Enoxacin, Thermo Scientific Chemicals
Enoxacin, Thermo Scientific Chemicals
Thermo Scientific Chemicals

Enoxacin, Thermo Scientific Chemicals

A quinolone antibacteral agent which acts on DNA gyrase
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Catalog number J61912.03
also known as J61912-03
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1 g
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Price (USD)/ Each
24.65
Special Offer
Online exclusive
Ends: 31-Dec-2024
28.70 
Save 4.05 (14%)
Add to cart
Enoxacin, Thermo Scientific Chemicals
Catalog numberJ61912.03
Price (USD)/ Each
24.65
Special Offer
Online exclusive
Ends: 31-Dec-2024
28.70 
Save 4.05 (14%)
-
Add to cart
Chemical Identifiers
CAS74011-58-8
IUPAC Name1-ethyl-6-fluoro-4-oxo-7-(piperazin-1-yl)-1,4-dihydro-1,8-naphthyridine-3-carboxylic acid
Molecular FormulaC15H17FN4O3
InChI KeyIDYZIJYBMGIQMJ-UHFFFAOYSA-N
SMILESCCN1C=C(C(O)=O)C(=O)C2=CC(F)=C(N=C12)N1CCNCC1
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SpecificationsSpecification SheetSpecification Sheet
FormPowder or crystals or crystalline powder
Assay from Supplier's CofA≥97.0%
Enoxacin is an antibacterial agent used in the treatment of gastro enteritis including infectious diarrhea, respiratory tract infections, gonorrhea and urinary tract infections. It is a bactericidal and its mode of action depends on blocking of bacterial DNA replication by binding itself to an enzyme called DNA gyrase.

This Thermo Scientific Chemicals brand product was originally part of the Alfa Aesar product portfolio. Some documentation and label information may refer to the legacy brand. The original Alfa Aesar product / item code or SKU reference has not changed as a part of the brand transition to Thermo Scientific Chemicals.

Applications
Enoxacin is an antibacterial agent used in the treatment of gastro enteritis including infectious diarrhea, respiratory tract infections, gonorrhea and urinary tract infections. It is a bactericidal and its mode of action depends on blocking of bacterial DNA replication by binding itself to an enzyme called DNA gyrase.

Solubility
50 mg/ml in 1 M NaOHSlightly soluble in sodium hydroxide, dimethyl sulfoxide, chloroform and methanol. Insoluble in water.

Notes
Store in cool place. Keep the container tightly closed in a dry and well-ventilated place.
RUO – Research Use Only

General References:

  1. Huang, W. Y.; Li, J.; Kong, S. L.; Wang, Z. C.; Zhu, H. L. Cu(II) and Co(II) ternary complexes of quinolone antimicrobial drug enoxacin and levofloxacin: structure and biological evaluation. RSC Adv. 2014, 4 (66), 35193-35204.
  2. Liu, X.; Qu, X.; Wu, C.; Zhai, Z.; Tian, B.; Li, H.; Ouyang, Z.; Xu, X.; Wang, W.; Fan, Q.; Tang, T.; Qin, A.; Dai, K. The effect of enoxacin on osteoclastogenesis and reduction of titanium particle-induced osteolysis via suppression of JNK signaling pathway. Biomaterials 2014, 35 (22), 5721-5730.