CHEBI:34613 - cefaloglycin

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ChEBI Name cefaloglycin
ChEBI ID CHEBI:34613
Definition A cephalosporin antibiotic containing at the 7β-position of the cephem skeleton an (R)-amino(phenyl)acetamido group.
Stars This entity has been manually annotated by the ChEBI Team.
Secondary ChEBI IDs CHEBI:164514
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Formula C18H19N3O6S
Net Charge 0
Average Mass 405.42500
Monoisotopic Mass 405.099
InChI InChI=1S/C18H19N3O6S/c1-9(22)27-7-11-8-28-17-13(16(24)21(17)14(11)18(25)26)20-15(23)12(19)10-5-3-2-4-6-10/h2-6,12-13,17H,7-8,19H2,1H3,(H,20,23)(H,25,26)/t12-,13-,17-/m1/s1
InChIKey FUBBGQLTSCSAON-PBFPGSCMSA-N
SMILES [H][C@]12SCC(COC(C)=O)=C(N1C(=O)[C@H]2NC(=O)[C@H](N)c1ccccc1)C(O)=O
Roles Classification
Biological Role(s): antimicrobial agent
A substance that kills or slows the growth of microorganisms, including bacteria, viruses, fungi and protozoans.
(via heterocyclic antibiotic )
drug allergen
Any drug which causes the onset of an allergic reaction.
(via cephalosporin )
Application(s): drug allergen
Any drug which causes the onset of an allergic reaction.
(via cephalosporin )
View more via ChEBI Ontology
ChEBI Ontology
Outgoing cefaloglycin (CHEBI:34613) has role antimicrobial agent (CHEBI:33281)
cefaloglycin (CHEBI:34613) is a cephalosporin (CHEBI:23066)
IUPAC Names
(6R,7R)-3-(acetoxymethyl)-7-{[(2R)-2-amino-2-phenylacetyl]amino}-8-oxo-5-thia-1-azabicyclo[4.2.0]oct-2-ene-2-carboxylic acid
3-acetoxymethyl-7β-[(2R)-2-amino-2-phenylacetamido]-3,4-didehydrocepham-4-carboxylic acid
INNs Sources
Cefaloglicina ChemIDplus
Cefaloglycine ChemIDplus
Cefaloglycinum ChemIDplus
Synonyms Sources
7-(2-D-alpha-Aminophenylacetamido)cephalosporanic acid ChemIDplus
7-(D-2-Amino-2-phenylacetamido)-3-acetoxymethyl-delta(sup3)-cephem-4-carboxylic acid ChemIDplus
7-(D-alpha-Aminophenyl-acetamido)cephalosporanic acid ChemIDplus
CEG KEGG DRUG
Cephaloglycine ChemIDplus
Cephaoglycin acid ChemIDplus
D-(-)-Cephaloglycin ChemIDplus
D-Cephaloglycine ChemIDplus
Database Links Databases
572 DrugCentral
C13440 KEGG COMPOUND
Cephaloglycin Wikipedia
D01949 KEGG DRUG
DB00689 DrugBank
View more database links
Registry Numbers Types Sources
3577-01-3 CAS Registry Number ChemIDplus
5405868 Reaxys Registry Number Reaxys
5405868 Beilstein Registry Number Beilstein
Citations Waiting for Citations Types Sources
2083978 PubMed citation Europe PMC
2133431 PubMed citation Europe PMC
6631918 PubMed citation ChEMBL
Last Modified
22 February 2017