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| Product | Description | |
|---|---|---|
| Enoxacin | 1g Pack Size. Group: Antibiotics, Bioactive Small Molecules. Formula: C15H17FN4O3. CAS No. 74011-58-8. Prepack ID 71188914-1g. Molecular Weight 320.32. See USA prepack pricing. |  |
| Enoxacin | A fluororquinolone antibacterial used to treat urinary tract infections and gonorrhea. Group: Biochemicals. Alternative Names: 1-Ethyl-6-fluoro-1,4-dihydro-4-oxo-7-(1-piperazinyl)-1,8-naphthyridine-3-carboxylic Acid; Enofloxacin; Enofloxacine; Enoksetin; Flumark; NSC 629661; PD 107779; Penetrex. Grades: Highly Purified. CAS No. 74011-58-8. Pack Sizes: 1g. US Biological Life Sciences. |  Worldwide |
| Enoxacin | Enoxacin is an oral broad-spectrum fluoroquinolone antibacterial agent used in the treatment of urinary tract infections and gonorrhea. Insomnia is a common adverse effect. Uses: Anti-bacterial agents. Synonyms: R41468; R41468; R-41468; PD 107779; PD-107779; PD107779; Penetrex; Enoxacine; Comprecin. Grades: >98%. CAS No. 74011-58-8. Molecular formula: C15H17FN4O3. Mole weight: 320.32. |  |
| Enoxacin glyconate | Heterocyclic Organic Compound. Alternative Names: ENOXACIN GLUCONATE;ENOXACIN GLYCONATE. CAS No. 104142-71-4. Molecular formula: C15H17FN4O3.C6H12O7. Mole weight: 534.491. Catalog: ACM104142714. |  |
| Enoxacin hydrate | Enoxacin hydrate (Enoxacin sesquihydrate), a fluoroquinolone, interferes with DNA replication and inhibits bacterial DNA gyrase (IC 50 =126 μg/ml) and topoisomerase IV (IC 50 =26.5 μg/ml). Enoxacin hydrate is a miRNA processing activator and enhances siRNA-mediated mRNA degradation and promotes the biogenesis of endogenous miRNAs. Enoxacin hydrate has potent activities against gram-positive and -negative bacteria. Enoxacin hydrate is a cancer-specific growth inhibitor that acts by enhancing TAR RNA-binding protein 2 (TRBP)-mediated microRNA processing [1] [2] [3] [4]. Uses: Scientific research. Group: Signaling pathways. Alternative Names: Enoxacin sesquihydrate; AT-2266 hydrate; CI-919 hydrate. CAS No. 84294-96-2. Pack Sizes: 100 mg; 500 mg. Product ID: HY-B0268A. |  |
| Enoxacin hydrate | Enoxacin hydrate is a synthetic antibiotic belonging to quinolone carboxylic acid compound. It is bactericidal and has a postantibiotischen effect. It is a broad-spectrum antibacterial agent and inhibited 90% Escherichia coli, Klebsiella sp., Aeromonas sp., Enterobacter spp., Serratia spp., Proteus mirabilis, and Morganella morganii at less than or equal to 0.8 micrograms/ml. Uses: Enoxacin hydrate is bactericidal and has a postantibiotischen effect. it is a broad-spectrum antibacterial agent. Synonyms: Enoxacin sesquihydrate;AT-2266 hydrate;CI-919 hydrate; AT 2266 hydrate;CI 919 hydrate; AT2266 hydrate;CI919 hydrate; 1-Ethyl-6-fluoro-1,4-dihydro-4-oxo-7-(1-piperazinyl)-1,8-naphthyridine-3-carboxylic Acid hydrate. Grades: >98%. CAS No. 84294-96-2. Molecular formula: C30H40F2N8O9. Mole weight: 694.694. | |
| Enoxacin Sesquihydrate | Enoxacin Sesquihydrate. Group: Biochemicals. Alternative Names: 1-Ethyl-6-fluoro-1,4-dihydro-4-oxo-7-(1-piperazinyl)-1,8-naphthyridine-3-carboxylic Acid Sesquihydrate. Grades: Highly Purified. CAS No. 84294-96-2. Pack Sizes: 5g, 10g, 25g, 50g, 100g. US Biological Life Sciences. | Worldwide |
| 3-(2,6-Dichloro-5-fluoropyridin-3-yl)-3-oxopropanoic Acid Ethyl Ester | Enoxacin intermediate. Group: Biochemicals. Grades: Highly Purified. CAS No. 96568-04-6. Pack Sizes: 1g, 10g, 25g, 50g, 100g. Molecular Formula: C??H?Cl?FNO?. US Biological Life Sciences. | Worldwide |
| Ciprofloxacin-d8 | Ciprofloxacin-d8 is the deuterium labeled Ciprofloxacin. Ciprofloxacin is a synthetic third-generation quinolone antibacterial drug with broad-spectrum antibacterial activity and good bactericidal effect. Its antibacterial activity against almost all bacteria is 2 to 4 times stronger than norfloxacin and enoxacin. It has antibacterial effects on Enterobacteriaceae, Pseudomonas aeruginosa, Haemophilus influenzae, Neisseria gonorrhoeae, Streptococcus, Legionella, and Staphylococcus aureus. Group: Isotope-labeled environmental contaminants. Alternative Names: Bay-09867-d8. CAS No. 1130050-35-9. Molecular formula: C17H10D8FN3O3. Mole weight: 339.39. Appearance: Solid. Canonical SMILES: O=C1C2=CC (F)=C (N3C ([2H]) ([2H])C ([2H]) ([2H])NC ([2H]) ([2H])C3 ([2H])[2H])C=C2N (C4CC4)C=C1C (O)=O. Catalog: ACM1130050359. | |
| Ciprofloxacin HCI | Ciprofloxacin hydrochloride is the hydrochloride of ciprofloxacin, which belongs to the second generation of synthetic quinolone antibacterial drugs. It has broad spectrum antibacterial activity and good bactericidal effect. Its antibacterial activity against almost all bacteria is 2 ~ 4 times stronger than that of norfloxacin and enoxacin. It has antibacterial effect on enterobacter, Pseudomonas aeruginosa, Haemophilus influenzae, gonococcus, Streptococcus, Legionella and Staphylococcus aureus. CAS No. 93107-08-5. Product ID: PAP-0062. Molecular formula: C17H18FN3O3.HCl. Category: Antibiotic. Product Keywords: Antibacterial, Anti-inflammatory and Antiviral Series; Ciprofloxacin HCI; PAP-0062; Antibiotic; C17H18FN3O3.HCl; 93107-08-5. Appearance: Crystalline Solid. Standard: USP/EP. Grade: CEP/ISO. Color: White or yellowish. Physical State: crystalline powder. Solubility: insoluble in EtOH; ≥33.87 mg/mL in H2O; ≥9.34 mg/mL in DMSO with ultrasonic. Storage: Sealed in dry,Room Temperature. Applications: It has a broad spectrum and efficient antibacterial effect, a wide range of treatment, good oral absorption, low toxicity, and is mainly used in the treatment of urinary tract infection, biliary tract infection and intestinal infection. Melting Point: >300 ºC. |  |
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