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Ozenoxacin

Catalog No. T7902 CAS 245765-41-7

Synonyms: T-3912

Ozenoxacin is a quinolone Antibacterial. It shows potent activities against the main microorganisms isolated from soft tissue and skin infections.

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Ozenoxacin, CAS 245765-41-7

Pack Size	Availability	Price/USD
1 mg	In stock	$ 31.00
5 mg	In stock	$ 72.00
10 mg	In stock	$ 113.00
25 mg	In stock	$ 222.00
50 mg	In stock	$ 377.00
100 mg	In stock	$ 563.00
500 mg	In stock	$ 1,190.00
1 mL * 10 mM (in DMSO)	In stock	$ 62.00

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Purity: 99.56%

Purity: 99.33%

Biological Description

Chemical Properties

Storage & Solubility Information

Description

Ozenoxacin is a quinolone antibacterial. It shows potent activities against the main microorganisms isolated from soft tissue and skin infections.

In vitro

Ozenoxacin shows potent antibacterial activities against clinical isolates of Gram-positive microorganisms (MICs: 0.008 to 4 mg/L). Ozenoxacin shows good activities against strains of MRSA, MSSA, MSSE, and MRSE with 2, 3, or 4 mutations in the gyrA and grlA (parC) genes [1]. Ozenoxacin inhibits MSSA strains and S. agalactiae strains, with the rates of resistance of >10?10 and 5.3?×?10?10, respectively. The maximum MIC value for mutant strains is 8 mg/L for Ozenoxacin [2].

Synonyms	T-3912
Molecular Weight	363.41
Formula	C21H21N3O3
CAS No.	245765-41-7

Storage

Powder: -20°C for 3 years | In solvent: -80°C for 2 years

Solubility Information

DMSO: 5 mg/mL (13.76 mM), Need ultrasonic and warming

( < 1 mg/ml refers to the product slightly soluble or insoluble )

References and Literature

1. López Y, et al. In vitro activity of Ozenoxacin against quinolone-susceptible and quinolone-resistant gram-positive bacteria. Antimicrob Agents Chemother. 2013 Dec;57(12):6389-92. 2. López Y, et al. In vitro selection of mutants resistant to ozenoxacin compared with levofloxacin and ciprofloxacin in Gram-positive cocci. J Antimicrob Chemother. 2015 Jan;70(1):57-61

Related compound libraries

This product is contained In the following compound libraries：

Drug-induced Liver Injury (DILI) Compound Library FDA-Approved Drug Library Clinical Compound Library Bioactive Compounds Library Max Anti-Bacterial Compound Library ReFRAME Related Library FDA-Approved & Pharmacopeia Drug Library Approved Drug Library Pediatric Drug Library NO PAINS Compound Library

Related Products

Related compounds with same targets

6-Ethoxychelerythrine 6-Diazo-5-oxo-L-nor-Leucine Trovafloxacin (Z)-Ligustilide Nanchangmycin Salinomycin sodium salt Eravacycline Durlobactam Triethylamine

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Method for preparing DMSO master liquid: mg drug pre-dissolved in μL DMSO (Master liquid concentration mg/mL)，Please contact us first if the concentration exceeds the DMSO solubility of the batch of drug.

Method for preparing in vivo formulation：Take μL DMSO master liquid, next add μL PEG300， mix and clarify, next add μL Tween 80，mix and clarify, next add μL ddH₂O, mix and clarify.

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Please see Inhibitor Handling Instructions for more frequently ask questions. Topics include: how to prepare stock solutions, how to store products, and cautions on cell-based assays & animal experiments, etc.

Keywords

Ozenoxacin 245765-41-7 Microbiology/Virology Antibacterial Inhibitor T 3912 Bacterial inhibit T-3912 T3912 inhibitor

Products are chemical reagents for research use only and are not intended for human use. We do not sell to patients.