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Details

Stereochemistry ABSOLUTE
Molecular Formula C23H24N6O5S2
Molecular Weight 528.604
Optical Activity UNSPECIFIED
Defined Stereocenters 2 / 2
E/Z Centers 1
Charge 0

SHOW SMILES / InChI
Structure of CEFQUINOME

SMILES

[H][C@]12SCC(C[N+]3=C4CCCCC4=CC=C3)=C(N1C(=O)[C@H]2NC(=O)C(=N/OC)\C5=CSC(N)=N5)C([O-])=O

InChI

InChIKey=YWKJNRNSJKEFMK-PQFQYKRASA-N
InChI=1S/C23H24N6O5S2/c1-34-27-16(14-11-36-23(24)25-14)19(30)26-17-20(31)29-18(22(32)33)13(10-35-21(17)29)9-28-8-4-6-12-5-2-3-7-15(12)28/h4,6,8,11,17,21H,2-3,5,7,9-10H2,1H3,(H3-,24,25,26,30,32,33)/b27-16-/t17-,21-/m1/s1

HIDE SMILES / InChI

Molecular Formula C23H24N6O5S2
Molecular Weight 528.604
Charge 0
Count
Stereochemistry ABSOLUTE
Additional Stereochemistry No
Defined Stereocenters 2 / 2
E/Z Centers 1
Optical Activity UNSPECIFIED

Cefquinome is a 4th generation cephalosporin which is active against a broad spectrum of Gram positive and Gram negative bacteria. As many cephalosporin it acts by binding to bacterial PBP and thus inhibiting the cell wall synthesis. Cefquinome is approved for veterinary use in cattles with respiratory tract infections, skin infections, bacterial mastitis and septicaemia.

Approval Year

TargetsConditions

Conditions

ConditionModalityTargetsHighest PhaseProduct
Curative
COBACTAN

Approved Use

Treatment of infections caused by bacteria sensitive to cefquinome, such as: (1) Respiratory tract infections caused by Pasteurella multocida and Mannheimia haemolytica. (2) Digital dermatitis, infectious bulbar necrosis and interdigital necrobacillosis (foul in foot). (3) Acute E.coli mastitis with signs of systemic involvement. (4) Calf-E.coli septicaemia.

Launch Date

1.15611835E12
Curative
COBACTAN

Approved Use

Treatment of infections caused by bacteria sensitive to cefquinome, such as: (1) Respiratory tract infections caused by Pasteurella multocida and Mannheimia haemolytica. (2) Digital dermatitis, infectious bulbar necrosis and interdigital necrobacillosis (foul in foot). (3) Acute E.coli mastitis with signs of systemic involvement. (4) Calf-E.coli septicaemia.

Launch Date

1.15611835E12
Curative
COBACTAN

Approved Use

Treatment of infections caused by bacteria sensitive to cefquinome, such as: (1) Respiratory tract infections caused by Pasteurella multocida and Mannheimia haemolytica. (2) Digital dermatitis, infectious bulbar necrosis and interdigital necrobacillosis (foul in foot). (3) Acute E.coli mastitis with signs of systemic involvement. (4) Calf-E.coli septicaemia.

Launch Date

1.15611835E12
Curative
COBACTAN

Approved Use

Treatment of infections caused by bacteria sensitive to cefquinome, such as: (1) Respiratory tract infections caused by Pasteurella multocida and Mannheimia haemolytica. (2) Digital dermatitis, infectious bulbar necrosis and interdigital necrobacillosis (foul in foot). (3) Acute E.coli mastitis with signs of systemic involvement. (4) Calf-E.coli septicaemia.

Launch Date

1.15611835E12
Curative
COBACTAN

Approved Use

Treatment of infections caused by bacteria sensitive to cefquinome, such as: (1) Respiratory tract infections caused by Pasteurella multocida and Mannheimia haemolytica. (2) Digital dermatitis, infectious bulbar necrosis and interdigital necrobacillosis (foul in foot). (3) Acute E.coli mastitis with signs of systemic involvement. (4) Calf-E.coli septicaemia.

Launch Date

1.15611835E12
Curative
COBACTAN

Approved Use

Treatment of infections caused by bacteria sensitive to cefquinome, such as: (1) Respiratory tract infections caused by Pasteurella multocida and Mannheimia haemolytica. (2) Digital dermatitis, infectious bulbar necrosis and interdigital necrobacillosis (foul in foot). (3) Acute E.coli mastitis with signs of systemic involvement. (4) Calf-E.coli septicaemia.

Launch Date

1.15611835E12
PubMed

PubMed

TitleDatePubMed
Antibacterial activities in vitro and in vivo and pharmacokinetics of cefquinome (HR 111V), a new broad-spectrum cephalosporin.
1991 Jan
In vitro activities of cephalosporins and quinolones against Escherichia coli strains isolated from diarrheic dairy calves.
1999 Mar
Selection and persistence of CTX-M-producing Escherichia coli in the intestinal flora of pigs treated with amoxicillin, ceftiofur, or cefquinome.
2008 Oct
Factors affecting cure when treating bovine clinical mastitis with cephalosporin-based intramammary preparations.
2009 May
Development and validation of a high-performance liquid chromatography method for determination of cefquinome concentrations in sheep plasma and its application to pharmacokinetic studies.
2011 Feb
Development of stability-indicating methods for cefquinome sulphate.
2013 Sep
Comparative Pharmacokinetics of Cefquinome (Cobactan 2.5%) following Repeated Intramuscular Administrations in Sheep and Goats.
2014
Stability-indicating HPLC method for the determination of cefquinome sulfate.
2014 Mar-Apr
Patents

Sample Use Guides

1 mg cefquinome/kg (2ml/50 kg body wt.) or 2 mg cefquinome/kg (4ml/50 kg body wt.) given by intramuscular injection (2,5% Cobactan solution).
Route of Administration: Intramuscular
In Vitro Use Guide
The MICs of cefquinome against single laboratory strains of gram-positive and gram-negative anaerobic bacteria were determined. The values were (MIC50): 0.781 ug/ml for Staphylococcus aureus (Methicillin susceptible); 12.5 ug/ml for Staphylococcus aureus (Methicillin resistant); <0.006 ug/ml for Streptococcus spp.; 4.0 ug/ml for Enterococci; 0.049 ug/ml for E.Coli and Klebsiella spp.; 0.098 ug/ml for Salmonella spp., Enterobacter spp. and Proteus mirabilis; 0.195 ug/ml for Serratia marcescens and Proteus spp.; 0.002 ug/ml for Streptococcus pyogenes; 0.008 ug/ml for Streptococcus pneumoniae and Klebsiella pneumoniae; 0.078 ug/ml for Pasteurella multocida, Proteus mirabilis ATCC 14273; 0.03 ug/ml for Escherichia coli 078 and 0.06 ug/ml for Salmonella typhimurium MZ II.
Substance Class Chemical
Created
by admin
on Fri Dec 15 16:12:29 UTC 2023
Edited
by admin
on Fri Dec 15 16:12:29 UTC 2023
Record UNII
Z74S078CWP
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
CEFQUINOME
INN   MI  
INN  
Official Name English
1-(((6R,7R)-7-(2-(2-AMINO-4-THIAZOLYL)GLYOXYLAMIDO)-2-CARBOXY-8-OXO-5-THIA-1-AZABICYCLO(4.2.0)OCT-2-EN-3-YL)METHYL)-5,6,7,8-TETRAHYDROQUINOLINIUM HYDROXIDE, INNER SALT, 72-(Z)-(O-METHYLOXIME)
Common Name English
cefquinome [INN]
Common Name English
COBACTAN
Brand Name English
QUINOLINIUM, 1-((7-(((2-AMINO-4-THIAZOLYL)(METHOXYIMINO)ACETYL)AMINO)-2-CARBOXY-8-OXO-5-THIA-1-AZABICYCLO(4.2.0)OCT-2-EN-3-YL)METHYL)-5,6,7,8-TETRAHYDRO-, HYDROXIDE, INNER SALT, (6R-(6.ALPHA.,7.BETA.(Z)))-
Common Name English
HR111V
Code English
CEFQUINOME [MI]
Common Name English
Classification Tree Code System Code
WHO-VATC QJ51DE90
Created by admin on Fri Dec 15 16:12:29 UTC 2023 , Edited by admin on Fri Dec 15 16:12:29 UTC 2023
WHO-VATC QG51AA07
Created by admin on Fri Dec 15 16:12:29 UTC 2023 , Edited by admin on Fri Dec 15 16:12:29 UTC 2023
WHO-VATC QJ01DE90
Created by admin on Fri Dec 15 16:12:29 UTC 2023 , Edited by admin on Fri Dec 15 16:12:29 UTC 2023
NCI_THESAURUS C357
Created by admin on Fri Dec 15 16:12:29 UTC 2023 , Edited by admin on Fri Dec 15 16:12:29 UTC 2023
Code System Code Type Description
INN
6287
Created by admin on Fri Dec 15 16:12:29 UTC 2023 , Edited by admin on Fri Dec 15 16:12:29 UTC 2023
PRIMARY
NCI_THESAURUS
C79564
Created by admin on Fri Dec 15 16:12:29 UTC 2023 , Edited by admin on Fri Dec 15 16:12:29 UTC 2023
PRIMARY
MERCK INDEX
m3214
Created by admin on Fri Dec 15 16:12:29 UTC 2023 , Edited by admin on Fri Dec 15 16:12:29 UTC 2023
PRIMARY Merck Index
PUBCHEM
5464355
Created by admin on Fri Dec 15 16:12:29 UTC 2023 , Edited by admin on Fri Dec 15 16:12:29 UTC 2023
PRIMARY
WIKIPEDIA
Cefquinome
Created by admin on Fri Dec 15 16:12:29 UTC 2023 , Edited by admin on Fri Dec 15 16:12:29 UTC 2023
PRIMARY
SMS_ID
100000081830
Created by admin on Fri Dec 15 16:12:29 UTC 2023 , Edited by admin on Fri Dec 15 16:12:29 UTC 2023
PRIMARY
FDA UNII
Z74S078CWP
Created by admin on Fri Dec 15 16:12:29 UTC 2023 , Edited by admin on Fri Dec 15 16:12:29 UTC 2023
PRIMARY
CAS
84957-30-2
Created by admin on Fri Dec 15 16:12:29 UTC 2023 , Edited by admin on Fri Dec 15 16:12:29 UTC 2023
PRIMARY
MESH
C068212
Created by admin on Fri Dec 15 16:12:29 UTC 2023 , Edited by admin on Fri Dec 15 16:12:29 UTC 2023
PRIMARY
EPA CompTox
DTXSID00894103
Created by admin on Fri Dec 15 16:12:29 UTC 2023 , Edited by admin on Fri Dec 15 16:12:29 UTC 2023
PRIMARY
ChEMBL
CHEMBL1631107
Created by admin on Fri Dec 15 16:12:29 UTC 2023 , Edited by admin on Fri Dec 15 16:12:29 UTC 2023
PRIMARY
EVMPD
SUB07416MIG
Created by admin on Fri Dec 15 16:12:29 UTC 2023 , Edited by admin on Fri Dec 15 16:12:29 UTC 2023
PRIMARY
Related Record Type Details
SALT/SOLVATE -> PARENT
Related Record Type Details
ACTIVE MOIETY