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Bioorg Med Chem Lett ; 30(13): 127237, 2020 07 01.
Article in English | MEDLINE | ID: mdl-32386981

ABSTRACT

Twenty benzothiazole derivatives bearing a 1,3,4-oxadiazole moiety were synthesized and evaluated for their anti-oxidant and anti-inflammatory activities. Among these compounds, 8h and 8l were appeared to have high radical scavenging efficacies as 0.05 ± 0.02 and 0.07 ± 0.03 mmol/L of IC50 values in ABTS+ bioassay, respectively. In anti-inflammatory tests, compound 8h displayed good activity with 57.35% inhibition after intraperitoneal administration, which was more potent than the reference drug (indomethacin). Molecular modeling studies were performed to investigate the binding mode of the representative compound 8h into COX-2 enzyme. In vitro enzyme study implied that compound 8h exerted its anti-inflammatory activity through COX-2 inhibition.


Subject(s)
Anti-Inflammatory Agents/therapeutic use , Benzothiazoles/therapeutic use , Free Radical Scavengers/therapeutic use , Inflammation/drug therapy , Oxadiazoles/therapeutic use , Animals , Anti-Inflammatory Agents/chemical synthesis , Anti-Inflammatory Agents/metabolism , Benzothiazoles/chemical synthesis , Benzothiazoles/metabolism , Cyclooxygenase 2/metabolism , Cyclooxygenase 2 Inhibitors/chemical synthesis , Cyclooxygenase 2 Inhibitors/metabolism , Cyclooxygenase 2 Inhibitors/therapeutic use , Free Radical Scavengers/chemical synthesis , Free Radical Scavengers/metabolism , Humans , Mice , Molecular Docking Simulation , Molecular Structure , Oxadiazoles/chemical synthesis , Oxadiazoles/metabolism , Structure-Activity Relationship
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