Ciprofloxacin
Synonyms: ciprofloxacin, Ciprofloxacine", "Ciprobay", "Ciproxan", "Cipro", "Ciprofloxacina", "Ciprofloxacino", "Ciprofloxacinum", "Cipro IV", "Ciproquinol", "Cipromycin", "Ciprocinol", "Septicide", "Bacquinor", "Ciprodar", "Cifloxin", "Ciproxina", "Ciprinol", "Bernoflox", "Cipro XR", "Roxytal", "Italnik", "Fimoflox", "Corsacin", "Citopcin", "Ciprogis", "Zumaflox", "Ciproxine", "Ciprolin", "Spitacin", "Quintor", "Quinolid", "Proflaxin", "Probiox", "Ipiflox", "Superocin", "Ciprowin", "Ciprolon", "Ciproflox", "Ciprecu", "BAY q 3939", "Ciplus", "Baflox", "Rancif", "Ciriax", "Cycin", "Cixan", "Loxan", "Cilab", "Unex", "Sophixin Ofteno".
Source: Ciprofloxacin is a drug with rapid bactericidal action and a broad spectrum of activity.
Identifiers:
IUPAC Name: 1-cyclopropyl-6-fluoro-4-oxo-7-piperazin-1-ylquinoline-3-carboxylic acid
CAS Number: 85721-33-1
PubChem ID: 2764
InChiKey: MYSWGUAQZAJSOK-UHFFFAOYSA-N
Canonical SMILES: C1CC1N2C=C(C(=O)C3=CC(=C(C=C32)N4CCNCC4)F)C(=O)O
Structural Properties:
Molecular Formula: C17H18FN3O3
Molecular Weight: 331.34
Pharmacophore Features:
Number of bond donors: 2
Number of bond acceptors: 7
Number of atoms different from hydrogen: 24
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Evidence Supporting This Chemical as an Emerging Contaminant
Sussuchi, E. M., Carvalho, S. W., Gimenez, I. F., & SantAnna, M. V. (2019, May). Synthesis of CdTe Semiconductor Nanocrystals on Hydrotalcite Matrix Surface for Electrochemical Detection of Ciprofloxacin. In?Meeting Abstracts?(No. 43, pp. 2068-2068). The Electrochemical Society.
Feng, N. X., Yu, J., Xiang, L., Yu, L. Y., Zhao, H. M., Mo, C. H., ... & Li, Q. X. (2019). Co-metabolic degradation of the antibiotic ciprofloxacin by the enriched bacterial consortium XG and its bacterial community composition. Science of the Total Environment, 665, 41-51.
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