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Ozenoxacin

CAS No.
245765-41-7
Chemical Name:
Ozenoxacin
Synonyms
T 3912;M-5120;Ozenoxacin;Ozefloxacin;GF-00100100;GF-001001-00;Ozenoxacin, >Ozenoxacin, >90%;Ozenoxacin(T 3912);Ozenoxacin USP/EP/BP
CBNumber:
CB62498834
Molecular Formula:
C21H21N3O3
Molecular Weight:
363.41
MDL Number:
MFCD18633255
MOL File:
245765-41-7.mol
Last updated:2024-11-04 20:04:50

Ozenoxacin Properties

Melting point >255°C (dec.)
Boiling point 573.5±50.0 °C(Predicted)
Density 1.372±0.06 g/cm3(Predicted)
storage temp. 2-8°C(protect from light)
solubility DMSO (Slightly)
pka 6.46±0.50(Predicted)
form Solid
color Off-White
FDA UNII V0LH498RFO
ATC code D06AX14

SAFETY

Risk and Safety Statements

Symbol(GHS)  GHS hazard pictograms
GHS07
Signal word  Warning
Hazard statements  H302-H315-H319-H335
Precautionary statements  P261-P280-P301+P312-P302+P352-P305+P351+P338

Ozenoxacin price

Manufacturer Product number Product description CAS number Packaging Price Updated Buy
TRC O880100 Ozenoxacin,>90% 245765-41-7 250mg $970 2021-12-16 Buy
ChemScene CS-0003657 Ozenoxacin 99.00% 245765-41-7 5mg $90 2021-12-16 Buy
AK Scientific 3780CR Ozenoxacin 245765-41-7 5mg $104 2021-12-16 Buy
ChemScene CS-0003657 Ozenoxacin 99.00% 245765-41-7 10mg $140 2021-12-16 Buy
ChemScene CS-0003657 Ozenoxacin 99.00% 245765-41-7 25mg $270 2021-12-16 Buy
Product number Packaging Price Buy
O880100 250mg $970 Buy
CS-0003657 5mg $90 Buy
3780CR 5mg $104 Buy
CS-0003657 10mg $140 Buy
CS-0003657 25mg $270 Buy

Ozenoxacin Chemical Properties,Uses,Production

Description

Ozenoxacin is used to treat impetigo (a skin infection caused by bacteria) in adults and children 2 months of age and older. Ozenoxacin is in a class of medications called antibacterials. It works by killing and stopping the growth of bacteria on the skin. To date, ozenoxacin has been used in trials studying the treatment of impetigo. As of December 11, 2017 the FDA approved Ferrer Internacional S.A.'s Xepi (ozenoxacin 1%) as a topically applied cream indicated for the treatment of impetigo caused by Staphylococccus aureus or Streptococcus pyogenes in adult and pediatric patients 2 months of age and older.

Pharmacokinetics

Although the exposure response relationship for ozenoxacin after it has been applied topically has not yet been studied, a formal relationship is unlikely because systemic exposure of ozenoxacin following its topical application has been measured to be negligible .

Mechanism of action

Ozenoxacin is a quinolone antibiotic drug. And, like most quinolones, ozenoxacin predominately executes its mechanism of action by entering into bacterial cells and acting to inhibit the bacterial DNA replication enzymes DNA gyrase A and topoisomerase IV . As DNA gyrase A and topoisomerase IV are essential to bacterial DNA replication activities including supercoiling, supercoil relaxation, chromosomal condensation, chromosomal decatenation and more, their inhibition is the principal action of ozenoxacin's mechanism and it has been demonstrated to be bactericidal against S. aureus and S. pyogenes organisms.

Description

Ozenoxacin is a novel, nonfluorinated quinolone antibiotic discovered by Toyama Chemical Co. Ltd. and developed by Maruho Co. Ltd. Ozenoxacin was approved by the PMDA of Japan in September 2015 for the treatment of acne and skin infections. Ozenoxacin shows potent antibacterial activity against anaerobic and aerobic, gram-positive and -negative bacteria, especially those implicated in superficial skin infections such as S. aureus, Staphylococcus epidermidis, and Propionibacterium acnes. The mechanism of action of ozenoxacin involves the drug’s affinity for DNA gyrase and DNA topoisomerase IV and upon binding triggers bacterial apoptosis.

Uses

Ozenoxacin is a non-fluorinated topical quinolone. It exhibits antimicrobial activity against?propionibacteria and staphylococci. Ozenoxacin can be used to treat acne and superficial skin infections.

Definition

ChEBI: Ozenoxacin is a member of quinolines.

Synthesis

A U.S. patent filed by co-workers at Toyama describes the only publicly disclosed synthetic approach to this drug.12 The drug?ˉs assembly hinges upon a key Stille coupling between a quinolonyl bromide and a stannylpyridine. Buchwald-Hartwig coupling of commercially available 2,6- dibromotoluene (22) and cyclopropylamine (23) gave Ncyclopropyl- 3-bromo-2-methylaniline 24 in 84% yield , and this step was followed by reaction with diethyl ethoxymethylenemalonate (25) and subsequent cyclization under acidic conditions to secure bromoquinoline 26 in 43% yield over the two-step sequence. Stille coupling of 27 with bromoquinoline 26 resulted in pyridyl quinoline adduct 28 in 80% yield. Saponification of ester 28 followed by acidic removal of the N-acetyl group delivered the active pharmaceutical ingredient ozenoxacin (III) in 75% yield.
The preparation of key stannane 27, which is not commercially available and began with the conversion of commercially available 5-bromo-2- chloro-3-methylpyridine (30) to aminopyridine derivative 31 upon treatment with aqueous methylamine at elevated temperature in a sealed vessel. The resulting aminopyridine was subjected to acetic anhydride in pyridine, resulting in acetamide 32 in good yield, and this coupling was followed by a modest-yielding palladium-catalyzed installation of the stannyl group to deliver subunit 27.

Synthesis_245765-41-7

Ozenoxacin Preparation Products And Raw materials

Raw materials

Preparation Products

Global( 184)Suppliers
Supplier Tel Email Country ProdList Advantage
Hebei Chuanghai Biotechnology Co,.LTD
+86-13131129325 sales1@chuanghaibio.com China 5893 58
shandong perfect biotechnology co.ltd
+86-53169958659; +8618596095638 sales@sdperfect.com China 294 58
Jinan Million Pharmaceutical Co., Ltd
0531-68659554 +8613031714605 info@millionpharm.com China 252 58
Hebei Xinsheng New Material Technology Co., LTD.
+86-16632316109 xinshengkeji@xsmaterial.com China 1085 58
hebei hongtan Biotechnology Co., Ltd
+86-86-1913198-3935 +8617331935328 sales03@chemcn.cn China 970 58
Hebei Saisier Technology Co., LTD
+86-18400010335 +86-18034520335 admin@hbsaisier.cn China 1015 58
Apeloa production Co.,Limited
+8619933239880 admin@apcl.com.cn China 852 58
Hebei Longbang Technology Co., LTD
+86-18633929156 +86-18633929156 admin@hblongbang.com China 941 58
Hangzhou FandaChem Co.,Ltd.
+8615858145714 FandaChem@Gmail.com China 9218 55
Shanghai Yingrui Biopharma Co., Ltd.
+86-21-33585366 - 03@ sales03@shyrchem.com CHINA 738 60

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  • Toxicity of Ozenoxacin
  • Ozenoxacin is in a class of medications called antibacterials. It works by killing and stopping the growth of bacteria on the ....
  • Oct 11,2019

View Lastest Price from Ozenoxacin manufacturers

Image Update time Product Price Min. Order Purity Supply Ability Manufacturer
Ozenoxacin  pictures 2024-11-07 Ozenoxacin
245765-41-7
US $6.00 / kg 1kg More than 99% 2000KG/Month Hebei Longbang Technology Co., Ltd
Ozenoxacin pictures 2024-11-07 Ozenoxacin
245765-41-7
US $80.00-60.00 / KG 1KG 99.9% 1000 hebei hongtan Biotechnology Co., Ltd
Ozenoxacin pictures 2024-11-07 Ozenoxacin
245765-41-7
US $1.00-0.50 / KG 2KG 99% 200KG Jinan Million Pharmaceutical Co., Ltd
  • Ozenoxacin  pictures
  • Ozenoxacin
    245765-41-7
  • US $6.00 / kg
  • More than 99%
  • Hebei Longbang Technology Co., Ltd
  • Ozenoxacin pictures
  • Ozenoxacin
    245765-41-7
  • US $80.00-60.00 / KG
  • 99.9%
  • hebei hongtan Biotechnology Co., Ltd
  • Ozenoxacin pictures
  • Ozenoxacin
    245765-41-7
  • US $1.00-0.50 / KG
  • 99%
  • Jinan Million Pharmaceutical Co., Ltd

245765-41-7(Ozenoxacin)Related Search:

Ozenoxacin T 3912 :3-Quinolinecarboxylic acid, 1-cyclopropyl-1,4-dihydro-8-methyl-7-[5-methyl-6-(methylamino)-3-pyridinyl]-4-oxo- Ozenoxacin(T 3912) 1-cyclopropyl-8-methyl-7-[5-methyl-6-(methylamino)pyridin-3-yl]-4-oxoquinoline-3-carboxylic acid Ozenoxacin , T 3912,UNII-V0LH498RFO Ozenoxacin Impurity 1 organic materials Ozenoxacin Ozenoxacin, > 1-cyclopropyl-8-methyl-7-(5-methyl-6-(methylamino)pyridin-3-yl)-4-oxo-1,4-dihydroquinoline-3-carboxylic acid Ozenoxacin USP/EP/BP Ozenoxacin, >90% Ozefloxacin GF-00100100 GF-001001-00 M-5120 245765-41-7