CHEBI:135716 - ceftezole

Main ChEBI Ontology Automatic Xrefs Reactions Pathways Models
ChEBI Name ceftezole
ChEBI ID CHEBI:135716
Definition A first-generation cephalosporin antibiotic having (1,3,4-thiadiazol-2-ylsulfanyl)methyl and [2-(1H-tetrazol-1-yl)acetamido side groups located at positions 3 and 7 respectively.
Stars This entity has been manually annotated by the ChEBI Team.
Supplier Information
Download Molfile XML SDF
Wikipedia License
Waiting for wikipedia content
Read full article at Wikipedia
Formula C13H12N8O4S3
Net Charge 0
Average Mass 440.484
Monoisotopic Mass 440.01436
InChI InChI=1S/C13H12N8O4S3/c22-7(1-20-4-14-18-19-20)16-8-10(23)21-9(12(24)25)6(2-26-11(8)21)3-27-13-17-15-5-28-13/h4-5,8,11H,1-3H2,(H,16,22)(H,24,25)/t8-,11-/m1/s1
InChIKey DZMVCVMFETWNIU-LDYMZIIASA-N
SMILES C(O)(=O)C=1N2[C@@]([C@@H](C2=O)NC(CN3C=NN=N3)=O)(SCC1CSC4=NN=CS4)[H]
Roles Classification
Biological Role(s): drug allergen
Any drug which causes the onset of an allergic reaction.
(via cephalosporin )
antimicrobial agent
A substance that kills or slows the growth of microorganisms, including bacteria, viruses, fungi and protozoans.
(via heterocyclic antibiotic )
Application(s): drug allergen
Any drug which causes the onset of an allergic reaction.
(via cephalosporin )
View more via ChEBI Ontology
ChEBI Ontology
Outgoing ceftezole (CHEBI:135716) is a cephalosporin (CHEBI:23066)
ceftezole (CHEBI:135716) is a thiadiazoles (CHEBI:38099)
IUPAC Name
7-[2-(1H-tetrazol-1-yl)acetamido]-3-[(1,3,4-thiadiazol-2-ylsulfanyl)methyl]-3,4-didehydrocepham-4-carboxylic acid
INNs Sources
ceftezol ChemIDplus
ceftézole WHO MedNet
ceftezole ChemIDplus
ceftezolum WHO MedNet
Synonyms Sources
(6R,7R)-8-oxo-7-[2-(1H-tetrazol-1-yl)acetamido]-3-[(1,3,4-thiadiazol-2-ylsulfanyl)methyl]-5-thia-1-azabicyclo[4.2.0]oct-2-ene-2-carboxylic acid IUPAC
ceftezol DrugCentral
demethyl cefazolin DrugCentral
demethylcefazolin DrugCentral
Manual Xrefs Databases
Ceftezole Wikipedia
CN101544659 Patent
View more database links
Registry Numbers Types Sources
26973-24-0 CAS Registry Number ChemIDplus
4046849 Reaxys Registry Number Reaxys
Citations Waiting for Citations Types Sources
17671744 PubMed citation Europe PMC
29017833 PubMed citation Europe PMC
783103 PubMed citation Europe PMC
825020 PubMed citation Europe PMC
Last Modified
14 March 2018