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Ciprofloxacin

Summarized by Plex Health
Last Updated: 02 May 2022
ciprofloxacin derivatives affect parasite cell division and increase the survival of mice infected with toxoplasma gondii. "ciprofloxacin derivatives affect parasite cell division and increase the survival of mice infected with toxoplasma gondii.", by Martins-Duarte ES, Dubar F, Lawton P, da Silva CF, Soeiro Mde N, de Souza W, Biot C, Vommaro RC. pone.0125705.g004: Cipro derivatives affected parasite daughter cells scission process.Immunofluorescence microscopy of LLC-MK2 cells infected with tachyzoites of T. gondii and treated for 24 h with Cipro derivatives. Parasites were labeled with anti-HSP60 (recognizing the apicoplast,...

Ciprofloxacin is a fluoroquinolone antibiotic, it is used to deal with different types of bacterial infections. Fluoroquinolone prescription antibiotics can cause major or disabling side effects that may not be relatively easy to fix. Ciprofloxacin needs to be used only for infections that can not be treated with a safer antibiotic. If you have a history of myasthenia gravis, tell your physician. Ciprofloxacin may cause tearing or swelling of a ligament, particularly in the Achilles' ligament of the heel. If you take normal tablets or oral suspension: Take the medication as quickly as you can, yet avoid the missed out on dosage if your following dose schedules in less than 6 hrs. The most common side effects of ciprofloxacin tablets and fluid are feeling sick and diarrhoea. Ciprofloxacin is a fluoroquinolone antibacterial active versus a broad spectrum of gram-positive and gram-negative eye pathogens. It is available as the monohydrochloride monohydrate salt of 1-cyclopropyl-6fluoro-1,4-dihydro-4 oxo-73quinoline-carboxylic acid. It is a faint to light yellow crystalline powder with a molecular weight of 385. 8 Its empirical formula is C17H18FN3O3HClH2O and its chemical structure is as follows: Ciprofloxacin varies from other quinolones in that it has a fluorine atom at the 6-position, a piperazine moiety at the 7-position, and a cyclopropyl ring at the 1-position. Each mL of Ciprofloxacin Ophthalmic Solution, USP consists of: Active: Ciprofloxacin HCl, USP 3. 5 mg matching to 3 mg base. Preservative: Benzalkonium Chloride 0. 006%. Inactives: Acetic Acid, Edetate Disodium 0. 05%, Mannitol 4. 6%, Sodium Acetate, Hydrochloric Acid and/or Sodium Hydroxide and Water for Injection.

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PubChem - CovalentUnitCount

(Table source)
CIDMolecularFormulaMolecularWeightCanonicalSMILESIsomericSMILESInChIInChIKeyIUPACNameXLogPExactMassMonoisotopicMassTPSAComplexityChargeHBondDonorCountHBondAcceptorCountRotatableBondCountHeavyAtomCountIsotopeAtomCountAtomStereoCountDefinedAtomStereoCountUndefinedAtomStereoCountBondStereoCountDefinedBondStereoCountUndefinedBondStereoCountCovalentUnitCount
2764C17H18FN3O3331.34C1CC1N2C=C(C(=O)C3=CC(=C(C=C32)N4CCNCC4)F)C(=O)OC1CC1N2C=C(C(=O)C3=CC(=C(C=C32)N4CCNCC4)F)C(=O)OInChI=1S/C17H18FN3O3/c18-13-7-11-14(8-15(13)20-5-3-19-4-6-20)21(10-1-2-10)9-12(16(11)22)17(23)24/h7-10,19H,1-6H2,(H,23,24)MYSWGUAQZAJSOK-UHFFFAOYSA-N1-cyclopropyl-6-fluoro-4-oxo-7-piperazin-1-ylquinoline-3-carboxylic acid-1.1331.13321961331.1332196172.957102732400000001
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