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Details

Stereochemistry ABSOLUTE
Molecular Formula C16H16N4O8S
Molecular Weight 424.385
Optical Activity UNSPECIFIED
Defined Stereocenters 2 / 2
E/Z Centers 1
Charge 0

SHOW SMILES / InChI
Structure of CEFUROXIME

SMILES

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

InChI

InChIKey=JFPVXVDWJQMJEE-IZRZKJBUSA-N
InChI=1S/C16H16N4O8S/c1-26-19-9(8-3-2-4-27-8)12(21)18-10-13(22)20-11(15(23)24)7(5-28-16(17)25)6-29-14(10)20/h2-4,10,14H,5-6H2,1H3,(H2,17,25)(H,18,21)(H,23,24)/b19-9-/t10-,14-/m1/s1

HIDE SMILES / InChI
Molecular Formula C16H16N4O8S
Molecular Weight 424.385
Charge 0
Count
Stereochemistry ABSOLUTE
Additional Stereochemistry No
Defined Stereocenters 2 / 2
E/Z Centers 1
Optical Activity UNSPECIFIED

Approval Year

Unknown
86413
Substance Class Chemical
Created
by admin
on Fri Dec 15 14:59:25 UTC 2023
Edited
by admin
on Fri Dec 15 14:59:25 UTC 2023
Record UNII
O1R9FJ93ED
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
CEFUROXIME
INN   MART.   MI   USAN   VANDF   WHO-DD  
USAN   INN  
Official Name English
CEFUROXIME [MI]
Common Name English
640/359
Code English
CEFUROXIME [USP IMPURITY]
Common Name English
Cefuroxime [WHO-DD]
Common Name English
CEFUROXIME AXETIL IMPURITY D [EP IMPURITY]
Common Name English
CEFUROXIME [MART.]
Common Name English
cefuroxime [INN]
Common Name English
CEFUROXIME [USAN]
Common Name English
CEFUROXIME ACID
Common Name English
CEFUROXIME [VANDF]
Common Name English
Classification Tree Code System Code
WHO-VATC QJ01DC02
Created by admin on Fri Dec 15 14:59:25 UTC 2023 , Edited by admin on Fri Dec 15 14:59:25 UTC 2023
NCI_THESAURUS C357
Created by admin on Fri Dec 15 14:59:25 UTC 2023 , Edited by admin on Fri Dec 15 14:59:25 UTC 2023
WHO-VATC QS01AA27
Created by admin on Fri Dec 15 14:59:25 UTC 2023 , Edited by admin on Fri Dec 15 14:59:25 UTC 2023
NDF-RT N0000011161
Created by admin on Fri Dec 15 14:59:25 UTC 2023 , Edited by admin on Fri Dec 15 14:59:25 UTC 2023
LIVERTOX NBK548358
Created by admin on Fri Dec 15 14:59:25 UTC 2023 , Edited by admin on Fri Dec 15 14:59:25 UTC 2023
NDF-RT N0000011161
Created by admin on Fri Dec 15 14:59:25 UTC 2023 , Edited by admin on Fri Dec 15 14:59:25 UTC 2023
WHO-ATC J01RA03
Created by admin on Fri Dec 15 14:59:25 UTC 2023 , Edited by admin on Fri Dec 15 14:59:25 UTC 2023
NDF-RT N0000011161
Created by admin on Fri Dec 15 14:59:25 UTC 2023 , Edited by admin on Fri Dec 15 14:59:25 UTC 2023
NDF-RT N0000011161
Created by admin on Fri Dec 15 14:59:25 UTC 2023 , Edited by admin on Fri Dec 15 14:59:25 UTC 2023
NDF-RT N0000011161
Created by admin on Fri Dec 15 14:59:25 UTC 2023 , Edited by admin on Fri Dec 15 14:59:25 UTC 2023
WHO-ATC J01DC02
Created by admin on Fri Dec 15 14:59:25 UTC 2023 , Edited by admin on Fri Dec 15 14:59:25 UTC 2023
NDF-RT N0000011161
Created by admin on Fri Dec 15 14:59:25 UTC 2023 , Edited by admin on Fri Dec 15 14:59:25 UTC 2023
LIVERTOX NBK548666
Created by admin on Fri Dec 15 14:59:25 UTC 2023 , Edited by admin on Fri Dec 15 14:59:25 UTC 2023
NDF-RT N0000011161
Created by admin on Fri Dec 15 14:59:25 UTC 2023 , Edited by admin on Fri Dec 15 14:59:25 UTC 2023
LIVERTOX NBK547862
Created by admin on Fri Dec 15 14:59:25 UTC 2023 , Edited by admin on Fri Dec 15 14:59:25 UTC 2023
NDF-RT N0000011161
Created by admin on Fri Dec 15 14:59:25 UTC 2023 , Edited by admin on Fri Dec 15 14:59:25 UTC 2023
NDF-RT N0000011161
Created by admin on Fri Dec 15 14:59:25 UTC 2023 , Edited by admin on Fri Dec 15 14:59:25 UTC 2023
NDF-RT N0000011161
Created by admin on Fri Dec 15 14:59:25 UTC 2023 , Edited by admin on Fri Dec 15 14:59:25 UTC 2023
WHO-ATC S01AA27
Created by admin on Fri Dec 15 14:59:25 UTC 2023 , Edited by admin on Fri Dec 15 14:59:25 UTC 2023
WHO-VATC QJ01RA03
Created by admin on Fri Dec 15 14:59:25 UTC 2023 , Edited by admin on Fri Dec 15 14:59:25 UTC 2023
NDF-RT N0000011161
Created by admin on Fri Dec 15 14:59:25 UTC 2023 , Edited by admin on Fri Dec 15 14:59:25 UTC 2023
NDF-RT N0000011161
Created by admin on Fri Dec 15 14:59:25 UTC 2023 , Edited by admin on Fri Dec 15 14:59:25 UTC 2023
WHO-VATC QJ51DC02
Created by admin on Fri Dec 15 14:59:25 UTC 2023 , Edited by admin on Fri Dec 15 14:59:25 UTC 2023
NDF-RT N0000175488
Created by admin on Fri Dec 15 14:59:25 UTC 2023 , Edited by admin on Fri Dec 15 14:59:25 UTC 2023
Code System Code Type Description
ChEMBL
CHEMBL1436
Created by admin on Fri Dec 15 14:59:25 UTC 2023 , Edited by admin on Fri Dec 15 14:59:25 UTC 2023
PRIMARY
EPA CompTox
DTXSID5022774
Created by admin on Fri Dec 15 14:59:25 UTC 2023 , Edited by admin on Fri Dec 15 14:59:25 UTC 2023
PRIMARY
MESH
D002444
Created by admin on Fri Dec 15 14:59:25 UTC 2023 , Edited by admin on Fri Dec 15 14:59:25 UTC 2023
PRIMARY
USAN
U-22
Created by admin on Fri Dec 15 14:59:25 UTC 2023 , Edited by admin on Fri Dec 15 14:59:25 UTC 2023
PRIMARY
MERCK INDEX
m3226
Created by admin on Fri Dec 15 14:59:25 UTC 2023 , Edited by admin on Fri Dec 15 14:59:25 UTC 2023
PRIMARY Merck Index
DRUG BANK
DB01112
Created by admin on Fri Dec 15 14:59:25 UTC 2023 , Edited by admin on Fri Dec 15 14:59:25 UTC 2023
PRIMARY
DAILYMED
O1R9FJ93ED
Created by admin on Fri Dec 15 14:59:25 UTC 2023 , Edited by admin on Fri Dec 15 14:59:25 UTC 2023
PRIMARY
SMS_ID
100000092667
Created by admin on Fri Dec 15 14:59:25 UTC 2023 , Edited by admin on Fri Dec 15 14:59:25 UTC 2023
PRIMARY
RXCUI
2194
Created by admin on Fri Dec 15 14:59:25 UTC 2023 , Edited by admin on Fri Dec 15 14:59:25 UTC 2023
PRIMARY RxNorm
INN
3902
Created by admin on Fri Dec 15 14:59:25 UTC 2023 , Edited by admin on Fri Dec 15 14:59:25 UTC 2023
PRIMARY
ECHA (EC/EINECS)
259-560-1
Created by admin on Fri Dec 15 14:59:25 UTC 2023 , Edited by admin on Fri Dec 15 14:59:25 UTC 2023
PRIMARY
EVMPD
SUB07433MIG
Created by admin on Fri Dec 15 14:59:25 UTC 2023 , Edited by admin on Fri Dec 15 14:59:25 UTC 2023
PRIMARY
LACTMED
Cefuroxime
Created by admin on Fri Dec 15 14:59:25 UTC 2023 , Edited by admin on Fri Dec 15 14:59:25 UTC 2023
PRIMARY
CAS
55268-75-2
Created by admin on Fri Dec 15 14:59:25 UTC 2023 , Edited by admin on Fri Dec 15 14:59:25 UTC 2023
PRIMARY
DRUG CENTRAL
565
Created by admin on Fri Dec 15 14:59:25 UTC 2023 , Edited by admin on Fri Dec 15 14:59:25 UTC 2023
PRIMARY
NCI_THESAURUS
C61669
Created by admin on Fri Dec 15 14:59:25 UTC 2023 , Edited by admin on Fri Dec 15 14:59:25 UTC 2023
PRIMARY
CHEBI
3515
Created by admin on Fri Dec 15 14:59:25 UTC 2023 , Edited by admin on Fri Dec 15 14:59:25 UTC 2023
PRIMARY
WIKIPEDIA
Cefuroxime
Created by admin on Fri Dec 15 14:59:25 UTC 2023 , Edited by admin on Fri Dec 15 14:59:25 UTC 2023
PRIMARY
FDA UNII
O1R9FJ93ED
Created by admin on Fri Dec 15 14:59:25 UTC 2023 , Edited by admin on Fri Dec 15 14:59:25 UTC 2023
PRIMARY
PUBCHEM
5479529
Created by admin on Fri Dec 15 14:59:25 UTC 2023 , Edited by admin on Fri Dec 15 14:59:25 UTC 2023
PRIMARY
Related Record Type Details
Structure of CEFUROXIME SODIUM
SALT/SOLVATE -> PARENT
Structure of CEFUROXIME BUTYL AMMONIUM
SALT/SOLVATE -> PARENT
PLASMA PROTEIN FRACTION (HUMAN)
BINDER->LIGAND
BINDING
PENICILLIN-BINDING PROTEIN 1A
TARGET -> INHIBITOR
Structure of CEFUROXIME
EXCRETED UNCHANGED
Metabolically stable
Related Record Type Details
Structure of CEFUROXIME AXETIL
PRODRUG -> METABOLITE ACTIVE
Related Record Type Details
Structure of CEFUROXIME AXETIL
PARENT -> IMPURITY
CHROMATOGRAPHIC PURITY (HPLC/UV)
USP
Related Record Type Details
Structure of CEFUROXIME
ACTIVE MOIETY
Name Property Type Amount Referenced Substance Defining Parameters References
Biological Half-life PHARMACOKINETIC
NIH
NCATS
PRIVACY ACT
ACCESSIBILITY
DISCLAIMER
HHS VULNERABILITY DISCLOSURE
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