scholarly journals Chiral Derivatives of Xanthones: Investigation of Enantioselectivity as Inhibitors of Cyclooxygenases (COX-1 and COX-2) and Binding Interaction with Human Serum Albumin

2016 ◽  
Author(s):  
Madalena Pinto ◽  
Carla Fernandes ◽  
Andreia Palmeira ◽  
Inês Ramos ◽  
Carlos Carneiro ◽  
...  
Keyword(s):  
Human Serum Albumin ◽  
Serum Albumin ◽  
Human Serum ◽  
Binding Interaction ◽  
Cox 2 ◽  
Derivatives Of ◽  
Cox 1

scholarly journals Chiral Derivatives of Xanthones: Investigation of the Effect of Enantioselectivity on Inhibition of Cyclooxygenases (COX-1 and COX-2) and Binding Interaction with Human Serum Albumin

2017 ◽  
Vol 10 (4) ◽  
pp. 50 ◽  
Author(s):  
Carla Fernandes ◽  
Andreia Palmeira ◽  
Inês Ramos ◽  
Carlos Carneiro ◽  
Carlos Afonso ◽  
...  
Keyword(s):  
Human Serum Albumin ◽  
Serum Albumin ◽  
Human Serum ◽  
Binding Interaction ◽  
Cox 2 ◽  
Derivatives Of ◽  
Cox 1

scholarly journals The Influence of Glycosylation of Natural and Synthetic Prenylated Flavonoids on Binding to Human Serum Albumin and Inhibition of Cyclooxygenases COX-1 and COX-2

Molecules ◽  
2017 ◽  
Vol 22 (7) ◽  
pp. 1230 ◽  
Author(s):  
Tomasz Tronina ◽  
Paulina Strugała ◽  
Jarosław Popłoński ◽  
Aleksandra Włoch ◽  
Sandra Sordon ◽  
...  
Keyword(s):  
Human Serum Albumin ◽  
Serum Albumin ◽  
Human Serum ◽  
Prenylated Flavonoids ◽  
Cox 2 ◽  
Cox 1 ◽  
Natural And Synthetic

Phosphonate monoesters on a thiacalix[4]arene framework as potential inhibitors of protein tyrosine phosphatase 1B

2015 ◽  
Vol 13 (33) ◽  
pp. 8803-8806 ◽  
Author(s):  
Viacheslav V. Trush ◽  
Sergiy G. Kharchenko ◽  
Vsevolod Yu. Tanchuk ◽  
Vitaly I. Kalchenko ◽  
Andriy I. Vovk
Keyword(s):  
Human Serum Albumin ◽  
Serum Albumin ◽  
Human Serum ◽  
Protein Tyrosine Phosphatase ◽  
Tyrosine Phosphatase ◽  
Methylphosphonic Acid ◽  
Protein Tyrosine Phosphatase 1B ◽  
Protein Tyrosine ◽  
Potential Inhibitors ◽  
Derivatives Of

Monoester derivatives of thiacalix[4]arene tetrakis(methylphosphonic) acid were found to be capable of inhibiting protein tyrosine phosphatase 1B. In addition, these compounds can strongly bind to human serum albumin.

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