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• W2147591855 abstract "The synthesis of new 4-[2-(alkylamino)ethylthio]pyrrolo[1,2-a]quinoxaline derivatives la-1 is described in five or six steps starting from various substituted nitroanilines 2a-e. The bioisostere 5-[2-(alkylamino)ethylthio]pyrrolo[1,2- a]thieno[3,2-e]pyrazine 1m was also prepared. The new derivatives were evaluated as efflux pump inhibitors (EPIs) in a model targeting the NorA system of Staphylococcus aureus. The antibiotic susceptibility of two strains overproducing NorA, SA-1199B and SA-1, was determined alone and in combination with the neo-synthesised compounds by the agar diffusion method and MIC determination, in comparison with reserpine and omeprazole taken as reference EPIs. A preliminary structure-activity relationship study firstly allowed to clarify the influence of the substituents at positions 7 and/or 8 of the pyrrolo[1,2-a]quinoxaline nucleus. Methoxy substituted compounds, 1b and 1g, were more potent EPIs than the unsubstituted compounds (1a and 1f), followed by chlorinated derivatives (1c-d and 1h). Moreover, the replacement of the N,N-diethylamino group (compounds 1a-e) by a bioisostere such as pyrrolidine (compounds 1f-h) enhanced the EPI activity, in contrast with the replacement by a piperidine moiety (compounds 1i-k). Finally, the pyrrolo[1,2-a]thieno[3,2-e]pyrazine compound 1m exhibited a higher EPI activity than its pyrrolo[1,2-a]quinoxaline analogue la, opening the way to further pharmacomodulation." @default.
• W2147591855 created "2016-06-24" @default.
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• W2147591855 date "2007-01-01" @default.
• W2147591855 modified "2023-09-23" @default.
• W2147591855 title "Synthesis of new 4-[2-(alkylamino)ethylthio]pyrrolo[1,2-<i>a</i>]quinoxaline and 5-[2-(alkylamino)ethylthio]pyrrolo[1,2-<i>a</i>]thieno[3,2-<i>e</i>]pyrazine derivatives, as potential bacterial multidrug resistance pump inhibitors" @default.
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• W2147591855 doi "https://doi.org/10.1080/14756360701485406" @default.
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