449-9818
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About
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Research Areas
  • Natural product bioactivities and synthesis
  • Plant biochemistry and biosynthesis
  • Bioactive Compounds and Antitumor Agents
  • Phytochemical compounds biological activities
  • Click Chemistry and Applications
  • Phytochemistry and Bioactive Compounds
  • Synthesis and biological activity
  • Biological Activity of Diterpenoids and Biflavonoids
  • Monoclonal and Polyclonal Antibodies Research
  • Synthesis and Characterization of Pyrroles
  • Chemical Synthesis and Analysis

Palacký University Olomouc
2014-2022

Institute of Molecular and Translational Medicine
2018-2022

Faculty (United Kingdom)
2018

University Hospital Olomouc
2018

Abstract This Focus Review summarizes recent advances in the synthesis of betulinic acid derivatives with modified A‐rings. It also focuses on their application as potential therapeutic agents for treatment cancer and other diseases. Betulinic (BA) exhibits therapeutically interesting biological properties, including antitumor, anti‐HIV, antiprotozoal, hepato‐ or nephroprotective activity; however, its clinical use has been severely limited by higher IC 50 value worse pharmacological...

10.1002/ajoc.201800163 article EN Asian Journal of Organic Chemistry 2018-05-09

Abstract A total of 41 new triterpenoids were prepared from allobetulone, methyl betulonate, oleanonate, and oleanonic acid to study their influence on cancer cells. Each 3‐oxotriterpene was brominated at C2 substituted with thiocyanate; subsequent cyclization the appropriate ammonium salts gave N‐substituted thiazoles. All compounds tested for in vitro cytotoxic activity eight cell lines two non‐cancer fibroblasts. 2‐Bromoallobetulone ( 2 b ) 2‐bromobetulonate 3 ), 2‐bromooleanonic 5...

10.1002/cmdc.201600626 article EN ChemMedChem 2017-01-13

A set of fifteen triterpenoid pyrazines and pyridines was prepared from parent 3-oxoderivatives (betulonic acid, dihydrobetulonic oleanonic moronic ursonic heterobetulonic allobetulone). Cytotoxicity all compounds tested in eight cancer two non-cancer cell lines. Evaluation the structure-activity relationships revealed that core determined whether final molecule is active or not, while heterocycle able to increase activity modulate specificity. Five (1b, 1c, 2b, 2c, 8) were found be...

10.1016/j.ejmech.2022.114777 article EN cc-by European Journal of Medicinal Chemistry 2022-09-23

An easy, good-yielding access to functionalized enantiomerically pure 1,2,3-triazole derivatives of amino acids using commercially available ketones and esters is described.

10.1039/c8ob00533h article EN Organic & Biomolecular Chemistry 2018-01-01
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