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Interdiscip Sci ; 4(4): 268-72, 2012 Dec.
Article in English | MEDLINE | ID: mdl-23354815

ABSTRACT

The anti inflammatory potential of the human and microbial biotransformed derivatives of berberine were determined by molecular docking. It was revealed that almost all derivatives formed as a result of biotransformation showed increase in phospholipase A(2) binding affinity compared to berberine. The newly introduced -OH group/groups establish stronger hydrogen bonding interactions and more number of van der Waals contacts with the protein. As phospholipase A(2) is a target of anti inflammatory drugs, it might be concluded that certain biotransformed derivatives of berberine could be better anti inflammatory agents compared to berberine.


Subject(s)
Anti-Inflammatory Agents/pharmacology , Berberine/pharmacology , Phospholipases A2/chemistry , Plant Extracts/pharmacology , Anti-Inflammatory Agents/chemistry , Berberine/analogs & derivatives , Berberine/chemistry , Biotransformation , Computer Simulation , Humans , Hydrogen Bonding , Hydroxyl Radical/chemistry , Models, Molecular , Phospholipases A2/metabolism , Plant Extracts/chemistry , Protein Binding
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