Synthesis, anti-mycobacterial and cytotoxic evaluation of substituted isoindoline-1,3-dione-4-aminoquinolines coupled via alkyl/amide linkers.
RSC Adv
; 9(15): 8515-8528, 2019 Mar 12.
Article
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| MEDLINE
| ID: mdl-35518673
ABSTRACT
A series of secondary amine-substituted isoindoline-1,3-dione-4-aminoquinolines were prepared via microwave heating and assayed for their anti-mycobacterial activities. The compound with a butyl chain as a spacer between the two pharmacophores and piperidine as the secondary amine component on the isoindoline ring was the most potent and non-cytotoxic among the synthesized compounds, exhibiting a minimum inhibitory concentration (MIC99) of 6.25 µg mL-1 against Mycobacterium tuberculosis.
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RSC Adv
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2019
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Article