8-Hydroxy Moxifloxacin Hydrobromide

Product Name 8-Hydroxy Moxifloxacin Hydrobromide
Alternate Names Moxifloxacin Impurities, Impurities of Moxifloxacin
CAT No. CS-T-79636
CAS No. 1292904-74-5
Category Impurities
Stock IN-Stock
Mol. Wt. 468.32 g/mol
Mol. For. C20H23BrFN3O4
Hazardous This is a Hazardous Compound
COA View Sample COA
MSDS View Sample MSDS
Parent API Moxifloxacin
Smileys O=C(C1=CN(C2CC2)C3=C(C=C(F)C(N(C4)C[C@]5([H])[C@@]4([H])CCCN5)=C3O)C1=O)O.[H]Br
Canonical Smiles C1CC2CN(CC2NC1)C3=C(C=C4C(=C3O)N(C=C(C4=O)C(=O)O)C5CC5)F.Br
InchIKey VJTHCZDXAAGHAF-OEQYQXMYSA-N
Inchl InChI=1S/C20H22FN3O4.BrH/c21-14-6-12-16(24(11-3-4-11)8-13(18(12)25)20(27)28)19(26)17(14)23-7-10-2-1-5-22-15(10)9-23;/h6,8,10-11,15,22,26H,1-5,7,9H2,(H,27,28);1H/t10-,15+;/m0./s1
IUPAC 7-[(4aS,7aS)-1,2,3,4,4a,5,7,7a-octahydropyrrolo[3,4-b]pyridin-6-yl]-1-cyclopropyl-6-fluoro-8-hydroxy-4-oxoquinoline-3-carboxylic acid;hydrobromide
Controlled No
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8-Hydroxy Moxifloxacin Hydrobromide is a potent antibiotic agent that is used to treat a wide range of bacterial infections. It is a derivative of the fluoroquinolone class of antibiotics, which work by inhibiting bacterial DNA synthesis and preventing the growth and replication of bacteria. This compound is typically administered orally or intravenously, depending on the severity of the infection. It is commonly used to treat respiratory tract infections, skin infections, urinary tract infections, and intra-abdominal infections. The chemical structure of 8-Hydroxy Moxifloxacin Hydrobromide includes a hydroxyl group and a fluorine atom in the quinolone ring, which enhances its antibacterial activity. It is highly soluble in water and is stable under acidic and basic conditions. This compound has a strong affinity for bacterial DNA gyrase and topoisomerase IV, which are essential enzymes for bacterial replication. It binds to these enzymes and causes DNA strand breaks, leading to bacterial death. In terms of safety, 8-Hydroxy Moxifloxacin Hydrobromide has been found to have a low risk of adverse effects. However, it is not recommended for use in pregnant women or children under 18 years of age due to potential harmful effects on bone and cartilage development. Overall, 8-Hydroxy Moxifloxacin Hydrobromide is a highly effective antibiotic agent that is widely used in clinical practice to treat bacterial infections. Its chemical properties and mechanism of action make it a valuable tool in the fight against bacterial diseases.

Related Compounds

Moxifloxacin Hydrochloride Monohydrate | Moxifloxacin Impurity 1 | Moxifloxacin Nitroso R,R Isomer impurity | Moxifloxacin Nitroso impurity 3 ( R,R Isomer) | N-Nitroso Moxifloxacin Related compound-B | Moxifloxacin Related Compound B | Moxifloxacin Methyl Ester | Moxifloxacin Related Compound H | N-Nitroso-Moxifloxacin | Mono-Nitroso-Pyrrolopiperidine | Moxifloxacin EP Impurity D HCl salt | Moxifloxacin Related Compound G HCl salt | Di-Nitroso- Pyrrolopiperidine | Moxifloxacin N-methyl Impurity | Moxifloxacin Nitroso impurity 4 | N-Methyl Moxifloxacin Hydrochloride | Moxifloxacin Impurity D Hydrochloride (8-Fluoro-6-Methoxy Moxifloxacin) | Moxifloxacin EP Impurity D | N-Nitroso Moxifloxacin methyl ester | N-Nitroso Desmethyl Moxifloxacin methyl ester | N-formyl moxifloxacin | Moxifloxacin Difluoro Hydroxy Impurity | Moxifloxacin Nitroso impurity 1 ( R,R Isomer) | Moxifloxacin Nitroso Impurity 2 | N-Nitroso Moxifloxacin Related compound-A | Moxifloxacin EP impurity E | N-Nitroso Moxifloxacin Related compound-C | Moxifloxacin Related Compound F | ent-Moxifloxacin Hydrochloride | Moxifloxacin EP Impurity A | Moxifloxacin Nitroso impurity 2 ( R,R Isomer) | Moxifloxacin Impurity 38 | N-Nitroso Moxifloxacin Related compound-D | Moxifloxacin Impurity 69 | Moxifloxacin Impurity 2 | N-Allyloxycarbonyl Moxifloxacin | Moxifloxacin EP impurity B |

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