Chemodex

Moxifloxacin hydrochloride

CHF 88.00
In stock
CDX-M0189-M05050 mgCHF 88.00
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Product Details
Synonyms BAY 12-8039; Alelox; 1-Cyclopropyl-6-fluoro-8-methoxy-7-[(4aS,7aS)-octahydropyrrolo[3,4-b]pyridin-6-yl]-4-oxo-1,4-dihydroquinoline-3-carboxylic acid hydrochloride
Product Type Chemical
Properties
Formula C21H24FN3O4 . HCl
MW 401.43 . 36.46
CAS 186826-86-8
RTECS VB1983750
Source/Host Chemicals Synthetic
Purity Chemicals ≥97% (NMR)
Appearance Light yellow powder.
Solubility Soluble in DMSO (10mg/ml) or water (5mg/ml).
Identity Determined by 1H-NMR.
Declaration Manufactured by Chemodex.
Other Product Data

Click here for Original Manufacturer Product Datasheet
Our product description may differ slightly from the original manufacturers product datasheet.

InChi Key IDIIJJHBXUESQI-DFIJPDEKSA-N
Smiles O=C1C(C(O)=O)=CN(C2CC2)C3=C(OC)C([NH+]4C[C@](NCCC5)([H])[C@]5([H])C4)=C(F)C=C31.[Cl-]
Shipping and Handling
Shipping AMBIENT
Short Term Storage +4°C
Long Term Storage -20°C
Handling Advice Protect from light and moisture.
Use/Stability Stable for at least 2 years after receipt when stored at -20°C.
Documents
MSDS Download PDF
Product Specification Sheet
Datasheet Download PDF
Description

Moxifloxacin is a fourth-generation synthetic broad-spectrum fluoroquinolone antibiotic. It is used against both Gram-positive and Gram-negative bacteria and to treat bacterial infections associated with bronchitis, sinusitis, and other conditions. Fluoroquinolones stabilize DNA strand breaks created by DNA gyrase (Topo II) and topoisomerase IV by binding to the enzyme-DNA complex. Compared to mammalian DNA gyrase, moxifloxacin has 100 times higher affinity for bacterial DNA gyrase. Can also be used as reference compound.

Product References

(1) M. Souli, et al.; Int. J. Antimicrob. Agents. 10, 23 (1998) | (2) C. Ballow, et al.; Clin. Ther. 21, 513 (1999) | (3) A. Dalhoff, et al.; Clin. Infect. Dis. 32, S22 (2001) | (4) R. Kishii, et al.; Antimicrob. Agents Chemother. 47, 77 (2003) | (5) M. Miravitlles; J. Chron. Obstruct. Pulmon. Dis. 2, 191 (2007) | (6) M. Miravitlles & A. Anzueto; Expert Opin. Pharmacother. 9, 1755 (2008) (Review) | (7) H. Takiff & E. Guerrero; Antimicrob. Agents Chemother. 55, 5421 (2011) | (8) M.M. Al Omari, et al.; Profiles Drug Subst. Excip. Relat. Methodol. 39, 299 (2014) (Review)

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