2018
DOI: 10.1016/j.imbio.2017.10.008
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Immunobiological efficacy and immunotoxicity of novel synthetically prepared fluoroquinolone ethyl 6-fluoro-8-nitro-4-oxo-1,4-dihydroquinoline-3-carboxylate

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Cited by 7 publications
(2 citation statements)
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“…A new synthetically prepared fluoroquinolone derivative 6-fluoro-8-nitro-4-oxo-1,4-dihydroquinoline-3-carboxylate (6FN) could induce RAW 264.7 macrophages cell-release of pro- and anti-inflammatory TH1, TH2 and TH17 cytokines with anti-cancer and/or anti-infection activities. A significant inhibition of growth in cancer cells HeLa was detected [116].…”
Section: Development Of Therapy By Targeting Tamsmentioning
confidence: 99%
“…A new synthetically prepared fluoroquinolone derivative 6-fluoro-8-nitro-4-oxo-1,4-dihydroquinoline-3-carboxylate (6FN) could induce RAW 264.7 macrophages cell-release of pro- and anti-inflammatory TH1, TH2 and TH17 cytokines with anti-cancer and/or anti-infection activities. A significant inhibition of growth in cancer cells HeLa was detected [116].…”
Section: Development Of Therapy By Targeting Tamsmentioning
confidence: 99%
“…A complete cell growth inhibition of the tested cell lines was observed at the higher concentrations applied (40–100 μM) after 48–72 hr of incubation. Cell growth inhibition was reported to be a result of apoptosis induction through activation of caspase‐9 and ‐3 . Substitution of ciprofloxacin at the piperazinyl N‐ 4 with aryl and alkyl carbamoylmethyl derivatives yielded potent antiproliferative compounds against non‐small cell lung cancer A549 cell line.…”
Section: Fluoroquinolone Derivatives With Anticancer Activitymentioning
confidence: 99%