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CAS RN: 86393-32-0 | 產品號碼: C2227
Ciprofloxacin Hydrochloride Monohydrate
 
									 
							
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| 產品號碼 | C2227 | 
| 純度/分析方法   | >98.0%(T)(HPLC) | 
| 分子式 / 分子量 | C__1__7H__1__8FN__3O__3·HCl·H__2O = 385.83 | 
| 外觀與形狀(20°C) | Solid | 
| 儲存條件   | Room Temperature (Recommended in a cool and dark place, <15°C) | 
| 應避免的情況 | Light Sensitive | 
| CAS RN | 86393-32-0 | 
| 相關CAS RN   | 85721-33-1 | 
| Reaxys-RN | 4627629 | 
| PubChem Substance ID | 87560207 | 
| SDBS (AIST Spectral DB) | 52167 | 
| Merck Index(14) | 2314 | 
| MDL編號 | MFCD00242856 | 
產品規格
		  | Appearance | White to Light yellow powder to crystal | 
| Purity(HPLC) | min. 98.0 area% | 
| Purity(Neutralization titration) | min. 98.0 % | 
| Water | 4.7 to 6.7 % | 
| NMR | confirm to structure | 
		性質
	 
						 GHS
						  
								 相關法規
							    
						運輸資料
							| HS編碼* | 2933.59-000 | 
			Application
		
			Quorum sensing research / Biofilm research
		
		References
- Ciprofloxacin-Loaded Mixed Polymeric Micelles as Antibiofilm Agents
- Sub-Inhibitory Concentrations of Ciprofloxacin Alone and Combinations with Plant-Derived Compounds against P. aeruginosa Biofilms and Their Effects on the Metabolomic Profile of P. aeruginosa Biofilms
- Evolution of Antibiotic Resistance in Biofilm and Planktonic Pseudomonas aeruginosa Populations Exposed to Subinhibitory Levels of Ciprofloxacin
- Subinhibitory concentration of ciprofloxacin targets quorum sensing system of Pseudomonas aeruginosa causing inhibition of biofilm formation & reduction of virulence
- Role of Antibiotic Penetration Limitation in Klebsiella pneumoniae Biofilm Resistance to Ampicillin and Ciprofloxacin
- Investigation of Ciprofloxacin Penetration into Pseudomonas aeruginosa Biofilms
			Application
		
			Studies on the Antibacterial Activities of Ciprofloxacin
		
		References
- Comparison of the antibacterial activities of the quinolones Bay 12-8039, gatifloxacin (AM 1155), trovafloxacin, clinafloxacin, levofloxacin and ciprofloxacin
- Activity of acyclovir, ciprofloxacin and organotin polymers derived from acyclovir and ciprofloxacin against Herpes simplex virus (HSV-1) and Varicella Zoster virus (VZV)				     				 - M. R. Roner, C. E. Carraher, Jr., A. Zhao, J. L. Roehr, K. D. Bassett, D. W. Siegmann-Louda, PMSE Prepr. 2004, 90, 515.
 
- Mechanism of inhibition of DNA gyrase by quinolone antibacterials: a cooperative drug-DNA binding model
- In vitro activity of Bay 09867, a new quinoline derivative, compared with those of other antimicrobial agents
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