CHEBI:9321 - sulbactam

Main ChEBI Ontology Automatic Xrefs Reactions Pathways Models
ChEBI Name sulbactam
ChEBI ID CHEBI:9321
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 C8H11NO5S
Net Charge 0
Average Mass 233.24200
Monoisotopic Mass 233.036
InChI InChI=1S/C8H11NO5S/c1-8(2)6(7(11)12)9-4(10)3-5(9)15(8,13)14/h5-6H,3H2,1-2H3,(H,11,12)/t5-,6+/m1/s1
InChIKey FKENQMMABCRJMK-RITPCOANSA-N
SMILES [H][C@@]12CC(=O)N1[C@@H](C(O)=O)C(C)(C)S2(=O)=O
Roles Classification
Chemical Role(s): Bronsted acid
A molecular entity capable of donating a hydron to an acceptor (Bronsted base).
(via oxoacid )
Biological Role(s): antimicrobial agent
A substance that kills or slows the growth of microorganisms, including bacteria, viruses, fungi and protozoans.
(via heterocyclic antibiotic )
View more via ChEBI Ontology
ChEBI Ontology
Outgoing sulbactam (CHEBI:9321) is a penicillanic acids (CHEBI:25865)
Incoming sultamicillin (CHEBI:51770) has functional parent sulbactam (CHEBI:9321)
tazobactam (CHEBI:9421) has functional parent sulbactam (CHEBI:9321)
IUPAC Name
2,2-dimethyl-1,1-dioxidopenam-3α-carboxylic acid
INNs Sources
sulbactam ChemIDplus
sulbactamum ChemIDplus
Synonyms Sources
(2S,5R)-3,3-dimethyl-7-oxo-4-thia-1-azabicyclo(3.2.0)heptane-2-carboxylic acid 4,4-dioxide ChemIDplus
(2S,5R)-3,3-dimethyl-7-oxo-4-thia-1-azabicyclo[3.2.0]heptane-2-carboxylic acid 4,4-dioxide IUPAC
penicillanic acid 1,1-dioxide ChEBI
penicillanic acid sulfone ChEBI
Manual Xrefs Databases
2492 DrugCentral
BE867859 Patent
C07770 KEGG COMPOUND
C14001 KEGG COMPOUND
D02223 KEGG DRUG
D08533 KEGG DRUG
LSM-5553 LINCS
Sulbactam Wikipedia
US4234579 Patent
View more database links
Registry Numbers Types Sources
4192832 Beilstein Registry Number Beilstein
68373-14-8 CAS Registry Number ChemIDplus
Last Modified
22 February 2017