Chemodex

Marbofloxacin

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CDX-M0172-M100100 mgCHF 97.00
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Product Details
Synonyms 9-Fluoro-2,3-dihydro-3-methyl-10-(4-methyl-piperazino)-7-oxo-7H-pyrido[1,2,3-ij][1,2,4]benzoxadiazine-6-carboxylic acid; Marbocyl; Zeniquin; Aurizon; CID 60651
Product Type Chemical
Properties
Formula C17H19FN4O4
MW 362.36
CAS 115550-35-1
RTECS UU8815140
Source/Host Chemicals Synthetic
Purity Chemicals ≥ 98% (HPLC)
Appearance White to beige to brown powder.
Solubility Soluble in DMF (20mg/ml) or DMSO (20 mg/ml). Slightly soluble in ethanol (1 mg/ml) or PBS (1mg/ml).
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 BPFYOAJNDMUVBL-UHFFFAOYSA-N
Smiles O=C1C=2C3=C(C(=C(F)C2)N4CCN(C)CC4)OCN(C)N3C=C1C(O)=O
Shipping and Handling
Shipping AMBIENT
Short Term Storage +20°C
Long Term Storage +4°C
Handling Advice Protect from light and moisture.
Use/Stability Stable for at least 2 years after receipt when stored at +4°C.
Documents
Product Specification Sheet
Datasheet Download PDF
Description
Marbofloxacin is a broad-spectrum fluoroquinolone antibiotic active against Gram-negative, Gram-positive and Mycoplasma spp. bacteria. It acts by inhibiting the activity of DNA gyrase and topoisomerase IV, enzymes fundamental to the replication and transcription of bacterial DNA. Thus, the inhibition of these enzymes leads to the death of the bacteria. Marbofloxacin has also been shown to exhibit antileishmanial activity in a canine model. Marbofloxacin has low toxicity and limited development of bacterial resistance. Compound can be used as analytical reference material.
Product References
(1) M. Spreng, et al.; J. Vet. Pharmacol. Ther. 18, 284 (1995) | (2) A.A. Ferran, et al.; Vet. Microbiol. 148, 292 (2011) | (3) J. Shen, et al.; Acta Crystallogr. 68, 998 (2012) | (4) C. Pineda, et al.; PLoS One 12, e0185981 (2017) | (5) Z. Lei, et al.; Front. Pharmacol. 8, 1 (2017) | (6) T.L.A. da Silva, et al.; J. AOAC Int. 105, 456 (2022)
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