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Bioorg Chem ; 87: 465-473, 2019 06.
Article in English | MEDLINE | ID: mdl-30927587

ABSTRACT

An efficient and convenient Meglumine catalyzed procedure for the synthesis of bis(indolyl) methanes at ambient temperature under aqueous conditions in high yields. The catalytic reaction proceeds very smoothly. Clean reaction, ease of product isolation/purification, easily available reactants, metal free and environmentally friendly reaction conditions are the notable advantages of the present methodology. All the entitled compounds were characterized by IR, 1H, 13C NMR, mass spectra and evaluated for their antioxidant (DPPH, H2O2 and NO scavenging methods). They exhibited potent in vitro antioxidant activity dose-dependently. The binding interactions and molecular docking studies for entitled compounds were studied against 3MNG protein. 4d exhibited marked binding affinity with excellent docking score of -7.6 K.cal/mol and emerged as a lead compound.


Subject(s)
Antioxidants/pharmacology , Indoles/pharmacology , Meglumine/chemistry , Methane/pharmacology , Molecular Docking Simulation , Antioxidants/chemical synthesis , Antioxidants/chemistry , Benzothiazoles/antagonists & inhibitors , Catalysis , Dose-Response Relationship, Drug , Humans , Hydrogen Peroxide/antagonists & inhibitors , Indoles/chemistry , Methane/analogs & derivatives , Methane/chemistry , Molecular Structure , Nitric Oxide/antagonists & inhibitors , Structure-Activity Relationship , Sulfonic Acids/antagonists & inhibitors
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