Voer een woord of zin in in een taal naar keuze 👆
Taal:
Vertaling en analyse van woorden door kunstmatige intelligentie ChatGPT
Op deze pagina kunt u een gedetailleerde analyse krijgen van een woord of zin, geproduceerd met behulp van de beste kunstmatige intelligentietechnologie tot nu toe:
- hoe het woord wordt gebruikt
- gebruiksfrequentie
- het wordt vaker gebruikt in mondelinge of schriftelijke toespraken
- opties voor woordvertaling
- Gebruiksvoorbeelden (meerdere zinnen met vertaling)
- etymologie
Wat (wie) is quinolone - definitie
ANY CHEMICAL COMPOUND HAVING 2-QUINOLONE OR 4-QUINOLONE SKELETON IN ITS STRUCTURE
Quinolones; Kinolone; Quinolinone
fluoroquinolone
![[[Levofloxacin]]](https://commons.wikimedia.org/wiki/Special:FilePath/Levofloxacin.svg?width=200 "[[Levofloxacin]]")
![Nalidixic acid. Although technically a [[naphthyridine]], it is considered the predecessor of all subsequently developed quinolone antibiotics.](https://commons.wikimedia.org/wiki/Special:FilePath/Nalidixic acid.png?width=200 "Nalidixic acid. Although technically a [[naphthyridine]], it is considered the predecessor of all subsequently developed quinolone antibiotics.")
![Sites of substitution in second-generation fluoroquinolone antibiotics: Here, and in following the orientation of the quinolones are flipped with respect to horizontal and vertical axes, relative to earlier images; the nitrogen (N)-containing pyridine ring is now on the left, and the N-1 atom and C-6 carbonyl are at 12 o'clock and 6 o'clock in the pyridine ring. The characteristic 6-fluoro group is shown in red. For instance, in ciprofloxacin, above, the R substituent attached to the N-1 atom is a [[cyclopropyl]] group, the R substituent in blue is a [[piperazine]] moiety, and the remaining substitution sites (R groups) are hydrogen atoms.](https://commons.wikimedia.org/wiki/Special:FilePath/Quinolone.svg?width=200 "Sites of substitution in second-generation fluoroquinolone antibiotics: Here, and in following the orientation of the quinolones are flipped with respect to horizontal and vertical axes, relative to earlier images; the nitrogen (N)-containing pyridine ring is now on the left, and the N-1 atom and C-6 carbonyl are at 12 o'clock and 6 o'clock in the pyridine ring. The characteristic 6-fluoro group is shown in red. For instance, in ciprofloxacin, above, the R substituent attached to the N-1 atom is a [[cyclopropyl]] group, the R substituent in blue is a [[piperazine]] moiety, and the remaining substitution sites (R groups) are hydrogen atoms.")
![[[Trovafloxacin]]](https://commons.wikimedia.org/wiki/Special:FilePath/Trovafloxacin.svg?width=200 "[[Trovafloxacin]]")
CLASS OF PHARMACEUTICAL DRUGS, SUBGROUP OF QUINOLONES
Fluoroquinolones; Fluoroquinolone; Quinolone anitbiotics; Quinolone antibiotics; Quinolone-induced tendonopathy; Fluoroquinolone toxicity; Quinolone toxicity syndrome; Fluoroquinolone Toxicity Syndrome; FQTS; Fluoroquinolone toxicity syndrome; Fluoroquinolone Toxicity; Adverse effects of fluoroquinolones; Adverse reaction to fluoroquinolone; Fluoroquinolone adverse reactions; Adverse effects of quinolones; Fluoroquinolone antibiotic; Fluoroquinolone antibiotics; Fluoroquinolone-associated disability; FQAD; 2- and 4-Quinolones; Flouroquinolone
[?fl??r??'kw?n?l??n, ?fl?:-]
¦ noun an antibiotic used especially in the treatment of systemic infections.
Wikipedia
Quinolone
Quinolone may refer to:
- 2-Quinolone
- 4-Quinolone
- Quinolone antibiotics
