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The free radical scavenging properties of these derivatives were evaluated to elucidate structure-activity relationships.
The inhibition properties of BPP derivatives were evaluated also by polarization resistance method.
All the synthesized pyrrolone derivatives were evaluated for their possible antibacterial, antifungal and antitubercular activities.
Some derivatives were evaluated for their fluorescent potentiality and showed some fluorescent emission properties.
The cytotoxicity against MT-4 cells and anti-HIV properties of new derivatives were evaluated.
The wound repair properties of these derivatives were evaluated using in vitro and in vivo assays.
The anti-cancer activities of the generated triazolonaphthalimide derivatives were evaluated with five cancer cell lines.
These derivatives were evaluated for their in vitro antimicrobial properties against human pathogens.
The synthesized benzimidazole derivatives were evaluated for their in vitro antitubercular activity against Mycobacterium tuberculosis H37Rv (NCFT/TB/537).
The synthesized 1,4-disubstituted piperidine derivatives were evaluated for their affinity at both σ1 and σ2 receptors.
These derivatives were evaluated for their in vitro antibacterial activities against a panel of Staphylococcus aureus and Staphylococcus epidermidis.
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