1979
DOI: 10.1007/bf00789527
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Synthesis and antibacterial activity of substituted quinoxaline N-oxides with methyl or methoxy substituents in the benzene ring

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“…The more active the chemical, the less negative the reduction potential is a well‐grounded statement for those compounds that have shown promising biological action in which chlorine atom substituted on 6th and 7th position of the heterocyclic ring with substitution of 2‐phenylethyl on CONH 2 exhibited highly potent activity (Torres et al, 2011). Musatova et al experimentally discovered that QdNOs containing dimethyl ( 14 ; Figure 3), methyl, acetoxymethyl, or hydroxymethyl ( 15 ; Figure 3) groups in positions 2 or 2,3 exhibit significant antibacterial action (Musatova et al, 1979).…”
Section: Biological Activitiesmentioning
confidence: 99%
“…The more active the chemical, the less negative the reduction potential is a well‐grounded statement for those compounds that have shown promising biological action in which chlorine atom substituted on 6th and 7th position of the heterocyclic ring with substitution of 2‐phenylethyl on CONH 2 exhibited highly potent activity (Torres et al, 2011). Musatova et al experimentally discovered that QdNOs containing dimethyl ( 14 ; Figure 3), methyl, acetoxymethyl, or hydroxymethyl ( 15 ; Figure 3) groups in positions 2 or 2,3 exhibit significant antibacterial action (Musatova et al, 1979).…”
Section: Biological Activitiesmentioning
confidence: 99%