ChemInform Abstract: Hydrophobicity and Self-Association of Bile Acids with a Special Emphasis on Oxo Derivatives of 5β-Cholanic Acid

ChemInform ◽  
2013 ◽  
Vol 44 (8) ◽  
pp. no-no
Author(s):  
Mihalj Posa
1984 ◽  
Vol 49 (7) ◽  
pp. 1617-1621 ◽  
Author(s):  
Růžena Míčková

The paper describes decarboxylation of derivatives of 3α,12α-dihydroxy-5β-cholanic acid to 24-norchol-22-ene, and conversion of this key intermediate to pregnane derivatives.


In this work the bile acids and certain of their derivatives have been studied with regard to their bacteriostatic power and relative activities in removing the Gram-positive complex from yeast. No correlation between these properties was obtained. A simple relationship was apparent, however, between the bacteriostatic activities of the compounds and their ability to depress the surface tension of the metabolism medium. The limiting dilution at which the 'active' bile acids were bacteriostatic for Staphylococcus aureus corresponded to a depression of the surface tension of the medium by approximately 4∙5 dynes. The relationship between bacteriostatic power and surface activity was only valid for this particular series of compounds of closely related molecular structure.


Molecules ◽  
2018 ◽  
Vol 23 (3) ◽  
pp. 679 ◽  
Author(s):  
Oksana Salomatina ◽  
Irina Popadyuk ◽  
Alexandra Zakharenko ◽  
Olga Zakharova ◽  
Dmitriy Fadeev ◽  
...  
Keyword(s):  

2020 ◽  
Author(s):  
Bojana R. Vasiljević ◽  
Edward T. Petri ◽  
Sofija S. Bekić ◽  
Andjelka S. Ćelić ◽  
Ljubica M. Grbović ◽  
...  

Green synthesis of bile acids derivatives and 5β-cholanic acid was achieved under microwave irradiation, and the binding affinity for the ligand binding domain of the glucocorticoid receptor was measured.


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