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

Details

Stereochemistry ABSOLUTE
Molecular Formula C19H17N5O7S3
Molecular Weight 523.563
Optical Activity UNSPECIFIED
Defined Stereocenters 2 / 2
E/Z Centers 1
Charge 0

SHOW SMILES / InChI
Structure of CEFTIOFUR

SMILES

[H][C@]12SCC(CSC(=O)C3=CC=CO3)=C(N1C(=O)[C@H]2NC(=O)C(=N/OC)\C4=CSC(N)=N4)C(O)=O

InChI

InChIKey=ZBHXIWJRIFEVQY-IHMPYVIRSA-N
InChI=1S/C19H17N5O7S3/c1-30-23-11(9-7-34-19(20)21-9)14(25)22-12-15(26)24-13(17(27)28)8(5-32-16(12)24)6-33-18(29)10-3-2-4-31-10/h2-4,7,12,16H,5-6H2,1H3,(H2,20,21)(H,22,25)(H,27,28)/b23-11-/t12-,16-/m1/s1

HIDE SMILES / InChI

Molecular Formula C19H17N5O7S3
Molecular Weight 523.563
Charge 0
Count
Stereochemistry ABSOLUTE
Additional Stereochemistry No
Defined Stereocenters 2 / 2
E/Z Centers 1
Optical Activity UNSPECIFIED

Approval Year

Substance Class Chemical
Created
by admin
on Sat Dec 16 16:19:43 UTC 2023
Edited
by admin
on Sat Dec 16 16:19:43 UTC 2023
Record UNII
83JL932I1C
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
CEFTIOFUR
HSDB   INN   MART.   MI   WHO-DD  
INN  
Official Name English
CEFTIOFUR [EMA EPAR VETERINARY]
Common Name English
ceftiofur [INN]
Common Name English
CEFTIOFUR [HSDB]
Common Name English
Ceftiofur [WHO-DD]
Common Name English
CEFTIOFUR CRYSTALLINE FREE ACID [GREEN BOOK]
Common Name English
CEFTIOFUR [MI]
Common Name English
5-THIA-1-AZABICYCLO(4.2.0)OCT-2-ENE-2-CARBOXYLIC ACID, 7-(((2-AMINO-4-THIAZOLYL)(METHOXYIMINO)ACETYL)AMINO)-3-(((2-FURANYLCARBONYL)THIO)METHYL)-8-OXO-, (6R-(6.ALPHA.,7.BETA.(Z)))-
Common Name English
CEFTIOFUR CRYSTALLINE FREE ACID
GREEN BOOK  
Common Name English
CEFTIOFUR [MART.]
Common Name English
(6R,7R)-7-(2-(2-AMINO-4-THIAZOLYL)GLYOXYLAMIDO)-3-(MERCAPTOMETHYL)-8-OXO-5-THIA-1-AZABICYCLO(4.2.0)OCT-2-ENE-2-CARBOXYLIC ACID, 7(SUP 2)-(Z)-(O-METHYLOXIME), 2-FUROATE (ESTER)
Common Name English
NAXCEL
Brand Name English
Classification Tree Code System Code
WHO-VATC QJ01DD90
Created by admin on Sat Dec 16 16:19:43 UTC 2023 , Edited by admin on Sat Dec 16 16:19:43 UTC 2023
CFR 21 CFR 522.313
Created by admin on Sat Dec 16 16:19:43 UTC 2023 , Edited by admin on Sat Dec 16 16:19:43 UTC 2023
EMA VETERINARY ASSESSMENT REPORTS NAXCEL [AUTHORIZED]
Created by admin on Sat Dec 16 16:19:43 UTC 2023 , Edited by admin on Sat Dec 16 16:19:43 UTC 2023
CFR 21 CFR 556.113
Created by admin on Sat Dec 16 16:19:43 UTC 2023 , Edited by admin on Sat Dec 16 16:19:43 UTC 2023
CFR 21 CFR 526.313
Created by admin on Sat Dec 16 16:19:43 UTC 2023 , Edited by admin on Sat Dec 16 16:19:43 UTC 2023
EMA VETERINARY ASSESSMENT REPORTS NAXCEL [AUTHORIZED]
Created by admin on Sat Dec 16 16:19:43 UTC 2023 , Edited by admin on Sat Dec 16 16:19:43 UTC 2023
CFR 21 CFR 522.313A
Created by admin on Sat Dec 16 16:19:43 UTC 2023 , Edited by admin on Sat Dec 16 16:19:43 UTC 2023
WHO-VATC QJ01DD99
Created by admin on Sat Dec 16 16:19:43 UTC 2023 , Edited by admin on Sat Dec 16 16:19:43 UTC 2023
NCI_THESAURUS C357
Created by admin on Sat Dec 16 16:19:43 UTC 2023 , Edited by admin on Sat Dec 16 16:19:43 UTC 2023
WHO-VATC QJ51DD90
Created by admin on Sat Dec 16 16:19:43 UTC 2023 , Edited by admin on Sat Dec 16 16:19:43 UTC 2023
Code System Code Type Description
SMS_ID
100000081834
Created by admin on Sat Dec 16 16:19:43 UTC 2023 , Edited by admin on Sat Dec 16 16:19:43 UTC 2023
PRIMARY
ChEMBL
CHEMBL222913
Created by admin on Sat Dec 16 16:19:43 UTC 2023 , Edited by admin on Sat Dec 16 16:19:43 UTC 2023
PRIMARY
HSDB
7445
Created by admin on Sat Dec 16 16:19:43 UTC 2023 , Edited by admin on Sat Dec 16 16:19:43 UTC 2023
PRIMARY
FDA UNII
83JL932I1C
Created by admin on Sat Dec 16 16:19:43 UTC 2023 , Edited by admin on Sat Dec 16 16:19:43 UTC 2023
PRIMARY
PUBCHEM
6328657
Created by admin on Sat Dec 16 16:19:43 UTC 2023 , Edited by admin on Sat Dec 16 16:19:43 UTC 2023
PRIMARY
DRUG BANK
DB11485
Created by admin on Sat Dec 16 16:19:43 UTC 2023 , Edited by admin on Sat Dec 16 16:19:43 UTC 2023
PRIMARY
NCI_THESAURUS
C81036
Created by admin on Sat Dec 16 16:19:43 UTC 2023 , Edited by admin on Sat Dec 16 16:19:43 UTC 2023
PRIMARY
EPA CompTox
DTXSID7046702
Created by admin on Sat Dec 16 16:19:43 UTC 2023 , Edited by admin on Sat Dec 16 16:19:43 UTC 2023
PRIMARY
CAS
80370-57-6
Created by admin on Sat Dec 16 16:19:43 UTC 2023 , Edited by admin on Sat Dec 16 16:19:43 UTC 2023
PRIMARY
INN
5703
Created by admin on Sat Dec 16 16:19:43 UTC 2023 , Edited by admin on Sat Dec 16 16:19:43 UTC 2023
PRIMARY
MERCK INDEX
m3221
Created by admin on Sat Dec 16 16:19:43 UTC 2023 , Edited by admin on Sat Dec 16 16:19:43 UTC 2023
PRIMARY Merck Index
WIKIPEDIA
CEFTIOFUR
Created by admin on Sat Dec 16 16:19:43 UTC 2023 , Edited by admin on Sat Dec 16 16:19:43 UTC 2023
PRIMARY
EVMPD
SUB07426MIG
Created by admin on Sat Dec 16 16:19:43 UTC 2023 , Edited by admin on Sat Dec 16 16:19:43 UTC 2023
PRIMARY
RXCUI
1311521
Created by admin on Sat Dec 16 16:19:43 UTC 2023 , Edited by admin on Sat Dec 16 16:19:43 UTC 2023
PRIMARY RxNorm
DAILYMED
83JL932I1C
Created by admin on Sat Dec 16 16:19:43 UTC 2023 , Edited by admin on Sat Dec 16 16:19:43 UTC 2023
PRIMARY
Related Record Type Details
SALT/SOLVATE -> PARENT
SALT/SOLVATE -> PARENT
Related Record Type Details
ACTIVE MOIETY