Skip to Content
Merck
CN

SML3649

Ozenoxacin

≥98% (HPLC)

Synonym(s):

1-Cyclopropyl-8-methyl-7-(5-methyl-6-methylamino-pyridin-3-yl)-4-oxo1,4-dihydro-quinoline-3-carboxylic acid

Sign In to View Organizational & Contract Pricing.

Select a Size

About This Item

Empirical Formula (Hill Notation):
C21H21N3O3
CAS Number:
245765-41-7
Molecular Weight:
363.41
UNSPSC Code:
51111800
NACRES:
NA.25
MDL number:
MFCD18633255

Key Documents

View All Documentation
Technical Service
Need help? Our team of experienced scientists is here for you.
Let Us Assist
Technical Service
Need help? Our team of experienced scientists is here for you.
Let Us Assist

SMILES string

[n]2(c3c([c](c(c2)C(=O)O)=O)ccc(c3C)c4cnc(c(c4)C)NC)C1CC1

InChI

1S/C21H21N3O3/c1-11-8-13(9-23-20(11)22-3)15-6-7-16-18(12(15)2)24(14-4-5-14)10-17(19(16)25)21(26)27/h6-10,14H,4-5H2,1-3H3,(H,22,23)(H,26,27)

InChI key

XPIJWUTXQAGSLK-UHFFFAOYSA-N

assay

≥98% (HPLC)

form

powder

color

white to beige

solubility

DMSO: 2 mg/mL, clear (Warmed)

storage temp.

-10 to -25°C

Quality Level

100

Looking for similar products? Visit Product Comparison Guide

Related Categories

Biochem/physiol Actions

Ozenoxacin is a quinolone antimicrobial that inhibits bacterial DNA replication enzymes, DNA gyrase A and topoisomerase IV
Quinolone antimicrobial that inhibits bacterial DNA replication enzymes, DNA gyrase A and topoisomerase IV

Storage Class

11 - Combustible Solids

wgk

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

Regulatory Information

新产品
This item has

Choose from one of the most recent versions:

Certificates of Analysis (COA)

Lot/Batch Number
0000236329
0000236330
0000230411
0000236329
0000236330

Don't see the Right Version?

If you require a particular version, you can look up a specific certificate by the Lot or Batch number.

Search for a COA

Already Own This Product?

Find documentation for the products that you have recently purchased in the Document Library.

Visit the Document Library

Y López et al.
Antimicrobial agents and chemotherapy, 57(12), 6389-6392 (2013-10-02)
In vitro activity of ozenoxacin, a novel nonfluorinated topical (L. D. Saravolatz and J. Leggett, Clin. Infect. Dis. 37:1210-1215, 2003) quinolone, was compared with the activities of other quinolones against well-characterized quinolone-susceptible and quinolone-resistant Gram-positive bacteria. Ozenoxacin was 3-fold to

Our team of scientists has experience in all areas of research including Life Science, Material Science, Chemical Synthesis, Chromatography, Analytical and many others.

Contact Technical Service