U.S. Department of Health & Human Services Divider Arrow National Institutes of Health Divider Arrow NCATS

Details

Stereochemistry ABSOLUTE
Molecular Formula C17H19N5O6S2
Molecular Weight 453.493
Optical Activity UNSPECIFIED
Defined Stereocenters 3 / 3
E/Z Centers 1
Charge 0

SHOW SMILES / InChI
Structure of CEFOVECIN

SMILES

[H][C@]12SCC([C@@H]3CCCO3)=C(N1C(=O)[C@H]2NC(=O)C(=N/OC)\C4=CSC(N)=N4)C(O)=O

InChI

InChIKey=ZJGQFXVQDVCVOK-QFKLAVHZSA-N
InChI=1S/C17H19N5O6S2/c1-27-21-10(8-6-30-17(18)19-8)13(23)20-11-14(24)22-12(16(25)26)7(5-29-15(11)22)9-3-2-4-28-9/h6,9,11,15H,2-5H2,1H3,(H2,18,19)(H,20,23)(H,25,26)/b21-10-/t9-,11+,15+/m0/s1

HIDE SMILES / InChI

Molecular Formula C17H19N5O6S2
Molecular Weight 453.493
Charge 0
Count
Stereochemistry ABSOLUTE
Additional Stereochemistry No
Defined Stereocenters 3 / 3
E/Z Centers 1
Optical Activity UNSPECIFIED

Description
Curator's Comment: description was created based on several sources, including: http://www.zora.uzh.ch/40272/4/Cefovecin.pdf | http://www.ema.europa.eu/docs/en_GB/document_library/EPAR_-_Scientific_Discussion/veterinary/000098/WC500062064.pdf

Cefovecin is a third generation cephalosporin with a broad-spectrum of activity against Gram-positive and Gram-negative bacteria. Cefovecin differs from other cephalosporins in that it is highly protein bound and has a long duration of activity. As with all cephalosporins, the bactericidal action of cefovecin results from the inhibition of bacterial cell wall synthesis through binding to the penicillin-binding proteins (PBPs). It is indicated for the treatment of skin infections secondary superficial pyoderma, abscesses and wounds. Some gastrointestinal adverse effects like vomiting, anorexia or diarrhea were observed.

Originator

Curator's Comment: # Pfizer, Inc.

Approval Year

TargetsConditions

Conditions

ConditionModalityTargetsHighest PhaseProduct
Curative
Convenia

Approved Use

CONVENIA is indicated for the treatment of skin infections (secondary superficial pyoderma, abscesses, and wounds) in dogs caused by susceptible strains of Staphylococcus intermedius and Streptococcus canis and skin infections (wounds and abscesses) in cats, caused by susceptible strains of Pasteurella multocida.

Launch Date

2008
Curative
Convenia

Approved Use

CONVENIA is indicated for the treatment of skin infections (secondary superficial pyoderma, abscesses, and wounds) in dogs caused by susceptible strains of Staphylococcus intermedius and Streptococcus canis and skin infections (wounds and abscesses) in cats, caused by susceptible strains of Pasteurella multocida.

Launch Date

2008
Curative
Convenia

Approved Use

CONVENIA is indicated for the treatment of skin infections (secondary superficial pyoderma, abscesses, and wounds) in dogs caused by susceptible strains of Staphylococcus intermedius and Streptococcus canis and skin infections (wounds and abscesses) in cats, caused by susceptible strains of Pasteurella multocida.

Launch Date

2008
PubMed

PubMed

TitleDatePubMed
Pharmacokinetics and pharmacodynamics of cefovecin in dogs.
2006 Dec
Pharmacokinetics of cefovecin in cats.
2006 Dec
Patents

Sample Use Guides

A single injection of 8 mg/kg body weight. A second injection of 8 mg/kg may be administered if response to therapy is not complete.
Route of Administration: Other
The minimum inhibitory concentrations (MICs) were determined for 45 clinical Pasteurella multocida isolates from infections in cats using applicable Clinical and Laboratory Standards Institute (CLSI) standards. The MIC90 for P. multocida was ≤ 0.06 ug/mL.
Substance Class Chemical
Created
by admin
on Sat Dec 16 16:48:25 GMT 2023
Edited
by admin
on Sat Dec 16 16:48:25 GMT 2023
Record UNII
0D1OL46ZIE
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
CEFOVECIN
INN   MI  
INN  
Official Name English
CEFOVECIN [MI]
Common Name English
(6R,7R)-7-(((2Z)-2-(2-AMINO-1,3-THIAZOL-4-YL)-2-(METHOXYIMINO)ACETYL)AMINO)-8-OXO-3-((2S)-TETRAHYDROFURAN-2-YL)-5-THIA-1-AZABICYCLO(4.2.0)OCT-2-ENE-2-CARBOXYLIC ACID
Systematic Name English
CONVENIA
Brand Name English
cefovecin [INN]
Common Name English
5-THIA-1-AZABICYCLO(4.2.0)OCT-2-ENE-2-CARBOXYLIC ACID, 7-(((2Z)-2-(2-AMINO-4-THIAZOLYL)-2-(METHOXYIMINO)-1-OXOETHYL)AMINO)-8-OXO-3-((2S)-TETRAHYDRO-2-FURANYL)-, (6R,7R)-
Common Name English
CEFOVECIN (EMA EPAR: VETERINARY)
Common Name English
Classification Tree Code System Code
NCI_THESAURUS C357
Created by admin on Sat Dec 16 16:48:25 GMT 2023 , Edited by admin on Sat Dec 16 16:48:25 GMT 2023
CFR 21 CFR 522.311
Created by admin on Sat Dec 16 16:48:25 GMT 2023 , Edited by admin on Sat Dec 16 16:48:25 GMT 2023
EMA VETERINARY ASSESSMENT REPORTS CONVENIA (AUTHORISED)
Created by admin on Sat Dec 16 16:48:25 GMT 2023 , Edited by admin on Sat Dec 16 16:48:25 GMT 2023
WHO-VATC QJ01DD91
Created by admin on Sat Dec 16 16:48:25 GMT 2023 , Edited by admin on Sat Dec 16 16:48:25 GMT 2023
EMA VETERINARY ASSESSMENT REPORTS CONVENIA (AUTHORISED)
Created by admin on Sat Dec 16 16:48:25 GMT 2023 , Edited by admin on Sat Dec 16 16:48:25 GMT 2023
Code System Code Type Description
FDA UNII
0D1OL46ZIE
Created by admin on Sat Dec 16 16:48:25 GMT 2023 , Edited by admin on Sat Dec 16 16:48:25 GMT 2023
PRIMARY
CAS
234096-34-5
Created by admin on Sat Dec 16 16:48:25 GMT 2023 , Edited by admin on Sat Dec 16 16:48:25 GMT 2023
PRIMARY
NCI_THESAURUS
C76035
Created by admin on Sat Dec 16 16:48:25 GMT 2023 , Edited by admin on Sat Dec 16 16:48:25 GMT 2023
PRIMARY
EPA CompTox
DTXSID00177963
Created by admin on Sat Dec 16 16:48:25 GMT 2023 , Edited by admin on Sat Dec 16 16:48:25 GMT 2023
PRIMARY
PUBCHEM
6336480
Created by admin on Sat Dec 16 16:48:25 GMT 2023 , Edited by admin on Sat Dec 16 16:48:25 GMT 2023
PRIMARY
ChEMBL
CHEMBL2110625
Created by admin on Sat Dec 16 16:48:25 GMT 2023 , Edited by admin on Sat Dec 16 16:48:25 GMT 2023
PRIMARY
SMS_ID
300000023753
Created by admin on Sat Dec 16 16:48:25 GMT 2023 , Edited by admin on Sat Dec 16 16:48:25 GMT 2023
PRIMARY
DAILYMED
0D1OL46ZIE
Created by admin on Sat Dec 16 16:48:25 GMT 2023 , Edited by admin on Sat Dec 16 16:48:25 GMT 2023
PRIMARY
INN
8225
Created by admin on Sat Dec 16 16:48:25 GMT 2023 , Edited by admin on Sat Dec 16 16:48:25 GMT 2023
PRIMARY
RXCUI
1591901
Created by admin on Sat Dec 16 16:48:25 GMT 2023 , Edited by admin on Sat Dec 16 16:48:25 GMT 2023
PRIMARY RxNorm
MESH
C516253
Created by admin on Sat Dec 16 16:48:25 GMT 2023 , Edited by admin on Sat Dec 16 16:48:25 GMT 2023
PRIMARY
WIKIPEDIA
Cefovecin
Created by admin on Sat Dec 16 16:48:25 GMT 2023 , Edited by admin on Sat Dec 16 16:48:25 GMT 2023
PRIMARY
MERCK INDEX
m3207
Created by admin on Sat Dec 16 16:48:25 GMT 2023 , Edited by admin on Sat Dec 16 16:48:25 GMT 2023
PRIMARY Merck Index
Related Record Type Details
SALT/SOLVATE -> PARENT
Related Record Type Details
ACTIVE MOIETY